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1. Full Text G.P.15
by van Engelen, B.G and Voet, N and Janssen, B and Bleijenberg, G and Hendriks, J and de Groot, I and Padberg, G and Heerschap, A and Geurts, A
Neuromuscular Disorders, ISSN 0960-8966, 2014, Volume 24, Issue 9, pp. 798 - 799
The aim of this study was to investigate the effect of aerobic exercise training (AET) and cognitive behavior therapy (CBT) on chronic fatigue in patients with... 
Neurology | Cognitive therapy | Exercise
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2. Full Text Characterization of sarcoplasmic reticulum Ca.sup.2+ ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy
by Guglielmi, V and Oosterhof, A and Voermans, N.C and Cardani, R and Molenaar, J.P and van Kuppevelt, T.H and Meola, G and van Engelen, B.G and Tomelleri, G and Vattemi, G
Neuromuscular Disorders, ISSN 0960-8966, 06/2016, Volume 26, Issue 6, p. 378
* SERCA impairment has been suggested to occur in DM and in hypothyroid myopathy. * SERCA activity and expression of SERCA1 and SERCA2 are not altered in these... 
Hypothyroidism | Adenosine triphosphatase | Oligomers | Medical research | Myotonic dystrophy | Muscles | Medicine, Experimental
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3. Full Text Neuromuscular properties of the thigh muscles in patients with Ehlers-Danlos syndrome
by Gerrits, K.H.L and Voermans, N.C and de Haan, A and van Engelen, B.G
Muscle and Nerve, ISSN 0148-639X, 2013, Volume 47, Issue 1, pp. 96 - 104
Introduction: Ehlers-Danlos syndrome (EDS), a connective tissue disorder, may lead to impaired contractile function of lower limb muscles. Methods: To test... 
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4. Full Text Compound heterozygous mutations of the TNXB gene cause primary myopathy
by Voermans, N.C and Gerrits, K.H.L and van Engelen, B.G and de Haan, A
Neuromuscular Disorders, ISSN 0960-8966, 2014, Volume 24, pp. 88 - 89
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5. Full Text Coffee and muscle cramps
by Voermans, N.C and van Engelen, B.G
Neuromuscular Disorders, ISSN 0960-8966, 2011, Volume 21, Issue 12, pp. 832 - 832
Neurology | CAFFEINE | NEUROSCIENCES | CLINICAL NEUROLOGY | Female | Male | Coffee - adverse effects | Coffea - adverse effects | Humans | Muscle Cramp - etiology
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6. Full Text G.P.15: Aerobic exercise and cognitive behavior therapy reduce fatigue and slow progression of muscle MR fatty infiltration in FSHD
by van Engelen, B.G and Voet, N and Janssen, B and Bleijenberg, G and Hendriks, J and de Groot, I and Padberg, G and Heerschap, A and Geurts, A
Neuromuscular Disorders, ISSN 0960-8966, 10/2014, Volume 24, Issue 9-10, pp. 798 - 799
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7. Full Text Titin-based stiffening of muscle fibers in Ehlers-Danlos Syndrome
by Ottenheijm, C.A.C and Voermans, N.C and Hudson, B.D and Irving, T and Stienen, G.J.M and van Engelen, B.G and Granzier, H
Journal of Applied Physiology, ISSN 8750-7587, 2012, Volume 112, Issue 7, pp. 1157 - 1165
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8. Full Text EM.P.3.08 Matrix matters in man and mouse
by Voermans, N.C and van Engelen, B.G
Neuromuscular Disorders, ISSN 0960-8966, 2009, Volume 19, Issue 8, pp. 576 - 576
Neurology
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9. Full Text Diagnostic yield of muscle fibre conduction velocity in myopathies
by Blijham, P.J and van Engelen, B.G and st, G and Stegeman, D.F and Schelhaas, H.J and Zwarts, M.J
Journal of the Neurological Sciences, ISSN 0022-510X, 2011, Volume 309, Issue 1-2, pp. 40 - 44
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10. Full Text Muscle characteristics and altered myofascial force transmission in tenascin-X deficient mice, a mouse model of Ehlers-Danlos syndrome
by Huijing, P.A.J.B.M and Voermans, N.C and Baan, G.C and Buse-Pot, T.E and van Engelen, B.G and de Haan, A
Journal of Applied Physiology, ISSN 8750-7587, 2010, Volume 109, Issue 4, pp. 986 - 995
The Ehlers-Danlos syndrome is a group of inherited connective tissue disorders caused by defects in collagens or tenascin-X (TNX). Muscle involvement can be... 
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11. Full Text Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy
by Cats, E.A and Pol, W.L. van der and Piepers, S and Franssen, H and Jacobs, B.C and Berg-Vos, R.M. van den and Kuks, J.B.M and Doorn, P.A. van and Engelen, B.G.M. van and Verschuuren, J.J and Wokke, J.H.J and Veldink, J.H and Berg, L.H. van den
Neurology, ISSN 0028-3878, 2010, Volume 75, Issue 9, pp. 818 - 825
OBJECTIVE: Identification and examination of all patients with multifocal motor neuropathy (MMN) in the Netherlands to document the clinical spectrum and... 
ANTIBODIES | IMMUNOGLOBULIN TREATMENT | DISEASE | DOUBLE-BLIND | IMMUNE-MEDIATED POLYNEUROPATHIES | CONDUCTION BLOCK | GANGLIOSIDE | GRADUATED TUNING FORK | INTRAVENOUS IMMUNOGLOBULINS | SEVERITY | CLINICAL NEUROLOGY | Cross-Sectional Studies | Humans | Middle Aged | Immunoglobulins, Intravenous - administration & dosage | Male | Neural Conduction - physiology | Treatment Outcome | Muscle Fatigue - drug effects | Adult | Female | Motor Neuron Disease - drug therapy | Aged | Neural Conduction - drug effects | Motor Neuron Disease - physiopathology | Muscle Fatigue - physiology
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12. Full Text Repeatability and reliability of muscle relaxation properties induced by motor cortical stimulation
by Molenaar, J.P and Voermans, N.C and Jong, L.A de and Stegeman, D.F and Doorduin, J and Engelen, B.G.M. van
Journal of Applied Physiology, ISSN 8750-7587, 2018, Volume 124, Issue 6, pp. 1597 - 1604
Impaired muscle relaxation is a feature of many neuromuscular disorders. However, few tests arc available to quantify muscle relaxation. Transcranial magnetic... 
Muscle relaxation | Muscle cooling | Transcranial magnetic stimulation | Muscle fatigue | ENZYME-ACTIVITIES | SPORT SCIENCES | SILENT PERIOD | PHYSIOLOGY | transcranial magnetic stimulation | HUMAN SKELETAL-MUSCLE | SUPRASPINAL FATIGUE | MAGNETIC STIMULATION | FIBER-TYPE COMPOSITION | ELECTRICAL-STIMULATION | muscle cooling | VOLUNTARY ACTIVATION | SEX-DIFFERENCES | muscle fatigue | muscle relaxation | ADDUCTOR POLLICIS MUSCLE
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13. Full Text Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome
by Guglielmi, V and Voermans, N.C and Oosterhof, A and Nowis, D and Engelen, B.G.M. van and Tomelleri, G and Vattemi, G
Neuropathology and Applied Neurobiology, ISSN 0305-1846, 2018, Volume 44, Issue 5, pp. 533 - 536
Brody disease (BD, OMIM #601003) is an inherited skeletal muscle disease clinically characterized by exercise-induced impairment of muscle relaxation and... 
SKELETAL-MUSCLE | UNFOLDED PROTEIN RESPONSE | SERCA1 | RETICULUM | PATHOLOGY | NEUROSCIENCES | CA2+ HOMEOSTASIS | CLINICAL NEUROLOGY | Analysis | Stress (Physiology)
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14. Full Text The predictive value of respiratory function tests for non-invasive ventilation in amyotrophic lateral sclerosis
by Tilanus, T. B. M and Groothuis, J. T and TenBroek-Pastoor, J. M. C and Feuth, T. B and Heija, Y. F and Slenders, J. P. L and Doorduin, J and van Engelen, B. G and Kampelmacher, M. J and Raaphorst, J
Respiratory research, ISSN 1465-9921, 2017, Volume 18, Issue 1, pp. 144 - 10
Background: Non-invasive ventilation (NIV) improves survival and quality of life in amyotrophic lateral sclerosis (ALS) patients. The timing of referral to a... 
ALS | Non-invasive ventilation | Respiratory function tests | NASAL-INSPIRATORY PRESSURE | STANDARDS | SPIROMETRY | MOTOR-NEURON DISEASE | FLOW | IMPAIRMENT | VARIABILITY | PROGRESSIVE MUSCULAR-ATROPHY | NEUROMUSCULAR DISEASE | MUSCLE STRENGTH | RESPIRATORY SYSTEM | Predictive Value of Tests | Cough - physiopathology | Amyotrophic Lateral Sclerosis - physiopathology | Area Under Curve | Humans | Middle Aged | Respiratory Muscles - physiopathology | Amyotrophic Lateral Sclerosis - diagnosis | Male | Patient Selection | Time Factors | Clinical Decision-Making | Female | Retrospective Studies | Muscle Strength | Reproducibility of Results | Time-to-Treatment | Amyotrophic Lateral Sclerosis - therapy | Respiratory Function Tests - methods | Lung - physiopathology | Disease Progression | Maximal Respiratory Pressures | Noninvasive Ventilation | Vital Capacity | ROC Curve | Aged | Care and treatment | Usage | Patient outcomes | Physiological aspects | Amyotrophic lateral sclerosis | Pulmonary function tests | Research | Artificial respiration | Neuromuscular diseases | Respiratory function | Cut-off | Indication | Data processing | Patients | Pressure | Cough | Quality of life | Studies | Hypercapnia | Hypoventilation | Medical prognosis | Ventilation | Respiration | Health risk assessment
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15. Full Text Implementation of multidisciplinary advince to allied health care professionals regarding the management of their patients with neuromuscular diseases
by Cup, E.H and Pieterse, A.J and Henicks, H.T and van Engelen, B.G and Oostendorp, R.A and van der Wilt, G.J
Disability and Rehabilitation, ISSN 0963-8288, 2011, Volume 33, Issue 9, pp. 787 - 795
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16. Full Text PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose
by Voermans, N.C and Preisler, N and Madsen, K.L and Janssen, M.C.H and Kusters, B and Abu Bakar, N and Conte, F and Lamberti, V.M.L and Nusman, F and van Engelen, B.G and van Scherpenzeel, M and Vissing, J and Lefeber, D.J
Neuromuscular Disorders, ISSN 0960-8966, 2017, Volume 27, Issue 4, pp. 370 - 376
Highlights • PGM1 deficiency is associated with severe exercise intolerance due to a block in skeletal muscle glycogenolytic capacity. • Oral galactose... 
Neurology | Phosphoglucomutase 1 | Glycogen Storage Disease type XIV | Oral galactose treatment | Congenital disorder of protein N-glycosylation | PGM1 deficiency | Galactose - pharmacology | Glycogen Storage Disease - drug therapy | Humans | Middle Aged | Male | Exercise - physiology | Glycogen Storage Disease - metabolism | Muscles | Galactose
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17. Full Text Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire study
by van Ruitenbeek, E and Custers, J.A.E and Verhaak, C and Snoeck, M and Erasmus, C.E and Kamsteeg, E.J and Schouten, M.I and Coleman, C and Treves, S and Van Engelen, B.G and Jungbluth, H and Voermans, N.C
Neuromuscular Disorders, ISSN 0960-8966, 01/2019, Volume 29, Issue 1, pp. 30 - 38
Mutations in are a common genetic cause of non-dystrophic neuromuscular disorders. To obtain baseline data concerning the prevalence of fatigue, the... 
MELAS | Functional impairment | Quality of life | RYR1-related myopathies | MALIGNANT HYPERTHERMIA | MUSCULAR-DYSTROPHY | HOSPITAL ANXIETY | CANCER | NEUROSCIENCES | CLINICAL NEUROLOGY | SKELETAL-MUSCLE | DISEASE | MUTATION | PSYCHOLOGICAL DISTRESS | HEALTH | MYOTONIC-DYSTROPHY
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18. Full Text Living with Myotonic Dystrophy; what can be learned form couples? A qualitative study
by Cup, E.H and Kinebanian, A and Satink, T and Pieterse, A.J and Henicks, H.T and Oostendorp, R.A and van der Wilt, G.J and van Engelen, B.G
BMC Neurology, ISSN 1471-2377, 2011, Volume 13
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19. Full Text KBTBD13: a novel gene implicated in cardiomyopathy
by de Winter, J.M and van den Berg, M.P and Strohm, J and Jongbloed, J.D and van der Roest, W and van Wijngaarden, J and Timmermans, J and Kamsteeg, E.J and van Engelen, B.G and van der Pijl, R.J and Granzier, H and Voermans, N.C and van Spaendonck-Zwarts, K and Ottenheijm, C.A.C
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 07/2018, Volume 120, pp. 6 - 6
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20. Full Text Effects of shared medical appointments on quality of life and cost-effectiveness for patients with a chronic neuromuscular disease. Study protocol of a randomized controlled trial
by Seesing, F.M and st, G and van der Wilt, G.J and van Engelen, B.G
BMC Neurology, ISSN 1471-2377, 2011, Volume 32, Issue 11
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