المؤلفون: AkdoÄŸan, Neslihan, Duygulu, Serap, Anlar, Banu, Ayter, Şükriye, Aksoy, M. Cemalettin

مصطلحات موضوعية: Neurofibromatosis 1, Neurofibroma

العلاقة: Kitap - Ulusal; https://hdl.handle.net/20.500.11851/11572Test

الإتاحة: https://doi.org/20.500.11851/11572Test
https://hdl.handle.net/20.500.11851/11572Test

المؤلفون: Kuorilehto, Tommi, Pöyhönen, Minna, Keski-Nisula, Leo, Laurikka, Jari, Salenius, Juha-Pekka

المساهمون: Lääketieteellisen genetiikan ja perinnöllisyyslääketieteen osasto, HUSLAB, Minna Pöyhönen / Vastuullinen tutkija, Medicum

مصطلحات موضوعية: Ehlers-Danlos Syndrome, +complications, +genetics, Marfan Syndrome, Neurofibromatosis 1, Vascular Diseases, +etiology, +surgery

وصف الملف: application/pdf

العلاقة: Kuorilehto , T , Pöyhönen , M , Keski-Nisula , L , Laurikka , J & Salenius , J-P 2011 , ' Marfanin oireyhtymään, Ehlers-Danlosin oireyhtymään ja neurofibromatoosi 1:een liittyvät verisuonimuutokset ja niiden kirurginen hoito ' , Duodecim , Vuosikerta. 127 , Nro 21 , Sivut 2280-2286 . < http://www.terveysportti.fi/xmedia/duo/duo99875.pdfTest >; RIS: urn:2B41A283B6629220B6A2220CBD677DB2; ORCID: /0000-0003-2037-2744/work/93604545; b60e4adc-4bb3-420c-9715-0d1a477a0325; http://hdl.handle.net/10138/329734Test

الإتاحة: http://hdl.handle.net/10138/329734Test

المؤلفون: Hartson, Mary Reed

مصطلحات موضوعية: Sabin, Albert B. (Albert Bruce), 1906-1993 -- Correspondence, Hartson, Mary Reed -- Correspondence, Reichmann's Disease, Von Recklinghausen Disease, Neurofibromatosis 1, Addison Disease

الوقت: 1944

وصف الملف: paper; application/pdf

العلاقة: The Albert B. Sabin Archives; Sabin Archives. Correspondence, Miscellaneous. Box 02. File 08 (1944); http://hdl.handle.net/2374.UC/667669Test

الإتاحة: http://hdl.handle.net/2374.UC/667669Test

المؤلفون: Persu, A., Canning, C., Prejbisz, A., Dobrowolski, P., Amar, L., Chrysochou, C., Kądziela, J., Litwin, M., van Twist, D., Van der Niepen, P., Wuerzner, G., de Leeuw, P., Azizi, M., Januszewicz, M., Januszewicz, A.

المصدر: Hypertension, vol. 78, no. 4, pp. 898-911

مصطلحات موضوعية: aneurysm, arteriovenous fistula, dissection, hypertension, renovascular, neurofibromatosis 1

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34455817; info:eu-repo/semantics/altIdentifier/eissn/1524-4563; https://serval.unil.ch/notice/serval:BIB_D89900C18765Test; urn:issn:0194-911X

الإتاحة: https://doi.org/10.1161/HYPERTENSIONAHA.121.17004Test
https://serval.unil.ch/notice/serval:BIB_D89900C18765Test

المؤلفون: Wimmer, K

المساهمون: Abteilung Humangenetik des Klinischen Instituts für Medizinische und Chemische Labordiagnostik (KIMCL), Medizinische Universität Wien, Wien, Austria

مصطلحات موضوعية: Chromosome 17, Von Recklinghausen neurofibromatosis (alias), Peripheral neurofibromatosis (alias), Cancer Prone Diseases Section, Genes, Neurofibromatosis 1, Bone Marrow Diseases, Heredodegenerative Disorders, Nervous System, Myelodysplastic Syndromes, Myosarcoma, Neoplasms, Connective and Soft Tissue, Germ Cell and Embryonal, Muscle Tissue, Nerve Tissue, Neoplastic Syndromes, Hereditary, Nerve Sheath Neoplasms, Neuroectodermal Tumors, Neuroendocrine Tumors, Neurofibroma, Neurofibromatoses, Paraganglioma, Peripheral Nervous System Diseases, Pheochromocytoma, Rhabdomyosarcoma, Sarcoma

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Kprones/NF1ID10006.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2006, Vol. 10, N° 3; p. 206-207; http://hdl.handle.net/2042/38337Test; https://doi.org/10.4267/2042/38337Test

الإتاحة: https://doi.org/10.4267/2042/38337Test
http://hdl.handle.net/2042/38337Test

المؤلفون: Wimmer, K

المساهمون: Abteilung Humangenetik des Klinischen Instituts für Medizinische und Chemische Labordiagnostik (KIMCL), Medizinische Universität Wien, Wien, Austria

مصطلحات موضوعية: Chromosome 17, NF1 gene, Genes Section, Genes, Neoplasm, Neurofibromatosis 1, Tumor Suppressor, Heredodegenerative Disorders, Nervous System, Neoplasms, Nerve Tissue, Neoplastic Syndromes, Hereditary, Nerve Sheath Neoplasms, Neurofibroma

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Genes/NF1ID134.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2006, Vol. 10, N° 3; p. 171-172; http://hdl.handle.net/2042/38320Test; https://doi.org/10.4267/2042/38320Test

الإتاحة: https://doi.org/10.4267/2042/38320Test
http://hdl.handle.net/2042/38320Test

المؤلفون: Patil, DP, Kundu, GC

المساهمون: National Center for Cell Science, NCCS Complex, Ganeshkhind, Pune 411007, India

مصطلحات موضوعية: Chromosome 1, LCK gene, P56-LCK LSK (T cell-specific protein-tyrosine kinase) (alias), lck tyrosine kinase (AA 1-142) (alias), membrane associated protein tyrosine kinase (alias), proto-oncogene LCK (alias), protein-tyrosine kinase (alias), put. ptk (135aa), tyrosine kinase (alias), Genes Section, Genes, Neoplasm, Neurofibromatosis 1, Tumor Suppressor, Leukemia, Lymphoid, T-Cell, Lymphoproliferative Disorders

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Genes/LCKID14ch1p34.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2005, Vol. 9, N° 3; p. 228-230; http://hdl.handle.net/2042/38212Test; https://doi.org/10.4267/2042/38212Test

الإتاحة: https://doi.org/10.4267/2042/38212Test
http://hdl.handle.net/2042/38212Test

المؤلفون: Boyer, J

المساهمون: Laboratoire d'Hématologie, CH du MANS, France

مصطلحات موضوعية: Chromosome 1, Chromosome 7, Leukemia Section, T-ALL (class disease), Genes, Neurofibromatosis 1, Chromosome Aberrations, Translocation, Genetic

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/t0107p34q34ID1045.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2003, Vol. 7, N° 4; p. 264-265; http://hdl.handle.net/2042/38022Test; https://doi.org/10.4267/2042/38022Test

الإتاحة: https://doi.org/10.4267/2042/38022Test
http://hdl.handle.net/2042/38022Test

المؤلفون: Gimenez-Roqueplo, AP

المساهمون: Département de Génétique Moléculaire, Hôpital Européen Georges Pompidou, 20-40, rue Leblanc, 75908 Paris cedex 15, France

مصطلحات موضوعية: Chromosome 1, Chromosome 3, Chromosome 10, Chromosome 11, Chromosome 17, Catecholamine-secreting paraganglioma (alias), Functional paraganglioma (alias), Solid Tumors Section, Genes, Neurofibromatosis 1, RET protein, human, SDHB protein, SDHD protein, VHL protein, Multiple Endocrine Neoplasia Type 2a, Neoplastic Syndromes, Hereditary, Nerve Sheath Neoplasms, von Hippel-Lindau Disease

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Tumors/pheochromocytomaID5026.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2003, Vol. 7, N° 2; p. 127-130; http://hdl.handle.net/2042/37972Test; https://doi.org/10.4267/2042/37972Test

الإتاحة: https://doi.org/10.4267/2042/37972Test
http://hdl.handle.net/2042/37972Test

المؤلفون: Kaneko, Y

المساهمون: Department of Cancer Chemotherapy, Saitama Cancer Center Hospital, 818 Komuro, Ina, Saitama, 362-0806, Japan

مصطلحات موضوعية: Solid Tumors Section, MYCN protein, human, Beckwith-Wiedemann Syndrome, Ganglioneuroblastoma, Ganglioneuroma, Kidney Neoplasms, Myosarcoma, Neoplastic Syndromes, Hereditary, Neuroectodermal Tumors, Primitive, Peripheral, Neurofibromatosis 1, Sarcoma, Ewing's, Urogenital Neoplasms, Urologic Neoplasms, Wilms Tumor

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Tumors/neurob5002.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2002, Vol. 6, N° 1; p. 37-39; http://hdl.handle.net/2042/37818Test; https://doi.org/10.4267/2042/37818Test

الإتاحة: https://doi.org/10.4267/2042/37818Test
http://hdl.handle.net/2042/37818Test