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I Rapin

Showing results (91-100 of 121) with videos related to

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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 casesY Lindenbaum, D Dickson, P Rosenbaum, et al.
Annals of Neurology|May 1, 1981
Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological featuresJ E Goldman, D Katz, I Rapin, et al.
Cancer|March 1, 1976
Primary intracranial Burkitt's lymphoma in an infantM P Valsamis, P H Levine, I Rapin, et al.
Neurology|February 24, 2001
Cockayne syndrome and xeroderma pigmentosumI 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 patientsJ E Goldman, T Yamanaka, I Rapin, et al.
Neurology|July 13, 2005
Epileptiform EEG abnormalities in children with language regressionK 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 familyK 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 fibrosisD M Silverstein, L Zacharowicz, M Edelman, et al.
Acta Neuropathologica|December 19, 1975
GM2-gangliosidosis, AB variant: clinico-pathological study of a caseC 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 dystrophyK M Weidenheim, L Goodman, D W Dickson, et al.
Pageof 13

Showing results (91-100 of 121) with videos related to

Sort By:
Pageof 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 casesY Lindenbaum, D Dickson, P Rosenbaum, et al.
Annals of Neurology|May 1, 1981
Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological featuresJ E Goldman, D Katz, I Rapin, et al.
Cancer|March 1, 1976
Primary intracranial Burkitt's lymphoma in an infantM P Valsamis, P H Levine, I Rapin, et al.
Neurology|February 24, 2001
Cockayne syndrome and xeroderma pigmentosumI 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 patientsJ E Goldman, T Yamanaka, I Rapin, et al.
Neurology|July 13, 2005
Epileptiform EEG abnormalities in children with language regressionK 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 familyK 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 fibrosisD M Silverstein, L Zacharowicz, M Edelman, et al.
Acta Neuropathologica|December 19, 1975
GM2-gangliosidosis, AB variant: clinico-pathological study of a caseC 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 dystrophyK M Weidenheim, L Goodman, D W Dickson, et al.
Pageof 13