肌中央軸空病 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "肌中央軸空病" in Chinese language version.

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archive.org

Quinlivan RM, Muller CR, Davis M, et al. Central core disease: clinical, pathological, and genetic features. Arch. Dis. Child. 2003, 88 (12): 1051–5. PMC 1719384 . PMID 14670767. doi:10.1136/adc.88.12.1051.

doi.org

Quinlivan RM, Muller CR, Davis M, et al. Central core disease: clinical, pathological, and genetic features. Arch. Dis. Child. 2003, 88 (12): 1051–5. PMC 1719384 . PMID 14670767. doi:10.1136/adc.88.12.1051.
Magee KR, Shy GM. A new congenital non-progressive myopathy. Brain. 1956, 79 (4): 610–21. CiteSeerX 10.1.1.1026.496 . PMID 13396066. doi:10.1093/brain/79.4.610.
Robinson, Rl; Brooks, C; Brown, Sl; Ellis, Fr; Halsall, Pj; Quinnell, Rj; Shaw, Ma; Hopkins, Pm. RYR1 mutations causing central core disease are associated with more severe malignant hyperthermia in vitro contracture test phenotypes. Human Mutation. August 2002, 20 (2): 88–97. PMID 12124989. doi:10.1002/humu.10098.

mercksource.com

道兰氏医学词典中的central core disease

nih.gov

ncbi.nlm.nih.gov

Quinlivan RM, Muller CR, Davis M, et al. Central core disease: clinical, pathological, and genetic features. Arch. Dis. Child. 2003, 88 (12): 1051–5. PMC 1719384 . PMID 14670767. doi:10.1136/adc.88.12.1051.
Magee KR, Shy GM. A new congenital non-progressive myopathy. Brain. 1956, 79 (4): 610–21. CiteSeerX 10.1.1.1026.496 . PMID 13396066. doi:10.1093/brain/79.4.610.
Robinson, Rl; Brooks, C; Brown, Sl; Ellis, Fr; Halsall, Pj; Quinnell, Rj; Shaw, Ma; Hopkins, Pm. RYR1 mutations causing central core disease are associated with more severe malignant hyperthermia in vitro contracture test phenotypes. Human Mutation. August 2002, 20 (2): 88–97. PMID 12124989. doi:10.1002/humu.10098.
Talwalkar, SS; Parker, JR; Heffner, RR; Parker, JC. Adult central core disease. Clinical, histologic and genetic aspects: case report and review of the literature.. Clin Neuropathol. 2006, 25 (4): 180–4. PMID 16866299.

psu.edu

citeseerx.ist.psu.edu

Magee KR, Shy GM. A new congenital non-progressive myopathy. Brain. 1956, 79 (4): 610–21. CiteSeerX 10.1.1.1026.496 . PMID 13396066. doi:10.1093/brain/79.4.610.