Search research articles
Contact Us
Filters
Showing results (11-20 of 38) with videos related to
Page
of 4
Sort By:
Neuropediatrics
|
November 10, 2004
Hypovitaminosis D-related myopathy in immigrant teenagers
J J C van der Heyden, A Verrips, H J ter Laak, et al.
Stroke
|
October 1, 1993
Familial cerebrovascular accidents due to concomitant hyperhomocysteinemia and protein C deficiency type 1
D G Franken, A Vreugdenhil, G H Boers, et al.
Human Molecular Genetics
|
January 4, 2001
Autosomal dominant transmission of GLUT1 deficiency
J Klepper, M Willemsen, A Verrips, et al.
Neuropediatrics
|
June 21, 2001
Scheie syndrome presenting as myopathy
A Verrips, B G van Engelen, H ter Laak, et al.
European Journal of Pediatrics
|
May 14, 1998
Treatment and follow-up of children with cerebrotendinous xanthomatosis
A F van Heijst, A Verrips, R A Wevers, et al.
Neuromuscular Disorders : NMD
|
June 1, 2007
Quantitative skeletal muscle ultrasound: diagnostic value in childhood neuromuscular disease
S Pillen, A Verrips, N van Alfen, et al.
European Journal of Pediatrics
|
December 2, 2008
A previously healthy 11-year-old girl with behavioural disturbances, desquamation of the skin and loss of teeth
A A A van der Linde, C A W Lewiszong-Rutjens, A Verrips, et al.
The Netherlands Journal of Medicine
|
August 27, 1998
Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
J A Hiel, A Verrips, A Keyser, et al.
Journal of Inherited Metabolic Disease
|
January 5, 2002
Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophy
M E Rubio-Gozalbo, D A van Waardenburg, P P Forget, et al.
Neuromuscular Disorders : NMD
|
May 2, 2016
No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndrome
J van Vliet, A Verrips, A A Tieleman, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Neuropediatrics
|
November 10, 2004
Hypovitaminosis D-related myopathy in immigrant teenagers
J J C van der Heyden, A Verrips, H J ter Laak, et al.
Stroke
|
October 1, 1993
Familial cerebrovascular accidents due to concomitant hyperhomocysteinemia and protein C deficiency type 1
D G Franken, A Vreugdenhil, G H Boers, et al.
Human Molecular Genetics
|
January 4, 2001
Autosomal dominant transmission of GLUT1 deficiency
J Klepper, M Willemsen, A Verrips, et al.
Neuropediatrics
|
June 21, 2001
Scheie syndrome presenting as myopathy
A Verrips, B G van Engelen, H ter Laak, et al.
European Journal of Pediatrics
|
May 14, 1998
Treatment and follow-up of children with cerebrotendinous xanthomatosis
A F van Heijst, A Verrips, R A Wevers, et al.
Neuromuscular Disorders : NMD
|
June 1, 2007
Quantitative skeletal muscle ultrasound: diagnostic value in childhood neuromuscular disease
S Pillen, A Verrips, N van Alfen, et al.
European Journal of Pediatrics
|
December 2, 2008
A previously healthy 11-year-old girl with behavioural disturbances, desquamation of the skin and loss of teeth
A A A van der Linde, C A W Lewiszong-Rutjens, A Verrips, et al.
The Netherlands Journal of Medicine
|
August 27, 1998
Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
J A Hiel, A Verrips, A Keyser, et al.
Journal of Inherited Metabolic Disease
|
January 5, 2002
Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophy
M E Rubio-Gozalbo, D A van Waardenburg, P P Forget, et al.
Neuromuscular Disorders : NMD
|
May 2, 2016
No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndrome
J van Vliet, A Verrips, A A Tieleman, et al.
Page
of 4