B G van Engelen
Overview
Explore the profile of B G van Engelen including associated specialties, affiliations and a list of published articles.
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Articles
112
Citations
1568
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Recent Articles
1.
van de Geest-Buit W, Rasing N, Mul K, Deenen J, Vincenten S, Siemann I, et al.
Disabil Rehabil
. 2022 Jul;
45(15):2507-2516.
PMID: 35815498
Purpose: To assess the psychosocial outcomes of facial weakness in facioscapulohumeral muscular dystrophy (FSHD). Materials And Methods: A cross-sectional survey study. The severity of facial weakness was assessed by patients...
2.
Voermans N, Vriens-Munoz Bravo M, Padberg G, Laforet P, van Alfen N, Attarian S, et al.
Neuromuscul Disord
. 2021 Aug;
31(9):907-918.
PMID: 34404575
No abstract available.
3.
Voermans N, van der Bilt R, IJspeert J, Hogrel J, Jeanpierre M, Behin A, et al.
J Neurol
. 2019 Sep;
266(12):2987-2996.
PMID: 31471688
Objective: To study scapular winging or other forms of scapular dyskinesis (condition of alteration of the normal position and motion of the scapula) in myotonic dystrophy type 1 (DM1), which...
4.
van Ruitenbeek E, Custers J, Verhaak C, Snoeck M, Erasmus C, Kamsteeg E, et al.
Neuromuscul Disord
. 2018 Dec;
29(1):30-38.
PMID: 30578099
Mutations in RYR1 are a common genetic cause of non-dystrophic neuromuscular disorders. To obtain baseline data concerning the prevalence of fatigue, the psychological disease burden and quality of life associated...
5.
Molenaar J, Voermans N, de Jong L, Stegeman D, Doorduin J, van Engelen B
J Appl Physiol (1985)
. 2018 Mar;
124(6):1597-1604.
PMID: 29543137
Impaired muscle relaxation is a feature of many neuromuscular disorders. However, few tests are available to quantify muscle relaxation. Transcranial magnetic stimulation (TMS) of the motor cortex can induce muscle...
6.
Guglielmi V, Voermans N, Oosterhof A, Nowis D, van Engelen B, Tomelleri G, et al.
Neuropathol Appl Neurobiol
. 2017 Aug;
44(5):533-536.
PMID: 28801956
No abstract available.
7.
Tilanus T, Groothuis J, TenBroek-Pastoor J, Feuth T, Heijdra Y, Slenders J, et al.
Respir Res
. 2017 Jul;
18(1):144.
PMID: 28743265
Background: Non-invasive ventilation (NIV) improves survival and quality of life in amyotrophic lateral sclerosis (ALS) patients. The timing of referral to a home ventilation service (HVS), which is in part...
8.
Voermans N, Preisler N, Madsen K, Janssen M, Kusters B, Abu Bakar N, et al.
Neuromuscul Disord
. 2017 Feb;
27(4):370-376.
PMID: 28190645
Mutations in PGM1 (phosphoglucomutase 1) cause Glycogen Storage Disease type XIV, which is also a congenital disorder of protein N-glycosylation. It presents throughout life as myopathy with additional systemic symptoms....
9.
Demirdas S, Dulfer E, Robert L, Kempers M, van Beek D, Micha D, et al.
Clin Genet
. 2016 Sep;
91(3):411-425.
PMID: 27582382
The tenascin-X (TNX) deficient type Ehlers-Danlos syndrome (EDS) is similar to the classical type of EDS. Because of the limited awareness among geneticists and the challenge of the molecular analysis...
10.
Guglielmi V, Oosterhof A, Voermans N, Cardani R, Molenaar J, van Kuppevelt T, et al.
Neuromuscul Disord
. 2016 May;
26(6):378-85.
PMID: 27133661
Sarcoplasmic/endoplasmic reticulum Ca(2+) ATPase (SERCA) pumps play the major role in lowering cytoplasmic calcium concentration in skeletal muscle by catalyzing the ATP-dependent transport of Ca(2+) from the cytosol to the...