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Results: 1-9 |
Results: 9

Authors: Kaye, EM
Citation: Em. Kaye, Update on white matter genetic disorders - Response, PED NEUROL, 25(4), 2001, pp. 348-348

Authors: Kaye, EM
Citation: Em. Kaye, Update on genetic disorders affecting white matter, PED NEUROL, 24(1), 2001, pp. 11-24

Authors: Kang, PB Hunter, JV Kaye, EM
Citation: Pb. Kang et al., Lactic acid elevation in extramitochondrial childhood neurodegenerative diseases, J CHILD NEU, 16(9), 2001, pp. 657-660

Authors: Folkerth, RD Alroy, J Bhan, I Kaye, EM
Citation: Rd. Folkerth et al., Infantile G(M1) gangliosidosis complete morphology and histochemistry of two autopsy cases, with particular reference to delayed central nervous system myelination, PEDIATR D P, 3(1), 2000, pp. 73-86

Authors: Sena-Esteves, M Camp, SM Alroy, J Breakefield, XO Kaye, EM
Citation: M. Sena-esteves et al., Correction of acid beta-galactosidase deficiency in GM(1) gangliosidosis human fibroblasts by retrovirus vector-mediated gene transfer: Higher efficiency of release and cross-correction by the murine enzyme, HUM GENE TH, 11(5), 2000, pp. 715-727

Authors: Selak, MA de Chadarevian, JP Melvin, JJ Grover, WD Salganicoff, L Kaye, EM
Citation: Ma. Selak et al., Mitochondrial activity in Pompe's disease, PED NEUROL, 23(1), 2000, pp. 54-57

Authors: Katsetos, CD Fincke, JE Legido, A Lischner, HW de Chadarevian, JP Kaye, EM Platsoucas, CD Oleszak, EL
Citation: Cd. Katsetos et al., Angiocentric CD3(+) T-cell infiltrates in human immunodeficiency virus type 1-associated central nervous system disease in children, CL DIAG LAB, 6(1), 1999, pp. 105-114

Authors: Libenson, MH Kaye, EM Rosman, NP Gilmore, HE
Citation: Mh. Libenson et al., Acetazolamide and furosemide for posthemorrhagic hydrocephalus of the newborn, PED NEUROL, 20(3), 1999, pp. 185-191

Authors: Ross, BD Kaye, EM
Citation: Bd. Ross et Em. Kaye, Creatin' news, NEUROLOGY, 53(2), 1999, pp. 249-250
Risultati: 1-9 |