Campbell KP - Search Results

1

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.

Cirak S, Foley AR, Herrmann R, Willer T, Yau S, Stevens E, Torelli S, Brodd L, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nürnberg P; UK10K Consortium; Michele DE, Plagnol V, Hurles M, Moore SA, Sewry CA, Campbell KP, Voit T, Muntoni F. Cirak S, et al. Among authors: campbell kp. Brain. 2013 Jan;136(Pt 1):269-81. doi: 10.1093/brain/aws312. Epub 2013 Jan 3. Brain. 2013. PMID: 23288328 Free PMC article.

2

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities.

Sunada Y, Edgar TS, Lotz BP, Rust RS, Campbell KP. Sunada Y, et al. Among authors: campbell kp. Neurology. 1995 Nov;45(11):2084-9. doi: 10.1212/wnl.45.11.2084. Neurology. 1995. PMID: 7501163

3

Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy.

Sewry CA, Matsumura K, Campbell KP, Dubowitz V. Sewry CA, et al. Among authors: campbell kp. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):401-9. doi: 10.1016/0960-8966(94)90079-5. Neuromuscul Disord. 1994. PMID: 7881285 Clinical Trial.

4

Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy.

Sewry CA, Sansome A, Matsumura K, Campbell KP, Dubowitz V. Sewry CA, et al. Among authors: campbell kp. Neuromuscul Disord. 1994 Mar;4(2):121-9. doi: 10.1016/0960-8966(94)90003-5. Neuromuscul Disord. 1994. PMID: 8012192

5

Neurosensory hearing loss in secondary adhalinopathy.

Oexle K, Herrmann R, Dodé C, Leturcq F, Hübner C, Kaplan JC, Mizuno Y, Ozawa E, Campbell KP, Voit T. Oexle K, et al. Among authors: campbell kp. Neuropediatrics. 1996 Feb;27(1):32-6. doi: 10.1055/s-2007-973744. Neuropediatrics. 1996. PMID: 8677023

6

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

Carrié A, Piccolo F, Leturcq F, de Toma C, Azibi K, Beldjord C, Vallat JM, Merlini L, Voit T, Sewry C, Urtizberea JA, Romero N, Tomé FM, Fardeau M, Sunada Y, Campbell KP, Kaplan JC, Jeanpierre M. Carrié A, et al. Among authors: campbell kp. J Med Genet. 1997 Jun;34(6):470-5. doi: 10.1136/jmg.34.6.470. J Med Genet. 1997. PMID: 9192266 Free PMC article.

7

The sarcoglycan complex in limb-girdle muscular dystrophy.

Lim LE, Campbell KP. Lim LE, et al. Among authors: campbell kp. Curr Opin Neurol. 1998 Oct;11(5):443-52. doi: 10.1097/00019052-199810000-00006. Curr Opin Neurol. 1998. PMID: 9847993 Review.

8

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.

Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Durbeej M, et al. Among authors: campbell kp. Mol Cell. 2000 Jan;5(1):141-51. doi: 10.1016/s1097-2765(00)80410-4. Mol Cell. 2000. PMID: 10678176 Free article.

9

Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.

Barresi R, Moore SA, Stolle CA, Mendell JR, Campbell KP. Barresi R, et al. Among authors: campbell kp. J Biol Chem. 2000 Dec 8;275(49):38554-60. doi: 10.1074/jbc.M007799200. J Biol Chem. 2000. PMID: 10993904 Free article.

10

Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb--girdle muscular dystrophies.

Piccolo F, Moore SA, Ford GC, Campbell KP. Piccolo F, et al. Among authors: campbell kp. Ann Neurol. 2000 Dec;48(6):902-12. Ann Neurol. 2000. PMID: 11117547

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