Hermanova M - Search Results

1

An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRI.

Vondracek P, Hermanova M, Vodickova K, Fajkusova L, Blakely EL, He L, Turnbull DM, Taylor RW, Tajsharghi H. Vondracek P, et al. Among authors: hermanova m. Eur J Paediatr Neurol. 2007 Nov;11(6):381-4. doi: 10.1016/j.ejpn.2007.01.010. Epub 2007 Mar 29. Eur J Paediatr Neurol. 2007. PMID: 17395506

2

[Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)].

Lukás Z, Vojtísková M, Fajkusová L, Bednarík J, Kadanka Z, Hájek J, Hermanová M, Vohánka S, Vytopil M. Lukás Z, et al. Among authors: hermanova m. Cesk Patol. 2001 Nov;37(4):137-45. Cesk Patol. 2001. PMID: 11813630 Czech.

3

[A unique case of congenital muscular dystrophy].

Hermanová M, Vondrácek P, Lukás Z. Hermanová M, et al. Cesk Patol. 2004 Apr;40(2):57-62. Cesk Patol. 2004. PMID: 15233018 Czech.

4

Mutations in Czech LGMD2A patients revealed by analysis of calpain3 mRNA and their phenotypic outcome.

Chrobáková T, Hermanová M, Kroupová I, Vondrácek P, Maríková T, Mazanec R, Zámecník J, Stanek J, Havlová M, Fajkusová L. Chrobáková T, et al. Among authors: hermanova m. Neuromuscul Disord. 2004 Oct;14(10):659-65. doi: 10.1016/j.nmd.2004.05.005. Neuromuscul Disord. 2004. PMID: 15351423

5

X-linked Charcot-Marie-Tooth disease: phenotypic expression of a novel mutation Ile127Ser in the GJB1 (connexin 32) gene.

Vondracek P, Seeman P, Hermanova M, Fajkusova L. Vondracek P, et al. Among authors: hermanova m. Muscle Nerve. 2005 Feb;31(2):252-5. doi: 10.1002/mus.20166. Muscle Nerve. 2005. PMID: 15468313

6

Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients.

Hermanová M, Zapletalová E, Sedlácková J, Chrobáková T, Letocha O, Kroupová I, Zámecník J, Vondrácek P, Mazanec R, Maríková T, Vohánka S, Fajkusová L. Hermanová M, et al. Muscle Nerve. 2006 Mar;33(3):424-32. doi: 10.1002/mus.20480. Muscle Nerve. 2006. PMID: 16372320

7

Quantitative analysis of CAPN3 transcripts in LGMD2A patients: involvement of nonsense-mediated mRNA decay.

Stehlíková K, Zapletalová E, Sedlácková J, Hermanová M, Vondrácek P, Maríková T, Mazanec R, Zámecník J, Vohánka S, Fajkus J, Fajkusová L. Stehlíková K, et al. Among authors: hermanova m. Neuromuscul Disord. 2007 Feb;17(2):143-7. doi: 10.1016/j.nmd.2006.10.001. Epub 2006 Dec 8. Neuromuscul Disord. 2007. PMID: 17157502

8

Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophy.

Vondracek P, Hermanova M, Sedlackova J, Fajkusova L, Stary D, Michenkova A, Gaillyova R, Seeman P, Mazanec R. Vondracek P, et al. Among authors: hermanova m. Eur J Neurol. 2007 Oct;14(10):1182-5. doi: 10.1111/j.1468-1331.2007.01917.x. Eur J Neurol. 2007. PMID: 17880576

9

Point mutations in Czech DMD/BMD patients and their phenotypic outcome.

Sedlácková J, Vondrácek P, Hermanová M, Zámecník J, Hrubá Z, Haberlová J, Kraus J, Maríková T, Hedvicáková P, Vohánka S, Fajkusová L. Sedlácková J, et al. Among authors: hermanova m. Neuromuscul Disord. 2009 Nov;19(11):749-53. doi: 10.1016/j.nmd.2009.08.011. Epub 2009 Sep 26. Neuromuscul Disord. 2009. PMID: 19783145

10

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic.

Stehlíková K, Skálová D, Zídková J, Mrázová L, Vondráček P, Mazanec R, Voháňka S, Haberlová J, Hermanová M, Zámečník J, Souček O, Ošlejšková H, Dvořáčková N, Solařová P, Fajkusová L. Stehlíková K, et al. Among authors: hermanova m. BMC Neurol. 2014 Aug 19;14:154. doi: 10.1186/s12883-014-0154-7. BMC Neurol. 2014. PMID: 25135358 Free PMC article.

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