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R T Leshner

Showing results (21-30 of 32) with videos related to

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Journal of Neuropathology and Experimental Neurology|September 1, 1989
Remyelination in the human central nervous systemN R Ghatak, R T Leshner, A C Price, et al.
Muscle & Nerve|January 1, 1988
Intraoperative electroneurography: management of ulnar neuropathy at the elbowW W Campbell, S K Sahni, R M Pridgeon, et al.
Clinical Chemistry|April 1, 1989
Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studiesT W Prior, P A Blasco, J L Dove, et al.
Annals of Neurology|April 1, 1980
Myelopathy in mucopolysaccharidosis type II (Hunter syndrome)C E Ballenger, T R Swift, R T Leshner, et al.
Applied Neurophysiology|January 1, 1987
CT-guided stereotactic biopsies of lesions in the medulla and a case of Leigh's diseaseK S Sahni, N R Ghatak, A N Gulati, et al.
Annals of Neurology|November 1, 1985
Biotinidase deficiency: initial clinical features and rapid diagnosisB Wolf, G S Heard, K A Weissbecker, et al.
Annals of Neurology|March 1, 1987
Adrenoleukodystrophy: dietary oleic acid lowers hexacosanoate levelsW B Rizzo, M W Phillips, A L Dammann, et al.
American Journal of Clinical Pathology|November 1, 1985
Prediction of carrier status in Duchenne dystrophy by creatine kinase measurementH D Gruemer, W G Miller, V M Chinchilli, et al.
Clinical Chemistry|May 1, 1984
Are reference limits for serum creatine kinase valid in detection of the carrier state for Duchenne muscular dystrophy?H D Gruemer, W G Miller, V M Chinchilli, et al.
Neurology|February 20, 1999
Plasma exchange versus intravenous immunoglobulin treatment in myasthenic crisisA I Qureshi, M A Choudhry, M S Akbar, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Journal of Neuropathology and Experimental Neurology|September 1, 1989
Remyelination in the human central nervous systemN R Ghatak, R T Leshner, A C Price, et al.
Muscle & Nerve|January 1, 1988
Intraoperative electroneurography: management of ulnar neuropathy at the elbowW W Campbell, S K Sahni, R M Pridgeon, et al.
Clinical Chemistry|April 1, 1989
Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studiesT W Prior, P A Blasco, J L Dove, et al.
Annals of Neurology|April 1, 1980
Myelopathy in mucopolysaccharidosis type II (Hunter syndrome)C E Ballenger, T R Swift, R T Leshner, et al.
Applied Neurophysiology|January 1, 1987
CT-guided stereotactic biopsies of lesions in the medulla and a case of Leigh's diseaseK S Sahni, N R Ghatak, A N Gulati, et al.
Annals of Neurology|November 1, 1985
Biotinidase deficiency: initial clinical features and rapid diagnosisB Wolf, G S Heard, K A Weissbecker, et al.
Annals of Neurology|March 1, 1987
Adrenoleukodystrophy: dietary oleic acid lowers hexacosanoate levelsW B Rizzo, M W Phillips, A L Dammann, et al.
American Journal of Clinical Pathology|November 1, 1985
Prediction of carrier status in Duchenne dystrophy by creatine kinase measurementH D Gruemer, W G Miller, V M Chinchilli, et al.
Clinical Chemistry|May 1, 1984
Are reference limits for serum creatine kinase valid in detection of the carrier state for Duchenne muscular dystrophy?H D Gruemer, W G Miller, V M Chinchilli, et al.
Neurology|February 20, 1999
Plasma exchange versus intravenous immunoglobulin treatment in myasthenic crisisA I Qureshi, M A Choudhry, M S Akbar, et al.
Pageof 4