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Epilepsia
|
July 22, 1998
Intractable epilepsy in a population-based series of mentally retarded children
U Steffenburg, A Hedström, A Lindroth, et al.
Journal of Medical Genetics
|
September 6, 2005
Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)
J Schoumans, C Ruivenkamp, E Holmberg, et al.
European Child & Adolescent Psychiatry
|
December 1, 1996
Transient psychosis in a girl with epilepsy and continuous spikes and waves during slow sleep (CSWS)
M Kyllerman, A Nydén, N Praquin, et al.
Acta Paediatrica Scandinavica
|
January 1, 1985
Children of alcoholic mothers. Growth and motor performance compared to matched controls
M Kyllerman, M Aronson, K G Sabel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene
T Martinsson, A Oldfors, N Darin, et al.
Lakartidningen
|
February 1, 1995
[Gene amplification in viral CNS infections. Rapid diagnostic identification of herpesviruses]
T Bergström, S Olofsson, M Studahl, et al.
Neurology
|
March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age
H Tajsharghi, L-E Thornell, N Darin, et al.
Lakartidningen
|
September 14, 1977
[Alcohol and pregnancy]
M Aronsson, C Carlsson, P R Johansson, et al.
Clinical Genetics
|
May 1, 1990
X-linked myotubular myopathy: a linkage study
C Darnfors, H E Larsson, A Oldfors, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1994
Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations
M Kyllerman, O H Skjeldal, M Lundberg, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 80) with videos related to
Sort By:
Page
of 8
Epilepsia
|
July 22, 1998
Intractable epilepsy in a population-based series of mentally retarded children
U Steffenburg, A Hedström, A Lindroth, et al.
Journal of Medical Genetics
|
September 6, 2005
Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)
J Schoumans, C Ruivenkamp, E Holmberg, et al.
European Child & Adolescent Psychiatry
|
December 1, 1996
Transient psychosis in a girl with epilepsy and continuous spikes and waves during slow sleep (CSWS)
M Kyllerman, A Nydén, N Praquin, et al.
Acta Paediatrica Scandinavica
|
January 1, 1985
Children of alcoholic mothers. Growth and motor performance compared to matched controls
M Kyllerman, M Aronson, K G Sabel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene
T Martinsson, A Oldfors, N Darin, et al.
Lakartidningen
|
February 1, 1995
[Gene amplification in viral CNS infections. Rapid diagnostic identification of herpesviruses]
T Bergström, S Olofsson, M Studahl, et al.
Neurology
|
March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age
H Tajsharghi, L-E Thornell, N Darin, et al.
Lakartidningen
|
September 14, 1977
[Alcohol and pregnancy]
M Aronsson, C Carlsson, P R Johansson, et al.
Clinical Genetics
|
May 1, 1990
X-linked myotubular myopathy: a linkage study
C Darnfors, H E Larsson, A Oldfors, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1994
Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations
M Kyllerman, O H Skjeldal, M Lundberg, et al.
Page
of 8