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Arquivos De Neuro-Psiquiatria
|
March 1, 1989
Periodic hypersomnia, congenital ectodermal disorders and multiple exostosis
R Reimão, A Diament
Arquivos De Neuro-Psiquiatria
|
June 1, 1995
DOPA-sensitive progressive dystonia of childhood with diurnal fluctuations of symptoms: a case report
J L Gherpelli, L M Nagae, A Diament
Arquivos De Neuro-Psiquiatria
|
June 1, 1997
[Angelman syndrome: a frequently undiagnosed cause of mental retardation and epilepsy. Case report]
C Fridman, F Kok, A Diament, et al.
Arquivos De Neuro-Psiquiatria
|
September 1, 1993
[Infantile spinal amyotrophy with atypical course: report of 2 cases]
L M Ferreira, U C Reed, L J Silva, et al.
Journal of Medical Genetics
|
July 1, 1990
Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation
C P Koiffmann, A Diament, D H de Souza, et al.
American Journal of Medical Genetics
|
June 22, 2000
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients
C Fridman, M C Varela, F Kok, et al.
Arquivos De Neuro-Psiquiatria
|
June 1, 1988
Multiple sclerosis with early childhood onset. A case report
M I Vergani, R Reimão, A M Silva, et al.
Human Genetics
|
December 1, 1990
In search of a genetic basis for the Rett syndrome
P S Martinho, P G Otto, F Kok, et al.
Revista Do Hospital Das Clinicas
|
September 1, 1992
[Centronuclear (myotubular) myopathy: a case report]
U C Reed, A M Tsanaclis, L M Ferreira, et al.
Brain & Development
|
January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency
U C Reed, S K Marie, M Vainzof, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Arquivos De Neuro-Psiquiatria
|
March 1, 1989
Periodic hypersomnia, congenital ectodermal disorders and multiple exostosis
R Reimão, A Diament
Arquivos De Neuro-Psiquiatria
|
June 1, 1995
DOPA-sensitive progressive dystonia of childhood with diurnal fluctuations of symptoms: a case report
J L Gherpelli, L M Nagae, A Diament
Arquivos De Neuro-Psiquiatria
|
June 1, 1997
[Angelman syndrome: a frequently undiagnosed cause of mental retardation and epilepsy. Case report]
C Fridman, F Kok, A Diament, et al.
Arquivos De Neuro-Psiquiatria
|
September 1, 1993
[Infantile spinal amyotrophy with atypical course: report of 2 cases]
L M Ferreira, U C Reed, L J Silva, et al.
Journal of Medical Genetics
|
July 1, 1990
Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation
C P Koiffmann, A Diament, D H de Souza, et al.
American Journal of Medical Genetics
|
June 22, 2000
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients
C Fridman, M C Varela, F Kok, et al.
Arquivos De Neuro-Psiquiatria
|
June 1, 1988
Multiple sclerosis with early childhood onset. A case report
M I Vergani, R Reimão, A M Silva, et al.
Human Genetics
|
December 1, 1990
In search of a genetic basis for the Rett syndrome
P S Martinho, P G Otto, F Kok, et al.
Revista Do Hospital Das Clinicas
|
September 1, 1992
[Centronuclear (myotubular) myopathy: a case report]
U C Reed, A M Tsanaclis, L M Ferreira, et al.
Brain & Development
|
January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency
U C Reed, S K Marie, M Vainzof, et al.
Page
of 3