Campbell KP - Search Results

1

A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI.

Murakami T, Hayashi YK, Ogawa M, Noguchi S, Campbell KP, Togawa M, Inoue T, Oka A, Ohno K, Nonaka I, Nishino I. Murakami T, et al. Among authors: campbell kp. Brain Dev. 2009 Jun;31(6):465-8. doi: 10.1016/j.braindev.2008.08.005. Epub 2008 Sep 19. Brain Dev. 2009. PMID: 18804929 Free PMC article.

2

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy.

Matsumura K, Nonaka I, Campbell KP. Matsumura K, et al. Among authors: campbell kp. Lancet. 1993 Feb 27;341(8844):521-2. doi: 10.1016/0140-6736(93)90279-p. Lancet. 1993. PMID: 8094772

3

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Michele DE, et al. Among authors: campbell kp. Nature. 2002 Jul 25;418(6896):417-22. doi: 10.1038/nature00837. Nature. 2002. PMID: 12140558

4

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I. Kim DS, et al. Among authors: campbell kp. Neurology. 2004 Mar 23;62(6):1009-11. doi: 10.1212/01.wnl.0000115386.28769.65. Neurology. 2004. PMID: 15037715

5

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. Barresi R, et al. Among authors: campbell kp. Nat Med. 2004 Jul;10(7):696-703. doi: 10.1038/nm1059. Epub 2004 Jun 6. Nat Med. 2004. PMID: 15184894 Free article.

6

Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.

Matsumoto H, Hayashi YK, Kim DS, Ogawa M, Murakami T, Noguchi S, Nonaka I, Nakazawa T, Matsuo T, Futagami S, Campbell KP, Nishino I. Matsumoto H, et al. Among authors: campbell kp. Neuromuscul Disord. 2005 May;15(5):342-8. doi: 10.1016/j.nmd.2005.01.009. Neuromuscul Disord. 2005. PMID: 15833426

7

Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy.

Saito F, Blank M, Schröder J, Manya H, Shimizu T, Campbell KP, Endo T, Mizutani M, Kröger S, Matsumura K. Saito F, et al. Among authors: campbell kp. FEBS Lett. 2005 Apr 25;579(11):2359-63. doi: 10.1016/j.febslet.2005.03.033. FEBS Lett. 2005. PMID: 15848172 Free article.

8

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness.

Murakami T, Hayashi YK, Noguchi S, Ogawa M, Nonaka I, Tanabe Y, Ogino M, Takada F, Eriguchi M, Kotooka N, Campbell KP, Osawa M, Nishino I. Murakami T, et al. Among authors: campbell kp. Ann Neurol. 2006 Nov;60(5):597-602. doi: 10.1002/ana.20973. Ann Neurol. 2006. PMID: 17036286

9

A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity.

Jimenez-Mallebrera C, Torelli S, Feng L, Kim J, Godfrey C, Clement E, Mein R, Abbs S, Brown SC, Campbell KP, Kröger S, Talim B, Topaloglu H, Quinlivan R, Roper H, Childs AM, Kinali M, Sewry CA, Muntoni F. Jimenez-Mallebrera C, et al. Among authors: campbell kp. Brain Pathol. 2009 Oct;19(4):596-611. doi: 10.1111/j.1750-3639.2008.00198.x. Epub 2008 Aug 7. Brain Pathol. 2009. PMID: 18691338 Free PMC article.

10

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.

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