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Nemaline myopathy 8
- ... Testing Registry: Nemaline myopathy 7 Genetic Testing Registry: Nemaline myopathy 8 Genetic Testing Registry: Nemaline myopathy 9 Nemaline myopathy ... 4B, AUTOSOMAL RECESSIVE; CMYP4B CONGENITAL MYOPATHY 23; CMYP23 NEMALINE MYOPATHY 8; NEM8 NEMALINE MYOPATHY 9; NEM9 NEMALINE MYOPATHY 10; ...
- ... beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. Neuromuscul Disord. 2002 Feb;12(2):151-8. doi: 10.1016/s0960-8966(01)00252-8. ... H, Ohlsson M, Lindberg C, Oldfors A. Congenital myopathy with nemaline rods ... Neurol. 2007 Sep;64(9):1334-8. doi: 10.1001/archneur.64.9.1334. Citation ...
- ... explains the absence of cardiac involvement in ACTA1 nemaline myopathy. Neuromuscul Disord. 2005 Dec;15(12):829-35. doi: 10.1016/j.nmd.2005.08.004. Epub 2005 Nov 8. Citation on PubMed Kaimaktchiev V, Goebel H, Laing ...
- ... myopathy Congenital myopathy with excess of thin filaments Nemaline myopathy 3 ... myopathy with actin filament deposits. Acta Neuropathol. 1996 Jul;92(1):104-8. doi: 10.1007/s004010050496. Citation on PubMed Feng ...
- ... gene (ACTA1). Neuromuscul Disord. 2003 Sep;13(7-8):519-31. doi: 10.1016/s0960-8966(03)00101-9. Citation on PubMed Weeks DA, Nixon RR, Kaimaktchiev V, Mierau GW. Intranuclear rod myopathy, a rare and morphologically striking variant of nemaline rod myopathy. Ultrastruct Pathol. 2003 May-Jun;27( ...
- ... molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy. Biochem J. 2012 Feb 15;442(1):231- ...
- ... gene are also associated with a condition called nemaline myopathy. People with nemaline myopathy typically have muscle weakness throughout their body, including ...