Muscle biopsy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Muscle biopsy" in English language version.

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Gonorazky, HD; Bönnemann, CG; Dowling, JJ (2018). The genetics of congenital myopathies. Handbook of Clinical Neurology. Vol. 148. pp. 549–564. doi:10.1016/B978-0-444-64076-5.00036-3. ISBN 9780444640765. PMID 29478600.
Jungbluth, Heinz; Treves, Susan; Zorzato, Francesco; Sarkozy, Anna; Ochala, Julien; Sewry, Caroline; Phadke, Rahul; Gautel, Mathias; Muntoni, Francesco (2 February 2018). "Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction". Nature Reviews Neurology. 14 (3): 151–167. doi:10.1038/nrneurol.2017.191. hdl:11392/2382654. PMID 29391587. S2CID 3542904.
Pierson CR, Tomczak K, Agrawal P, Moghadaszadeh B, Beggs AH (July 2005). "X-linked myotubular and centronuclear myopathies". J. Neuropathol. Exp. Neurol. 64 (7): 555–64. doi:10.1097/01.jnen.0000171653.17213.2e. PMID 16042307.
Bitoun M, Maugenre S, Jeannet PY, et al. (November 2005). "Mutations in dynamin 2 cause dominant centronuclear myopathy" (PDF). Nat. Genet. 37 (11): 1207–9. doi:10.1038/ng1657. PMID 16227997. S2CID 37842933.

Jungbluth, Heinz; Treves, Susan; Zorzato, Francesco; Sarkozy, Anna; Ochala, Julien; Sewry, Caroline; Phadke, Rahul; Gautel, Mathias; Muntoni, Francesco (2 February 2018). "Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction". Nature Reviews Neurology. 14 (3): 151–167. doi:10.1038/nrneurol.2017.191. hdl:11392/2382654. PMID 29391587. S2CID 3542904.

Bitoun M, Maugenre S, Jeannet PY, et al. (November 2005). "Mutations in dynamin 2 cause dominant centronuclear myopathy" (PDF). Nat. Genet. 37 (11): 1207–9. doi:10.1038/ng1657. PMID 16227997. S2CID 37842933.

Gonorazky, HD; Bönnemann, CG; Dowling, JJ (2018). The genetics of congenital myopathies. Handbook of Clinical Neurology. Vol. 148. pp. 549–564. doi:10.1016/B978-0-444-64076-5.00036-3. ISBN 9780444640765. PMID 29478600.
Jungbluth, Heinz; Treves, Susan; Zorzato, Francesco; Sarkozy, Anna; Ochala, Julien; Sewry, Caroline; Phadke, Rahul; Gautel, Mathias; Muntoni, Francesco (2 February 2018). "Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction". Nature Reviews Neurology. 14 (3): 151–167. doi:10.1038/nrneurol.2017.191. hdl:11392/2382654. PMID 29391587. S2CID 3542904.
Pierson CR, Tomczak K, Agrawal P, Moghadaszadeh B, Beggs AH (July 2005). "X-linked myotubular and centronuclear myopathies". J. Neuropathol. Exp. Neurol. 64 (7): 555–64. doi:10.1097/01.jnen.0000171653.17213.2e. PMID 16042307.
Bitoun M, Maugenre S, Jeannet PY, et al. (November 2005). "Mutations in dynamin 2 cause dominant centronuclear myopathy" (PDF). Nat. Genet. 37 (11): 1207–9. doi:10.1038/ng1657. PMID 16227997. S2CID 37842933.

Jungbluth, Heinz; Treves, Susan; Zorzato, Francesco; Sarkozy, Anna; Ochala, Julien; Sewry, Caroline; Phadke, Rahul; Gautel, Mathias; Muntoni, Francesco (2 February 2018). "Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction". Nature Reviews Neurology. 14 (3): 151–167. doi:10.1038/nrneurol.2017.191. hdl:11392/2382654. PMID 29391587. S2CID 3542904.
Bitoun M, Maugenre S, Jeannet PY, et al. (November 2005). "Mutations in dynamin 2 cause dominant centronuclear myopathy" (PDF). Nat. Genet. 37 (11): 1207–9. doi:10.1038/ng1657. PMID 16227997. S2CID 37842933.

Jungbluth, Heinz; Treves, Susan; Zorzato, Francesco; Sarkozy, Anna; Ochala, Julien; Sewry, Caroline; Phadke, Rahul; Gautel, Mathias; Muntoni, Francesco (2 February 2018). "Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction". Nature Reviews Neurology. 14 (3): 151–167. doi:10.1038/nrneurol.2017.191. hdl:11392/2382654. PMID 29391587. S2CID 3542904.