يعرض 1 - 20 نتائج من 69 نتيجة بحث عن '"Bausch B"', وقت الاستعلام: 0.93s تنقيح النتائج
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    Academic Journal

    المصدر: JAMA network open. 2(8):e198898

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    Academic Journal
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    Academic Journal

    المساهمون: von Dobschuetz, E, Leijon, H, Schalin Jäntti, C, Schiavi, Francesca, Brauckhoff, M, Peczkowska, M, Spiazzi, G, Demattè, S, Cecchini, Me, Sartorato, P, Krajewska, J, Hasse Lazar, K, Roszkowska Purska, K, Taschin, E, Malinoc, A, Akslen, La, Arola, J, Lange, D, Fassina, Ambrogio, Pennelli, Gianmaria, Barbareschi, M, Luettges, J, Prejbisz, A, Januszewicz, A, Strate, T, Bausch, B, Castinetti, F, Jarzab, B, Opocher, Giuseppe, Eng, C, Neumann, Hp

    Relation: info:eu-repo/semantics/altIdentifier/pmid/25595276; info:eu-repo/semantics/altIdentifier/wos/WOS:000354624100010; ispartofbook:Endocrine-related cancer; volume:22; journal:ENDOCRINE-RELATED CANCER; http://hdl.handle.net/11577/3148562; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84929326593

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    Conference

    المصدر: ESBS 2005: Skull Base Surgery: An Interdisciplinary Challenge; 7th Congress of the European Skull Base Society held in association with the 13th Congress of the German Society of Skull Base Surgery; 20050518-20050521; Fulda; DOC05esbs68 /20090127/

    Relation: Astuti D, Douglas F, Lennard TW, et al. Germline SDHD mutation in familial pheochromocytoma. Lancet. 2001;357:1181-2.; Astuti D, Latif F, Dallol A, et al. Gene mutations in the succinate dehydrogenase subunit B cause susceptibility to familial ppheochromocytoma and to familial paraganglioma. Am J Hum Genet. 2001;69:49-54.; Au HC, Ream-Robinson D, Bellew LA, Broomfield E, Saghbini M, Scheffler IE. Structural organization of the gene encoding the human iron-sulfur subunit of succinate dehydrogenase. Gene. 1995;159:249-53.; Bauters C, Vantyghem M, Leteurtre E, et al. Hereditary pheochromocytomas and paragangliomas: a study of five susceptibility genes. J Med Genet. 2003;40:e75.; Baysal BE, Ferrel RE; Willett-Brozick JE, et al. Mutations in SDHD; a mitochondrial complex II gene, in hereditary paraganglioma. Science. 2000;287:848-51.; Baysal BE, Willett-Brozick JE, Lawrence EC, et al. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. J Med Genet. 2002;39:178-83.; Baysal BE, Willett-Brozick JE, Filho PA, et al. An Alu mediated partial SDHC deletion causes familial and sporadic paraganglioma. J Med Genet. 2004;41:703-9.; Bourgeron T, Rustin P, Chretien D, et al. Mutation of nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. Nat Genet. 1995;11:144-9.; Dannenberg H, Dinjens WN, Abbou M, et al. Freuquent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma. Clin Cancer Res. 2002;8:2061-6.; Drovdlic CM, Myers EN, Peters JA, et al. Proportion of hereditable paraganglioma cases and associated clinical characteristics. Laryngoscope. 2001;111:1822-7.; Elbehti-Green A, Au HC, Mascarello JT, Ream-Robinson D, Scheffler IE. Characterization of the human SDHC gene, encoding one of the integral membrane proteins of succinate-quinone oxidoreductase in mitochondria. Gene. 1998;213:133-40.; Hensen EF, Jordanova ES, Van Minderhout IJ, et al. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and pheochromocytoma families. Oncogene. 2004;23:4076-83.; Hirawake H, Taniwaki M, Tamura A, Kojima S, Kita K. Cytochrome b in human complex II (succinate-ubiquinone-oxidoreductase):cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and the small (SDHD) subunits to 1q21 and 11q23. Cytogenet Cell Genet. 1997;79:132-8.; Lack EE, Cubilla A, Woodruff JM. Paragangliomas of the head and neck region. A pathologic study of tumors from 71 patients. Hum Pathol. 1979;10:191-218.; Lee JH, Barich F, Karnell LH, et al. Chemodectomas of the head and neck. In: Batsakis JG, editor. Tumors of the head and neck. Clinical and pathological considerations. Baltimore MD: Williams and Wilkins; 1979. p. 280-8.; Mariman EC, van Beersum SE, Cremers CW, Struycken PM, Ropers HH. Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1:evidence forbgenetic heterogeneity. Hum Genet. 1995:56-62.; McCaffrey TC, Meyer FB, Michels VV. Familial paragangliomas of the head and neck. Arch Otolaryngool Head Neck Surg. 1994;120:1211-6.; McWhinney SR, Pilarski RT, Forrester SR, et al. Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma. J Clin Endocrinol Metab. 2004;89:5694-9.; Neumann HP, Pawlu C, Peczkowska M, et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA. 2004;292:943-51.; Neumann HP, Bausch B, McWhinney SR, et al. Germ-line mutations in non-syndromic pheochromocytoma. N Engl J Med. 2002;346:1459-66.; Niemann S, Steinberger D, Müller U. PGl 3, a third, not maternally imprinted locus in autosomal dominant paraganglioma. Neurogenetics. 1999;2:167-70.; Niemann S, Müller U, Engelhardt D, Lohse P. Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. Hum Genet. 2003;113:92-4.; Niemann S, Müller U. Mutations in SDHC cause autosomal dominant paraganglioma type 3. Nat Genet. 2000;26:268-70.; Taschner PE, Jansen JC, Baysal BE, et al. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. Genes Chromosomes Cancer. 2001;31:274-81.; Van der Mey AG, Maaswinkel-Mooy PD, Cornelisse CJ, Schmidt PH, Van de Kamp J. Genomic imprinting in hereditary glomus tumors:evidence for new genetic theory. Lancet. 1989;2:1291-4.; Vanharanta S, Buchta M, McWhinney SR, et al. Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. Am J Hum Genet. 2004;74:153-9.; http://dx.doi.org/10.3205/05esbs68; http://nbn-resolving.de/urn:nbn:de:0183-05esbs688; http://www.egms.de/en/meetings/esbs2005/05esbs68.shtml

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    Conference

    المصدر: 77. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e.V.; 20060524-20060528; Mannheim; DOC06hnod113 /20060424/

    مصطلحات موضوعية: ddc: 610

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    Academic Journal

    المصدر: Steurer, J; Held, U; Spaar, A; Bausch, B; Zoller, M; Hunziker, R; Bachmann, L M (2011). A decision aid to rule out pneumonia and reduce unnecessary prescriptions of antibiotics in primary care patients with cough and fever. BMC Medicine, 9:56.

    وصف الملف: application/pdf

    Relation: https://www.zora.uzh.ch/id/eprint/53268/1/1741-7015-9-56.pdf; info:pmid/21569472; urn:issn:1741-7015

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    Academic Journal
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    Academic Journal

    المساهمون: Bausch, B, Wellner, U, Peyre, M, Boedeker, Cc, Hes, Fj, Anglani, M, de Campos, Jm, Kanno, H, Maher, Er, Krauss, T, Sansó, G, Barontini, M, Letizia, Claudio, Hader, C, Schiavi, F, Zanoletti, E, Suárez, C, Offergeld, C, Malinoc, A, Zschiedrich, S, Glasker, S, Bobin, S, Sterkers, O, Tran Ba Huy, P, Giraud, S, Links, T, Eng, C, Opocher, G, Richard, S, Neumann, Hp, International ELST, Consortium

    Relation: journal:HEAD & NECK; http://hdl.handle.net/11573/782014

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    Academic Journal

    المساهمون: Castinetti, F, Qi, Xp, Walz, Mk, Maia, Al, Sansó, G, Peczkowska, M, Hasse Lazar, K, Links, Tp, Dvorakova, S, Toledo, Ra, Mian, Caterina, Bugalho, Mj, Wohllk, N, Kollyukh, O, Canu, L, Loli, P, Bergmann, Sr, Costa, Jb, Makay, O, Patocs, A, Pfeifer, M, Shah, N, Cuny, T, Brauckhoff, M, Bausch, B, von Dobschuetz, E, Letizia, C, Barczynski, M, Alevizaki, Mk, Czetwertynska, M, Ugurlu, Mu, Valk, G, Plukker, Jt, Sartorato, P, Siqueira, Dr, Barontini, M, Szperl, M, Jarzab, B, Verbeek, Hh, Zelinka, T, Vlcek, P, Toledo, Sp, Coutinho, Fl, Mannelli, M, Recasens, M, Demarquet, L, Petramala, L, Yaremchuk, S, Zabolotnyi, D, Schiavi, F, Opocher, Giuseppe, Racz, K, Januszewicz, A, Weryha, G, Henry, Jf, Brue, T, Conte Devolx, B, Eng, C, Neumann, Hp

    Relation: info:eu-repo/semantics/altIdentifier/pmid/24745698; info:eu-repo/semantics/altIdentifier/wos/WOS:000335512100052; volume:15; issue:6; firstpage:648; lastpage:655; numberofpages:8; journal:THE LANCET ONCOLOGY; http://hdl.handle.net/11577/2827263; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84899970790

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    Academic Journal

    المساهمون: Bausch, B, Wellner, U, Bausch, D, Schiavi, F, Barontini, M, Sanso, G, Walz, Mk, Peczkowska, M, Weryha, G, Dall'Igna, P, Cecchetto, G, Bisogno, G, Moeller, Lc, Bockenhauer, D, Patocs, A, Rácz, K, Zabolotnyi, D, Yaremchuk, S, Dzivite-Krisane, I, Castinetti, F, Taieb, D, Malinoc, A, von Dobschuetz, E, Roessler, J, Schmid, Kw, Opocher, G, Eng, C, Neumann, Hp

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000334279600009; volume:21; issue:1; firstpage:17; lastpage:25; numberofpages:9; journal:ENDOCRINE-RELATED CANCER; http://hdl.handle.net/11586/311730; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84893617173

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    Academic Journal

    المساهمون: Bausch, B, Borozdin, W, Mautner, Vf, Hoffmann, Mm, Boehm, D, Robledo, M, Cascon, A, Harenberg, T, Schiavi, F, Pawlu, C, Peczkowska, M, Letizia, C, Calvieri, S, Arnaldi, G, KLINGENBERG NOFTZ, Rd, Reisch, N, Fassina, Ambrogio, Brunaud, L, Walter, Ma, Mannelli, M, Macgregor, G, Palazzo, Ff, Barontini, M, Walz, Mk, Kremens, B, Brabant, G, Pfffle, R, Koschker, Ac, Lohoefner, F, Mohaupt, M, Gimm, O, Jarzab, B, Mcwhinney, Sr, Opocher, Giuseppe, Januzewicz, A, Kohlhase, J, Eng, C, Neumann, Hp

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/pmid/17426081; info:eu-repo/semantics/altIdentifier/wos/WOS:000247851000059; volume:92; issue:7; firstpage:2784; lastpage:2792; numberofpages:9; journal:THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; http://hdl.handle.net/11577/2470734; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-34447114512

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    Academic Journal

    المساهمون: Schiavi, F, Boedeker, Cc, Bausch, B, Peczkowska, M, Gomez, Cf, Strassburg, T, Pawlu, C, Buchta, M, Salzmann, M, Hoffmann, Mm, Berlis, A, Brink, I, Cybulla, M, Muresan, M, Walter, Ma, Forrer, F, Valimaki, M, Kawecki, A, Szutkowski, Z, Schipper, J, Walz, Mk, Pigny, P, Bauters, C, WILLET BROZICK, Je, Baysal, Be, Januszewicz, A, Eng, C, Opocher, Giuseppe, Neumann, Hp, EUROPEAN AMERICAN PARAGANGLIOMA STUDY, Group

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/pmid/16249420; info:eu-repo/semantics/altIdentifier/wos/WOS:000232778900026; volume:294; issue:16; firstpage:2057; lastpage:2063; numberofpages:7; journal:JAMA; http://hdl.handle.net/11577/1425771; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-27244446452

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    Academic Journal

    المساهمون: Neumann, Hp, Pawlu, C, Peczkowska, M, Bausch, B, Mcwhinney, Sr, Muresan, M, Buchta, M, Franke, G, Klisch, J, Bley, Ta, Hoegerle, S, Boedeker, Cc, Opocher, Giuseppe, Schipper, J, Januszewicz, A, Eng, C, EUROPEAN AMERICAN PARAGANGLIOMA STUDY, Group

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/pmid/15328326; info:eu-repo/semantics/altIdentifier/wos/WOS:000223429200019; volume:292; issue:8; firstpage:943; lastpage:951; numberofpages:9; journal:JAMA; http://hdl.handle.net/11577/1360164; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-4143105824

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    Academic Journal
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    Academic Journal