Miopatía nemalínica (Spanish Wikipedia)

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

refsWebsite

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12nih.gov

4^th place

1google.es

5,088^th place

361^st place

1web.archive.org

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1edu.

low place

1jst.go.jp

1,903^rd place

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edu.

moon.ouhsc.edu.

Department of Pathology, University of Oklahoma Health Sciences Center. «Nemaline Myopathy». Archivado desde el original el 20 de febrero de 2009. Consultado el 24 de diciembre 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

jst.go.jp

journalarchive.jst.go.jp

Oishi M, Mochizuki Y (1998). Magnetic resonance imaging findings of the skeletal muscle of a patient with nemaline myopathy (37). PMID 9804088.

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.
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.
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 el 25 de diciembre 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.
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.

web.archive.org

Department of Pathology, University of Oklahoma Health Sciences Center. «Nemaline Myopathy». Archivado desde el original el 20 de febrero de 2009. Consultado el 24 de diciembre de 2008.