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المؤلفون: Fabrice Jardin, Jean-Michel Vallat, Didier Hannequin, Annie Laquerrière, Olivier Martinaud, Anne-Laure Bedat-Millet, Lucile Musset, Snejana Jurici
المصدر: Case Reports in Neurology
Case Reports in Neurology, Vol 3, Iss 3, Pp 294-300 (2011)مصطلحات موضوعية: Waldenström macroglobulinemia, Pathology, medicine.medical_specialty, biology, business.industry, Anti mag, Waldenstrom macroglobulinemia, Autopsy case, Anti-MAG, Amyotrophic lateral sclerosis, medicine.disease, Published: December, 2011, lcsh:RC346-429, Monoclonal gammopathy, nervous system, Immunoglobulin M, Gammopathy, medicine, biology.protein, Neurology (clinical), Antibody, medicine.symptom, business, lcsh:Neurology. Diseases of the nervous system
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862f296793a53acd18d8df1c4b99aad2Test
https://doi.org/10.1159/000335004Test -
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المؤلفون: Cécile Acquaviva-Bourdain, Bruno Eymard, Odile Boespflug-Tanguy, Isabelle Pénisson-Besnier, Brage S. Andresen, Anne-Laure Bedat-Millet, Anne Lombès, Anthony Behin, Christine Vianey-Saban, Denys Chaigne, Isabelle Delevaux, Michèle Brivet, Cécile Laroche, Pascal Laforêt, Brigitte Chabrol, Odile Rigal
المصدر: laforet, P, Acquaviva-Bourdain, C, Rigal, O, Brivet, M, Penisson-Besnier, I, Chabrol, B, Chaigne, D, Boespflug-Tanguy, O, Laroche, C, Bedat-Millet, A, Behin, A, Delevaux, I, Lombès, A, Andresen, B S, Eymard, B & Vianey-Saban, C 2009, ' Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-coenzyme A dehydrogenase (VLCAD) deficiency ', Neuromuscular Disorders, vol. 19, pp. 324-329 .
مصطلحات موضوعية: Adult, Male, Heterozygote, medicine.medical_specialty, Mitochondrial Diseases, Adolescent, Genotype, DNA Mutational Analysis, Metabolic myopathy, Exercise intolerance, Biology, Compound heterozygosity, Rhabdomyolysis, Very Long-Chain Acyl-CoA Dehydrogenase Deficiency, Young Adult, Muscular Diseases, Carnitine, Internal medicine, medicine, Humans, Genetic Testing, Child, Beta oxidation, Cells, Cultured, Genetics (clinical), Exercise Tolerance, Muscle Weakness, Acyl-CoA Dehydrogenase, Long-Chain, Homozygote, Acyl CoA dehydrogenase, Middle Aged, medicine.disease, Endocrinology, Neurology, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, Female, Neurology (clinical), medicine.symptom, Differential diagnosis, Biomarkers, Metabolism, Inborn Errors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88752006eafbb4137e6ba00eac515201Test
https://doi.org/10.1016/j.nmd.2009.02.007Test