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Bulletin De L'Academie Nationale De Medecine
|
August 7, 1999
[Recessive dopa-responsive form of dystonia due to a mutation of the tyrosine hydroxylase gene]
P Rondot, R A Wevers
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
April 9, 1998
Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines
K J Lamers, R A Wevers
Clinical Chemistry
|
July 1, 1994
High-resolution 1H-NMR spectroscopy of blood plasma for metabolic studies
R A Wevers, U Engelke, A Heerschap
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 1988
An immunobioluminescence assay for gamma-gamma enolase activity in human serum and cerebrospinal fluid
R A Wevers, A W Theunisse, G Rijksen
The Journal of Pediatrics
|
March 10, 2001
L-dopa and selegiline for tyrosine hydroxylase deficiency
M Häussler, G F Hoffmann, R A Wevers
The American Journal of Psychiatry
|
March 1, 1988
Use of arylsulfatase A in chronic psychiatric patients
M J Hoes, K J Lamers, R A Wevers
Journal of Inherited Metabolic Disease
|
April 7, 2025
CLPB Deficiency, a Mitochondrial Chaperonopathy With Neutropenia and Neurological Presentation
D Mróz, J Jagłowska, R A Wevers, et al.
Neuropediatrics
|
June 25, 1998
Cerebrospinal fluid investigations for neurometabolic disorders
G F Hoffmann, R A Surtees, R A Wevers
Neuropediatrics
|
May 1, 1991
Infective acute transverse myelopathy. Report of two cases
W H Linssen, F J Gabreëls, R A Wevers
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 1983
A bioluminescent assay for enolase (EC 4.2.1.11) activity in human serum and cerebrospinal fluid
R A Wevers, A A Jacobs, O R Hommes
Page
of 23
Search research articles
Search
Showing results (1-10 of 222) with videos related to
Sort By:
Page
of 23
Bulletin De L'Academie Nationale De Medecine
|
August 7, 1999
[Recessive dopa-responsive form of dystonia due to a mutation of the tyrosine hydroxylase gene]
P Rondot, R A Wevers
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
April 9, 1998
Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines
K J Lamers, R A Wevers
Clinical Chemistry
|
July 1, 1994
High-resolution 1H-NMR spectroscopy of blood plasma for metabolic studies
R A Wevers, U Engelke, A Heerschap
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 1988
An immunobioluminescence assay for gamma-gamma enolase activity in human serum and cerebrospinal fluid
R A Wevers, A W Theunisse, G Rijksen
The Journal of Pediatrics
|
March 10, 2001
L-dopa and selegiline for tyrosine hydroxylase deficiency
M Häussler, G F Hoffmann, R A Wevers
The American Journal of Psychiatry
|
March 1, 1988
Use of arylsulfatase A in chronic psychiatric patients
M J Hoes, K J Lamers, R A Wevers
Journal of Inherited Metabolic Disease
|
April 7, 2025
CLPB Deficiency, a Mitochondrial Chaperonopathy With Neutropenia and Neurological Presentation
D Mróz, J Jagłowska, R A Wevers, et al.
Neuropediatrics
|
June 25, 1998
Cerebrospinal fluid investigations for neurometabolic disorders
G F Hoffmann, R A Surtees, R A Wevers
Neuropediatrics
|
May 1, 1991
Infective acute transverse myelopathy. Report of two cases
W H Linssen, F J Gabreëls, R A Wevers
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 1983
A bioluminescent assay for enolase (EC 4.2.1.11) activity in human serum and cerebrospinal fluid
R A Wevers, A A Jacobs, O R Hommes
Page
of 23