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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 17, 2004
Hereditary porencephaly: clinical and MRI findings in two Dutch families
G M S Mancini, I F M de Coo, M H Lequin, et al.
Journal of Medical Genetics
|
April 3, 2007
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease
M J Blok, L Spruijt, I F M de Coo, et al.
European Journal of Medical Genetics
|
January 4, 2011
Lung disease in FLNA mutation: confirmatory report
M C Y de Wit, H A W M Tiddens, I F M de Coo, et al.
Human Reproduction Update
|
October 4, 2005
The transmission of OXPHOS disease and methods to prevent this
L J A M Jacobs, G de Wert, J P M Geraedts, et al.
Annals of Neurology
|
March 24, 2005
Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease
Farid Meggouh, Marianne de Visser, Willem F M Arts, et al.
Neurogenetics
|
April 23, 2009
Movement disorder and neuronal migration disorder due to ARFGEF2 mutation
M C Y de Wit, I F M de Coo, D J J Halley, et al.
Journal of Immunological Methods
|
August 21, 2007
A simplified and reliable assay for complex I in human blood lymphocytes
L E A de Wit, L Spruijt, G C Schoonderwoerd, et al.
Clinical Genetics
|
March 9, 2016
Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder
M Nguyen, I Boesten, D M E I Hellebrekers, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2009
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects
M C Y de Wit, J M Kros, D J J Halley, et al.
Journal of Clinical and Experimental Neuropsychology
|
October 7, 2005
Increased prevalences of left-handedness and left-eye sighting dominance in individuals with Williams-Beuren syndrome
J W Van Strien, G C Lagers-Van Haselen, J M Van Hagen, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 41) with videos related to
Sort By:
Page
of 5
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 17, 2004
Hereditary porencephaly: clinical and MRI findings in two Dutch families
G M S Mancini, I F M de Coo, M H Lequin, et al.
Journal of Medical Genetics
|
April 3, 2007
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease
M J Blok, L Spruijt, I F M de Coo, et al.
European Journal of Medical Genetics
|
January 4, 2011
Lung disease in FLNA mutation: confirmatory report
M C Y de Wit, H A W M Tiddens, I F M de Coo, et al.
Human Reproduction Update
|
October 4, 2005
The transmission of OXPHOS disease and methods to prevent this
L J A M Jacobs, G de Wert, J P M Geraedts, et al.
Annals of Neurology
|
March 24, 2005
Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease
Farid Meggouh, Marianne de Visser, Willem F M Arts, et al.
Neurogenetics
|
April 23, 2009
Movement disorder and neuronal migration disorder due to ARFGEF2 mutation
M C Y de Wit, I F M de Coo, D J J Halley, et al.
Journal of Immunological Methods
|
August 21, 2007
A simplified and reliable assay for complex I in human blood lymphocytes
L E A de Wit, L Spruijt, G C Schoonderwoerd, et al.
Clinical Genetics
|
March 9, 2016
Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder
M Nguyen, I Boesten, D M E I Hellebrekers, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2009
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects
M C Y de Wit, J M Kros, D J J Halley, et al.
Journal of Clinical and Experimental Neuropsychology
|
October 7, 2005
Increased prevalences of left-handedness and left-eye sighting dominance in individuals with Williams-Beuren syndrome
J W Van Strien, G C Lagers-Van Haselen, J M Van Hagen, et al.
Page
of 5