Miopatía nemalínica (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Miopatía nemalínica" in Galician language version.

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12nih.gov

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moon.ouhsc.edu.

Department of Pathology, University of Oklahoma Health Sciences Center. "Nemaline Myopathy". Arquivado dende o orixinal o 20 de febreiro de 2009. Consultado o 24 de decembro de 2008.

google.es

books.google.es

Joanne Lynn, Herbert B. Newton, Alexander Rae-Grant (2003). The 5-minute Neurology Consult. Lippincott Williams & Wilkins. ISBN 0-683-30723-1. Ver en Google Books

nih.gov

ncbi.nlm.nih.gov

Schnell C, Kan A, North KN. (2000). "An artefact gone awry': identification of the first case of nemaline myopathy by Dr R.D.K. Reye". Neuromuscul Disord. 10 ((4-5)). PMID 10838259.
Anderson SL, Ekstein J, Donnelly MC, Keefe EM, Toto NR, LeVoci LA, Rubin BY. (2004). "Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene". Hum genet 115 (3). PMID 15221447.
Johnston JJ, Kelley RI, Crawford TO, Morton DH, Agarwala R, Koch T, Schäffer AA, Francomano CA, Biesecker LG. (2000). "A novel nemaline myopathy in the Amish caused by a mutation in troponin T1". Am J Hum Genet. 67 (4). PMID 1095287. Arquivado dende o orixinal o 12 de setembro de 2019. Consultado o 30 de abril de 2015.
North KN, Laing NG, Wallgren-Pettersson C. (1997). "Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy". J Med Genet. 34 (9). PMID 9321754. Arquivado dende o orixinal o 12 de setembro de 2019. Consultado o 30 de abril de 2015.
North, Kathryn (2002). "Nemaline Myopathy". Gene Reviews. PMID.
Ryan MM, Ilkovski B, Strickland CD, Schnell C, Sanoudou D, Midgett C, Houston R, Muirhead D, Dennett X, Shield LK, De Girolami U, Iannaccone ST, Laing NG, North KN, Beggs AH (2003). "Clinical course correlates poorly with muscle pathology in nemaline myopathy". Neurology (60). PMID 12601110.
Wallgren-Pettersson C. (2002). "Nemaline and myotubular myopathies". Semin Pediatr Neurol. 9 (2). PMID 12138997.
"OMIM #161800". Consultado o 25 de decembro de 2008.
Feng JJ, Marston S. (2008). "Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies". Neuromuscul Disord. PMID 18976909.
Oishi M, Mochizuki Y (1998). "Magnetic resonance imaging findings of the skeletal muscle of a patient with nemaline myopathy" (37). PMID 9804088.

pubmedcentral.nih.gov

Johnston JJ, Kelley RI, Crawford TO, Morton DH, Agarwala R, Koch T, Schäffer AA, Francomano CA, Biesecker LG. (2000). "A novel nemaline myopathy in the Amish caused by a mutation in troponin T1". Am J Hum Genet. 67 (4). PMID 1095287. Arquivado dende o orixinal o 12 de setembro de 2019. Consultado o 30 de abril de 2015.
North KN, Laing NG, Wallgren-Pettersson C. (1997). "Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy". J Med Genet. 34 (9). PMID 9321754. Arquivado dende o orixinal o 12 de setembro de 2019. Consultado o 30 de abril de 2015.

web.archive.org

Johnston JJ, Kelley RI, Crawford TO, Morton DH, Agarwala R, Koch T, Schäffer AA, Francomano CA, Biesecker LG. (2000). "A novel nemaline myopathy in the Amish caused by a mutation in troponin T1". Am J Hum Genet. 67 (4). PMID 1095287. Arquivado dende o orixinal o 12 de setembro de 2019. Consultado o 30 de abril de 2015.
North KN, Laing NG, Wallgren-Pettersson C. (1997). "Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy". J Med Genet. 34 (9). PMID 9321754. Arquivado dende o orixinal o 12 de setembro de 2019. Consultado o 30 de abril de 2015.
Department of Pathology, University of Oklahoma Health Sciences Center. "Nemaline Myopathy". Arquivado dende o orixinal o 20 de febreiro de 2009. Consultado o 24 de decembro de 2008.