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E M Kaye

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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 14, 1999
Infantile G(M1) gangliosidosis: complete morphology and histochemistry of two autopsy cases, with particular reference to delayed central nervous system myelinationR D Folkerth, J Alroy, I Bhan, et al.
Pediatric Neurology|September 1, 1985
Seizures in bacterial meningitis: prevalence, patterns, pathogenesis, and prognosisN P Rosman, D B Peterson, E M Kaye, et al.
Pediatric Neurology|July 1, 1985
Chronic epidural hematomas in childhood: increased recognition and non-surgical managementE M Kaye, P R Cass, E Dooling, et al.
Annals of Neurology|February 1, 1989
Transient neonatal hyperglycinemiaR Schiffmann, E M Kaye, J K Willis, et al.
Annals of Neurology|December 1, 1994
Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy: clinical and molecular studiesE M Kaye, R F Doll, M R Natowicz, et al.
Pediatric Neurology|April 20, 1999
Acetazolamide and furosemide for posthemorrhagic hydrocephalus of the newbornM H Libenson, E M Kaye, N P Rosman, et al.
Annals of Neurology|May 1, 1988
Nervous system involvement in Fabry's disease: clinicopathological and biochemical correlationE M Kaye, E H Kolodny, E L Logigian, et al.
Annals of Neurology|August 1, 1986
Type 2 and type 3 Gaucher disease: a morphological and biochemical studyE M Kaye, M D Ullman, E R Wilson, et al.
Virchows Archiv : an International Journal of Pathology|January 1, 1995
Retarded bone formation in GM1-gangliosidosis: a study of the infantile form and comparison with two canine modelsJ Alroy, K Knowles, S H Schelling, et al.
Neurology|December 1, 1992
Possible use of CSF glycosphingolipids for the diagnosis and therapeutic monitoring of lysosomal storage diseasesE M Kaye, M D Ullman, E H Kolodny, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 14, 1999
Infantile G(M1) gangliosidosis: complete morphology and histochemistry of two autopsy cases, with particular reference to delayed central nervous system myelinationR D Folkerth, J Alroy, I Bhan, et al.
Pediatric Neurology|September 1, 1985
Seizures in bacterial meningitis: prevalence, patterns, pathogenesis, and prognosisN P Rosman, D B Peterson, E M Kaye, et al.
Pediatric Neurology|July 1, 1985
Chronic epidural hematomas in childhood: increased recognition and non-surgical managementE M Kaye, P R Cass, E Dooling, et al.
Annals of Neurology|February 1, 1989
Transient neonatal hyperglycinemiaR Schiffmann, E M Kaye, J K Willis, et al.
Annals of Neurology|December 1, 1994
Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy: clinical and molecular studiesE M Kaye, R F Doll, M R Natowicz, et al.
Pediatric Neurology|April 20, 1999
Acetazolamide and furosemide for posthemorrhagic hydrocephalus of the newbornM H Libenson, E M Kaye, N P Rosman, et al.
Annals of Neurology|May 1, 1988
Nervous system involvement in Fabry's disease: clinicopathological and biochemical correlationE M Kaye, E H Kolodny, E L Logigian, et al.
Annals of Neurology|August 1, 1986
Type 2 and type 3 Gaucher disease: a morphological and biochemical studyE M Kaye, M D Ullman, E R Wilson, et al.
Virchows Archiv : an International Journal of Pathology|January 1, 1995
Retarded bone formation in GM1-gangliosidosis: a study of the infantile form and comparison with two canine modelsJ Alroy, K Knowles, S H Schelling, et al.
Neurology|December 1, 1992
Possible use of CSF glycosphingolipids for the diagnosis and therapeutic monitoring of lysosomal storage diseasesE M Kaye, M D Ullman, E H Kolodny, et al.
Pageof 4