AAAAAA
Results: 1-25/43
Authors:
Matsumoto, N
Tamura, S
Moser, A
Moser, HW
Braverman, N
Suzuki, Y
Shimozawa, N
Kondo, N
Fujiki, Y
Citation: N. Matsumoto et al., The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6, J HUM GENET, 46(5), 2001, pp. 273-277
Authors:
Berger, J
Moser, HW
Forss-Petter, S
Citation: J. Berger et al., Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment, CURR OP NEU, 14(3), 2001, pp. 305-312
Authors:
Watkins, PA
Hamilton, JA
Leaf, A
Spector, AA
Moore, SA
Anderson, RE
Moser, HW
Noetzel, MJ
Katz, R
Citation: Pa. Watkins et al., Brain uptake and utilization of fatty acids - Applications to peroxisomal biogenesis diseases, J MOL NEURO, 16(2-3), 2001, pp. 87-92
Authors:
Faust, PL
Su, HM
Moser, A
Moser, HW
Citation: Pl. Faust et al., The peroxisome deficient PEX2 Zellweger mouse - Pathologic and biochemicalcorrelates of lipid dysfunction, J MOL NEURO, 16(2-3), 2001, pp. 289-297
Authors:
Katz, R
Hamilton, JA
Spector, AA
Moore, SA
Moser, HW
Noetzel, MJ
Watkins, PA
Citation: R. Katz et al., Brain uptake and utilization of fatty acids - Recommendations for future research, J MOL NEURO, 16(2-3), 2001, pp. 333-335
Authors:
Bezman, L
Moser, AB
Raymond, GV
Rinaldo, P
Watkins, PA
Smith, KD
Kass, NE
Moser, HW
Citation: L. Bezman et al., Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening, ANN NEUROL, 49(4), 2001, pp. 512-517
Authors:
Powers, JM
Rosenblatt, DS
Schmidt, RE
Cross, AH
Black, JT
Moser, AB
Moser, HW
Morgan, DJ
Citation: Jm. Powers et al., Neurological and neuropathologic heterogeneity in two brothers with cobalamin C deficiency, ANN NEUROL, 49(3), 2001, pp. 396-400
Authors:
van Geel, BM
Bezman, L
Loes, DJ
Moser, HW
Raymond, GV
Citation: Bm. Van Geel et al., Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy, ANN NEUROL, 49(2), 2001, pp. 186-194
Authors:
Melhem, ER
Gotwald, TF
Itoh, R
Zinreich, SJ
Moser, HW
Citation: Er. Melhem et al., T2 relaxation measurements in X-linked adrenoleukodystrophy performed using dual-echo fast fluid-attenuated inversion recovery MR imaging, AM J NEUROR, 22(4), 2001, pp. 773-776
Authors:
Ito, R
Melhem, ER
Mori, S
Eichler, FS
Raymond, GV
Moser, HW
Citation: R. Ito et al., Diffusion tensor brain MR imaging in X-linked cerebral adrenoleukodystrophy, NEUROLOGY, 56(4), 2001, pp. 544-547
Authors:
Powers, JM
DeCiero, DP
Cox, C
Richfield, EK
Ito, M
Boser, AB
Moser, HW
Citation: Jm. Powers et al., The dorsal root ganglia in adrenomyeloneuropathy: Neuronal atrophy and abnormal mitochondria, J NE EXP NE, 60(5), 2001, pp. 493-501
Authors:
Ito, M
Blumberg, BM
Mock, DJ
Goodman, AD
Moser, AB
Moser, HW
Smith, KD
Powers, JM
Citation: M. Ito et al., Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: Morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation, J NE EXP NE, 60(10), 2001, pp. 1004-1019
Authors:
Williard, DE
Nwankwo, JO
Kaduce, TL
Harmon, SD
Irons, M
Moser, HW
Raymond, GV
Spector, AA
Citation: De. Williard et al., Identification of a fatty acid Delta(6)-desaturase deficiency in human skin fibroblasts, J LIPID RES, 42(4), 2001, pp. 501-508
Authors:
Su, HM
Moser, AB
Moser, HW
Watkins, PA
Citation: Hm. Su et al., Peroxisomal straight-chain acyl-CoA oxidase and D-bifunctional protein areessential for the retroconversion step in docosahexaenoic acid synthesis, J BIOL CHEM, 276(41), 2001, pp. 38115-38120
Authors:
Moser, HW
Raymond, GV
Citation: Hw. Moser et Gv. Raymond, Docosahexaenoic acid therapy for disorders of peroxisome biogenesis, NUTR HLTH, 2001, pp. 257-271
Authors:
Moser, HW
Citation: Hw. Moser, Molecular genetics of peroxisomal disorders, FRONT BIOSC, 5, 2000, pp. D298-D306
Authors:
Lachtermacher, MBR
Seuanez, HN
Moser, AB
Moser, HW
Smith, KD
Citation: Mbr. Lachtermacher et al., Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described, HUM MUTAT, 15(4), 2000, pp. 348-353
Authors:
Kaufmann, WE
Moser, HW
Citation: We. Kaufmann et Hw. Moser, Dendritic anomalies in disorders associated with mental retardation, CEREB CORT, 10(10), 2000, pp. 981-991
Authors:
Lachtermacher, MBR
Seuanez, HN
Moser, HW
Smith, KD
Citation: Mbr. Lachtermacher et al., One-step multiplex PCR strategy for identification of mutations by SSCP and DNA sequencing, BIOTECHNIQU, 29(2), 2000, pp. 234
Authors:
Yeager, AM
Uhas, KA
Coles, CD
Davis, PC
Krause, WL
Moser, HW
Citation: Am. Yeager et al., Bone marrow transplantation for infantile ceramidase deficiency (Farber disease), BONE MAR TR, 26(3), 2000, pp. 357-363
Authors:
Santos, MJ
Henderson, SC
Moser, AB
Moser, HW
Lazarow, PB
Citation: Mj. Santos et al., Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger Syndrome: A confocal laser scanning microscopy study, BIO CELL, 92(2), 2000, pp. 85-94
Authors:
Melhem, ER
Loes, DJ
Georgiades, CS
Raymond, GV
Moser, HW
Citation: Er. Melhem et al., X-linked adrenoleukodystrophy: The role of contrast-enhanced MR imaging inpredicting disease progression, AM J NEUROR, 21(5), 2000, pp. 839-844
Authors:
Moser, HW
Loes, DJ
Melhem, ER
Raymond, GV
Bezman, L
Cox, CS
Lu, SE
Citation: Hw. Moser et al., X-linked adrenoleukodystrophy: Overview and prognosis as a function of ageand brain magnetic resonance imaging abnormality. A study involving 372 patients, NEUROPEDIAT, 31(5), 2000, pp. 227-239
Authors:
Moser, HW
Bezman, L
Lu, SE
Raymond, GV
Citation: Hw. Moser et al., Therapy of X-linked adrenoleukodystrophy: Prognosis based upon age and MRIabnormality and plans for placebo-controlled trials, J INH MET D, 23(3), 2000, pp. 273-277
Authors:
Powers, JM
DeCiero, DP
Ito, M
Moser, AB
Moser, HW
Citation: Jm. Powers et al., Adrenomyeloneuropathy: A neuropathologic review featuring its noninflammatory myelopathy, J NE EXP NE, 59(2), 2000, pp. 89-102