Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy von Loes, D J, Fatemi, A, Melhem, E R, Gupte, N, Bezman, L, Moser, H W, Raymond, G V

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Adrenoleukodystrophy : phenotype, genetics, pathogenesis and therapy von MOSER, H. W

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Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls von Moser, Ann B., Kreiter, Nancy, Bezman, Lena, Lu, Shou-En, Raymond, Gerald V., Naidu, Sakkubai, Moser, Hugo W.

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Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy von EICHLER, F. S, BARKER, P. B, COX, C, EDWIN, D, ULUG, A. M, MOSER, H. W, RAYMOND, G. V

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Increase of pollinator attraction by means of a visual signal in the sexually deceptive orchid, Ophrys heldreichii (Orchidaceae) von Spaethe, J., Moser, W. H., Paulus, H. F.

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PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts von Steinberg, S. J, Snowden, A, Braverman, N. E, Chen, L, Watkins, P. A, Clayton, P. T, Setchell, K. D. R, Heubi, J. E, Raymond, G. V, Moser, A. B, Moser, H. W

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MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy von FATEMI, A, BARKER, P. B, ULUG, A. M, NAGAE-POETSCHER, L. M, BEAUCHAMP, N. J, MOSER, A. B, RAYMOND, G. V, MOSER, H. W, NAIDU, S

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Mutations in the PTS1 receptor gene, PXR1 , define complementation group 2 of the peroxisome biogenesis disorders von Dodt, Gabriele, Braverman, Nancy, Wong, Candice, Moser, Ann, Moser, Hugo W, Watkins, Paul, Valle, David, Gould, Stephen J

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Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy von POWERS, JAMES M, DECIERO, DAVID P, ITO, MASUMI, MOSER, ANN B, MOSER, HUGO W

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X-linked adrenoleukodystrophy : Overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patients von MOSER, H. W, LOES, D. J, MELHEM, E. R, RAYMOND, G. V, BEZMAN, Lena, COX, Christiane S, LU, Shou-En

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Diffusion tensor brain MR imaging in X-linked cerebral adrenoleukodystrophy von ITO, R, MELHEM, E. R, MORI, S, EICHLER, F. S, RAYMOND, G. V, MOSER, H. W

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Neuroimaging studies in Rett syndrome von Naidu, S., Kaufmann, W.E., Abrams, M.T., Pearlson, G.D., Lanham, D.C., Fredericksen, K.A., Barker, P.B., Horska, A., Golay, X., Mori, S., Wong, D.F., Yablonski, M., Moser, H.W., Johnston, M.V.

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Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders von Reuber, Bernadette E, Germain-Lee, Emily, Collins, Cynthia S, Morrell, James C, Ameritunga, Rohan, Moser, Hugo W, Valle, David, Gould, Stephen J

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Spectroscopic evidence of cerebral axonopathy in patients with pure adrenomyeloneuropathy von DUBEY, P, FATEMI, A, RAYMOND, G. V, BARKER, P. B, DEGAONKAR, M, TROEGER, M, ZACKOWSKI, K, BASTIAN, A, SMITH, S. A, POMPER, M. G, MOSER, H. W

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Dendritic Anomalies in Disorders Associated with Mental Retardation von Kaufmann, Walter E., Moser, Hugo W.

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Peroxisomal Bifunctional Protein Deficiency Revisited: Resolution of Its True Enzymatic and Molecular Basis von van Grunsven, E.G., van Berkel, E., Mooijer, P.A.W., Watkins, P.A., Moser, H.W., Suzuki, Y., Jiang, L.L., Hashimoto, T., Hoefler, G., Adamski, J., Wanders, R.J.A.

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Bone marrow transplantation for infantile ceramidase deficiency (Farber disease) von YEAGER, A. M, UHAS, K. A, COLES, C. D, DAVIS, P. C, KRAUSE, W, MOSER, H. W

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Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening von Bezman, Lena, Moser, Ann B., Raymond, Gerald V., Piero Rinaldo, Watkins, Paul A., Smith, Kirby D., Kass, Nancy E., Moser, Hugo W.

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Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders von Warren, Daniel S., Morrell, James C., Moser, Hugo W., Valle, David, Gould, Stephen J.

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The Inflammatory Myelinopathy of Adreno-Leukodystrophy: Cells, Effector Molecules, and Pathogenetic Implications von POWERS, JAMES M, LIU, YAN, MOSER, ANN B, MOSER, HUGO W

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