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

European journal of paediatric neurology, 2007-11, Vol.11 (6), p.381-384

2007

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Mechanisms of the host immune response and helminth-induced pathology during Trichobilharzia regenti (Schistosomatidae) neuroinvasion in mice

PLoS pathogens, 2022-02, Vol.18 (2), p.e1010302-e1010302

2022

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Differential proteomic analysis of laser-microdissected penetration glands of avian schistosome cercariae with a focus on proteins involved in host invasion

International journal for parasitology, 2022-05, Vol.52 (6), p.343-358

2022

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Immature stages of the genus Oxythyrea (Coleoptera: Scarabaeidae: Cetoniinae) with a key to third instar larvae, and notes on the biology of the genus

Zootaxa, 2018-10, Vol.4486 (4), p.401

2018

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Cryptic diversity of Oxythyrea flower chafers and its implication for conservation of non‐forest biotopes in the Balkans

Insect conservation and diversity, 2023-01, Vol.16 (1), p.133-146

2023

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Proton pencil-beam scanning radiotherapy in the treatment of nasopharyngeal cancer: dosimetric parameters and 2-year results

European archives of oto-rhino-laryngology, 2021-03, Vol.278 (3), p.763-769

2021

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Effects of silymarin flavonolignans and synthetic silybin derivatives on estrogen and aryl hydrocarbon receptor activation

Toxicology (Amsterdam), 2005-11, Vol.215 (1), p.80-89

2005

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Role of miR-653 and miR-29c in downregulation of CYP1A2 expression in hepatocellular carcinoma

Pharmacological reports, 2022-02, Vol.74 (1), p.148-158

2022

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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

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

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

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

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

Mechanisms of the host immune response and helminth-induced pathology during Trichobilharzia regenti (Schistosomatidae) neuroinvasion in mice

Differential proteomic analysis of laser-microdissected penetration glands of avian schistosome cercariae with a focus on proteins involved in host invasion

Immature stages of the genus Oxythyrea (Coleoptera: Scarabaeidae: Cetoniinae) with a key to third instar larvae, and notes on the biology of the genus

Cryptic diversity of Oxythyrea flower chafers and its implication for conservation of non‐forest biotopes in the Balkans

Proton pencil-beam scanning radiotherapy in the treatment of nasopharyngeal cancer: dosimetric parameters and 2-year results

Effects of silymarin flavonolignans and synthetic silybin derivatives on estrogen and aryl hydrocarbon receptor activation

Role of miR-653 and miR-29c in downregulation of CYP1A2 expression in hepatocellular carcinoma

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