Powers, James M.

A mouse model for X-linked adrenoleukodystrophy

Lu, J.-F., Lawler, A. M., Watkins, P. A., Powers, J. M., Moser, A. B., Moser, H. W., & Smith, K. D. (1997) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 293

The Inflammatory Myelinopathy of Adreno-Leukodystrophy: Cells, Effector Molecules, and Pathogenetic Implications

POWERS, J. M., LIU, Y., MOSER, A. B., & MOSER, H. W. (1992) · Journal of Neuropathology and Experimental Neurology

Multiple Sclerosis Research StudiesNeuroinflammation and Neurodegeneration Mechanisms

Cited by 265

Peroxisomal Disorders: Genotype, Phenotype, Major Neuropathologic Lesions, and Pathogenesis

Powers, J. M., & Moser, H. W. (1998) · Brain Pathology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 208

Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy

Powers, J. M., DeCiero, D. P., Ito, M., Moser, A. B., & Moser, H. W. (2000) · Journal of Neuropathology & Experimental Neurology

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 204

Leukoencephalopathy with vanishing white matter: a review

Bugiani, M., Boor, I., Powers, J. M., Scheper, G. C., & van der Knaap, M. S. (2010) · Journal of Neuropathology & Experimental Neurology

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 189

Phospholipids in X-linked adrenoleukodystrophy white matter: Fatty acid abnormalities before the onset of demyelination

Theda, C., Moser, A. B., Powers, J. M., & Moser, H. W. (1992) · Journal of the Neurological Sciences

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 99

The Dorsal Root Ganglia in Adrenomyeloneuropathy: Neuronal Atrophy and Abnormal Mitochondria

Powers, J. M., Deciero, D. P., Cox, C., Richfield, E. K., Ito, M., Moser, A. B., & Moser, H. W. (2001) · Journal of Neuropathology & Experimental Neurology

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 96

Head trauma can initiate the onset of adreno-leukodystrophy

Raymond, G. V., Seidman, R., Monteith, T. S., Kolodny, E., Sathe, S., Mahmood, A., & Powers, J. M. (2010) · Journal of the Neurological Sciences

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 90

Human leukocyte antigens and cytokine expression in cerebral inflammatory demyelinative lesions of X-linked adrenoleukodystrophy and multiple sclerosis

McGuinness, M. C., Powers, J. M., Bias, W. B., Schmeckpeper, B. J., Segal, A. H., Gowda, V. C., Wesselingh, S. L., Berger, J., Griffin, D. E., & Smith, K. D. (1997) · Journal of Neuroimmunology

Multiple Sclerosis Research StudiesLysosomal Storage Disorders Research

Cited by 89

PRESIDENTIAL ADDRESS: The Pathology of Peroxisomal Disorders with Pathogenetic Considerations

Powers, J. M. (1995) · Journal of Neuropathology and Experimental Neurology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 67

Histochemical characteristics of the striated inclusions of adrenoleukodystrophy

Johnson, A. B., Schaumburg, H. H., & Powers, J. M. (1976) · Journal of Histochemistry & Cytochemistry

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 66

Cerebellar atrophy in chronic rhizomelic chondrodysplasia punctata: a potential role for phytanic acid and calcium in the death of its Purkinje cells

Powers, J. M., Kenjarski, T. P., Moser, A. B., & Moser, H. W. (1999) · Acta Neuropathologica

Metabolism and Genetic DisordersGenetic Neurodegenerative Diseases

Cited by 49

Fetal adrenoleukodystrophy: the significance of pathologic lesions in adrenal gland and testis

Powers, J. M., Moser, H. W., Moser, A. B., & Schaumburg, H. H. (1982) · Human Pathology

Metabolism and Genetic DisordersAdrenal Hormones and Disorders

Cited by 49

Adreno-leukodystrophy: A personal historical note

Powers, J. M. (2005) · Acta Neuropathologica

Adrenal Hormones and DisordersMetabolism and Genetic Disorders

Cited by 15

THE MYELONEUROPATHY VARIANT OF ADRENOLEUKODYSTROPHY: 26

Schaumburq, H. H., Powers, J. M., Spencer, P. S., Raine, C. S., Prineas, J. W., & Boehme, D. M. (1976) · Journal of Neuropathology and Experimental Neurology

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 7