Browsing by Author "Mul, K."

The many faces of facioscapulohumeral muscular dystrophy: opportunities and challenges on the road to therapies

2019, Dissertation

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

Goselink, R.J.M.; Mul, K. ; Kernebeek, C.R. van ; Lemmers, R.; Maarel, S.M. van der; Schreuder, T.H.A. ; Erasmus, C.E. ; Padberg, G.W. ; Statland, J.M.; Voermans, N.C. ; et al.

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2019, Article / Letter to editor (Neurology, vol. 92, iss. 4, (2019), pp. e378-e385)

Effects of weakness of orofacial muscles on swallowing and communication in FSHD

Mul, K. ; Berggren, K.N.; Sills, M.Y.; McCalley, A.; Engelen, B.G.M. van ; Johnson, N.E.; Statland, J.M.

2019, Article / Letter to editor (Neurology, vol. 92, iss. 9, (2019), pp. e957-e963)

Specific muscle strength is reduced in facioscapulohumeral dystrophy: An MRI based musculoskeletal analysis

Marra, M.A.; Heskamp, L.; Mul, K. ; Lassche, S.; Engelen, B.G.M. van ; Heerschap, A. ; Verdonschot, N.J.

2018, Article / Letter to editor (Neuromuscular Disorders, vol. 28, iss. 3, (2018), pp. 238-245)

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

Mul, K. ; Horlings, G.C. ; Vincenten, S.C.C.; Voermans, N.C. ; Engelen, B.G.M. van ; Alfen, N. van

2018, Article / Letter to editor (Journal of Neurology, vol. 265, iss. 11, (2018), pp. 2646-2655)

FSHD type 2 and Bosma arhinia microphthalmia syndrome Two faces of the same mutation

Mul, K. ; Lemmers, Richard J. L. F.; Kriek, M.; Vliet, P.J. van der; Boogaard, M.L. van den; Badrising, U.A.; Voermans, N.C. ; Engelen, B.G.M. van ; Horlings, G.C. ; Shaw, N.D.; et al.

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2018, Article / Letter to editor (Neurology, vol. 91, iss. 6, (2018), pp. E562-E570)

Electrical impedance myography in facioscapulohumeral muscular dystrophy: A 1-year follow-up study

Mul, K. ; Heatwole, C.; Eichinger, K.; Dilek, N.; Martens, W.B.; Engelen, B.G.M. van ; Tawil, R.; Statland, J.M.

2018, Article / Letter to editor (Muscle and Nerve, vol. 58, iss. 2, (2018), pp. 213-218)

Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2

Lemmers, Richard J. L. F.; Vliet, P.J. van der; Balog, J.; Goeman, J.J. ; Arindrarto, W.; Krom, Y.D.; Mul, K. ; Engelen, B.G.M. van ; Tawil, R.; Maarel, S.M. van der

2018, Article / Letter to editor (European Journal of Human Genetics, vol. 26, iss. 1, (2018), pp. 94-106)

Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1

Mul, K. ; Voermans, N.C. ; Lemmers, Richard J. L. F.; Jonker, M.A.; Vliet, Patrick J. van der; Padberg, G.W. ; Maarel, Silvere M. van der; Horlings, G.C.

2018, Article / Letter to editor (Clinical Genetics, vol. 94, iss. 6, (2018), pp. 521-527)

Lifetime endogenous estrogen exposure and disease severity in female patients with facioscapulohumeral muscular dystrophy

Mul, K. ; Horlings, G.C. ; Voermans, N.C. ; Schreuder, T.H.A. ; Engelen, B.G.M. van

2018, Article / Letter to editor (Neuromuscular Disorders, vol. 28, iss. 6, (2018), pp. 508-511)

A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy

Goselink, R.J.M.; Kernebeek, C.R. van ; Mul, K. ; Lemmers, R.J.L.F.; Maarel, S.M. van der; Brouwer, O.F.; Voermans, N.C. ; Padberg, G.W.A.M. ; Erasmus, C.E. ; Engelen, B.G.M. van

2018, Article / Letter to editor (European Journal of Paediatric Neurology, vol. 22, iss. 5, (2018), pp. 782-785)

225th ENMC international workshop:: A global FSHD registry framework, 18-20 November 2016, Heemskerk, The Netherlands

Mul, K. ; Kinoshita, J.; Dawkins, H.; Engelen, B.G.M. van ; Tupler, R.

2017, Article / Letter to editor (Neuromuscular Disorders, vol. 27, iss. 8, (2017), pp. 782-790)

Adding quantitative muscle MRI to the FSHD clinical trial toolbox

Mul, K. ; Vincenten, S.C.C.; Voermans, N.C. ; Lemmers, R.; Vliet, P.J.C. Van; Maarel, S.M. van der; Padberg, G.W.A.M. ; Horlings, G.C. ; Engelen, B.G.M. van

2017, Article / Letter to editor (Neurology, vol. 89, iss. 20, (2017), pp. 2057-2065)

Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)

Goselink, R.J.M.; Schreuder, T.H.A. ; Mul, K. ; Voermans, N.C. ; Pelsma, M.; Groot, I.J.M. de ; Alfen, N. van ; Franck, B.A.M.; Theelen, T. ; Lemmers, R.J.; et al.

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2016, Article / Letter to editor (BMC Neurology, vol. 16, (2016), pp. 138)

What's in a name? The clinical features of facioscapulohumeral muscular dystrophy

Mul, K. ; Lassche, S.; Voermans, N.C. ; Padberg, G.W. ; Horlings, G.C. ; Engelen, B.G.M. van

2016, Article / Letter to editor (Practical Neurology, vol. 16, iss. 3, (2016), pp. 201-207)

Integrating clinical and genetic observations in facioscapulohumeral muscular dystrophy

Mul, K. ; Boogaard, M.L. van den; Maarel, S.M. van der; Engelen, B.G.M. van

2016, Article / Letter to editor (Current Opinion in Neurology, vol. 29, iss. 5, (2016), pp. 606-613)

Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatum

Mul, K. ; Padberg, G.W. ; Voermans, N.C.

2015, Article / Letter to editor (European Journal of Medical Genetics, vol. 58, iss. 4, (2015), pp. 203-204)

Ulcus cruris als uiting van de ziekte van Waldenström

Mul, K. ; Vlot, A.; Vissers, M.

2014, Article / Letter to editor (Nederlands Tijdschrift voor Dermatologie & Venereologie, vol. 25, iss. 6, (2014), pp. 4)

Calcipotriol/betamethasone dipropionate ointment in mild-to-moderate paediatric psoriasis: long-term daily clinical practice data in a prospective cohort

Geel, M.J. van; Mul, K. ; Oostveen, A.M.; Kerkhof, P.C. van de ; Jong, E.M. de ; Seyger, M.M.B.

2014, Article / Letter to editor (British Journal of Dermatology, vol. 171, iss. 2, (2014), pp. 363-369)

Management of sporadic duodenal adenomas and the association with colorectal neoplasms: a retrospective cohort study.

Heumen, B.W.H van ; Mul, K. ; Nagtegaal, I.D. ; Kouwen, M.C.A. van ; Nagengast, F.M.

2012, Article / Letter to editor (Journal of Clinical Gastroenterology, vol. 46, iss. 5, (2012), pp. 390-396)

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