Suchergebnisse - Moore, Steven A

What Every Neuropathologist Needs to Know: The Muscle Biopsy von Nix, James S, Moore, Steven A

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Unilateral carrageenan injection into muscle or joint induces chronic bilateral hyperalgesia in rats von Radhakrishnan, Rajan, Moore, Steven A., Sluka, Kathleen A.

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The inflammatory pathology of dysferlinopathy is distinct from calpainopathy, Becker muscular dystrophy, and inflammatory myopathies von Becker, Nicole, Moore, Steven A., Jones, Karra A.

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Dystrophinopathy muscle biopsies in the genetic testing era: one center’s data von Carlson, Courtney R, Moore, Steven A, Mathews, Katherine D

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A novel CAPN3 mutation in late-onset limb-girdle muscular dystrophy with early respiratory insufficiency von Martinez-Thompson, Jennifer M., Moore, Steven A., Liewluck, Teerin

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Clinical Reasoning: A 30-year-old man with progressive weakness and atrophy von Quinn, Colin, Moore, Steven A., Bardakjian, Tanya M., Karam, Chafic

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Dystrophinopathy presenting with arrhythmia in an asymptomatic 34-year-old man: a case report von Wakefield, Seth E, Dimberg, Elliot L, Moore, Steven A, Tseng, Brian S

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Muscle Fatigue Increases the Probability of Developing Hyperalgesia in Mice von Yokoyama, Takeshi, Lisi, Tammy L., Moore, Steven A., Sluka, Kathleen A.

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Child Neurology: LAMA2 muscular dystrophy without contractures von Dean, Marissa, Rashid, Salman, Kupsky, William, Moore, Steven A., Jiang, Huiyuan

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ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles von Liewluck, Teerin, Niu, Zhiyv, Moore, Steven A., Alsharabati, Mohammad, Milone, Margherita

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CLIA Laboratory Testing for Facioscapulohumeral Dystrophy: A Retrospective Analysis von Rieken, Autumn, Bossler, Aaron D., Mathews, Katherine D., Moore, Steven A.

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Infantile onset CMT2D/dSMA V in monozygotic twins due to a mutation in the anticodon binding domain of GARS von Eskuri, Jamie M., Stanley, Christine M., Moore, Steven A., Mathews, Katherine D.

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CARDIAC PATHOLOGY EXCEEDS SKELETAL MUSCLE PATHOLOGY IN TWO CASES OF LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 2I von Margeta, Marta, Connolly, Anne M., Winder, Thomas L., Pestronk, Alan, Moore, Steven A.

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A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation‐prone Ano5 peptide von Xu, Jing, Xu, Li, Lau, Yeh S, Gao, Yandi, Moore, Steven A, Han, Renzhi

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Elevated Oxidative Membrane Damage Associated with Genetic Modifiers of Lyst-Mutant Phenotypes von Trantow, Colleen M., Hedberg-Buenz, Adam, Iwashita, Sachiyo, Moore, Steven A., Anderson, Michael G.

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Astrocytes in the Rat Nucleus Tractus Solitarii Are Critical for Cardiovascular Reflex Control von Lin, Li-Hsien, Moore, Steven A., Jones, Susan Y., McGlashon, Jacob, Talman, William T.

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Sudden Death and Myocardial Lesions after Damage to Catecholamine Neurons of the Nucleus Tractus Solitarii in Rat von Talman, William T., Dragon, Deidre Nitschke, Jones, Susan Y., Moore, Steven A., Lin, Li-Hsien

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Cardiac damage after lesions of the nucleus tractus solitarii von Nayate, Ameya, Moore, Steven A., Weiss, Robert, Taktakishvili, Otar M., Lin, Li-Hsien, Talman, William T.

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Allele-specific RNAi Mitigates Phenotypic Progression in a Transgenic Model of Alzheimer's Disease von Rodríguez-Lebrón, Edgardo, Gouvion, Cynthia M, Moore, Steven A, Davidson, Beverly L, Paulson, Henry L

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Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex von Cohn, Ronald D., Durbeej, Madeleine, Moore, Steven A., Coral-Vazquez, Ramón, Prouty, Sally, Campbell, Kevin P.

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