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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 5, 2002
Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases
Y Lindenbaum, D Dickson, P Rosenbaum, et al.
Annals of Neurology
|
May 1, 1981
Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features
J E Goldman, D Katz, I Rapin, et al.
Cancer
|
March 1, 1976
Primary intracranial Burkitt's lymphoma in an infant
M P Valsamis, P H Levine, I Rapin, et al.
Neurology
|
February 24, 2001
Cockayne syndrome and xeroderma pigmentosum
I Rapin, Y Lindenbaum, D W Dickson, et al.
Acta Neuropathologica
|
January 1, 1980
The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients
J E Goldman, T Yamanaka, I Rapin, et al.
Neurology
|
July 13, 2005
Epileptiform EEG abnormalities in children with language regression
K A McVicar, K Ballaban-Gil, I Rapin, et al.
Journal of Child Neurology
|
January 1, 1988
Spino-cerebellar degeneration with polyneuropathy associated with ceroid lipofuscinosis in one family
K E Wisniewski, R E Madrid, M Dambska, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 23, 1998
Joubert syndrome associated with multicystic kidney disease and hepatic fibrosis
D M Silverstein, L Zacharowicz, M Edelman, et al.
Acta Neuropathologica
|
December 19, 1975
GM2-gangliosidosis, AB variant: clinico-pathological study of a case
C M de Baecque, K Suzuki, I Rapin, et al.
Journal of Child Neurology
|
December 6, 2001
Etiology and pathophysiology of autistic behavior: clues from two cases with an unusual variant of neuroaxonal dystrophy
K M Weidenheim, L Goodman, D W Dickson, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 121) with videos related to
Sort By:
Page
of 13
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 5, 2002
Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases
Y Lindenbaum, D Dickson, P Rosenbaum, et al.
Annals of Neurology
|
May 1, 1981
Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features
J E Goldman, D Katz, I Rapin, et al.
Cancer
|
March 1, 1976
Primary intracranial Burkitt's lymphoma in an infant
M P Valsamis, P H Levine, I Rapin, et al.
Neurology
|
February 24, 2001
Cockayne syndrome and xeroderma pigmentosum
I Rapin, Y Lindenbaum, D W Dickson, et al.
Acta Neuropathologica
|
January 1, 1980
The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients
J E Goldman, T Yamanaka, I Rapin, et al.
Neurology
|
July 13, 2005
Epileptiform EEG abnormalities in children with language regression
K A McVicar, K Ballaban-Gil, I Rapin, et al.
Journal of Child Neurology
|
January 1, 1988
Spino-cerebellar degeneration with polyneuropathy associated with ceroid lipofuscinosis in one family
K E Wisniewski, R E Madrid, M Dambska, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 23, 1998
Joubert syndrome associated with multicystic kidney disease and hepatic fibrosis
D M Silverstein, L Zacharowicz, M Edelman, et al.
Acta Neuropathologica
|
December 19, 1975
GM2-gangliosidosis, AB variant: clinico-pathological study of a case
C M de Baecque, K Suzuki, I Rapin, et al.
Journal of Child Neurology
|
December 6, 2001
Etiology and pathophysiology of autistic behavior: clues from two cases with an unusual variant of neuroaxonal dystrophy
K M Weidenheim, L Goodman, D W Dickson, et al.
Page
of 13