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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
muscle strength dynamometer | myotonic dystrophy | myotonia | warm‐up | outcome measure | muscle relaxation | warm-up | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Myotonic dystrophy | Medical research | Myotonia | Clinical trials | Muscles | Dystrophy | Patients | Contraction | Relaxation time | Index Medicus
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2. Full Text SIM(2) and supergraphs
by Petráš, Stanislav and von Unge, Rikard and Vohánka, Jiří
The journal of high energy physics, ISSN 1126-6708, 7/2011, Volume 2011, Issue 7, pp. 1 - 30
Superspaces | Space-Time Symmetries | Quantum Physics | Quantum Field Theories, String Theory | Classical and Quantum Gravitation, Relativity Theory | Physics | Elementary Particles, Quantum Field Theory | Physical Sciences | Physics, Particles & Fields | Science & Technology | Physics - High Energy Physics - Theory
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3. Full Text The Association of methylprednisolone dosing to cessation of myotonia in a patient with myotonic dystrophy type 1
by Horáková, Magda and Horák, Tomáš and Bednařík, Josef and Voháňka, Stanislav
Neuromuscular disorders : NMD, ISSN 0960-8966, 05/2020, Volume 30, Issue 5, pp. 427 - 430
Therapy | Muscle relaxation | Corticosteroids | Myotonic dystrophy | Methylprednisolone | Myotonia | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Index Medicus
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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
LGMD2 | Calpain-3 | CAPN3 | Limb girdle muscular dystrophy | Sequence capture | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | 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 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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6. Full Text Poststroke delirium incidence and outcomes: Validation of the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU)
by Mitasova, Adela and Kostalova, Milena and Bednarik, Josef and Michalcakova, Radka and Kasparek, Tomas and Balabanova, Petra and Dusek, Ladislav and Vohanka, Stanislav and Ely, E Wesley
Critical care medicine, ISSN 0090-3493, 02/2012, Volume 40, Issue 2, pp. 484 - 490
diagnosis | intensive care | stroke | delirium | Life Sciences & Biomedicine | Critical Care Medicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | Intensive care medicine | Clinical death. Palliative care. Organ gift and preservation | Medical sciences | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy | Critical Care - methods | Delirium - epidemiology | Prospective Studies | Follow-Up Studies | Humans | Middle Aged | Stroke - diagnosis | Male | Delirium - therapy | Statistics, Nonparametric | Aged, 80 and over | Adult | Female | Stroke - mortality | Stroke - therapy | Severity of Illness Index | Intensive Care Units | Reproducibility of Results | Risk Assessment | Hospitals, University | Proportional Hazards Models | Survival Rate | Disease Progression | Confusion - classification | Neuropsychological Tests | Aged | Delirium - diagnosis | Cohort Studies | Index Medicus | Abridged Index Medicus
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7. Full Text Presymptomatic spondylotic cervical myelopathy: an updated predictive model
by Bednarik, Josef and Kadanka, Zdenek and Dusek, Ladislav and Kerkovsky, Milos and Vohanka, Stanislav and Novotny, Oldrich and Urbanek, Igor and Kratochvilova, Dagmar
European spine journal, ISSN 0940-6719, 3/2008, Volume 17, Issue 3, pp. 421 - 431
Surgical Orthopedics | Medicine & Public Health | Evoked potentials | Spondylotic cervical cord compression | Electromyography | Neurosurgery | Cervical spondylotic myelopathy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Orthopedics | Science & Technology | Predictive Value of Tests | Prognosis | Prospective Studies | Humans | Middle Aged | Evoked Potentials - physiology | Male | Aged, 80 and over | Radiculopathy - physiopathology | Adult | Female | Cervical Vertebrae - physiopathology | Neural Pathways - physiopathology | Spinal Cord Compression - diagnosis | Spinal Osteophytosis - diagnosis | Radiculopathy - diagnosis | Spinal Cord Compression - physiopathology | Electrodiagnosis - methods | Disease Progression | Magnetic Resonance Imaging | Cervical Vertebrae - pathology | Aged | Spinal Cord - physiopathology | Models, Neurological | Cohort Studies | Spinal Osteophytosis - physiopathology | Index Medicus | Original
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8. 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 and psychiatry, ISSN 0022-3050, 07/2011, Volume 82, Issue 7, pp. 779 - 781
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Surgery | Science & Technology | Injuries of the nervous system and the skull. Diseases due to physical agents | Neurology | Biological and medical sciences | Medical sciences | Traumas. Diseases due to physical agents | 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 | Mortality | Spinal cord injuries | Trauma | Index Medicus
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9. Full Text ‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab
by Vissing, John and Jacob, Saiju and Fujita, Kenji P and O’Brien, Fanny and Howard, James F and Mazia, Claudio Gabriel and Wilken, Miguel and Barroso, Fabio and Saba, Juliet and Rugiero, Marcelo and Bettini, Mariela and Chaves, Marcelo and Vidal, Gonzalo and Garcia, Alejana Dalila and de Bleecker, Jan and van den Abeele, Guy and de Koning, Kathy and de Mey, Katrien and Mercelis, Rudy and Mahieu, D. lphine and Wagemaekers, Linda and van Damme, Philip and Depreitere, Annelies and Schotte, Caroline and Smetcoren, Charlotte and Stevens, Olivier and van Daele, Sien and Vandenbussche, Nicolas and Vanhee, Annelies and Verjans, Sarah and Vynckier, Jan and D’Hont, Ann and Tilkin, Petra and Alves de Siqueira Carvalho, Alzira and Dias Brockhausen, Igor and Feder, David and Ambrosio, Daniel and César, Pamela and Melo, Ana Paula and Martins Ribeiro, Renata and Rocha, Rosana and Rosa, Bruno Bezerra and Veiga, Thabata and da Silva, Luiz Augusto and Santos Engel, Murilo and Gonçalves Geraldo, Jordana and da Penha Ananias Morita, Maria and van der Kooi, Anneke and de Visser, Marianne and Liu, Ye and REGAIN Study Grp and REGAIN study group and The REGAIN study group
Journal of neurology, ISSN 0340-5354, 2020, Volume 267, Issue 7, pp. 1991 - 2001
Refractory | Neurology | Myasthenia gravis | Clinical Neurology | Minimal symptom expression | Eculizumab | Acetylcholine receptor | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Activities of daily living | Acetylcholine receptors | Neuromuscular junctions | Myasthenia | Patients | Quality of life | Index Medicus | Original Communication
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10. 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 : NMD, ISSN 0960-8966, 2017, Volume 27, Issue 8, pp. 782 - 790
Neurology | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Muscular Dystrophy, Facioscapulohumeral - therapy | Congresses as Topic | Netherlands | Muscular Dystrophy, Facioscapulohumeral - diagnosis | Registries - statistics & numerical data | Humans | Conferences, meetings and seminars | Workshops (Educational programs) | Index Medicus
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11. Full Text Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
by Wood, L and Bassez, G and Bleyenheuft, Corinne and Campbell, C and Cossette, Louise and Jimenez-Moreno, A.C and Engelen, B.G.M. van and Vohanka, Stanislav and Lochmuller, H
Orphanet journal of rare diseases, ISSN 1750-1172, 2018, Volume 13, Issue 1, pp. 155 - 155
Clinical trials | Registries | Myotonic dystrophy | Trial readiness | Genetics & Heredity | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Clinical Trials as Topic | Rare Diseases | Education | Humans | Myotonic Dystrophy | Rare diseases | Evaluation | Medical research | Registries (in medicine) | Medicine, Experimental | Research | Datasets | Neuromuscular diseases | Mental disorders | Cognition & reasoning | Conferences | Collaboration | Cognitive ability | Data collection | Patients | Muscular dystrophy | Index Medicus
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12. Full Text Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
by Wood, Libby and Bassez, Guillaume and Bleyenheuft, Corinne and Campbell, Craig and Cossette, Louise and Jimenez-Moreno, Aura Cecilia and Dai, Yi and Dawkins, Hugh and Díaz-Manera, Jordi and Dogan, Celine and El Sherif, Rasha and Fossati, Barbara and Graham, Caroline and Hilbert, James and Kastreva, Kristinia and Kimura, En and Korngut, Lawrence and Kostera-Pruszczyk, Anna and Lindberg, Christopher and Lindvall, Bjorn and Luebbe, Elizabeth and Lusakowska, Anna and Mazanec, Radim and Meola, Giovani and Orlando, Liannna and Takahashi, Masanori P and Peric, Stojan and Puymirat, Jack and Rakocevic-Stojanovic, Vidosava and Rodrigues, Miriam and Roxburgh, Richard and Schoser, Benedikt and Segovia, Sonia and Shatillo, Andriy and Thiele, Simone and Tournev, Ivailo and van Engelen, Baziel and Vohanka, Stanislav and Lochmüller, Hanns
Orphanet journal of rare diseases, ISSN 1750-1172, 08/2019, Volume 14, Issue 1, pp. 199 - 199
Index Medicus
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13. Full Text Long‐term safety and efficacy of eculizumab in generalized myasthenia gravis
by Muppidi, Srikanth 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 Nowak, Richard J and Andersen, Henning and Casasnovas, Carlos and Vu, Tuan H and Mantegazza, Renato and O'Brien, Fanny L and Wang, Jing Jing and Fujita, Kenji P and Howard, James F and Mazia, Claudio Gabriel and Wilken, Miguel and Barroso, Fabio and Rugiero, Marcelo and Bettini, Mariela and Chaves, Marcelo and Vidal, Gonzalo and Garcia, Alejandra Dalila and Van den Abeele, Guy and de Koning, Kathy and De Mey, Katrien and Mercelis, Rudy and Mahieu, Délphine and Wagemaekers, Linda and Depreitere, Annelies and Smetcoren, Charlotte and Stevens, Olivier and Van Daele, Sien and Vandenbussche, Nicolas and Vanhee, Annelies and Verjans, Sarah and Vynckier, Jan and D'Hondt, Ann and Tilkin, Petra and Alves de Siqueira Carvalho, Alzira and Feder, David and Ambrosio, Daniel and César, Pamela and Martins Ribeiro, Renata and Rocha, Rosana and Bezerra Rosa, Bruno and Veiga, Thabata and da Silva, Luiz Augusto and Santos Engel, Murilo and Gonçalves Geraldo, Jordana and Nogueira Coelho, Erica and Pozo, Marina and Prando, Natalia and Martineli Torres, Debora Dada and Butinhao, Cristiani Fernanda and Duran, Gustavo and Gomes da Silva, Tamires Cristina and Otavio Maia Gonçalves, Luiz and Pazetto, Lucas Eduardo and Fialho, Tomás Augusto Suriane and Renata Cubas Volpe, Luciana and Souza Duca, Luciana and Gheller Friedrich, Maurício André and Guerreiro, Alexandre and Mohr, Henrique and Pereira Martins, Maurer and da Cruz Pacheco, Daiane and Ferreira, Luciana and Macagnan, Ana Paula and Pinto, Graziela and Santos, Aline and Souza Bulle Oliveira, Acary and Amaral Andrade, Ana Carolina and Annes, Marcelo and Cavalcante Lino, Valeria and Pinto, Wladimir and Assis, Natália and Carrara, Fernanda and Fernandes, Patricia and Siddiqi, Zaeem and Phan, Cecile and Narayan, Jeffrey and Blackmore, Derrick and Mallon, Ashley and Roderus, Rikki and Watt, Elizabeth and Vohanka, Stanislav and Bednarik, Josef and Chmelikova, Magda and Cierny, Marek and Toncrova, Stanislava and Junkerova, Jana and Kurkova, Barbora and Reguliova, Katarina and Zapletalova, Olga and Pitha, Jiri and ... and REGAIN Study Grp and Regain Study Group and for the Regain Study Group
Muscle & nerve, ISSN 0148-639X, 07/2019, Volume 60, Issue 1, pp. 14 - 24
MGC | myasthenia gravis | MG‐ADL | eculizumab | QMG | MG‐QOL15 | MG-ADL | MG-QOL15 | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Meningococcal Infections - epidemiology | Meningococcal Vaccines - therapeutic use | Humans | Middle Aged | Male | Aspergillosis - epidemiology | Activities of Daily Living | Aspergillosis - etiology | Heart Diseases - epidemiology | Meningococcal Infections - etiology | Adult | Female | Heart Diseases - chemically induced | Injection Site Reaction - epidemiology | Muscle Strength | Angioedema - epidemiology | Antibodies, Monoclonal, Humanized - therapeutic use | Injection Site Reaction - etiology | Meningococcal Infections - prevention & control | Treatment Outcome | Disease Progression | Myasthenia Gravis - physiopathology | Complement Inactivating Agents - therapeutic use | Quality of Life | Angioedema - chemically induced | Longitudinal Studies | Myasthenia Gravis - drug therapy | Myasthenia gravis | Effectiveness | Activities of daily living | Antibodies | Neuromuscular junctions | Remission | Myasthenia | Pharmacology | Safety | Muscular strength | Quality of life | Index Medicus | Clinical | Clinical s
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