Mohr M - Search Results

1

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.

Cossée M, Lagier-Tourenne C, Seguela C, Mohr M, Leturcq F, Gundesli H, Chelly J, Tranchant C, Koenig M, Mandel JL. Cossée M, et al. Among authors: mohr m. Neuromuscul Disord. 2009 Apr;19(4):255-60. doi: 10.1016/j.nmd.2009.02.003. Epub 2009 Mar 19. Neuromuscul Disord. 2009. PMID: 19303295

2

Muscle phosphorylase b kinase deficiency revisited.

Echaniz-Laguna A, Akman HO, Mohr M, Tranchant C, Talmant-Verbist V, Rolland MO, Dimauro S. Echaniz-Laguna A, et al. Among authors: mohr m. Neuromuscul Disord. 2010 Feb;20(2):125-7. doi: 10.1016/j.nmd.2009.11.004. Epub 2010 Jan 18. Neuromuscul Disord. 2010. PMID: 20080404

3

Myopathies in the elderly: a hospital-based study.

Echaniz-Laguna A, Mohr M, Lannes B, Tranchant C. Echaniz-Laguna A, et al. Among authors: mohr m. Neuromuscul Disord. 2010 Jul;20(7):443-7. doi: 10.1016/j.nmd.2010.05.003. Epub 2010 Jun 1. Neuromuscul Disord. 2010. PMID: 20621722

4

A novel variation in the Twinkle linker region causing late-onset dementia.

Echaniz-Laguna A, Chanson JB, Wilhelm JM, Sellal F, Mayençon M, Mohr M, Tranchant C, Mousson de Camaret B. Echaniz-Laguna A, et al. Among authors: mohr m. Neurogenetics. 2010 Feb;11(1):21-5. doi: 10.1007/s10048-009-0202-4. Epub 2009 Jun 10. Neurogenetics. 2010. PMID: 19513767

5

Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion.

Tranchant C, Mousson B, Mohr M, Dumoulin R, Welsch M, Weess C, Stepien G, Warter JM. Tranchant C, et al. Among authors: mohr m. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):561-6. doi: 10.1016/0960-8966(93)90116-2. Neuromuscul Disord. 1993. PMID: 8186712

6

Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease.

Echaniz-Laguna A, Mohr M, Epailly E, Nishino I, Charron P, Richard P, Guiraud-Chaumeil C, Tranchant C. Echaniz-Laguna A, et al. Among authors: mohr m. Muscle Nerve. 2006 Mar;33(3):393-7. doi: 10.1002/mus.20471. Muscle Nerve. 2006. PMID: 16372318

7

POLG1 variations presenting as multiple sclerosis.

Echaniz-Laguna A, Chassagne M, de Sèze J, Mohr M, Clerc-Renaud P, Tranchant C, Mousson de Camaret B. Echaniz-Laguna A, et al. Among authors: mohr m. Arch Neurol. 2010 Sep;67(9):1140-3. doi: 10.1001/archneurol.2010.219. Arch Neurol. 2010. PMID: 20837861

8

[Prion diseases].

Warter JM, Steinmetz G, Mohr M, Tranchant C. Warter JM, et al. Among authors: mohr m. Rev Neurol (Paris). 2002 Oct;158(10 Pt 1):998-1007. Rev Neurol (Paris). 2002. PMID: 12407310 Review. French.

9

Basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

Tranchant C, Geranton L, Guiraud-Chaumeil C, Mohr M, Warter JM. Tranchant C, et al. Among authors: mohr m. Neurology. 1999 Apr 12;52(6):1244-9. doi: 10.1212/wnl.52.6.1244. Neurology. 1999. PMID: 10214751

10

Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation.

Tranchant C, Sergeant N, Wattez A, Mohr M, Warter JM, Delacourte A. Tranchant C, et al. Among authors: mohr m. J Neurol Neurosurg Psychiatry. 1997 Aug;63(2):240-6. doi: 10.1136/jnnp.63.2.240. J Neurol Neurosurg Psychiatry. 1997. PMID: 9285466 Free PMC article.

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