Possible use of CSF glycosphingolipids for the diagnosis and therapeutic monitoring of lysosomal storage diseasesKAYE, E. M; ULLMAN, M. D; KOLODNY, E. H et al.Neurology. 1992, Vol 42, Num 12, pp 2290-2294, issn 0028-3878Article

Myelopathy in neonatal and infantile lupus erythematosusKAYE, E. M; BUTLER, I. J; CONLEY, S et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 7, pp 923-926, issn 0022-3050Article

Transient neonatal hyperglycinemiaSCHIFFMANN, R; KAYE, E. M; WILLIS, J. K. III et al.Annals of neurology. 1989, Vol 25, Num 2, pp 201-203, issn 0364-5134Article

Nervous system involvement in Fabry's disease: clinicopathological and biochemical correlationKAYE, E. M; KOLODNY, E. H; LOGIGIAN, E. L et al.Annals of neurology. 1988, Vol 23, Num 5, pp 505-509, issn 0364-5134Article

CT and MR appearance of the brain in two children with molybdenum cofactor deficiencyAPPIGNANI, B. A; KAYE, E. M; WOLPERT, S. M et al.American journal of neuroradiology. 1996, Vol 17, Num 2, pp 317-320, issn 0195-6108Article

Separation and quantitation of perbenzoylated glucocerebroside and galactocerebroside by high-performance liquid chromatographyKAYE, E. M; ULLMAN, M. D.Analytical biochemistry. 1984, Vol 138, Num 2, pp 380-385, issn 0003-2697Article

Mitochondrial activity in Pompe's diseaseSELAK, M. A; DE CHADAREVIAN, J. P; MELVIN, J. J et al.Pediatric neurology. 2000, Vol 23, Num 1, pp 54-57, issn 0887-8994Article

Acetazolamide and furosemide for posthemorrhagic hydrocephalus of the newbornLIBENSON, M. H; KAYE, E. M; ROSMAN, N. P et al.Pediatric neurology. 1999, Vol 20, Num 3, pp 185-191, issn 0887-8994Article

Childhood ataxia with diffuse central nervous system hypomyelinationSCHIFFMANN, R; MOLLER, J. R; HEISS, J. D et al.Annals of neurology. 1994, Vol 35, Num 3, pp 331-340, issn 0364-5134Article

A controlled trial of diazepam administered during febrile illnesses to prevent recurrence of febrile seizuresROSMAN, N. P; COLTON, T; LABAZZO, J et al.The New England journal of medicine. 1993, Vol 329, Num 2, pp 79-84, issn 0028-4793Article

TYpe 2 and type 3 Gaucher disease: a morphological and biochemical studyKAYE, E. M; ULLMAN, M. D; WILSON, E. R et al.Annals of neurology. 1986, Vol 20, Num 2, pp 223-230, issn 0364-5134Article

Congenital cardiomyopathy and pulmonary hypertension: Another fatal variant of cytochrome-c oxidase deficiencyVENDITTI, C. P; HARRIS, M. C; TAY, S et al.Journal of inherited metabolic disease. 2004, Vol 27, Num 6, pp 735-739, issn 0141-8955, 5 p.Article

Correction of acid β-galactosidase deficiency in GM₁ gangliosidosis human fibroblasts by retrovirus vector-mediated gene transfer : Higher efficiency of release and cross-correction by the murine enzymeSENA-ESTEVES, M; CAMP, S. M; ALROY, J et al.Human gene therapy. 2000, Vol 11, Num 5, pp 715-727, issn 1043-0342Article

Retarded bone formation in G_M1-gangliosidosis : a study of the infantile form and comparison with two canine modelsALROY, J; KNOWLES, K; SCHELLING, S. H et al.Virchows Archiv. 1995, Vol 426, Num 2, pp 141-148, issn 0945-6317Article

Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy : clinical and molecular studiesKAYE, E. M; DOLL, R. F; NATOWICZ, M. R et al.Annals of neurology. 1994, Vol 36, Num 6, pp 916-919, issn 0364-5134Article

Dysmyelinogenesis in animal model of GM₁ gangliosidosisKAYE, E. M; ALROY, J; RAGHAVAN, S. S et al.Pediatric neurology. 1992, Vol 8, Num 4, pp 255-261, issn 0887-8994Article

Neonatal idiopathic cerebral venous thrombosis : an unrecognized cause of transient seizures or lethargyRIVKIN, M. J; ANDERSON, M. L; KAYE, E. M et al.Annals of neurology. 1992, Vol 32, Num 1, pp 51-56, issn 0364-5134Article