نتائج البحث - "A.A. Tieleman"

1

Ancestral Origin of the First Indian Families with Myotonic Dystrophy Type 2

المؤلفون: Johanne M. Groothuismink, Manon Damen, Mascha M.V.A.P. Schijvenaars, Marlies Schimmel-Naber, A.A. Tieleman, Marieke J H Coenen

المصدر: Journal of Neuromuscular Diseases, 8, 715-722
Journal of Neuromuscular Diseases, 8, 4, pp. 715-722

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, India, Single-nucleotide polymorphism, 030105 genetics & heredity, Biology, 03 medical and health sciences, Young Adult, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, Genetic variation, SNP, Humans, Myotonic Dystrophy, Gene, Aged, Netherlands, Genetics, Suriname, Portugal, Haplotype, Intron, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Morocco, Neurology, Haplotypes, Inflammatory diseases Radboud Institute for Health Sciences [Radboudumc 5], Microsatellite, Female, Neurology (clinical), Trinucleotide repeat expansion, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6129650892a4acf407400b9ea40a10d8Test
https://hdl.handle.net/2066/236726Test

2

High incidence of falls in patients with myotonic dystrophy type 1 and 2: A prospective study

المؤلفون: Fran H.P. Smulders, A.A. Tieleman, Joost Raaphorst, Joost Berends, Baziel G.M. van Engelen, Nicol C. Voermans, Corinne G.C. Horlings

المساهمون: Neurology, Amsterdam Neuroscience - Neurodegeneration

المصدر: Neuromuscular Disorders, 29, 758-765
Neuromuscular disorders, 29(10). Elsevier Limited
Neuromuscular Disorders, 29, 10, pp. 758-765

مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, Myotonic dystrophy, Head trauma, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, 0302 clinical medicine, medicine, Humans, Myotonic Dystrophy, Clinical significance, Prospective Studies, Prospective cohort study, Genetics (clinical), Balance (ability), Muscle Weakness, business.industry, Incidence (epidemiology), Age Factors, Muscle weakness, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, 030104 developmental biology, Neurology, Pediatrics, Perinatology and Child Health, Accidental Falls, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Fall prevention

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cb2fd0c47cacebd58209292dda3a297Test
https://doi.org/10.1016/j.nmd.2019.08.012Test

3

Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2

المؤلفون: Hans Timmerman, A.A. Tieleman, Oliver H.G. Wilder-Smith, Judith van Vliet, Aad Verrips, Baziel G.M. van Engelen, Robert van Dongen

المصدر: van Vliet, J, Tieleman, A A, Verrips, A, Timmerman, H, van Dongen, R T M, van Engelen, B G M & Wilder-Smith, O H G 2018, ' Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2 ', Journal of Pain, vol. 19, no. 8, pp. 920-930 . https://doi.org/10.1016/j.jpain.2018.03.006Test
Journal of Pain, 19, 920-930
Journal of Pain, 19, 8, pp. 920-930

مصطلحات موضوعية: Adult, Male, Pain Threshold, musculoskeletal diseases, medicine.medical_specialty, Fibromyalgia, Central sensitization, Myotonic dystrophy type 2, quantitative sensory testing, Anxiety, Healthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18], 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, 0302 clinical medicine, Quality of life, Surveys and Questionnaires, Internal medicine, Humans, Myotonic Dystrophy, Medicine, pain, In patient, Muscle, Skeletal, Aged, 030203 arthritis & rheumatology, Central Nervous System Sensitization, fibromyalgia syndrome, Depression, business.industry, Catastrophization, Quantitative sensory testing, central sensitization, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, Disease control, Anesthesiology and Pain Medicine, Neurology, Hyperalgesia, Quality of Life, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64c530ca8aea05bf21eed3418c86743Test
https://doi.org/10.1016/j.jpain.2018.03.006Test

4

Graves' disease and celiac disease in a patient with myotonic dystrophy type 2

المؤلفون: M.J. Damen, A. F. G. van der Meer, A.A. Tieleman, Nicol C. Voermans

المصدر: Neuromuscular Disorders, 28, 10, pp. 878-880
Neuromuscular Disorders, 28, 878-880

مصطلحات موضوعية: musculoskeletal diseases, 0301 basic medicine, Hearing loss, Graves' disease, Myotonic dystrophy type 2, Inflammation, Disease, medicine.disease_cause, Diagnosis, Differential, 03 medical and health sciences, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, medicine, Humans, Myotonic Dystrophy, Progressive proximal muscle weakness, Genetics (clinical), Aged, Autoimmune disease, Mutation, business.industry, medicine.disease, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Graves Disease, Celiac Disease, 030104 developmental biology, Neurology, Pediatrics, Perinatology and Child Health, Immunology, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Inflammatory diseases Radboud Institute for Molecular Life Sciences [Radboudumc 5]

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f019720ce04250eece347554d243687bTest
https://doi.org/10.1016/j.nmd.2018.07.003Test

5

First familial Becker muscular dystrophy in Tanzania: Clinical and genetic features()

المؤلفون: William Howlett, H.A. van Duyvenvoorde, A.A. Tieleman, O.J. Igogo, Marieke C. J. Dekker, Ben C.J. Hamel

المصدر: Neuromuscular Disorders, 29, 317-320
Neuromuscular Disorders, 29, 4, pp. 317-320
Neuromuscular Disorders, 29(4), 317-320. PERGAMON-ELSEVIER SCIENCE LTD

مصطلحات موضوعية: 0301 basic medicine, Male, Pediatrics, medicine.medical_specialty, Weakness, Other Research Donders Center for Medical Neuroscience [Radboudumc 0], Global neurology, Muscle disorder, Medical care, Tanzania, 03 medical and health sciences, 0302 clinical medicine, Genotype, parasitic diseases, Medicine, Humans, Muscular dystrophy, Genetics (clinical), biology, business.industry, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], biology.organism_classification, medicine.disease, Pedigree, Muscular Dystrophy, Duchenne, 030104 developmental biology, Neurology, Becker muscular dystrophy, Pediatrics, Perinatology and Child Health, Africa, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0752a7384cf77838f3b6b66d836efc0Test
http://hdl.handle.net/2066/207145Test

6

Hearing impairment in patients with myotonic dystrophy type 2

المؤلفون: G. Bassez, Wim I. M. Verhagen, A.A. Tieleman, Judith van Vliet, George Lamas, Joost A.M. Engel, Elisabeth Mamelle, Baziel G.M. van Engelen, Tanya Stojkovic, Anthony Béhin, Bruno Eymard, Laurent Servais, Jan Meulstee

المساهمون: Département de pathologie [CHU Henri Mondor], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor, Institut de Myologie, Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Neurology
Neurology, 2018, 90 (7), pp.e615-e622. ⟨10.1212/WNL.0000000000004963⟩
Neurology, 90, 7, pp. E615-E622
Neurology, 90, E615-E622

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, [SDV]Life Sciences [q-bio], Population, Presbycusis, 030105 genetics & heredity, Audiology, Severity of Illness Index, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, otorhinolaryngologic diseases, Evoked Potentials, Auditory, Brain Stem, Medicine, Humans, Myotonic Dystrophy, education, Hearing Loss, Aged, education.field_of_study, Absolute threshold of hearing, medicine.diagnostic_test, business.industry, Hearing Tests, Age Factors, Tympanometry, Middle Aged, medicine.disease, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Cross-Sectional Studies, Cohort, Female, Neurology (clinical), Pure tone audiometry, Audiometry, business, 030217 neurology & neurosurgery, Cohort study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee90eb21eafbfb1f4322cb5d336091b3Test
https://hal.science/hal-03875067Test

7

No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndrome

المؤلفون: A.A. den Broeder, A.A. Tieleman, H. Cats, Hans Scheffer, Aad Verrips, J.A. van der Vliet, B.G.M. van Engelen

المصدر: Neuromuscular Disorders, 26, 370-3
Neuromuscular Disorders, 26, 6, pp. 370-3

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, musculoskeletal diseases, medicine.medical_specialty, Fibromyalgia, Adolescent, Cross-sectional study, 030105 genetics & heredity, Myotonic dystrophy, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Prevalence, medicine, Humans, Myotonic Dystrophy, Young adult, Creatine Kinase, Genetics (clinical), Aged, Genetic testing, medicine.diagnostic_test, business.industry, RNA-Binding Proteins, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, Myotonia, Rheumatology, Cross-Sectional Studies, Neurology, Pediatrics, Perinatology and Child Health, embryonic structures, Physical therapy, Population study, Female, Neurology (clinical), business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66bb2332328e49d80d2297d9ed47f06cTest
http://hdl.handle.net/2066/167988Test

8

Poor sleep quality and fatigue but no excessive daytime sleepiness in myotonic dystrophy type 2

المؤلفون: Baziel G.M. van Engelen, Hans Knoop, Anne-Els van de Logt, Gijs Bleijenberg, Sebastiaan Overeem, A.A. Tieleman

المصدر: Journal of Neurology, Neurosurgery, and Psychiatry, 81, 9, pp. 963-7
Journal of Neurology, Neurosurgery, and Psychiatry, 81, 963-7

مصطلحات موضوعية: Adult, Male, Sleep Wake Disorders, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Population, Excessive daytime sleepiness, Disorders of Excessive Somnolence, Severity of Illness Index, Myotonic dystrophy, Diagnosis, Differential, Pittsburgh Sleep Quality Index, Internal medicine, medicine, Humans, Myotonic Dystrophy, education, Fatigue, Aged, Sleep disorder, education.field_of_study, business.industry, Epworth Sleepiness Scale, Psychological determinants of chronic illness [NCEBP 8], Middle Aged, medicine.disease, Comorbidity, Psychiatry and Mental health, Physical therapy, Female, Surgery, Neurology (clinical), medicine.symptom, business, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06253a7e6a89ac9d3935dbdb4e4dde5eTest
https://doi.org/10.1136/jnnp.2009.192591Test

9

Gastrointestinal involvement is frequent in Myotonic Dystrophy type 2

المؤلفون: Anneke J. van der Kooi, A.A. Tieleman, Judith van Vliet, George F. Borm, Baziel G.M. van Engelen, Jan B.M.J. Jansen

المساهمون: ANS - Amsterdam Neuroscience, Neurology

المصدر: Neuromuscular disorders, 18(8), 646-649. Elsevier Limited
Neuromuscular Disorders, 18, 8, pp. 646-9
Neuromuscular Disorders, 18, 646-9

مصطلحات موضوعية: Adult, Male, Risk, musculoskeletal diseases, medicine.medical_specialty, Abdominal pain, Constipation, Gastrointestinal Diseases, Disease, Gastroenterology, Myotonic dystrophy, Proximal myotonic myopathy, Internal medicine, Surveys and Questionnaires, medicine, Perception and Action [DCN 1], Humans, Myotonic Dystrophy, Molecular gastro-enterology and hepatology [IGMD 2], Defecation, Gastrointestinal Transit, Genetics (clinical), Aged, Netherlands, Aged, 80 and over, Human Movement & Fatigue [NCEBP 10], Gastrointestinal tract, business.industry, Effective Hospital Care [EBP 2], Middle Aged, medicine.disease, Dysphagia, Health Surveys, Neuromuscular development and genetic disorders [UMCN 3.1], Surgery, Abdominal Pain, Neurology, Genetic defects of metabolism [UMCN 5.1], Evaluation of complex medical interventions [NCEBP 2], Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), medicine.symptom, business, Deglutition Disorders, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41226f054e01e1586459a9814abc5ecfTest
https://doi.org/10.1016/j.nmd.2008.05.010Test

10

Strong association between myotonic dystrophy type 2 and autoimmune diseases

المؤلفون: A.A. den Broeder, A-E van de Logt, B.G.M. van Engelen, A.A. Tieleman

المصدر: Journal of Neurology, Neurosurgery, and Psychiatry, 80, 11, pp. 1293-5
Journal of Neurology, Neurosurgery, and Psychiatry, 80, 1293-5

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::983465811f4569fdeb05ff2d68534846Test
https://doi.org/10.1136/jnnp.2008.156562Test

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