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A Verrips

Showing results (11-20 of 38) with videos related to

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Neuropediatrics|November 10, 2004
Hypovitaminosis D-related myopathy in immigrant teenagersJ 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 1D G Franken, A Vreugdenhil, G H Boers, et al.
Human Molecular Genetics|January 4, 2001
Autosomal dominant transmission of GLUT1 deficiencyJ Klepper, M Willemsen, A Verrips, et al.
Neuropediatrics|June 21, 2001
Scheie syndrome presenting as myopathyA 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 xanthomatosisA 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 diseaseS 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 teethA 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 episodesJ 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 adrenoleukodystrophyM 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 syndromeJ van Vliet, A Verrips, A A Tieleman, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Neuropediatrics|November 10, 2004
Hypovitaminosis D-related myopathy in immigrant teenagersJ 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 1D G Franken, A Vreugdenhil, G H Boers, et al.
Human Molecular Genetics|January 4, 2001
Autosomal dominant transmission of GLUT1 deficiencyJ Klepper, M Willemsen, A Verrips, et al.
Neuropediatrics|June 21, 2001
Scheie syndrome presenting as myopathyA 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 xanthomatosisA 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 diseaseS 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 teethA 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 episodesJ 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 adrenoleukodystrophyM 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 syndromeJ van Vliet, A Verrips, A A Tieleman, et al.
Pageof 4