Declarative and procedural learning in children and adolescents with posterior fossa tumours
- Eliana A Quintero-Gallego†1, 2Email author,
- Carlos M Gómez†2,
- Encarnación Vaquero Casares†2,
- Javier Márquez3 and
- Fco Javier Pérez-Santamaría2
© Quintero-Gallego et al; licensee BioMed Central Ltd. 2006
Received: 05 July 2005
Accepted: 15 March 2006
Published: 15 March 2006
This quasi-experimental study was designed to assess two important learning types – procedural and declarative – in children and adolescents affected by posterior fossa tumours (astrocytoma vs. medulloblastoma), given that memory has an important impact on the child's academic achievement and personal development.
We had three groups: two clinical (eighteen subjects) and one control (twelve subjects). The learning types in these groups were assessed by two experimental tasks evaluating procedural-implicit and declarative memory. A Serial Reaction-Time Task was used to measure procedural sequence learning, and the Spanish version  of the California Verbal Learning Test-Children's Version- CVLT-  to measure declarative-explicit learning. The learning capacity was assessed considering only the blocks that represent learning, and were compared with MANOVA in clinical and normal subjects. The Raven, simple reaction-time, finger-tapping test, and grooved pegboard tests were used to assess the overall functioning of subjects. The results were compared with those from a control group of the same age, and with Spanish norm-referenced tools where available
The results indicate the absence of procedural-implicit learning in both clinical groups, whereas declarative-explicit learning is maintained in both groups.
The clinical groups showed a conservation of declarative learning and a clear impairment of procedural learning. The results support the role of the cerebellum in the early phase of procedural learning.
Posterior fossa tumours constitute two thirds of all paediatric brain tumours . The main tumours appearing in this zone are medulloblastomas, pilocytic astrocytomas, and ependynomas, which together make up about 90% of the cases [4–6]. The most frequent are the astrocytoma and medulloblastoma. These tumours affect the cerebellum and/or its connections, so the study of cognitive and motor disturbances produced by this pathological status is important in assessing the neuropsychological profile of patients.
The principal interventions used with these tumours, and in general with most tumours, are surgery, chemotherapy, and radiotherapy. It has been demonstrated that these medical treatments cause not only motor alterations, but also deterioration in cognitive functions. Most of the relevant research has been focused on the long-term effects of radiotherapy because these are more general and severe, involving attention, memory, speed of mental processing, visuo-motor coordination [7–10], and a marked progressive impairment of overall intellectual functioning [8, 11]. Given that focal irradiation of the posterior fossa includes not only the brainstem and cerebellum but also parts of the temporal lobes and other structures, overall cognitive alteration could occur. It has been found that radiotherapy can affect the neuropsychological tests of children with medulloblastoma. In addition, psychosocial functions can be affected and academic difficulties presented. All these aspects lead to a decline in the quality of life of the individuals.
Anatomical studies: the cerebellum is connected to motor cortices, limbic areas, and polymodal associative cortex (prefrontal, parietal posterior, and superior temporal) [. e.g. ]. The functionality of these connections is dramatically expressed in the cerebellum-cerebral diaschisis phenomenon .
Neuroimaging studies during the performance of cognitive tasks have demonstrated a role of cerebellum in executive, attentional, perceptual, and language functions [e.g. ].
Studies related to populations with developmental disorders: populations diagnosed with hyperactivity or autism present morphometric disorders in some cerebellar structures: cerebellar vermis and/or hemispheres. When compared with control children, hyperactive children showed a decrease in the size of the posterior vermis lower portion (lobes VIII-X). In groups of autistic individuals, a decrease in the size of the vermis upper portion (lobes VI/VII) has been found [e.g. [21, 22]].
Studies related to mutism syndrome: this syndrome is presented in some cases of children suffering posterior fossa tumours (especially those affecting the vermis) who have been intervened. This is a clear sample of cognitive deterioration (generalised) after cerebellar damage. This syndrome is manifested approximately 4 days after surgery. Patients affected by it recover completely within a few weeks or months [23, 24].
Studies related to populations with cerebellar damage: Botez [25, 26] has indicated that cerebellar lesions affect three main neuropsychological aspects: a) visuo-spatial organisation (cerebellar-parietal circuit), b) executive functions for planning and programming activities (cerebellar-frontal circuit), and c) increased RTs for visual and auditory targets, indicating a reduced speed of information processing. The latter effect is less marked in unilateral lesions.
More specifically related with the objective of the present report is the cerebellum's role in learning and memory tasks. The role of the cerebellum in motor response learning acquisition has been clearly demonstrated [27, 28]. The cerebellum has a clear role in the acquisition of motor skills, in procedural learning (in close interaction with basal nuclei), and in the Pavlovian conditioning of certain motor responses (in close interaction with the hippocampus and cerebral cortex).
Specifically, a role in establishing the association between the different motor acts composing the sequence has been proposed . However, an important issue is whether the deficits are due to motor impairments. Previous work has demonstrated that the participation of the cerebellum is independent of the kind of motor processes involved in accomplishing the task . On the other hand, cerebellar activity during working memory tasks has been demonstrated , forming part of a circuit that includes prefrontal (Brodmann areas 6, 9, 44, and 46), parietal, temporal and anterior cingulated cortices, and cerebellum [32–35]. With regard to declarative memory, some authors attach importance to structures such as the cerebellum, besides the areas traditionally involved in these tasks .
The study's research aim was to test different types of learning task (procedural vs. declarative) in order to assess the learning potential in two clinical groups (medulloblastoma and astrocytoma tumours). Two different aspects would be considered: first, the assessment of learning and cognitive function capabilities after treatment would give some clues for establishing neuropsychological rehabilitation strategies after different types of treatment and tumour. Second, the results could give some information about the role of the cerebellum in procedural and declarative memory. In summary, this pathology could be considered an interesting model in which to study cerebellar functions and how the differential effects of certain medical therapies could also affect learning and cognitive functions.
Thirty individuals participated in this study: eighteen of them were clinical patients and twelve were controls. There were two clinical groups. The first (CE: astrocytoma) comprised eleven individuals (eight girls and three boys), the mean age being 11.54 years (S.D. = 3.20). In the second group (CE+: medulloblastoma) there were seven individuals (four girls and three boys); the mean age was 13.14 years (S.D. = 1.95) at the time of the evaluation. The control group (C) comprised twelve subjects (seven girls and five boys), the mean age being 10.66 years (S.D. = 2.22). There were no significant group differences with regard to age or sex.
Main characteristics of the clinical groups.
Histological tumor type
• Medulloblastoma (CE+ group)
n = 7
• Astrocitoma (CE group)
n = 11
n = 7
n = 3
n = 0
n = 7
• Not information
n = 0
n = 1
n = 3
n = 11
n = 4
n = 0
Chemo and radiotherapy
n = 2
n = 9
n = 5
n = 2
Subjective deficits referred to the parents
n = 0
n = 9
n = 7
n = 2
The members of the control group (C) were chosen from pupils of a private school in Seville. They were selected from a group of 50 children (from 6 to 16 years old) participating in a developmental-cognitive study, and who met the following criteria: standard educational opportunities, normal or corrected-to-normal visual acuity, and without any detected behavioural problems.
The present experimental protocol followed the norms of the Helsinki Declaration regarding experiments involving human subjects. The experimental protocol was approved by the ethics committee of the Virgen del Rocio Hospital.
Motor, visuo-motor, and IQ characteristics of the subjects
Descriptive values for general performance tasks. (In brackets is shown the standard deviation)
PEGBOARD (time to complete the task in seconds)
TAPPING (frequency in 20 seconds)
SIMPLE REACTION TIME (reaction time in milliseconds)
Finger-tapping task. The subjects had to tap a key of the computer keyboard rapidly and repeatedly for 20 seconds with the index finger (dominant and non-dominant hand). The variable obtained was the tapping number. The mean value of tapping number in the dominant and non-dominant hand was computed. One-way ANOVA (group factor) was performed for the tapping variables. There was no statistical difference between the three groups for tapping response.
The grooved pegboard. This consisted of a board having 25 holes with randomly positioned slots. Pegs, which had a key along one side, had to be rotated to match the hole before they could be inserted. The variable obtained from this test was the total time employed in filling all the holes using each hand. The mean value of the time needed to complete the task in the dominant and non-dominant hand was computed. Two children of the CE+ group did not end the task in the 300-second period required. The value of 300 seconds was assigned to these two subjects. One-way ANOVA (group factor) was performed for the pegboard. The effect of the group was statistically significant [F (2,27) = 5.48, p = 0.010]. The Scheffé post hoc test revealed that this effect was due to differences between the C and CE+ groups [p = 0.024].
Simple Reaction Time. This task tested whether subjects were able to complete visuo-motor reaction-time tasks. A single target (a fish in the centre of the screen) was presented, and the aim of the task was to respond with the index finger as fast as possible. The target duration was 1700 ms, and in order to reduce anticipations the ISI was randomised between 1500 and 2200 ms. One-way ANOVA (group factor) was performed on the RTs. The effect of the group was statistically significant [F (2,27) = 3.720 p = 0.038]. The post hoc test revealed that this effect was due to differences between the C and CE+ groups (p = 0.043).
A standard form of the Progressive Matrices of Raven was used. The score for each child was obtained taking into consideration the age of the child. The effect of the factor group was statistically significant [F (2,27 = 4.11, p = 0.028]. Post hoc comparisons indicated that this result was due to a significant difference between groups C and CE+ (p = 0.010).
The overall assessment indicated that there were no obvious motor, visuo-motor, or cognitive differences between the C and CE groups. The main differences were obtained between C and CE+ groups, while the CE group presented an intermediate status for all the performed tests. In any case, the obtained level of performance of the subjects was enough to participate and to complete the learning tests.
There are two possible interpretations of the differences between CE and CE+ groups described previously. First, there have been many reports that support general deficits associated to unspecific cortical and subcortical negative effects of chemo- and radiotherapy. Secondly, the type of surgery applied in these cases is generally more invasive, and could affect more input-output cerebellar pathways and cause post-surgery complications. With regard to the first point, some authors have suggested  that the general intellectual state could be diminished with time, and this could be associated with an impossibility for these children to acquire new skills at the same rate as control groups. In addition, there is some evidence of an association between reduced volumes of normal-appearing white matter (NAWM) and intellectual/academic deficits induced by radiotherapy . Reddick  has demonstrated that the primary consequence of reduced NAWM in paediatric patients treated for brain tumours is a decrease in attentional abilities, leading to a decline in IQ and academic achievement.
Putting together the obtained data on IQ, motor, and visuo-motor skills and the information in the previous paragraph, the decision was taken to consider the two clinical groups as two different clinical conditions.
Procedural learning (serial reaction-time task) . The serial reaction-time task (SRT) was used to measure the implicit sequence learning. Participants were seated in front of a computer screen at a distance of 53 cm. Four open circles subtending a visual angle of 16° and arranged horizontally were presented on the screen. The dominant hand was used to respond, using four keys, on the computer keyboard, aligned with the circles. In each trial in the sequence, a circle was filled in with solid red, and the participant had to press the corresponding key. The stimulus remained filled in until a key was pressed. If the key was not pressed in one second, the trial was ended. The duration of the stimulus was 1000 ms and the ISI were randomly obtained between 500 and 800 ms. The experiment consisted of five blocks of 40 trials. We presented an additional training block before starting the real test. The sequence of red-filled circles was randomised in blocks 1 and 5. In blocks 2, 3, and 4, the stimulus was presented according to a prearranged sequence consisting of 10 stimuli which were repeated 12 times during the 3 blocks. Subjects were asked at the end of the test if they had observed any kind of sequence in the stimulus presentation. None of the children had detected the sequence. The variables obtained were (according to the type of response) hits (accuracy), errors (responses given with any other key), omissions (no response), and anticipations (correct responses with RTs faster than 250 ms), and RTs for each of the blocks independently.
Declarative learning. (Spanish version by Benedet et al. . of California Verbal Learning Test-Children's Version- CVLT- by Delis et al. ). This test provides variables such as learning curve, learning stability through time, short- and long-term retention, learning strategies, recovery and storage, and interference susceptibility. In our study, we focused only on the learning curve in five trials, so the variable obtained was the quantity of remembered words in each trial.
The results were analysed using ANOVA and MANOVA tests, with the Scheffé test used for post hoc comparisons. The details of factors and levels are specific for each behavioural test. In order to improve the power of the analysis, all 3 "learning blocks" were included into MANOVA (block 2, 3 and 4 for the procedural task, and blocks 1 and 5 for the declarative task). The inter-subject variable was always the different clinical (CE and CE+) and control (C) groups. The normality of distributions was tested with the Shapiro-Wilk test, and the homocedasticity by means of the Levene test. As a result, the data obtained can be considered normally distributed and having similar variances (p = 0.05). For the RT analysis, when effects of the block were obtained t-tests (Bonferroni corrected for multiple comparison) were applied in order to test which block comparisons presented statistically significant differences.
Descriptive values for reaction times and response accuracy in learning blocks from the motor sequential task. (In brackets is shown the standard deviation)
GROUP/REACTION TIME (ms)
Analysis of the data for the factor accuracy revealed a significant effect of the group [F (2, 27) = 4.86; p = 0.016]. The post hoc comparisons showed that the CE+ group presented a lower number of correct responses than C (p = 0,016). No main effect of the block was obtained.
Analysis of RTs revealed significant effects of the block [F (2, 54) = 8.924; p < 0.001] and an interaction between block and group [F (4, 54) = 2.79; p = 0.035], but no main effect of the group was obtained. In order to clarify the groups where there was a change in RTs between blocks, paired t-tests (Bonferroni corrected for multiple comparisons) were performed to compare the three learning blocks for each subject group. For the C group the only obtained statistically significant differences was the block 2 with respect to block 4 (p < 0.003). However a trend to statistical significant differences were obtained when blocks 2 vs. 3 (p = 0.067) and blocks 3 vs. 4 (p = 0.095) were compared. For the CE group there was not any statistically significant differences between the different blocks, however there was a trend for statistical significance when the block 2 and 3 were compared (p = 0.064). For the CE+ group there was not any statistically significant differences between the different blocks
Descriptive values for frequency of remembered words in learning blocks from the declarative-verbal task. (In brackets is shown the standard deviation)
The present study was designed to assess procedural vs. declarative learning in children and adolescents with acquired pathology confined to the cerebellum (CE), and in children and adolescents with additional damage due to the chemotherapy and radiotherapy used (CE+). The characteristics of the clinical subjects included in the study did not show a major impairment of subjects that prevented their inclusion in the experiment. It should be noted that the conservation of basic motor skills, and of visuomotor and cognitive functioning of the two clinical groups, allows the testing of declarative and procedural learning.
Our results show differential alterations in learning capacity in children with posterior fossa tumours. The ANOVA of procedural data show that neither of the clinical groups was capable of learning motor sequences in spite of having sufficient basic visuo-motor skills to complete the task. The differences between clinical groups and controls could be explained by the involvement of cerebellar circuits in procedural learning. On the other hand, no statistical differences were found in the task related with declarative memory. The fact that the CE+ group showed a trend – non-statistically significant – towards being more affected than the CE group could be due to different factors such as the greater malignancy, the type of surgery employed, the post-surgical outcome, and coadjuvant treatments.
Our results support the broad evidence favouring the involvement of the cerebellum in procedural learning. There are many studies that indicate subcortical involvement in procedural learning, suggesting different roles for basal ganglia and cerebellum. Numerous studies with patients showing cerebellar disease or striatum degenerative disease support the relationship between these structures and procedural learning [40–44]. Gómez-Beldarrain et al.  have proposed functional cerebellar lateralised deficits due to cerebellar focal lesions. Children with neurodevelopmental disorders involving fronto-cerebellar lesions (e.g., autism) have also been shown to be impaired in procedural learning . In the latter two studies, a serial reaction-time task was used, as opposed to some other studies using more-clinically oriented tests. Daum  used two procedural learning tasks involving perceptual (mirror reading) and conceptual (Tower of Hanoi task) skill acquisition, and found that patients with cerebellar pathology showed no effect on skill acquisition. Daum's results could be interpreted as being that if more cognitive operations are involved in the two proposed tasks, then the procedural operations in the tasks could be compensated by cognitive functions. In our experiment, subjects were not aware of the hidden sequence, so that cognitive operations would have great difficulty in compensating the deficits in the serial task.
In line with these earlier studies showing that procedural learning is severely impaired in patients with different kinds of cerebellar damage are the experiments using positron emission tomography (PET), in which changes in cerebral metabolic activity have been observed in the striatum and the cerebellum during procedural learning [47–49]. In the same sense, it has been demonstrated that the interference of cerebellar activity by transcranial magnetic stimulation produces an interference of procedural learning of a serial sequence task .
Some recent studies using PET and fMRI have been interested in identifying the neural networks involved in different stages of sequential learning . A revised neurocognitive model of learning new sequences of motor control , based on a previous model , proposed that in the fast learning phase that occurs in motor learning during the first blocks of trials there is an involvement of cerebellar and striatal circuits. The learning progresses to a specialisation of the cerebellum in adaptation tasks, and a specialisation of striatal circuits in sequence learning. Present results of impaired sequential procedural learning support the involvement of the cerebellum in the early phase of sequential motor learning. However, the fact that the CE group presented a statistically significant trend for procedural learning when blocks 2 and 3 are compared suggest that, as proposed by current models of procedural learning [52, 53], the striatal circuit would play the most important role in sequential learning.
With regard to declarative learning, effective learning occurred in the two clinical groups. No interaction appeared between the effects of learning block and group. However, qualitatively it can be appreciated that CE+ performance was the lower, particularly in z-scores, but learning still remained within the score limits for a normal population.
The role of the cerebellum in declarative learning has been proved in tasks where visual memories must be formed and retrieved . More similarly to our study (because the encoded items were verbal), there are some neuroimaging studies that show an increase of activation in the cerebellum during memory tasks involving the encoding of sentences  or of auditory-verbal material . However, as far as we know, the only experiment that tried to find the areas correlated with the California Verbal Memory Test (similar to our declarative learning task) did not show an activation in the cerebellum . In the present report, in accord with other results, declarative memory is preserved in these clinical groups. In some studies that assess declarative learning from the sequence used to assess procedural learning , this kind of memory is conserved in adult clinical samples. By contrast, Parkinsonian patients and patients with cerebellar lesions failed to improve task performance when only procedural processes were used.
Our results can support the hypothesis of cerebellar involvement in the early phases of procedural learning acquisition [46, 52]. On the other hand, the early verbal declarative learning system was preserved. However, the cerebellum's role in motor learning  – but also in cognitive functions  – could be in reinforcement of the process rather than in the process itself. Thus it is possible that, with enough number of trials, procedural learning could still occur in cerebellar patients.
We thank Dr. Ana Maria Alvarez, Dr. Eduardo Quiroga, Dr. Charo Vázquez, and the staff of the Virgen del Rocio Hospital (Oncology Service and Neurosurgery Service) and ANDEX Foundation for their continuous support of this work. The work was possible thanks to financial support from the MEC (DGICYT).
- Benedet Alvarez MJ, Alejandre García M, Angeles , Pamos de la Hoz A: TAVECI. Test de Aprendizaje Verbal España Complutense Infantil. TEA Ediciones. 2001, MadridGoogle Scholar
- Delis DC, Kramer JH, Kaplan E, Ober BA: California verbal learning test children. 1994, San Antonio: The Psychological CorporationGoogle Scholar
- Danjoux CE, Jenkin RD, McLaughlin J, Grimard L, Gaspar L, Gaspar LE: Childhood medulloblastoma in Ontario, 1977–1987: population based results. Med Pediatr Onco. 1996, 26: 1-9. 10.1002/(SICI)1096-911X(199601)26:1<1::AID-MPO1>3.0.CO;2-Q.View ArticleGoogle Scholar
- Becker LE, Giangaspero F, Rorke LB: Embryonal tumors. Cancer incidence and survival among children and adolescents: United States SEER Program 1975–1995. Edited by: Keinhues P, Cavenee WK. 1995, NIH Pub No 99-46-49. Bethesda: National Cancer Institute, 51-63.Google Scholar
- Fuemmeler B, Elkin D, Mullins L: Survivors of childhood brain tumours: behavioural, emotional, and social adjustment. Clin Psychol Rev. 2002, 22 (4): 547-85. 10.1016/S0272-7358(01)00120-9.View ArticlePubMedGoogle Scholar
- McDonald T, Rood B, Santi M, Vezina G, Bingaman K, Cogen P, Packer R: Advances in the diagnosis, molecular genetics and treatment of pediatric embryonal CNS tumors. The oncologist. 2003, 8: 174-186. 10.1634/theoncologist.8-2-174.View ArticleGoogle Scholar
- Ris MD, Packer R, Goldwein J, Jones-Wallace D, Boyett JM: Intellectual outcome after reduced-dose radiation therapy plus adjuvant chemotherapy for medulloblastoma: a children's cancer group study. J Clin Oncol. 2001, 19 (15): 3470-3476.PubMedGoogle Scholar
- Palmer SL, Goloubeva O, Reddick WE, Glass JO, Gajjar A, Kun L: Patterns of intellectual development among survivors of paediatric medulloblastoma: a longitudinal analysis. J Clin Oncol. 2001, 19 (8): 2302-2308.PubMedGoogle Scholar
- Meyers CA, Geara F, Wong PF, Morrison WH: Neurocognitive effects of therapeutic irradiation for base of skull tumors. Int J Radiat Oncol Biol Phys. 2000, 46: 51-55. 10.1016/S0360-3016(99)00376-4.View ArticlePubMedGoogle Scholar
- Walter AW, Mulhern RK, Gajjar A, Heideman RL, Reardon D, Sanford RA: Survival and neurodevelopmental outcome of young children with medulloblastoma at St. Jude Children-s Research Hospital. J Clin Onc. 1999, 17 (12): 3720-3728.Google Scholar
- Zucchinelli V, Bouffet E: Academic future of children treated for brain tumors. Single-center study of 27 children. Arch Pediatr. 2000, 7 (9): 933-41. 10.1016/S0929-693X(00)90006-X.View ArticlePubMedGoogle Scholar
- Barrios M, Guàrdia J: Relación del cerebelo con las funciones cognitivas: evidencias neuroanatómicas, clínicas y de neuroimagen. Rev Neurol. 2001, 33 (6): 582-591.PubMedGoogle Scholar
- Yamaguchi S, Tsuchiya H, Kobayashi S: Visuospatial attention shift and motor responses in cerebellar disorders. J Cogn Neurosci. 1998, 10 (1): 95-107. 10.1162/089892998563806.View ArticlePubMedGoogle Scholar
- Siffert J, Poussaint TY, Goumnerova LC, Scott RM, LaValley B, Tarbell NJ, Pomeroy SL: Neurological dysfunction associated with postoperative cerebellar mutism. J Neurooncol. 2000, 48 (1): 75-81. 10.1023/A:1006483531811.View ArticlePubMedGoogle Scholar
- Levisohn L, Cronin-Golomb A, Schmahmann JD: Neuropsychological consequences of cerebellar tumour resection in children: cerebellar cognitive affective syndrome in a paediatric population. Brain. 2000, 123 (Pt 5): 1041-50. 10.1093/brain/123.5.1041.View ArticlePubMedGoogle Scholar
- Riva D, Giorgi C: The cerebellum contributes to higher functions during development: evidence from a series of children surgically treated for posterior fossa tumours. Brain. 2000, 123 (Pt 5): 1051-1061. 10.1093/brain/123.5.1051.View ArticlePubMedGoogle Scholar
- Karatekin C, Lazareff JA, Asarnow RF: Relevance of the cerebellar hemispheres for executive functions. Pediatr Neurol. 2000, 22 (2): 106-112. 10.1016/S0887-8994(99)00128-9.View ArticlePubMedGoogle Scholar
- Schmahmann JD, Pandya DN: The cerebrocerebellar system. Int Rev Neurobiol. 1997, 41: 31-60.View ArticlePubMedGoogle Scholar
- Boni S, Valle G, Cioggi RP, Bonetti MG, Perrone E, Tofani A: Crossed cerebello-cerebral diaschisis: a SPECT study. Nucl Med Commun. 1992, 13: 824-31.View ArticlePubMedGoogle Scholar
- Gebhart AL, Petersen SE, Thach WT: Role of the posterolateral cerebellum in language. Ann NY Acad Sci. 2002, 978: 318-33. 10.1111/j.1749-6632.2002.tb07577.x.View ArticlePubMedGoogle Scholar
- Mostofsky SH, Goldberg MC, Landa RJ, Denckla MB: Evidence for a deficit in procedural learning in children and adolescents with autism: implications for cerebellar contribution. J Int Neuropsychol Soc. 2000, 6 (7): 752-9. 10.1017/S1355617700677020.View ArticlePubMedGoogle Scholar
- Mostofsky SH, Reiss AL, Lockhart P, Denckla MB: Evaluation of cerebellar size in attention-deficit hyperactivity disorder. J Child Neurol. 1998, 13 (9): 434-9.View ArticlePubMedGoogle Scholar
- Turgut M: Transient "cerebellar" mutism. Childs Nerv Syst. 1998, 14 (4–5): 161-6. 10.1007/s003810050204.View ArticlePubMedGoogle Scholar
- Vandeinse D, Hornyak JE: Linguistic and cognitive deficits associated with cerebellar mutism. Pediatr-Rehabil. 1997, 1 (1): 41-4.PubMedGoogle Scholar
- Botez MI: The neuropsychology of the cerebellum: an emerging concept. Arch Neurol. 1992, 49: 1229-30.View ArticlePubMedGoogle Scholar
- Botez Marquard T, Leveille J, Botez MI: Neuropsychological functioning in unilateral cerebellar damage. Can J Neurol Sci. 1994, 21: 35-37.Google Scholar
- Frings M, Boenisch R, Gerwig M, Diener HC, Timmann D: Learning of sensory sequences in cerebellar patients. Learn Mem. 2004, 11 (3): 347-355. 10.1101/lm.66904.PubMed CentralView ArticlePubMedGoogle Scholar
- Molinari M, Leggio MG, Solida A, Ciorra R, Misciagna S, Silveri MC, Petrosini L: Cerebellum and procedural learning: evidence from focal cerebellar lesions. Brain. 1997, 120 (Pt 10): 1753-1762. 10.1093/brain/120.10.1753.View ArticlePubMedGoogle Scholar
- Shin JC, Ivry RB: Spatial and temporal sequence learning in patients with Parkinson's disease or cerebellar lesions. J Cogn Neurosci. 2003, 15 (8): 1232-43. 10.1162/089892903322598175.View ArticlePubMedGoogle Scholar
- Timmann D, Drepper J, Maschke M, Kolb FP, Boring D, Thilmann AF, Diener HC: Motor deficits cannot explain impaired cognitive associative learning in cerebellar patients. Neuropsychologia. 2002, 40 (7): 788-800. 10.1016/S0028-3932(01)00181-6.View ArticlePubMedGoogle Scholar
- Baddeley A: Working memory. C R Acad Sci III. 1998, 321 (2–3): 167-173.View ArticlePubMedGoogle Scholar
- Desmond JE, Gabrieli JD, Wagner AD, Ginier BL, Glover GH: Lobular patterns of cerebellar activation in verbal working-memory and finger-tapping tasks as revealed by functional MRI. J Neurosci. 1997, 17 (24): 9675-85.PubMedGoogle Scholar
- Grasby PM, Frith CD, Friston KJ, Simpson J, Fletcher PC, Frackowiak RS: A graded task approach to the functional mapping of brain areas implicated in auditory-verbal memory. Brain. 1994, 117: 1271-1282.View ArticlePubMedGoogle Scholar
- Fiez JA, Raife EA, Balota DA, Schwarz JP, Raichle ME, Petersen SE: A positron emission tomography study of the short-term maintenance of verbal information. J Neurosci. 1996, 16: 808-822.PubMedGoogle Scholar
- Schumacher EH, Lauber E, Awh E, Jonides J, Smith EE, Koeppe RA: PET evidence for an amodal verbal working memory system. NeuroImage. 1996, 3: 79-88. 10.1006/nimg.1996.0009.View ArticlePubMedGoogle Scholar
- Weis S, Klaver P, Reul J, Elger CE, Fernandez G: Temporal and cerebellar brain regions that support both declarative memory formation and retrieval. Cereb Cortex. 2004, 14 (3): 256-267. 10.1093/cercor/bhg125.View ArticlePubMedGoogle Scholar
- Mulhern RK, Palmer SL, Reddick WE, Glass JO, Kun LE, Taylor J, Langston J, Gajjar A: Risks of young age for selected neurocognitive deficits in medulloblastoma are associated with white matter loss. J Clin Oncol. 2001, 19 (2): 472-479.PubMedGoogle Scholar
- Reddick WE, White HA, Glass JO, Wheeler GC, Thompson SJ, Gajjar A, Leigh L, Mulhern RK: Developmental model relating white matter volume to neurocognitive deficits in pediatric brain tumour survivors. Cancer. 2003, 97 (10): 2512-2519. 10.1002/cncr.11355.View ArticlePubMedGoogle Scholar
- Niessen MJ, Bullemer P: Attentional requirements of learning: evidence from performance measures. Cogn Psychol. 1987, 19: 1-32. 10.1016/0010-0285(87)90002-8.View ArticleGoogle Scholar
- Doyon J, Laforce R, Gaudreau D, Castonguay M, Bédard PJ, Bouchard JP: Contribution of the striatum and cerebellum in visuomotor skill learning. Proceedings of Society for Neuroscience. 1993, 19: 1080-Google Scholar
- Fiez J, Petersen SE, Cheney MK, Raichle ME: Impaired non motor learning and error detection associated with cerebellar damage: A single case study. Brain. 1992, 115: 155-178.View ArticlePubMedGoogle Scholar
- Harrington DL, York Haaland K, Yeo RA, Marder E: Procedural memory in Parkinson's disease: Impaired motor but not visuoperceptual learning. J Clin Exp Neuropsychol. 1990, 12: 323-339.View ArticlePubMedGoogle Scholar
- Heindel WC, Butters N, Salmon DP: Impaired learning of a motor skill in patients with Huntington's disease. Behav Neurosci. 1988, 102: 141-146. 10.1037/0735-7044.102.1.141.View ArticlePubMedGoogle Scholar
- Pascual-Leone A, Grafman J, Clark K, Stewart M, Massaquoi S, Hallet M: Procedural visuomotor learning in Parkinson's disease and cerebellar degeneration. Ann Neurol. 1993, 34: 594-602. 10.1002/ana.410340414.View ArticlePubMedGoogle Scholar
- Gomez-Beldarrain M, Garcia-Monco JC, Rubio B, Pascual-Leone A: Effect of focal cerebellar lesions on procedural learning in the serial reaction time task. Exp Brain Res. 1998, 120 (1): 25-30. 10.1007/s002210050374.View ArticlePubMedGoogle Scholar
- Daum I, Ackermann H, Schugens MM, Reimold C, Dichgans J, Birbaumer N: The cerebellum and cognitive functions in humans. Behav Neurosci. 1993, 107 (3): 411-419. 10.1037/0735-7044.107.3.411.View ArticlePubMedGoogle Scholar
- Doyon J, Owen AM, Petrides M, Sziklas V, Evans AC: Functional anatomy of visuomotor skill learning in human subjects using positron emission tomography. Eur J Neurosci. 1996, 8: 637-648.View ArticlePubMedGoogle Scholar
- Jenkins IH, Brooks DJ, Nixon PD, Frackowiak RSJ, Passingham RE: Motor sequence learning: A study with positron emission tomography. J Neurosci. 14: 3775-90.Google Scholar
- Seitz RJ, Roland PE: Learning of sequential finger movements in man: a combined kinematic and positron emission tomography (PET) study. Eur J Neurosci. 1994, 4: 154-65.View ArticleGoogle Scholar
- Torriero S, Oliveri M, Koch G, Caltagirone C, Petrosini L: Interference of left and right cerebellar rTMS with procedural learning. J Cogn Neurosci. 2004, 16: 1605-1611. 10.1162/0898929042568488.View ArticlePubMedGoogle Scholar
- Hikosaka O, Nakahara H, Rand MK, Sakai K, Lu X, Nakamura K, Miyachi S, Doya K: Parallel neural networks for learning sequential procedures. Trends Neurosci. 1999, 22 (10): 464-471. 10.1016/S0166-2236(99)01439-3.View ArticlePubMedGoogle Scholar
- Doyon J, BenAli H: Reorganization and plasticity in the adult brain during learning of motor skills. Curr Opin Neurobiol. 2005, 15: 161-167. 10.1016/j.conb.2005.03.004.View ArticlePubMedGoogle Scholar
- Doyon J, Ungerleider LG: Functional anatomy of motor skill learning. Neuropsychology of memory. Edited by: Squire LR, Schacter DL. 2002, The Guilford Press, 225-238. NYGoogle Scholar
- Weis S, Klaver P, Reul J, Elger CE, Fernandez G: Temporal and cerebellar brain regions that support both declarative memory formation and retrieval. Cereb Cortex. 2004, 14 (3): 256-67. 10.1093/cercor/bhg125.View ArticlePubMedGoogle Scholar
- Bremner JD, Vythilingam M, Vermetten E, Vaccarino V, Charney D: Deficits in hippocampal and anterior cingulate functioning during verbal declarative memory encoding in midlife major depression. Am J Psychiatry. 2004, 161 (4): 637-45. 10.1176/appi.ajp.161.4.637.View ArticlePubMedGoogle Scholar
- Grasby PM, Frith CD, Friston KJ, Bench C, Frackowiak RS, Dolan RJ: Functional mapping of brain areas implicated in auditory – verbal memory function. Brain. 1993, 116 (Pt 1): 1-20.View ArticlePubMedGoogle Scholar
- Johnson SC, Saykin AJ, Flashman LA, McAllister TW, Sparling MB: Brain activation on fMRI and verbal memory ability: functional neuroanatomic correlates of CVLT performance. J Int Neuropsychol Soc. 2001, 7 (1): 55-62. 10.1017/S135561770171106X.View ArticlePubMedGoogle Scholar
- Doyon J, Gaudreau D, Laforce R, Castonguay M, Bedard PJ, Bedard F, Bouchard JP: Role of the striatum, cerebellum, and frontal lobes in the learning of a visuomotor sequence. Brain Cogn. 1997, 34 (2): 218-245. 10.1006/brcg.1997.0899.View ArticlePubMedGoogle Scholar
- Delgado-García JM, Gruart A: The role of interpositus nucleus in eyelid conditioned responses. Cerebellum. 2002, 1 (4): 289-308. 10.1080/147342202320883597.View ArticlePubMedGoogle Scholar
- Courchesne E, Allen G: Prediction and preparation, fundamental functions of the cerebellum. Learn Mem. 1997, 4 (1): 1-35.View ArticlePubMedGoogle Scholar
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