المؤلفون: Nicol C. Voermans, Thierry Kuntzer, Michel Delforge, Marie-Christiane Vekemans, Olivier Benveniste, Monique C. Minnema, Peter Van den Bergh, Véronique Leblond, Norma B. Romero, Jan Novy, Thomas Pabst, Françoise Bouhour, Henk M. Lokhorst, Bruno Eymard, Wouter Meersseman, Baziel G.M. van Engelen, Martin Lammens

المصدر: Neurology
Neurology, 83, 23, pp. 2133-9
Voermans, Nicol C; Benveniste, Olivier; Minnema, Monique C; Lokhorst, Henk; Lammens, Martin; Meersseman, Wouter; Delforge, Michel; Kuntzer, Thierry; Novy, Jan; Pabst, Thomas; Bouhour, Françoise; Romero, Norma; Leblond, Veronique; Bergh, Peter van den; Vekemans, Marie-Christiane; Engelen, Baziel G van; Eymard, Bruno (2014). Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT. Neurology, 83(23), pp. 2133-2139. Lippincott Williams & Wilkins 10.1212/WNL.0000000000001047 <http://dx.doi.org/10.1212/WNL.0000000000001047Test>
ResearcherID
Europe PubMed Central
Neurology, 83, 2133-9

مصطلحات موضوعية: Melphalan, Adult, Male, medicine.medical_specialty, Paraproteinemias, Late onset, 610 Medicine & health, Myopathies, Nemaline, Gastroenterology, Transplantation, Autologous, Autologous stem-cell transplantation, Nemaline myopathy, immune system diseases, Internal medicine, hemic and lymphatic diseases, Medicine, Humans, Age of Onset, Myopathy, Retrospective Studies, business.industry, Muscle weakness, medicine.disease, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Hematologic Response, 3. Good health, Surgery, Treatment Outcome, Female, Neurology (clinical), Human medicine, medicine.symptom, business, Case series, medicine.drug, Follow-Up Studies, Stem Cell Transplantation

وصف الملف: pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8519e93627827a67a1c17d2569a0441dTest
https://hdl.handle.net/10067/1221760151162165141Test

المؤلفون: Martin Lammens, Machiel J. Zwarts, B.G.M. van Engelen, A.A.W.M. Gabreëls-Festen, J.M.M. Gijtenbeek

المصدر: Neurology, 56, 1766-8
Neurology, 56, 12, pp. 1766-8

مصطلحات موضوعية: Axonal neuropathy, Neurofibromatosis 2, Pathology, medicine.medical_specialty, Schwann cell, Sural nerve biopsy, Sural Nerve, medicine, Humans, Tumor pathology, Neurofibromatosis type 2, Neuromusculaire en neurometabole aandoeningen, business.industry, Mononeuropathy Multiplex, Peripheral Nervous System Diseases, Tumor pathologie, Middle Aged, medicine.disease, Axons, Merlin (protein), Microscopy, Electron, Peripheral neuropathy, medicine.anatomical_structure, Neuromuscular and neurometabolic disorders, nervous system, Female, Schwann Cells, Neurology (clinical), business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94219edae5cf4f3e49219e4897bd0929Test
https://doi.org/10.1212/wnl.56.12.1766Test

المؤلفون: Martin W.I.M. Horstink, Alexis Brice, Martin Lammens, B.P.C. van de Warrenburg, Peter Praamstra, Niall Quinn, Jan Booij, C. B. Lücking, Pieter Wesseling, Patrice Denefle

المساهمون: Other departments

المصدر: Neurology, 56, 4, pp. 555--7
Neurology, 56, 555--7
Neurology, 56(4), 555-557. Lippincott Williams and Wilkins
ResearcherID

مصطلحات موضوعية: Male, Proband, Immunologische ontstekingsprocessen in de nier, Pathology, medicine.medical_specialty, Ubiquitin-Protein Ligases, Nonsense mutation, tau Proteins, Pathofysiologie van Hersenen en Gedrag, Substantia nigra, Pathophysiology of Brain and Behaviour, Biology, Polymerase Chain Reaction, Ligases, Loss of heterozygosity, Parkinsonian Disorders, Inflammatory reactions in the kidneys, medicine, Humans, Point Mutation, Missense mutation, Aged, Netherlands, Genetics, Neuromusculaire en neurometabole aandoeningen, Pars compacta, Point mutation, Parkinsonism, Brain, medicine.disease, nervous system diseases, Neuromuscular and neurometabolic disorders, nervous system, Astrocytes, Female, Neurology (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b898a7f0d4a1085d197675a4c95ac2a6Test
https://doi.org/10.1212/wnl.56.4.555Test

المؤلفون: I. Dehaene, Martin Lammens

المصدر: Scopus-Elsevier

مصطلحات موضوعية: medicine.medical_specialty, genetic structures, Pursuit eye movement, Eye disease, Autopsy, Audiology, Parietal Lobe, medicine, Paralysis, Saccades, Middle frontal gyrus, Humans, Aged, Ophthalmoplegia, business.industry, Precentral gyrus, Eye movement, Inferior parietal lobule, Anatomy, medicine.disease, Pursuit, Smooth, Frontal Lobe, Female, Neurology (clinical), medicine.symptom, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa26757b65f9962c48948c810d3e1c7Test
https://pubmed.ncbi.nlm.nih.gov/2006011Test

المؤلفون: P Verdru, Martin Lammens, Herwig Carton, A. Van Elsen, René Dom

المصدر: Neurology. 41:1382-1382

مصطلحات موضوعية: Adult, Pathology, medicine.medical_specialty, business.industry, Leukodystrophy, Cell, medicine.disease, Magnetic Resonance Imaging, Leukodystrophy, Globoid Cell, Degenerative disease, medicine.anatomical_structure, Galactosylceramidase, Genotype, medicine, Krabbe disease, Humans, Female, Dura Mater, Neurology (clinical), Age of onset, Adult type, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c51da38ad61291d29abc3b427b02d3e5Test
https://doi.org/10.1212/wnl.41.9.1382Test