Nicol C Voermans (N C Voermans)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 27

Top Topics

Coronavirus Disease

Clinical Practice

Ejection Fraction

Muscular Dystrophy

Top Venues

Acta neurologica Belgica

Clinical genetics

Practical neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, Joery P Molenaar, Hilde Braakman, Erik-Jan Kamsteeg, Richard J Rodenburg, Benno Kusters, Suzanne Koudijs, Baziel G M van Engelen, Corrie E Erasmus, Nicol C Voermans
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children. Neurology 102 (5) (2024)
Johanna C W Deenen, Joost Kools, Anna Greco, Renée Thewissen, Wiecke van de Put, Anke Lanser, Leo A B Joosten, Andre L M Verbeek, Baziel G M van Engelen, Nicol C Voermans
Living with facioscapulohumeral muscular dystrophy during the first two COVID-19 outbreaks: a repeated patient survey in the Netherlands. Acta neurologica Belgica 124 (2) (2024)
Johanna C W Deenen, Joost Kools, Anna Greco, Renée Thewissen, Wiecke van de Put, Anke Lanser, Leo A B Joosten, Andre L M Verbeek, Baziel G M van Engelen, Nicol C Voermans
Living with facioscapulohumeral muscular dystrophy during the first two COVID-19 outbreaks: a repeated patient survey in the Netherlands. Acta neurologica Belgica (2024)
Sanne C C Vincenten, Jeroen L M van Doorn, Sjan Teeselink, Nathaniël B Rasing, George W Padberg, Nicol C Voermans, Baziel G M van Engelen, Nens van Alfen, Karlien Mul
The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasound. Muscle & nerve (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics (2024)
Johanna C W Deenen, Joost Kools, Anna Greco, Renée Thewissen, Wiecke van de Put, Anke Lanser, Leo A B Joosten, Andre L M Verbeek, Baziel G M van Engelen, Nicol C Voermans
Living with facioscapulohumeral muscular dystrophy during the first two COVID-19 outbreaks: a repeated patient survey in the Netherlands. Acta neurologica Belgica 124 (2) (2024)
Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, Joery P Molenaar, Hilde Braakman, Erik-Jan Kamsteeg, Richard J Rodenburg, Benno Kusters, Suzanne Koudijs, Baziel G M van Engelen, Corrie E Erasmus, Nicol C Voermans
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children. Neurology 102 (5) (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Nicol C Voermans, Salman F Bhai, Pascal Laforet, John Vissing
Diagnostic workup of rhabdomyolysis: Genetic testing should precede neurophysiological testing. Muscle & nerve (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Johanna C W Deenen, Joost Kools, Anna Greco, Renée Thewissen, Wiecke van de Put, Anke Lanser, Leo A B Joosten, Andre L M Verbeek, Baziel G M van Engelen, Nicol C Voermans
Living with facioscapulohumeral muscular dystrophy during the first two COVID-19 outbreaks: a repeated patient survey in the Netherlands. Acta neurologica Belgica 124 (2) (2024)
Johanna C W Deenen, Joost Kools, Anna Greco, Renée Thewissen, Wiecke van de Put, Anke Lanser, Leo A B Joosten, Andre L M Verbeek, Baziel G M van Engelen, Nicol C Voermans
Living with facioscapulohumeral muscular dystrophy during the first two COVID-19 outbreaks: a repeated patient survey in the Netherlands. Acta neurologica Belgica 124 (2) (2024)
Nathaniël B Rasing, Willianne van de Geest-Buit, On Ying A Chan, Karlien Mul, Anke Lanser, Corrie E Erasmus, Jan T Groothuis, Judith Holler, Koen J A O Ingels, Bart Post, Ietske Siemann, Nicol C Voermans
Psychosocial functioning in patients with altered facial expression: a scoping review in five neurological diseases. Disability and rehabilitation (2023)
Walaa Karazi, Renata S Scalco, Mads G Stemmerik, Nicoline Løkken, Alejandro Lucia, Alfredo Santalla, Andrea Martinuzzi, Marinela Vavla, Gianluigi Reni, Antonio Toscano, Olimpia Musumeci, Carlyn V Kouwenberg, Pascal Laforêt, Beatriz San Millán, Irene Vieitez, Gabriele Siciliano, Enrico Kühnle, Rebecca Trost, Sabrina Sacconi, Hacer Durmus, Biruta Kierdaszuk, Andrew Wakelin, Antoni L Andreu, Tomàs Pinós, Ramon Marti, Ros Quinlivan, John Vissing, Nicol C Voermans, null null
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation. Orphanet journal of rare diseases 18 (1) (2023)
Jildou N Dijkstra, Eline Boon, Nick Kruijt, Esther Brusse, Sithara Ramdas, Heinz Jungbluth, Baziel G M van Engelen, Jon Walters, Nicol C Voermans
Muscle cramps and contractures: causes and treatment. Practical neurology (2022)
Joery P Molenaar, Elianne van Zandvoort, Baziel G M van Engelen, Nicol C Voermans, Jonne Doorduin
Reproducibility and robustness of motor cortical stimulation to assess muscle relaxation kinetics. Physiological reports 10 (20) (2022)
Jildou N Dijkstra, Eline Boon, Nick Kruijt, Esther Brusse, Sithara Ramdas, Heinz Jungbluth, Baziel G M van Engelen, Jon Walters, Nicol C Voermans
Muscle cramps and contractures: causes and treatment. Practical neurology 23 (1) (2022)
Sjan Teeselink, Sanne C C Vincenten, Nicol C Voermans, Jan T Groothuis, Jonne Doorduin, Peter J Wijkstra, Corinne Gosewina Cornelia Horlings, Baziel G M van Engelen, Karlien Mul
Long-term follow-up of respiratory function in facioscapulohumeral muscular dystrophy. Journal of neurology 269 (7) (2022)
Saskia L S Houwen-van Opstal, Ramon O Tak, Maaike Pelsma, Frederik M A van den Heuvel, Hermine A van Duyvenvoorde, Edith H C Cup, Lilian T L Sie, Johan S H Vles, Imelda J M de Groot, Nicol C Voermans, Michel A A P Willemsen
Long-term outcomes for females with early-onset dystrophinopathy. Developmental medicine and child neurology (2022)
Jildou N Dijkstra, Eline Boon, Nick Kruijt, Esther Brusse, Sithara Ramdas, Heinz Jungbluth, Baziel G M van Engelen, Jon Walters, Nicol C Voermans
Muscle cramps and contractures: causes and treatment. Practical neurology 23 (1) (2022)
Stacha F I Reumers, Frederik Braun, Jennifer L Spillane, Johann Böhm, Maartje Pennings, Meyke Schouten, Anneke J van der Kooi, A Reghan Foley, Carsten G Bonnemann, Erik-Jan Kamsteeg, Corrie E Erasmus, Ulrike Schara-Schmidt, Heinz Jungbluth, Nicol C Voermans
Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers: An International Questionnaire Study. Neurology 97 (5) (2021)
Sümeyye Sezer, Edith H C Cup, Lieve M Roets-Merken, Anke Lanser, Ietske Siemann, Janneke G Weikamp, Karlien Mul, Baziel G M van Engelen, Ton Satink, Nicol C Voermans
Experiences of patients with facioscapulohumeral dystrophy with facial weakness: a qualitative study. Disability and rehabilitation (2021)
Luuk R Van den Bersselaar, Marc M J Snoeck, Madelief Gubbels, Sheila Riazi, Erik-Jan Kamsteeg, Heinz Jungbluth, Nicol C Voermans
Anaesthesia and neuromuscular disorders: what a neurologist needs to know. Practical neurology (2020)
Nick Kruijt, Luuk R Van den Bersselaar, Erik-Jan Kamsteeg, W Verbeeck, M M J Snoeck, D S Everaerd, Wilson F Abdo, David R M Jansen, Corrie E Erasmus, Heinz Jungbluth, Nicol C Voermans
The etiology of rhabdomyolysis: an interaction between genetic susceptibility and external triggers. European journal of neurology 28 (2) (2020)
Nicol C Voermans, R C van der Bilt, J IJspeert, J Y Hogrel, M Jeanpierre, A Behin, P Laforet, T Stojkovic, B G van Engelen, G W Padberg, S Sacconi, R J L F Lemmers, S M van der Maarel, B Eymard, G Bassez
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations. Journal of neurology 266 (12) (2019)