Moser, H. W.
Kennedy Krieger Institute · Johns Hopkins University
7 papers on CoChat
Most cited papers
- Verified
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. (2003) · Neurology
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 268
- Verified
Adrenoleukodystrophy: Phenotypic variability and implications for therapy
Moser, H. W., Moser, A. B., Smith, K. D., Bergin, A., Borel, J., Shankroff, J., Stine, O. C., Merette, C., Ott, J., Krivit, W., et al. (1992) · Journal of Inherited Metabolic Disease
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 239
- Verified
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. (2000) · Neuropediatrics
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 210
- Verified
Nerve conduction studies in adrenomyeloneuropathy
Chaudhry, V, Moser, H. W., & Cornblath, D. R. (1996) · Journal of Neurology, Neurosurgery & Psychiatry
Hereditary Neurological DisordersPeripheral Neuropathies and Disorders
Cited by 73
- Verified
Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy
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. (2005) · Neurology
Advanced MRI Techniques and ApplicationsHereditary Neurological Disorders
Cited by 64
- Verified
Peroxisomal very long-chain fatty acid β-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders
Wanders, R. J. A., van Roermund, C. W. T., van Wijland, M. J. A., Heikoop, J., Schutgens, R. B. H., Schram, A. W., Tager, J. M., van den Bosch, H., Poll-Thé, B. T., Saudubray, J. M., et al. (1987) · Clinica Chimica Acta
Metabolism and Genetic DisordersGenetic and rare skin diseases.
Cited by 58
- Verified
Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment
Watkins, P. A., Naidu, S., & Moser, H. W. (1987) · Journal of Inherited Metabolic Disease
Metabolism and Genetic DisordersGenetic and rare skin diseases.
Cited by 20
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