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European Journal of Pediatrics
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May 14, 1998
Treatment and follow-up of children with cerebrotendinous xanthomatosis
A F van Heijst, A Verrips, R A Wevers, et al.
Muscle & Nerve
|
July 1, 1985
The relation between blood lactate and ammonia in ischemic handgrip exercise
S P Sinkeler, H A Daanen, R A Wevers, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome
M S van der Knaap, R A Wevers, L Monnens, et al.
Neuropediatrics
|
November 1, 1988
Acute transverse myelopathy as the initial manifestation of probable systemic lupus erythematosus in a child
W H Linssen, T J Fiselier, F J Gabreëls, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1987
Phenotypic expression in mucopolysaccharidosis VII
P L Bernsen, R A Wevers, F J Gabreëls, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1993
Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency
P J Poels, R A Wevers, J P Braakhekke, et al.
Human Molecular Genetics
|
March 1, 1994
Six novel mutations in the alpha-galactosidase A gene in families with Fabry disease
J K Ploos van Amstel, R P Jansen, J G de Jong, et al.
Journal of Inherited Metabolic Disease
|
November 10, 2009
Substrate deprivation therapy in juvenile Sandhoff disease
S B Wortmann, D J Lefeber, G Dekomien, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Ischaemic forearm testing in a patient with Ca(2+)-ATPase deficiency
R A Wevers, P J Poels, E M Joosten, et al.
Clinical Science (London, England : 1979)
|
April 1, 1987
AMP deaminase deficiency: study of the human skeletal muscle purine metabolism during ischaemic isometric exercise
S P Sinkeler, R A Binkhorst, E M Joosten, et al.
Page
of 23
Search research articles
Search
Showing results (81-90 of 222) with videos related to
Sort By:
Page
of 23
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.
Muscle & Nerve
|
July 1, 1985
The relation between blood lactate and ammonia in ischemic handgrip exercise
S P Sinkeler, H A Daanen, R A Wevers, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome
M S van der Knaap, R A Wevers, L Monnens, et al.
Neuropediatrics
|
November 1, 1988
Acute transverse myelopathy as the initial manifestation of probable systemic lupus erythematosus in a child
W H Linssen, T J Fiselier, F J Gabreëls, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1987
Phenotypic expression in mucopolysaccharidosis VII
P L Bernsen, R A Wevers, F J Gabreëls, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1993
Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency
P J Poels, R A Wevers, J P Braakhekke, et al.
Human Molecular Genetics
|
March 1, 1994
Six novel mutations in the alpha-galactosidase A gene in families with Fabry disease
J K Ploos van Amstel, R P Jansen, J G de Jong, et al.
Journal of Inherited Metabolic Disease
|
November 10, 2009
Substrate deprivation therapy in juvenile Sandhoff disease
S B Wortmann, D J Lefeber, G Dekomien, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Ischaemic forearm testing in a patient with Ca(2+)-ATPase deficiency
R A Wevers, P J Poels, E M Joosten, et al.
Clinical Science (London, England : 1979)
|
April 1, 1987
AMP deaminase deficiency: study of the human skeletal muscle purine metabolism during ischaemic isometric exercise
S P Sinkeler, R A Binkhorst, E M Joosten, et al.
Page
of 23