Baziel van Engelen - Publications#
H-index: 63 (Web of Science); 72 (Research gate), 82 (Google Scholar)
Selected contributions form the last 5 years
1. Stunnenberg BC, Raaphorst J, ... ,van Engelen BGM*, van der Wilt GJ* (* shared last authors). Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials. JAMA. 2018 Dec 11;320(22):2344-2353
2. Okkersen K, ..., van Engelen BGM. Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial. The Lancet Neurology, 2018 Aug;17(8): 671-680
3. van Eijk JJJ, Dalton HR, ..., van Engelen BGM. Clinical phenotype and outcome of hepatitis E virus-associated neuralgic amyotrophy. Neurology. 2017 Aug 29;89(9):909-917
4. Mul K, Vincenten SCC, ... , van Engelen BGM. Adding quantitative muscle MRI to the FSHD clinical trial toolbox. Neurology. 2017 Nov 14;89(20):2057-2065.
5. de Winter JM, ... , van Engelen BG*, Voermans NC*, Ottenheijm CA (*equal penultimate authors). KBTBD13 is an actin-binding protein that modulates muscle kinetics. J Clin Invest. 2020 Feb 3;130(2):754-767. doi: 10.1172/JCI124000.
6. Heskamp L, ... , van Engelen BGM*, Heerschap A* (* shared last authors). Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRI. Neurology. 2019 Jun 11;92(24
7. Goselink RJM, Mul K, ... , van Engelen BGM. Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy. Neurology. 2019 Jan 22;92(4):
8. Lilleker JB, Rietveld A, ... , van Engelen BG; all UKMYONET contributors. Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis. Ann Rheum Dis. 2017 May;76(5):862-868
9. Benveniste O, ..., van Engelen BG. Amyloid deposits and inflammatory infiltrates in sporadic inclusion body myositis: the inflammatory egg comes before the degenerative chicken. Acta Neuropathol. 2015 May;129(5):611-24.
10. Goselink RJM, ..., van Engelen BGM, Erasmus CE. Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study. Ann Neurol. 2018 Nov;84(5):627-637
