Straub V - Search Results

1

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.

Yoshida A, Kobayashi K, Manya H, Taniguchi K, Kano H, Mizuno M, Inazu T, Mitsuhashi H, Takahashi S, Takeuchi M, Herrmann R, Straub V, Talim B, Voit T, Topaloglu H, Toda T, Endo T. Yoshida A, et al. Among authors: straub v. Dev Cell. 2001 Nov;1(5):717-24. doi: 10.1016/s1534-5807(01)00070-3. Dev Cell. 2001. PMID: 11709191 Free article.

2

Direct visualization of the dystrophin network on skeletal muscle fiber membrane.

Straub V, Bittner RE, Léger JJ, Voit T. Straub V, et al. J Cell Biol. 1992 Dec;119(5):1183-91. doi: 10.1083/jcb.119.5.1183. J Cell Biol. 1992. PMID: 1447296 Free PMC article.

3

Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.

Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsöld R, Helliwell TR, Appleton R, et al. Voit T, et al. Among authors: straub v. Neuropediatrics. 1995 Jun;26(3):148-55. doi: 10.1055/s-2007-979745. Neuropediatrics. 1995. PMID: 7477753

4

Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry.

Herrmann R, Straub V, Meyer K, Kahn T, Wagner M, Voit T. Herrmann R, et al. Among authors: straub v. Eur J Pediatr. 1996 Nov;155(11):968-76. doi: 10.1007/BF02282889. Eur J Pediatr. 1996. PMID: 8911899

5

Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy.

Herrmann R, Straub V, Blank M, Kutzick C, Franke N, Jacob EN, Lenard HG, Kröger S, Voit T. Herrmann R, et al. Among authors: straub v. Hum Mol Genet. 2000 Sep 22;9(15):2335-40. doi: 10.1093/oxfordjournals.hmg.a018926. Hum Mol Genet. 2000. PMID: 11001938

6

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.

Haravuori H, Vihola A, Straub V, Auranen M, Richard I, Marchand S, Voit T, Labeit S, Somer H, Peltonen L, Beckmann JS, Udd B. Haravuori H, et al. Among authors: straub v. Neurology. 2001 Apr 10;56(7):869-77. doi: 10.1212/wnl.56.7.869. Neurology. 2001. PMID: 11294923

7

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.

Brockington M, Yuva Y, Prandini P, Brown SC, Torelli S, Benson MA, Herrmann R, Anderson LV, Bashir R, Burgunder JM, Fallet S, Romero N, Fardeau M, Straub V, Storey G, Pollitt C, Richard I, Sewry CA, Bushby K, Voit T, Blake DJ, Muntoni F. Brockington M, et al. Among authors: straub v. Hum Mol Genet. 2001 Dec 1;10(25):2851-9. doi: 10.1093/hmg/10.25.2851. Hum Mol Genet. 2001. PMID: 11741828

8

Deficiency of alpha-dystroglycan in muscle-eye-brain disease.

Kano H, Kobayashi K, Herrmann R, Tachikawa M, Manya H, Nishino I, Nonaka I, Straub V, Talim B, Voit T, Topaloglu H, Endo T, Yoshikawa H, Toda T. Kano H, et al. Among authors: straub v. Biochem Biophys Res Commun. 2002 Mar 15;291(5):1283-6. doi: 10.1006/bbrc.2002.6608. Biochem Biophys Res Commun. 2002. PMID: 11883957

9

Airway nitric oxide in Duchenne muscular dystrophy.

Straub V, Ratjen F, Amthor H, Voit T, Grasemann H. Straub V, et al. J Pediatr. 2002 Jul;141(1):132-4. doi: 10.1067/mpd.2002.125226. J Pediatr. 2002. PMID: 12091865

10

Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD.

Voit T, Parano E, Straub V, Schröder JM, Schaper J, Pavone P, Falsaperla R, Pavone L, Herrmann R. Voit T, et al. Among authors: straub v. Neuromuscul Disord. 2002 Oct;12(7-8):623-30. doi: 10.1016/s0960-8966(02)00018-4. Neuromuscul Disord. 2002. PMID: 12207929

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

491 results

Search Page