TDP-43 A315T mutation in familial motor neuron disease
Gitcho, Michael A., Baloh, Robert H., Chakraverty, Sumi, Mayo, Kevin, Norton, Joanne B., Levitch, Denise, Hatanpaa, Kimmo J., White III, Charles L., Bigio, Eileen H., Caselli, Richard, Baker, Matt, Al-Lozi, Muhammad T., Morris, John C., Pestronk, Alan, Rademakers, Rosa, Goate, Alison M., Cairns, Nigel J.
Published in Annals of neurology (01.04.2008)
Published in Annals of neurology (01.04.2008)
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Multifocal radiculoneuropathy during ipilimumab treatment of melanoma
Manousakis, Georgios, Koch, James, Sommerville, R. Brian, El-Dokla, Ahmed, Harms, Matthew B., Al-Lozi, Muhammad T., Schmidt, Robert E., Pestronk, Alan
Published in Muscle & nerve (01.09.2013)
Published in Muscle & nerve (01.09.2013)
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Clinical and laboratory features of neuropathies with serum IgM binding to TS-HDS
Pestronk, Alan, Schmidt, Robert E., Choksi, Rati M., Sommerville, R. Brian, Al-Lozi, Muhammad T.
Published in Muscle & nerve (01.06.2012)
Published in Muscle & nerve (01.06.2012)
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Phase 2 Trial of Rituximab in Acetylcholine Receptor Antibody-Positive Generalized Myasthenia Gravis: The BeatMG Study
Nowak, Richard J, Coffey, Christopher S, Goldstein, Jonathan M, Dimachkie, Mazen M, Benatar, Michael, Kissel, John T, Wolfe, Gil I, Burns, Ted M, Freimer, Miriam L, Nations, Sharon, Granit, Volkan, Smith, A Gordon, Richman, David P, Ciafaloni, Emma, Al-Lozi, Muhammad T, Sams, Laura Ann, Quan, Dianna, Ubogu, Eroboghene, Pearson, Brenda, Sharma, Aditi, Yankey, Jon W, Uribe, Liz, Shy, Michael, Amato, Anthony A, Conwit, Robin, O'Connor, Kevin C, Hafler, David A, Cudkowicz, Merit E, Barohn, Richard J
Published in Neurology (25.01.2022)
Published in Neurology (25.01.2022)
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Median and ulnar nerve conduction studies at the wrist: criterion validity of the NC-stat automated device
Armstrong, Theodore N, Dale, Ann M, Al-Lozi, Muhammad T, Franzblau, Alfred, Evanoff, Bradley A
Published in Journal of occupational and environmental medicine (01.07.2008)
Published in Journal of occupational and environmental medicine (01.07.2008)
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Journal Article
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy
Scoto, Mariacristina, Rossor, Alexander M, Harms, Matthew B, Cirak, Sebahattin, Calissano, Mattia, Robb, Stephanie, Manzur, Adnan Y, Martínez Arroyo, Amaia, Rodriguez Sanz, Aida, Mansour, Sahar, Fallon, Penny, Hadjikoumi, Irene, Klein, Andrea, Yang, Michele, De Visser, Marianne, Overweg-Plandsoen, W C G Truus, Baas, Frank, Taylor, J Paul, Benatar, Michael, Connolly, Anne M, Al-Lozi, Muhammad T, Nixon, John, de Goede, Christian G E L, Foley, A Reghan, Mcwilliam, Catherine, Pitt, Matthew, Sewry, Caroline, Phadke, Rahul, Hafezparast, Majid, Chong, W K Kling, Mercuri, Eugenio, Baloh, Robert H, Reilly, Mary M, Muntoni, Francesco
Published in Neurology (17.02.2015)
Published in Neurology (17.02.2015)
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Sensory neuropathy with monoclonal IgM binding to a trisulfated heparin disaccharide
Pestronk, Alan, Choksi, Rati, Logigian, Eric, Al-Lozi, Muhammad T.
Published in Muscle & nerve (01.02.2003)
Published in Muscle & nerve (01.02.2003)
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Journal Article
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
Kovach, Margaret J., Waggoner, Brook, Leal, Suzanne M., Gelber, David, Khardori, Romesh, Levenstien, Mark A., Shanks, Christy A., Gregg, Gregory, Al-Lozi, Muhammad T., Miller, Timothy, Rakowicz, Wojtek, Lopate, Glenn, Florence, Juliane, Glosser, Guila, Simmons, Zachary, Morris, John C., Whyte, Michael P., Pestronk, Alan, Kimonis, Virginia E.
Published in Molecular genetics and metabolism (01.12.2001)
Published in Molecular genetics and metabolism (01.12.2001)
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Brachio‐cervical inflammatory myopathies: Clinical, immune, and myopathologic features
Pestronk, Alan, Kos, Ksenija, Lopate, Glenn, Al‐Lozi, Muhammad T.
Published in Arthritis and rheumatism (01.05.2006)
Published in Arthritis and rheumatism (01.05.2006)
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Journal Article
P3-287: TDP-43 A315T mutation in familial motor neuron disease
Gitcho, Michael A, Baloh, Robert H, Chakraverty, Sumi, Mayo, Kevin, Norton, Joanne B, Levitch, Denise, Hatanpaa, Kimmo J, White, Charles H, Bigio, Eileen H, Caselli, Richard, Baker, Matt, Al-Lozi, Muhammad T, Morris, John C, Pestronk, Alan, Rademakers, Rosa, Goate, Alison M, Cairns, Nigel J
Published in Alzheimer's & dementia (01.07.2008)
Published in Alzheimer's & dementia (01.07.2008)
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Diagnostic criteria for late-onset (childhood and adult) pompe disease
Published in Muscle & nerve
(01.07.2009)
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Journal Article
Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation
Lopate, Glenn, Baloh, Robert H., Al-Lozi, Muhammad T., Miller, Timothy M., Fernandes Filho, J. Americo, Ni, Oliver, Leston, Alison, Florence, Julaine, Schierbecker, Jeanine, Allred, Peggy
Published in Amyotrophic lateral sclerosis (2010)
Published in Amyotrophic lateral sclerosis (2010)
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Correlates of HIV RNA concentrations in cerebrospinal fluid during antiretroviral therapy: a longitudinal cohort study
Livelli, Alessandro, Vaida, Florin, Ellis, Ronald J, Ma, Qing, Ferrara, Micol, Clifford, David B, Collier, Ann C, Gelman, Benjamin B, Marra, Christina M, McArthur, Justin C, McCutchan, J Allen, Morgello, Susan, Sacktor, Ned, Simpson, David M, Grant, Igor, Letendre, Scott L
Published in The lancet HIV (01.07.2019)
Published in The lancet HIV (01.07.2019)
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