Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy?

od Scalco, Renata S, Snoeck, Marc, Quinlivan, Ros, Treves, Susan, Laforét, Pascal, Jungbluth, Heinz, Voermans, Nicol C
Izdano u BMJ Open Sport Exerc Med (2016)

Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers

od Mul, Karlien, Horlings, Corinne G. C., Vincenten, Sanne C. C., Voermans, Nicol C., van Engelen, Baziel G. M., van Alfen, Nens
Izdano u J Neurol (2018)

Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy

od Lassche, Saskia, Voermans, Nicol C, Schreuder, Tim, Heerschap, Arend, Küsters, Benno, Ottenheijm, Coen AC, Hopman, Maria TE, van Engelen, Baziel GM
Izdano u Muscle Nerve (2020)

Anaesthesia and neuromuscular disorders: what a neurologist needs to know

od van den Bersselaar, Luuk R, Snoeck, Marc M J, Gubbels, Madelief, Riazi, Sheila, Kamsteeg, Erik-Jan, Jungbluth, Heinz, Voermans, Nicol C
Izdano u Pract Neurol (2020)

Titin-based stiffening of muscle fibers in Ehlers-Danlos Syndrome

od Ottenheijm, Coen A. C., Voermans, Nicol C., Hudson, Bryan D., Irving, Thomas, Stienen, Ger J. M., van Engelen, Baziel G., Granzier, Henk
Izdano 2012

Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD

od Lassche, Saskia, Küsters, Benno, Heerschap, Arend, Schyns, Maxime V.P., Ottenheijm, Coen A.C., Voermans, Nicol C., van Engelen, Baziel G.M.
Izdano u J Neuromuscul Dis (2020)

Clinical features, lectin staining, and a novel GNE frameshift mutation in HIBM

od Voermans, Nicol C., Guillard, M., Doedée, R., Lammens, M., Huizing, Marjan, Padberg, G.W., Wevers, R.A., van Engelen, B.G., Lefeber, D.J.
Izdano 2010

MRI-Guided Biopsy as a Tool for Diagnosis and Research of Muscle Disorders

od Lassche, Saskia, Janssen, Barbara H., IJzermans, Ties, Fütterer, Jurgen J., Voermans, Nicol C., Heerschap, Arend, Küsters, Benno, Mann, Ritse M., van Engelen, Baziel GM
Izdano u J Neuromuscul Dis (2018)

A novel role for the extracellular matrix glycoprotein‐Tenascin‐X in gastric function

od Aktar, Rubina, Peiris, Madusha, Fikree, Asma, Eaton, Simon, Kritas, Stamatiki, Kentish, Stephen J., Araujo, Eduardo J. A., Bacarin, Cristiano, Page, Amanda J., Voermans, Nicol C., Aziz, Qasim, Blackshaw, L. Ashley
Izdano u J Physiol (2019)

Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophy

od Lassche, Saskia, Stienen, Ger J.M., Irving, Tom C., van der Maarel, Silvère M., Voermans, Nicol C., Padberg, George W., Granzier, Henk, van Engelen, Baziel G.M., Ottenheijm, Coen A.C.
Izdano 2013

Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol

od Lassche, Saskia, Ottenheijm, Coen AC, Voermans, Nicol C, Westeneng, Henk-Jan, Janssen, Barbara H, van der Maarel, Silvère M, Hopman, Maria T, Padberg, George W, Stienen, Ger JM, van Engelen, Baziel GM
Izdano 2013

Dejerine–Sottas disease in childhood—Genetic and sonographic heterogeneity

od Hobbelink, Sanne M. R., Brockley, Cain R., Kennedy, Rachel A., Carroll, Kate, de Valle, Katy, Rao, Padma, Davis, Mark R., Laing, Nigel G., Voermans, Nicol C., Ryan, Monique M., Yiu, Eppie M.
Izdano u Brain Behav (2018)

The facioscapulohumeral muscular dystrophy Rasch‐built overall disability scale (FSHD‐RODS)

od Mul, Karlien, Hamadeh, Tatiana, Horlings, Corinne G. C., Tawil, Rabi, Statland, Jeffrey M., Sacconi, Sabrina, Corbett, Alastair J., Voermans, Nicol C., Faber, Catharina G., van Engelen, Baziel G. M., Merkies, Ingemar S. J.
Izdano u Eur J Neurol (2021)

Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy

od Lassche, Saskia, Voermans, Nicol C., van der Pijl, Robbert, van den Berg, Marloes, Heerschap, Arend, van Hees, Hieronymus, Kusters, Benno, van der Maarel, Silvère M., Ottenheijm, Coen A.C., van Engelen, Baziel G.M.
Izdano u Neurology (2020)

Intact transferrin and total plasma glycoprofiling for diagnosis and therapy monitoring in phosphoglucomutase-I deficiency

od Bakar, Nurulamin Abu, Voermans, Nicol C., Marquardt, Thorsten, Thiel, Christian, Janssen, Mirian C.H., Hansikova, Hana, Crushell, Ellen, Sykut-Cegielska, Jolanta, Bowling, Francis, Mørkrid, Lars, Vissing, John, Morava, Eva, van Scherpenzeel, Monique, Lefeber, Dirk J.
Izdano u Transl Res (2018)

Adding quantitative muscle MRI to the FSHD clinical trial toolbox

od Mul, Karlien, Vincenten, Sanne C.C., Voermans, Nicol C., Lemmers, Richard J.L.F., van der Vliet, Patrick J., van der Maarel, Silvère M., Padberg, George W., Horlings, Corinne G.C., van Engelen, Baziel G.M.
Izdano u Neurology (2017)

Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene

od Lemmers, Richard JLF, van der Vliet, Patrick J, Blatnik, Ana, Balog, Judit, Zidar, Janez, Henderson, Don, Goselink, Rianne, Tapscott, Stephen J., Voermans, Nicol C, Tawil, Rabi, Padberg, George W, van Engelen, Baziel GM, van der Maarel, Silvère M
Izdano u J Med Genet (2022)

Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy

od Goselink, Rianne J.M., Mul, Karlien, van Kernebeek, Caroline R., Lemmers, Richard J.L.F., van der Maarel, Silvère M., Schreuder, Tim H.A., Erasmus, Corrie E., Padberg, George W., Statland, Jeffrey M., Voermans, Nicol C., van Engelen, Baziel G.M.
Izdano u Neurology (2019)

Incidence, Prevalence, and Geographical Clustering of Motor Neuron Disease in the Netherlands

od de Jongh, Adriaan D., van Eijk, Ruben P.A., Peters, Susan M., van Es, Michael A., Horemans, Anja M.C., van der Kooi, Anneke J., Voermans, Nicol C., Vermeulen, Roel C.H., Veldink, Jan H., van den Berg, Leonard H.
Izdano u Neurology (2021)

Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice

od Zou, Yaqun, Zwolanek, Daniela, Izu, Yayoi, Gandhy, Shreya, Schreiber, Gudrun, Brockmann, Knut, Devoto, Marcella, Tian, Zuozhen, Hu, Ying, Veit, Guido, Meier, Markus, Stetefeld, Jörg, Hicks, Debbie, Straub, Volker, Voermans, Nicol C., Birk, David E., Barton, Elisabeth R., Koch, Manuel, Bönnemann, Carsten G.
Izdano 2014