Lecturer on Neurology, Boston Children's Hospital

Neurology

Edward Kaye is an expert in the field of Neurology. He graduated from Loyola University Chicago Stritch School of Medicine. Edward Kaye is also published. He has 46 publications published. The lastest publication: "Angiocentric CD3(+) T-cell infiltrates in human immunodeficiency virus type 1-associated central nervous system disease in children.'

Publications

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• Antisense oligonucleotides delivered to the mouse CNS ameliorate symptoms of severe spinal muscular atrophy.
• Niemann-Pick C disease: not your average lysosomal storage disease.
• Does gender parity exist in Fabry disease?
• Pediatric physical functioning reference curves.
• Where has all the white matter gone? Unraveling the mysteries of leukoencephalopathies.
• Newborn screening by tandem mass spectrometry for medium-chain Acyl-CoA dehydrogenase deficiency: a cost-effectiveness analysis.
• What does it mean to be a carrier for a metabolic disease?
• Gene therapy for the central nervous system in the lysosomal storage disorders.
• Infantile leukoencephalopathy owing to mitochondrial enzyme dysfunction.
• Lysosomal Storage Diseases.
• Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storage.
• Retarded bone formation in GM1-gangliosidosis: a study of the infantile form and comparison with two canine models.
• CT and MR appearance of the brain in two children with molybdenum cofactor deficiency.
• N. Paul Rosman, MD: scholar, teacher, clinician, and humanist.
• Neonatal idiopathic cerebral venous thrombosis: an unrecognized cause of transient seizures or lethargy.
• Transient neonatal hyperglycinemia.
• Creatin' news.
• Amino acids and the brain: too much, too little, or just inappropriate use of a good thing?
• Transient post-traumatic cortical blindness: brief v prolonged syndromes in childhood.
• Seizures in bacterial meningitis: prevalence, patterns, pathogenesis, and prognosis.
• Chronic epidural hematomas in childhood: increased recognition and non-surgical management.
• beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosis.
• Acetazolamide and furosemide for posthemorrhagic hydrocephalus of the newborn.
• Diagnosis and management of mitochondrial diseases.
• Hyaluronidase increases the biodistribution of acid alpha-1,4 glucosidase in the muscle of Pompe disease mice: an approach to enhance the efficacy of enzyme replacemen...
• Infantile G(M1) gangliosidosis: complete morphology and histochemistry of two autopsy cases, with particular reference to delayed central nervous system myelination.
• Neonatal herpes simplex meningoencephalitis associated with fetal monitor scalp electrodes.
• Modified encephaloduroarteriosynangiosis as a surgical treatment of childhood moyamoya disease: report of five cases.
• Therapeutic approaches to lysosomal storage diseases.
• Angiocentric CD3(+) T-cell infiltrates in human immunodeficiency virus type 1-associated central nervous system disease in children.
• Nervous system involvement in Fabry's disease: clinicopathological and biochemical correlation.
• Dysmyelinogenesis in animal model of GM1 gangliosidosis.
• Correction of acid beta-galactosidase deficiency in GM1 gangliosidosis human fibroblasts by retrovirus vector-mediated gene transfer: higher efficiency of release and ...
• Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency.
• Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy: clinical and molecular studies.
• Possible use of CSF glycosphingolipids for the diagnosis and therapeutic monitoring of lysosomal storage diseases.
• Type 2 and type 3 Gaucher disease: a morphological and biochemical study.
• Ultrastructural findings in skin from patients with Niemann-Pick disease, type C.
• Electron microscopic examination of skin biopsy as a cost-effective tool in the diagnosis of lysosomal storage diseases.
• Update on genetic disorders affecting white matter.
• Mitochondrial activity in Pompe's disease.
• Lactic acid elevation in extramitochondrial childhood neurodegenerative diseases.
• MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.
• Myelin lesions associated with lysosomal and peroxisomal disorders.
• [Central nervous system involvement in Gaucher disease].

Schools

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• Loyola University of Chicago Stritch School of Medicine

• Weill Cornell Medical College

• Foster McGaw

• Boston City Hospital

Doctors Specialties

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• Pediatric Neurology
• Pediatrics
• Neurology

Accepted Insurances

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Education

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• Boston University Medical Center
• Loyola University
• Loyola University Chicago Stritch School of Medicine

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