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Results: 1-14 |
Results: 14
GENETIC PEROXISOMAL DISORDERS - WHY, WHEN, AND HOW TO TEST
Authors: MOSER HW RAYMOND GV
Citation: Hw. Moser et Gv. Raymond, GENETIC PEROXISOMAL DISORDERS - WHY, WHEN, AND HOW TO TEST, Annals of neurology, 44(5), 1998, pp. 713-715
TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996
Authors: BEATY TH MAESTRI NE HETMANSKI JB WYSZYNSKI DF VANDERKOLK CA SIMPSON JC MCINTOSH I SMITH EA ZEIGER JS RAYMOND GV PANNY SR TIFFT CJ LEWANDA AF CRISTION CA WULFSBERG EA
Citation: Th. Beaty et al., TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996, The Cleft palate-craniofacial journal, 34(5), 1997, pp. 447-454
DOCOSAHEXAENOIC ACID THERAPY IN PEROXISOME BIOGENESIS DISORDERS
Authors: RAYMOND GV MOSER AB MOSER HW
Citation: Gv. Raymond et al., DOCOSAHEXAENOIC ACID THERAPY IN PEROXISOME BIOGENESIS DISORDERS, Annals of neurology, 42(3), 1997, pp. 41-41
CRYPTIC TERMINAL REARRANGEMENT OF CHROMOSOME 22Q13.32 DETECTED BY FISH IN 2 UNRELATED PATIENTS
Authors: DOHENY KF MCDERMID HE HARUM K THOMAS GH RAYMOND GV
Citation: Kf. Doheny et al., CRYPTIC TERMINAL REARRANGEMENT OF CHROMOSOME 22Q13.32 DETECTED BY FISH IN 2 UNRELATED PATIENTS, Journal of Medical Genetics, 34(8), 1997, pp. 640-644
ABNORMALITIES IN POLYUNSATURATED FATTY-ACIDS IN PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY
Authors: SOTO EG THEDA C MOSER AB MOSER HW RAYMOND GV
Citation: Eg. Soto et al., ABNORMALITIES IN POLYUNSATURATED FATTY-ACIDS IN PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY, American journal of human genetics, 61(4), 1997, pp. 1459-1459
PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY - AN ATYPICAL PRESENTATION
Authors: RAYMOND GV SOTO EG THEDA C MOSER AB MOSER HW
Citation: Gv. Raymond et al., PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY - AN ATYPICAL PRESENTATION, American journal of human genetics, 61(4), 1997, pp. 1512-1512
IMPROVED TISSUE CHARACTERIZATION IN ADRENOLEUKODYSTROPHY USING MAGNETIZATION-TRANSFER IMAGING
Authors: MELHEM ER BREITER SN ULUG AM RAYMOND GV MOSER HW
Citation: Er. Melhem et al., IMPROVED TISSUE CHARACTERIZATION IN ADRENOLEUKODYSTROPHY USING MAGNETIZATION-TRANSFER IMAGING, American journal of roentgenology, 166(3), 1996, pp. 689-695
HIPPOCAMPUS IN AUTISM - A GOLGI ANALYSIS
Authors: RAYMOND GV BAUMAN ML KEMPER TL
Citation: Gv. Raymond et al., HIPPOCAMPUS IN AUTISM - A GOLGI ANALYSIS, Acta Neuropathologica, 91(1), 1996, pp. 117-119
DISTINCTION BETWEEN PEROXISOMAL BIFUNCTIONAL ENZYME AND ACYL-COA OXIDASE DEFICIENCIES
Authors: WATKINS PA MCGUINNESS MC RAYMOND GV HICKS BA SISK JM MOSER AB MOSER HW
Citation: Pa. Watkins et al., DISTINCTION BETWEEN PEROXISOMAL BIFUNCTIONAL ENZYME AND ACYL-COA OXIDASE DEFICIENCIES, Annals of neurology, 38(3), 1995, pp. 472-477
TUMOR-NECROSIS-FACTOR-ALPHA AND X-LINKED ADRENOLEUKODYSTROPHY
Authors: MCGUINNESS MC GRIFFIN DE RAYMOND GV WASHINGTON CA MOSER HW SMITH KD
Citation: Mc. Mcguinness et al., TUMOR-NECROSIS-FACTOR-ALPHA AND X-LINKED ADRENOLEUKODYSTROPHY, Journal of neuroimmunology, 61(2), 1995, pp. 161-169
TERATOGEN UPDATE - ERGOT AND ERGOTAMINE
Authors: RAYMOND GV
Citation: Gv. Raymond, TERATOGEN UPDATE - ERGOT AND ERGOTAMINE, Teratology, 51(5), 1995, pp. 344-347
ANTICONVULSANT TERATOGENESIS .3. POSSIBLE METABOLIC BASIS
Authors: RAYMOND GV BUEHLER BA FINNELL RH HOLMES LB
Citation: Gv. Raymond et al., ANTICONVULSANT TERATOGENESIS .3. POSSIBLE METABOLIC BASIS, Teratology, 51(2), 1995, pp. 55-56
HEAD CIRCUMFERENCE STANDARDS IN NEONATES
Authors: RAYMOND GV HOLMES LB
Citation: Gv. Raymond et Lb. Holmes, HEAD CIRCUMFERENCE STANDARDS IN NEONATES, Journal of child neurology, 9(1), 1994, pp. 63-66
BIOCHEMICAL AND CLINICAL DISTINCTION BETWEEN PEROXISOMAL BIFUNCTIONALENZYME DEFICIENCY AND ACYL-COA OXIDASE DEFICIENCY
Authors: WATKINS PA MCGUINNESS MC RAYMOND GV RASMUSSEN M MOSER AB MOSER HW
Citation: Pa. Watkins et al., BIOCHEMICAL AND CLINICAL DISTINCTION BETWEEN PEROXISOMAL BIFUNCTIONALENZYME DEFICIENCY AND ACYL-COA OXIDASE DEFICIENCY, Annals of neurology, 36(3), 1994, pp. 492-492
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