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1. Full Text Quantitative myotonia assessment with a commercially available dynamometer in myotonic dystrophy types 1 and 2
by Horáková, Magda and Horák, Tomáš and Parmová, Olesja and Bednařík, Josef and Voháňka, Stanislav
Muscle & Nerve, ISSN 0148-639X, 04/2019, Volume 59, Issue 4, pp. 431 - 435
Introduction : The objective of this study was to develop a simple method for quantitative assessment of myotonia in patients with myotonic dystrophy type 1... 
muscle strength dynamometer | myotonic dystrophy | myotonia | warm‐up | outcome measure | muscle relaxation | warm-up | NEUROSCIENCES | CLINICAL NEUROLOGY | Myotonic dystrophy | Medical research | Myotonia | Clinical trials | Muscles | Dystrophy | Patients | Contraction | Relaxation time | Index Medicus
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2. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2016, Volume 79, Issue 2, p. 235
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3. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2016, Volume 79, Issue 6, p. 728
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4. Full Text Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
by Stehlíková, Kristýna and Stehlíková, Kristýna and Skálová, Daniela and Skálová, Daniela and Zídková, Jana and Zídková, Jana and Mrázová, Lenka and Mrázová, Lenka and VondráČek, Petr and Vondráček, Petr and Mazanec, Radim and Mazanec, Radim and Voháňka, Stanislav and Voháňka, Stanislav and Haberlová, Jana and Haberlová, Jana and Hermanová, Markéta and Hermanová, Markéta and Zámečník, Josef and ZámeČník, Josef and Souček, Ondřej and Souček, Ondřej and SouČek, Ondřej and Ošlejšková, Hana and Ošlejšková, Hana and DvořáČková, Nina and Dvořáčková, Nina and Solařová, Pavla and Solařová, Pavla and Fajkusová, Lenka and Fajkusová, Lenka
BMC neurology, ISSN 1471-2377, 2014, Volume 14, Issue 1, pp. 154 - 154
Background: Autosomal recessive limb-girdle muscular dystrophies (LGMD2) include a number of disorders with heterogeneous etiology that cause predominantly... 
LGMD2 | Calpain-3 | CAPN3 | Limb girdle muscular dystrophy | Sequence capture | LGMD2A PATIENTS | MUTATION ANALYSIS | ACTIVATED CHLORIDE CHANNEL | CALPAIN-3 GENE | PROTEIN GENE | LARGE COHORT | ANOCTAMIN 5 | CLINICAL NEUROLOGY | SKELETAL-MUSCLE | MESSENGER-RNA | SPECTRUM | Muscle Proteins - genetics | Proteins - genetics | Czech Republic | Sarcoglycans - genetics | DNA Mutational Analysis | Muscular Dystrophies, Limb-Girdle - genetics | Humans | Polymerase Chain Reaction | Genotype | Anoctamins | Chloride Channels - genetics | Calpain - genetics | Gene mutations | Analysis | Laboratories | Patients | Muscular dystrophy | Proteins | Medicine | Studies | Pathology | Neurology | Hospitals | Population | Genetics | Mutation | Genetic testing | Molecular biology | Deoxyribonucleic acid--DNA | Index Medicus
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5. Full Text SIM(2) and supergraphs
by Petráš, Stanislav and von Unge, Rikard and Vohánka, Jiří
Journal of High Energy Physics, ISSN 1126-6708, 7/2011, Volume 2011, Issue 7, pp. 1 - 30
We construct Feynman rules and Supergraphs in SIM(2) superspace. To test our methods we perform a one-loop calculation of the effective action of the SIM(2)... 
Superspaces | Space-Time Symmetries | Quantum Physics | Quantum Field Theories, String Theory | Classical and Quantum Gravitation, Relativity Theory | Physics | Elementary Particles, Quantum Field Theory | PHYSICS, PARTICLES & FIELDS | Physics - High Energy Physics - Theory
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6. Adultní forma Pompeho nemoci
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2014, Volume 77, Issue 6, pp. 667 - 676
Alpha glucosidase | Pompe disease | Limb-girdle muscle weakness | Lysosomal storage diseases
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7. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2014, Volume 77, Issue 4, p. 518
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8. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2014, Volume 77, Issue 1, p. 124
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9. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2014, Volume 77, Issue 2, p. 254
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10. Full Text CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel
by Skálová, Daniela and Zídková, Jana and Voháňka, Stanislav and Mazanec, Radim and Mušová, Zuzana and Vondráček, Petr and Mrázová, Lenka and Kraus, Josef and Réblová, Kamila and Fajkusová, Lenka
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, pp. e82549 - e82549
Myotonia congenita (MC) is a genetic disease caused by mutations in the skeletal muscle chloride channel gene (CLCN1) encoding the skeletal muscle chloride... 
GENE-MUTATIONS | CIC-1 | FAMILIES | HCLC-1 | MULTIDISCIPLINARY SCIENCES | VOLTAGE-DEPENDENCE | DOMINANT | SPECTRUM | CLC-1 | MISSENSE MUTATIONS | VARIABLE PENETRANCE | Chloride Channels - chemistry | Humans | Protein Multimerization | Models, Molecular | Male | Muscle, Skeletal - metabolism | Chloride Channels - genetics | Mutation, Missense | Chloride Channels - metabolism | Young Adult | Czech Republic | Phenotype | Adolescent | Adult | Female | Protein Conformation | Mutation | Myotonia Congenita - genetics | Myotonia Congenita - diagnosis | Muscles | Analysis | Genetic aspects | Myotonia | Amino acids | Homology | Monomers | Skeletal muscle | Proteins | Ethics | Musculoskeletal system | Neurology | Hospitals | Chloride | Missense mutation | Chlorides | Gene therapy | Molecular biology | Deoxyribonucleic acid--DNA | Structural analysis | Index Medicus | Deoxyribonucleic acid | DNA
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11. Full Text Quantitative myotonia assessment with a commercially available dynamometer in myotonic dystrophy types 1 and 2
: Myotonia in DM1 and DM2
by Horáková, Magda and Horák, Tomáš and Parmová, Olesja and Bednařík, Josef and Voháňka, Stanislav
Muscle & Nerve, ISSN 0148-639X, 04/2019, Volume 59, Issue 4, pp. 431 - 435
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12. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2013, Volume 76, Issue 1, p. 113
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13. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2013, Volume 76, Issue 3, p. 373
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14. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2013, Volume 76, Issue 2, p. 250
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15. Full Text Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study
by Howard, James F and Utsugisawa, Kimiaki and Benatar, Michael and Murai, Hiroyuki and Barohn, Richard J and Illa, Isabel and Jacob, Saiju and Vissing, John and Burns, Ted M and Kissel, John T and Muppidi, Srikanth and Nowak, Richard J and O'Brien, Fanny and Wang, Jing-Jing and Mantegazza, Renato and Mazia, Claudio Gabriel and Wilken, Miguel and Ortea, Carolina and Saba, Juliet and Rugiero, Marcelo and Bettini, Mariela and Vidal, Gonzalo and Vidal, Nuria and Garcia, Rebekah and Garcia, Sonia and Garcia, Alejandra Dalila and Lamont, Phillipa and Leong, Wai-Kuen and Boterhoven, Heidi and Fyfe, Beverly and Roberts, Leslie and Jasinarachchi, Mahi and Willlems, Natasha and Wanschitz, Julia and Löscher, Wolfgang and De Bleecker, Jan and Van den Abeele, Guy and de Koning, Kathy and De Mey, Katrien and Mercelis, Rudy and Wagemaekers, Linda and Mahieu, Delphine and Van Damme, Philip and Smetcoren, Charlotte and Stevens, Olivier and Verjans, Sarah and D'Hondt, Ann and Tilkin, Petra and Alves de Siqueira Carvalho, Alzira and Hasan, Rosa and Dias Brockhausen, Igor and Feder, David and Ambrosio, Daniel and Melo, Ana Paula and Rocha, Rosana and Rosa, Bruno and Veiga, Thabata and Augusto da Silva, Luiz and Gonçalves Geraldo, Jordana and da Penha Morita Ananias, Maria and Nogueira Coelho, Erica and Paiva, Gabriel and Pozo, Marina and Prando, Natalia and Dada Martineli Torres, Debora and Fernanda Butinhao, Cristiani and Coelho, Erica and Renata Cubas Volpe, Luciana and Duran, Gustavo and Gomes da Silva, Tamires Cristina and Otavio Maia Gonçalves, Luiz and Pazetto, Lucas Eduardo and Souza Duca, Luciana and Suriane Fialho, Tomás Augusto and Gheller Friedrich, Maurício André and Guerreiro, Alexandre and Mohr, Henrique and Pereira Martins, Maurer and da Cruz Pacheco, Daiane and Macagnan, Ana Paula and de Cassia Santos, Aline and Bulle Oliveira, Acary Souza and Amaral de Andrade, Ana Carolina and Annes, Marcelo and Cavalcante Lino, Valeria and Pinto, Wladimir and Miranda, Carolina and Carrara, Fernanda and Souza, Iandra and Genge, Angela and Massie, Rami and Campbell, Natasha and Bril, Vera and Katzberg, Hans and Soltani, Mehran and Ng, Eduardo and Siddiqi, Zaeem and Phan, Celile and Blackmore, Derrick and Vohanka, Stanislav and ... and REGAIN Study Grp and REGAIN Study Group
The Lancet Neurology, ISSN 1474-4422, 12/2017, Volume 16, Issue 12, pp. 976 - 986
Complement is likely to have a role in refractory generalised myasthenia gravis, but no approved therapies specifically target this system. Results from a... 
TRIAL | ENDPLATE | LOCALIZATION | COMPLEMENT INHIBITOR ECULIZUMAB | DAILY LIVING PROFILE | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | ACETYLCHOLINE-RECEPTOR | END-PLATE | CLINICAL NEUROLOGY | Severity of Illness Index | Antibodies, Monoclonal, Humanized - adverse effects | Double-Blind Method | Myasthenia Gravis - blood | Outcome Assessment (Health Care) | Autoantibodies - blood | Humans | Middle Aged | Male | Antibodies, Monoclonal, Humanized - administration & dosage | Myasthenia Gravis - physiopathology | Antibodies, Monoclonal, Humanized - pharmacology | Adult | Female | Receptors, Cholinergic - immunology | Aged | Myasthenia Gravis - drug therapy | Drug Resistance | Studies | Neurology | Immunoglobulins | Activities of daily living | Myasthenia gravis | Transplants & implants | Neuromuscular junctions | Acetylcholine | Myasthenia | Patients | Index Medicus
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16. Tick-borne meningitis complicated by a cardioembolic intraluminal carotid artery thrombus and stroke
by Cierny, M and Skorna, M and Peska, S and Polak, P and Vohanka, S
CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, ISSN 1210-7859, 2019, Volume 82, Issue 2, pp. 227 - 228
SURGERY | FREE-FLOATING THROMBUS | MANAGEMENT | ISCHEMIC-STROKE | NEUROSCIENCES
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17. Webové okénko
by Voháňka, Stanislav
Ceska a Slovenska Neurologie a Neurochirurgie, ISSN 1210-7859, 2012, Volume 75, Issue 4, p. 503
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18. Full Text Are subjects with spondylotic cervical cord encroachment at increased risk of cervical spinal cord injury after minor trauma?
by Bednařík, Josef and Sládková, Dagmar and Kadaňka, Zdeněk and Dušek, Ladislav and Keřkovský, Miloš and Voháňka, Stanislav and Novotný, Oldřich and Urbánek, Igor and Němec, Martin
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 07/2011, Volume 82, Issue 7, pp. 779 - 781
The aim of the study was to analyse the risk of symptomatic myelopathy after minor trauma in patients with asymptomatic spondylotic cervical spinal cord... 
SURGERY | MYELOPATHY | PSYCHIATRY | CLINICAL NEUROLOGY | Spondylosis - complications | Follow-Up Studies | Humans | Middle Aged | Male | Risk | Tomography, X-Ray Computed | Decompression, Surgical | Electrodiagnosis | Spondylosis - epidemiology | Spinal Cord Injuries - epidemiology | Aged, 80 and over | Pain - etiology | Adult | Female | Peripheral Nervous System Diseases - pathology | Retrospective Studies | Disability Evaluation | Muscle Weakness - etiology | Unconsciousness - complications | Spinal Fractures - epidemiology | Magnetic Resonance Imaging | Aged | Gait Disorders, Neurologic - etiology | Cohort Studies | Studies | Sports injuries | Pain | Surgery | Mortality | Spinal cord injuries | Trauma | Index Medicus
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19. Zvýšená hladina kreatinkinázy
by Voháňka, Stanislav
Interni Medicina pro Praxi, ISSN 1212-7299, 2012, Volume 14, Issue 8-9, pp. 322 - 326
Creatine kinase | Rhabdomyolysis | Muscle dystrophy | Myopathy
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20. Full Text 225th ENMC International Workshop: A global FSHD Registry framework 18-20 November 2016, Heemskerk, The Netherlands
by Mul, Karlien and Kinoshita, June and Dawkins, Hugh and van Engelen, Baziel and Tupler, Rossella and FSHD Consortium
Neuromuscular Disorders, ISSN 0960-8966, 2017, Volume 27, Issue 8, pp. 782 - 790
Highlights • The workshop focused on patient registries for facioscapulohumeral muscular dystrophy • The core dataset for international FSHD registries was... 
Neurology | FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY | NEUROSCIENCES | CLINICAL NEUROLOGY | Conferences, meetings and seminars | Workshops (Educational programs) | Index Medicus
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