about
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationDo the clinical features in infantile-onset saccade initiation delay (congenital ocular motor apraxia) correlate with brain magnetic resonance imaging findings?Neuroimaging Findings and Repeat Neuroimaging Value in Pediatric Chronic Ataxia.Ketogenic diet in Alpers-Huttenlocher syndrome.Anomalous development of brain structure and function in spina bifida myelomeningocele.Saccades in children.Idiopathic "benign" intracranial hypertension: case series and review.Should children with Bell's palsy be treated with corticosteroids? A systematic review.The cerebellum: it's about time! But timing is not everything--new insights into the role of the cerebellum in timing motor and cognitive tasks.The cerebellar dysplasia of Chiari II malformation as revealed by eye movementsVisual fixation in Chiari type II malformationUpper limb motor function in young adults with spina bifida and hydrocephalusUpper limb cerebellar motor function in children with spina bifidaThe Role of the Pediatric Cerebellum in Motor Functions, Cognition, and Behavior: A Clinical Perspective.Neuro-Ophthalmological Findings in Children and Adolescents with Chronic Ataxia.Recurrent Ataxia in Children and Adolescents.Can Latent Class Analysis Be Used to Improve the Diagnostic Process in Pediatric Patients with Chronic Ataxia?Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis.Lissencephaly with brainstem and cerebellar hypoplasia and congenital cataracts.The epidemiology of intermittent and chronic ataxia in children in Manitoba, Canada.Smooth pursuit eye movements in children.Epidemiology of Cerebellar Diseases and Therapeutic Approaches.Smooth ocular pursuit in Chiari type II malformation.Response to correspondence on "lissencephaly with brainstem and cerebellar hypoplasia and congenital cataracts".Infantile-onset saccade initiation delay (congenital ocular motor apraxia).Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.Claude syndrome 'plus' in an adolescent.Saccadic adaptation in children.Prolonged survival and serial magnetic resonance imaging/magnetic resonance spectroscopy changes in infantile Krabbe disease.Benign intracranial hypertension or communicating hydrocephalus: factors in pathogenesis.Early-onset neurodegenerative disease of the cerebellum and motor axons.New insights into the neuropathogenesis of molybdenum cofactor deficiency.Saccades in children with spina bifida and Chiari type II malformation.Novel diffusion tensor imaging findings in Krabbe disease.Is the prophylactic use of antiepileptic drugs in Sturge-Weber syndrome justified?Congenital Oculomotor Nerve Paresis With Isolated Cyclic Pupillary Spasms.Cerebellar malformations in children: determining long-term neurological outcomesCerebellar radiological abnormalities in children with neurofibromatosis type 1: part 1 - clinical and neuroimaging findingsCerebellar radiological abnormalities in children with neurofibromatosis type 1: part 2 - a neuroimaging natural history study with clinical correlationsMigraine and sickle-cell disorders: is there a cause for concern?
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Michael S Salman
@es
Michael S Salman
@nl
Michael S Salman
@sl
Michael S. Salman
@en
type
label
Michael S Salman
@es
Michael S Salman
@nl
Michael S Salman
@sl
Michael S. Salman
@en
prefLabel
Michael S Salman
@es
Michael S Salman
@nl
Michael S Salman
@sl
Michael S. Salman
@en
P106
P1153
35230667600
P21
P31
P496
0000-0002-0564-7044
P569
2000-01-01T00:00:00Z