المؤلفون: Dengler, N.F., Scholz, C., Beck, J., Uerschels, A.-K., Sure, U., Scheller, C., Strauss, C., Martin, D., Schackert, G., Heinen, C., Woitzik, J., McLean, A.L., Rosahl, S.K., Kolbenschlag, J., Heinzel, J., Schuhmann, M., Tatagiba, M.S., Guerra, W.K.-W., Schroeder, H.W.S., Vetrano, I.G., Ahmadi, R., Unterberg, A., Reinsch, J., Zdunczyk, A., Unteroberdoerster, M., Vajkoczy, P., Wehner, S., Becker, M., Matthies, C., Pérez-Tejón, J., Dubuisson, Annie, Barrone, D.G., Trivedi, R., Capone, C., Ferraresi, S., Kraschl, J., Kretschmer, T., Dombert, T., Staub, F., Ronellenfitsch, M., Marquardt, G., Prinz, V., Czabanka, M., Carolus, A., Braun, V., König, R., Antoniadis, G., Wirtz, C.R., Rasulic, L., Pedro, M.T.

المصدر: Neurological Research, 45 (1), 81 - 85 (2023)

مصطلحات موضوعية: neurofibroma, Peripheral nerve tumor, registry, schwannoma, leucine zipper like transcriptional regulator 1, protein, SWI/SNF related matrix associated actin dependent regulator of chromatin subfamily B member 1, unclassified drug, adolescent, Article, cancer registry, child, cohort analysis, computer assisted tomography, female, follow up, human, male, multicenter study, neurologic examination, nuclear magnetic resonance imaging, observational study, positron emission tomography, prospective study, quality of life, standardized uptake value, systematic review, tumor volume, clinical trial, Europe

العلاقة: urn:issn:0161-6412; urn:issn:1743-1328; https://orbi.uliege.be/handle/2268/303694Test; info:hdl:2268/303694; https://orbi.uliege.be/bitstream/2268/303694/1/Rational%20and%20design%20of%20the%20peripheral%20nerve%20tumor%20registry.pdfTest; scopus-id:2-s2.0-85139653540; info:pmid:36208460

الإتاحة: https://doi.org/10.1080/01616412.2022.2129762Test
https://orbi.uliege.be/handle/2268/303694Test
https://orbi.uliege.be/bitstream/2268/303694/1/Rational%20and%20design%20of%20the%20peripheral%20nerve%20tumor%20registry.pdfTest

المؤلفون: François Nobili, Lawrence R. Shoemaker, David V. Milford, Mitra Basiratnia, Anna Buck, Georges Deschênes, Isabel Cordeiro, Jorge M. Saraiva, Helen Fryssira, Anja Stein, Behzad Najafian, Natasa Stajic, Laura Massella, Joel Charrow, Glenda Hendson, Umakumaran Ponniah, Thomas Lücke, M. Semin Fenkçi, Doris Taha, Elena Levtchenko, J. Marietta Clewing, Pierre Frange, Yumi Asakura, Christine Kobelka, Jean Luc André, David M. Parham, Jonathan Zonana, Radovan Bogdanovic, Justin Weinkauf, Zhongxin Yu, C. Nur Semerci, Stefan Fründ, Arend Bökenkamp, Cornelius F. Boerkoel, Salman Kirmani, Dorothea Wand, Peter Stenzel, Kory Keller, David B. Lewis, Pierre Cochat, Marie Morimoto, Christy Mayfield, Encarna Guillén-Navarro, D. Ross McLeod, Andrew K. Gormley, Petra Lamfers, Dominique Bonneau

المساهمون: Pediatric surgery, ICaR - Circulation and metabolism

المصدر: Orphanet Journal of Rare Diseases, 7:70. BioMed Central
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 70 (2012)
Morimoto, M, Yu, Z X, Stenzel, P, Clewing, J M, Najafian, B, Mayfield, C, Hendson, G, Weinkauf, J G, Gormley, A K, Parham, D M, Ponniah, U, Andre, J L, Asakura, Y, Basiratnia, M, Bogdanovic, R, Bokenkamp, A, Bonneau, D, Buck, A, Charrow, J, Cochat, P, Cordeiro, I, Deschenes, G, Fenkci, M S, Frange, P, Frund, S, Fryssira, H, Guillen-Navarro, E, Keller, K, Kirmani, S, Kobelka, C, Lamfers, P, Levtchenko, E, Lewis, D B, Massella, L, Mcleod, D R, Milford, D V, Nobili, F, Saraiva, J M, Semerci, C N, Shoemaker, L, Stajic, N, Stein, A, Taha, D, Wand, D, Zonana, J, Lucke, T & Boerkoel, C F 2012, ' Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia? ', Orphanet Journal of Rare Diseases, vol. 7, 70 . https://doi.org/10.1186/1750-1172-7-70Test
Orphanet Journal of Rare Diseases

مصطلحات موضوعية: Male, Pathology, Nephrotic Syndrome, Arteriosclerosis, Gene mutation, Research & Experimental Medicine, GENETIC-DISEASES, fibroblast, medical record review, 0302 clinical medicine, MOUSE MODELS, nuclear protein, Genetics(clinical), Pharmacology (medical), Child, COSTELLO-SYNDROME, Genetics & Heredity, 0303 health sciences, adult, gene expression regulation, General Medicine, Hyperplasia, elastin binding protein, Immunohistochemistry, 3. Good health, emphysema, Medicine, Research & Experimental, SUPRAVALVULAR AORTIC-STENOSIS, Child, Preschool, histopathology, Autopsy, medicine.medical_specialty, gene sequence, Osteochondrodysplasias, Vascular disease, Schimke immuno-osseous dysplasia, CELL-PROLIFERATION, 03 medical and health sciences, Humans, human, protein expression, Science & Technology, autosomal recessive disorder, MUTATIONS, human cell, lcsh:R, DNA Helicases, Immunologic Deficiency Syndromes, Schimke immunoosseous dysplasia, school child, medicine.disease, major clinical study, myofibroblast, Elastin, aorta, vascular smooth muscle, smooth muscle fiber, Immunology, umbilical cord, Pulmonary Embolism, Nephrotic syndrome, 030217 neurology & neurosurgery, lung disease, genomic DNA, osteopontin, Medizin, lcsh:Medicine, preschool child, artery intima proliferation, single nucleotide polymorphism, SMARCAL1, gene mutation, Genetics (clinical), Medicine(all), messenger RNA, ELASTIN-BINDING-PROTEIN, article, artery, hyperplasia, unclassified drug, DEFICIENCY, female, Female, Life Sciences & Biomedicine, Adult, EXPRESSION, Pulmonary emphysema, Primary Immunodeficiency Diseases, binding protein, protein localization, lung parenchyma, gene expression profiling, medicine, IMMUNOOSSEOUS DYSPLASIA, 030304 developmental biology, Emphysema, business.industry, Research, human tissue, SWI SNF related matrix associated actin dependent regulator of chromatin subfamily a like 1, Dysplasia, business

وصف الملف: Electronic; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff0e0995712e817e2e461d654ddc339Test
https://lirias.kuleuven.be/handle/123456789/653703Test