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Critical illness polyneuromyopathy: the electrophysiological components of a complex entity

Intensive care medicine, 2003-09, Vol.29 (9), p.1505-1514

2003

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

Brain (London, England : 1878), 2013, Vol.136 (Pt 1), p.269-281

2013

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Health-Related Quality of Life in Children and Adolescents With Spinal Muscular Atrophy in the Czech Republic

Pediatric neurology, 2014-06, Vol.50 (6), p.591-594

2014

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Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)

Stem cell research, 2019-10, Vol.40, p.101562-101562, Article 101562

2019

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Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

BMC neurology, 2014-08, Vol.14 (1), p.154-154, Article 154

2014

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COMPASS-U Global Heat Balance Calculations

IEEE transactions on plasma science, 2023-03, Vol.51 (3), p.1-5

2023

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Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

American journal of human genetics, 2010-10, Vol.87 (4), p.513-522

2010

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CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel

PloS one, 2013-12, Vol.8 (12), p.e82549-e82549

2013

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Toroidal magnetic field ripple in the presence of misaligned toroidal field coils on the COMPASS-U tokamak

Fusion engineering and design, 2023-02, Vol.187, p.113378, Article 113378

2023

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

Muscle & nerve, 2005-02, Vol.31 (2), p.252-255

2005

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Toroidal magnetic field ripple in the presence of misaligned toroidal field coils on the COMPASS-U tokamak

Fusion engineering and design, 2022-12, Vol.187

2022

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Development of the diagnostic tools for the COMPASS-U tokamak and plans for the first plasma

Fusion engineering and design, 2023-06, Vol.191 (C), p.113545, Article 113545

2023

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Characterization of the DMD/BMD patient population in Czech Republic and Slovakia using an innovative registry approach

Neuromuscular disorders : NMD, 2009-04, Vol.19 (4), p.250-254

2009

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Risk factors for critical illness polyneuromyopathy

Journal of neurology, 2005-03, Vol.252 (3), p.343-351

2005

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Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients

Muscle & nerve, 2006-03, Vol.33 (3), p.424-432

2006

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First dedicated observations of runaway electrons in the COMPASS tokamak

Nukleonika, 2015-06, Vol.60 (2), p.249-255

2015

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COMPARISON BETWEEN 2D TURBULENCE MODEL ESEL AND EXPERIMENTAL DATA FROM AUG AND COMPASS TOKAMAKS

Acta polytechnica (Prague, Czech Republic : 1992), 2015-01, Vol.55 (2), p.128-135

2015

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Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy

Neuromuscular disorders : NMD, 2007-06, Vol.17 (6), p.476-481

2007

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Papillary fibroelastoma originating from the free left ventricular wall as the cause of recurrent stroke: Description of the case and literature review

Cor et vasa (English ed.), 2016-10, Vol.58 (5), p.e466-e469

2016

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Efficacy of pregabalin in neuropathic pain in paediatric oncological patients

European journal of paediatric neurology, 2009-07, Vol.13 (4), p.332-336

2009

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

Neuromuscular disorders : NMD, 2009-11, Vol.19 (11), p.749-753

2009

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Clinical and electrophysiological findings and long-term outcomes in paediatric patients with critical illness polyneuromyopathy

European journal of paediatric neurology, 2006-07, Vol.10 (4), p.176-181

2006

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Histopathological features in subsequent muscle biopsies in a warmblood mare with myotonic dystrophy

The Veterinary quarterly, 2012-09, Vol.32 (3-4), p.187-192

2012

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

Neuromuscular disorders : NMD, 2007-02, Vol.17 (2), p.143-147

2007

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

Neuromuscular disorders : NMD, 2004-10, Vol.14 (10), p.659-665

2004

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Critical illness polyneuromyopathy: the electrophysiological components of a complex entity

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

Health-Related Quality of Life in Children and Adolescents With Spinal Muscular Atrophy in the Czech Republic

Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

COMPASS-U Global Heat Balance Calculations

Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel

Toroidal magnetic field ripple in the presence of misaligned toroidal field coils on the COMPASS-U tokamak

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

Toroidal magnetic field ripple in the presence of misaligned toroidal field coils on the COMPASS-U tokamak

Development of the diagnostic tools for the COMPASS-U tokamak and plans for the first plasma

Characterization of the DMD/BMD patient population in Czech Republic and Slovakia using an innovative registry approach

Risk factors for critical illness polyneuromyopathy

Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients

First dedicated observations of runaway electrons in the COMPASS tokamak

COMPARISON BETWEEN 2D TURBULENCE MODEL ESEL AND EXPERIMENTAL DATA FROM AUG AND COMPASS TOKAMAKS

Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy

Papillary fibroelastoma originating from the free left ventricular wall as the cause of recurrent stroke: Description of the case and literature review

Efficacy of pregabalin in neuropathic pain in paediatric oncological patients

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

Clinical and electrophysiological findings and long-term outcomes in paediatric patients with critical illness polyneuromyopathy

Histopathological features in subsequent muscle biopsies in a warmblood mare with myotonic dystrophy

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

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

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