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Journal of Neurology
|
April 4, 2001
Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia
H J Schelhaas, P F Ippel, G Hageman, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
January 21, 2006
Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders
P J Blijham, H J ter Laak, H J Schelhaas, et al.
Journal of Intellectual Disability Research : JIDR
|
October 16, 2018
Classification of intellectual disability according to domains of adaptive functioning and between-domains discrepancy in adults with epilepsy
J S van Ool, F M Snoeijen-Schouwenaars, I Y Tan, et al.
Acta Neurologica Scandinavica
|
January 26, 2016
Botulinum toxin-A injections vs radiotherapy for drooling in ALS
J G Weikamp, D A X Schinagl, C C P Verstappen, et al.
European Journal of Neurology
|
May 7, 2010
Age-related changes in motor unit number estimates in adult patients with Charcot-Marie-Tooth type 1A
J P van Dijk, C Verhamme, I N van Schaik, et al.
Neuromuscular Disorders : NMD
|
March 27, 2007
Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation
S Overeem, H J Schelhaas, P J Blijham, et al.
Epilepsy & Behavior : E&B
|
May 26, 2015
Autism and behavior in adult patients with Dravet syndrome (DS)
J J L Berkvens, I Veugen, M J B M Veendrick-Meekes, et al.
Seizure
|
June 17, 2015
Carbamazepine and oxcarbazepine in adult patients with Dravet syndrome: Friend or foe?
F M Snoeijen-Schouwenaars, M J B M Veendrick, P van Mierlo, et al.
Neurology
|
September 24, 2011
Family history of neurodegenerative and vascular diseases in ALS: a population-based study
M H B Huisman, S W de Jong, M C Verwijs, et al.
Neurology
|
April 11, 2008
Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?
M C Ørngreen, H J Schelhaas, T D Jeppesen, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Journal of Neurology
|
April 4, 2001
Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia
H J Schelhaas, P F Ippel, G Hageman, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
January 21, 2006
Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders
P J Blijham, H J ter Laak, H J Schelhaas, et al.
Journal of Intellectual Disability Research : JIDR
|
October 16, 2018
Classification of intellectual disability according to domains of adaptive functioning and between-domains discrepancy in adults with epilepsy
J S van Ool, F M Snoeijen-Schouwenaars, I Y Tan, et al.
Acta Neurologica Scandinavica
|
January 26, 2016
Botulinum toxin-A injections vs radiotherapy for drooling in ALS
J G Weikamp, D A X Schinagl, C C P Verstappen, et al.
European Journal of Neurology
|
May 7, 2010
Age-related changes in motor unit number estimates in adult patients with Charcot-Marie-Tooth type 1A
J P van Dijk, C Verhamme, I N van Schaik, et al.
Neuromuscular Disorders : NMD
|
March 27, 2007
Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation
S Overeem, H J Schelhaas, P J Blijham, et al.
Epilepsy & Behavior : E&B
|
May 26, 2015
Autism and behavior in adult patients with Dravet syndrome (DS)
J J L Berkvens, I Veugen, M J B M Veendrick-Meekes, et al.
Seizure
|
June 17, 2015
Carbamazepine and oxcarbazepine in adult patients with Dravet syndrome: Friend or foe?
F M Snoeijen-Schouwenaars, M J B M Veendrick, P van Mierlo, et al.
Neurology
|
September 24, 2011
Family history of neurodegenerative and vascular diseases in ALS: a population-based study
M H B Huisman, S W de Jong, M C Verwijs, et al.
Neurology
|
April 11, 2008
Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?
M C Ørngreen, H J Schelhaas, T D Jeppesen, et al.
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of 3