Muhammad Al‐Lozi

<i>TDP‐43</i> A315T mutation in familial motor neuron disease

Michael A. Gitcho, Robert H. Baloh, Sumi Chakraverty et al. · Annals of Neurology · 2008 · 608 citations · Full text

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Margaret J. Kovach, Brook Waggoner, Suzanne M. Leal et al. · Molecular Genetics and Metabolism · 2001 · 197 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +12

Novel mutations expand the clinical spectrum of <i>DYNC1H1</i> -associated spinal muscular atrophy

Mariacristina Scoto, Alexander M. Rossor, Matthew B. Harms et al. · Neurology · 2015 · 127 citations · Full text

Treatment of Chronic Inflammatory Demyelinating Polyneuropathy With High-Dose Intermittent Intravenous Methylprednisolone

Glenn Lopate, Alan Pestronk, Muhammad Al‐Lozi · Archives of Neurology · 2005 · 115 citations

Multifocal radiculoneuropathy during ipilimumab treatment of melanoma

Georgios Manousakis, James P. Koch, R. Brian Sommerville et al. · Muscle & Nerve · 2013 · 76 citations · Full text