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

Volltext

Docosahexaenoic acid therapy in peroxisomal diseases: Results of a double-blind, randomized trial von PAKER, A. M, SUNNESS, J. S, BRERETON, N. H, SPEEDIE, L. J, ALBANNA, L, DHARMARAJ, S, MOSER, A. B, JONES, R. O, RAYMOND, G. V

Volltext

De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females von Webster, R., Cho, M.T., Retterer, K., Millan, F., Nowak, C., Douglas, J., Ahmad, A., Raymond, G.V., Johnson, M.R., Pujol, A., Begtrup, A., McKnight, D., Devinsky, O., Chung, W.K.

Volltext

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

Volltext

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients von GOROSPE, J. R, NAIDU, S, DE VIVO, D, VAN DER KNAAP, M. S, MESSING, A, BRENNER, M, HOFFMAN, E. P, JOHNSON, A. B, PURI, V, RAYMOND, G. V, JENKINS, S. D, PEDERSEN, R. C, LEWIS, D, KNOWLES, P, FERNANDEZ, R

Volltext

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.

Volltext

Hippocampus in autism : a Golgi analysis von RAYMOND, G. V, BAUMAN, M. L, KEMPER, T. L

Volltext

Newborn screening for X-linked adrenoleukodystrophy in New York State: Diagnostic protocol, surveillance protocol and treatment guidelines von Vogel, B.H., Bradley, S.E., Adams, D.J., D'Aco, K., Erbe, R.W., Fong, C., Iglesias, A., Kronn, D., Levy, P., Morrissey, M., Orsini, J., Parton, P., Pellegrino, J., Saavedra-Matiz, C.A., Shur, N., Wasserstein, M., Raymond, G.V., Caggana, M.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Intensity of MRI Gadolinium Enhancement in Cerebral Adrenoleukodystrophy: A Biomarker for Inflammation and Predictor of Outcome following Transplantation in Higher Risk Patients von Miller, W P, Mantovani, L F, Muzic, J, Rykken, J B, Gawande, R S, Lund, T C, Shanley, R M, Raymond, G V, Orchard, P J, Nascene, D R

Volltext

Childhood Cerebral Adrenoleukodystrophy: MR Perfusion Measurements and Their Use in Predicting Clinical Outcome after Hematopoietic Stem Cell Transplantation von McKinney, A M, Benson, J C, Nascene, D R, Eisengart, J, Salmela, M B, Loes, D J, Zhang, L, Patel, K, Raymond, G V, Miller, W P

Volltext

X-linked Adrenoleukodystrophy: The Role of Contrast-enhanced MR Imaging in Predicting Disease Progression von Melhem, Elias R, Loes, Daniel J, Georgiades, Christos S, Raymond, Gerald V, Moser, Hugo W

Volltext

Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy von FATEMI, A, SMITH, S. A, DUBEY, P, ZACKOWSKI, K. M, BASTIAN, A. J, VAN ZIJL, P. C, MOSER, H. W, RAYMOND, G. V, GOLAY, X

Volltext

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.

Volltext

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations von Kemp, Stephan, Pujol, Aurora, Waterham, Hans R., van Geel, Björn M., Boehm, Corinne D., Raymond, Gerald V., Cutting, Garry R., Wanders, Ronald J.A., Moser, Hugo W.

Volltext

Plasma and red blood cell fatty acids in peroxisomal disorders von MOSER, A. B, JONES, D. S, RAYMOND, G. V, MOSER, H. W

Volltext