Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy
Loes, D J, Fatemi, A, Melhem, E R, Gupte, N, Bezman, L, Moser, H W, Raymond, G V
Published in Neurology (12.08.2003)
Published in Neurology (12.08.2003)
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Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy
Eichler, F S, Barker, P B, Cox, C, Edwin, D, Ulug, A M, Moser, H W, Raymond, G V
Published in Neurology (26.03.2002)
Published in Neurology (26.03.2002)
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PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts
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
Published in Journal of inherited metabolic disease (01.02.2009)
Published in Journal of inherited metabolic disease (01.02.2009)
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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
Moser, H W, Loes, D J, Melhem, E R, Raymond, G V, Bezman, L, Cox, C S, Lu, S E
Published in Neuropediatrics (01.10.2000)
Published in Neuropediatrics (01.10.2000)
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Diffusion tensor brain MR imaging in X-linked cerebral adrenoleukodystrophy
Ito, R, Melhem, E R, Mori, S, Eichler, F S, Raymond, G V, Moser, H W
Published in Neurology (27.02.2001)
Published in Neurology (27.02.2001)
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Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
Moser, Ann B., Kreiter, Nancy, Bezman, Lena, Lu, Shou-En, Raymond, Gerald V., Naidu, Sakkubai, Moser, Hugo W.
Published in Annals of neurology (01.01.1999)
Published in Annals of neurology (01.01.1999)
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Journal Article
MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy
Fatemi, A, Barker, P B, Uluğ, A M, Nagae-Poetscher, L M, Beauchamp, N J, Moser, A B, Raymond, G V, Moser, H W, Naidu, S
Published in Neurology (22.04.2003)
Published in Neurology (22.04.2003)
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Spectroscopic evidence of cerebral axonopathy in patients with "pure" adrenomyeloneuropathy
Dubey, P, Fatemi, A, Barker, P B, Degaonkar, M, Troeger, M, Zackowski, K, Bastian, A, Smith, S A, Pomper, M G, Moser, H W, Raymond, G V
Published in Neurology (25.01.2005)
Published in Neurology (25.01.2005)
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Neuroimaging studies in Rett syndrome
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.
Published in Brain & development (Tokyo. 1979) (01.12.2001)
Published in Brain & development (Tokyo. 1979) (01.12.2001)
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Conference Proceeding
Mutations in the PTS1 receptor gene, PXR1 , define complementation group 2 of the peroxisome biogenesis disorders
Dodt, Gabriele, Braverman, Nancy, Wong, Candice, Moser, Ann, Moser, Hugo W, Watkins, Paul, Valle, David, Gould, Stephen J
Published in Nature genetics (01.02.1995)
Published in Nature genetics (01.02.1995)
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Journal Article
Peroxisomal Bifunctional Protein Deficiency Revisited: Resolution of Its True Enzymatic and Molecular Basis
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.
Published in American journal of human genetics (1999)
Published in American journal of human genetics (1999)
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Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
Reuber, Bernadette E, Germain-Lee, Emily, Collins, Cynthia S, Morrell, James C, Ameritunga, Rohan, Moser, Hugo W, Valle, David, Gould, Stephen J
Published in Nature genetics (01.12.1997)
Published in Nature genetics (01.12.1997)
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The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor
Yahraus, T., Braverman, N., Dodt, G., Kalish, J. E., Morrell, J. C., Moser, H. W., Valle, D., Gould, S. J.
Published in The EMBO journal (17.06.1996)
Published in The EMBO journal (17.06.1996)
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Journal Article
MR findings in adult-onset adrenoleukodystrophy
Kumar, AJ, Kohler, W, Kruse, B, Naidu, S, Bergin, A, Edwin, D, Moser, HW
Published in American journal of neuroradiology : AJNR (01.06.1995)
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Published in American journal of neuroradiology : AJNR (01.06.1995)
Journal Article
Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities
de Vet, E C, Ijlst, L, Oostheim, W, Dekker, C, Moser, H W, van Den Bosch, H, Wanders, R J
Published in Journal of lipid research (01.11.1999)
Published in Journal of lipid research (01.11.1999)
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