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Hugo Moser

Kennedy Krieger Institute, Baltimore, MD, United States 
Pediatric neurology, leukodystrophies
"Hugo Moser"


Mean distance: 14.27 (cluster 24)
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Steinberg SJ, Snowden A, Braverman NE, et al. (2009) A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts. Journal of Inherited Metabolic Disease. 32: 109-19
Smith SA, Golay X, Fatemi A, et al. (2009) Quantitative magnetization transfer characteristics of the human cervical spinal cord in vivo: application to adrenomyeloneuropathy. Magnetic Resonance in Medicine : Official Journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine. 61: 22-7
Pillion JP, Moser HW, Raymond GV. (2008) Auditory function in adrenomyeloneuropathy. Journal of the Neurological Sciences. 269: 24-9
Moser HW, Moser AB, Hollandsworth K, et al. (2007) "Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacy. Journal of Molecular Neuroscience : Mn. 33: 105-13
Mahmood A, Raymond GV, Dubey P, et al. (2007) Survival analysis of haematopoietic cell transplantation for childhood cerebral X-linked adrenoleukodystrophy: a comparison study. The Lancet. Neurology. 6: 687-92
Eichler F, Mahmood A, Loes D, et al. (2007) Magnetic resonance imaging detection of lesion progression in adult patients with X-linked adrenoleukodystrophy. Archives of Neurology. 64: 659-64
Moser HW, Mahmood A. (2007) New insights about hematopoietic stem cell transplantation in adrenoleukodystrophy. Archives of Neurology. 64: 631-2
Moser HW, Mahmood A, Raymond GV. (2007) X-linked adrenoleukodystrophy. Nature Clinical Practice. Neurology. 3: 140-51
Steinberg SJ, Dodt G, Raymond GV, et al. (2006) Peroxisome biogenesis disorders. Biochimica Et Biophysica Acta. 1763: 1733-48
Zackowski KM, Dubey P, Raymond GV, et al. (2006) Sensorimotor function and axonal integrity in adrenomyeloneuropathy. Archives of Neurology. 63: 74-80
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