Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nihat Bilginturan"'
Autor:
Herbert Schuster, Franz Rüschendorf, Carolin Schächterle, Hermann Haller, Anita Rauch, Thomas F. Wienker, Eireen Bartels-Klein, Fabrice Vandeput, Sylvia Bähring, Martin G. Bialer, Friedrich C. Luft, Thomas Liehr, Andreas Busjahn, Anja Weise, Stefan Mundlos, Jurg Ott, Irene Hollfinger, Matthew A. Movsesian, Astrid Mühl, Ramin Naraghi, Maolian Gong, Fatimunnisa Qadri, Enno Klussmann, Herbert Schulz, Jens Jordan, Jochen Hecht, Knut Mai, Martin Kann, Katharina Rittscher, Carsten Lindschau, Nihat Bilginturan, Ghislaine Plessis, Dmitri Parkhomchuk, Peter Krawitz, David Chitayat, Okan Toka, Jens Tank, Maxwell Hopp, Atakan Aydin, Martin Vaegler, Philipp G. Maass, Norbert Hubner, Hakan R. Toka, Yvette Wefeld-Neuenfeld, Lars O Hattenbach, Russell Hodge, Sigmar Stricker
Publikováno v:
Nature Genetics
Cardiovascular disease is the most common cause of death worldwide, and hypertension is the major risk factor(1). Mendelian hypertension elucidates mechanisms of blood pressure regulation. Here we report six missense mutations in PDE3A (encoding phos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b685bff7495f8caaf66c0e4cf9a9a5e6
https://doi.org/10.1038/ng.3302
https://doi.org/10.1038/ng.3302
Autor:
Özgür Öztekin, Okan Toka, Sylvia Bähring, Friedrich C. Luft, Ramin Naraghi, Hermann Haller, Andreas Busjahn, Hakan R. Toka, Hans Knoblauch, Thomas F. Wienker, Nihat Bilginturan, Herbert Schuster, Rudolf Fahlbusch
Publikováno v:
Scopus-Elsevier
Background and Purpose Autosomal dominant hypertension with brachydactyly features severe hypertension that causes stroke usually before the age of 50 years. We recently characterized the hypertension as featuring normal renin, aldosterone, and catec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d87420ffbec573a82955035e10f511d5
https://doi.org/10.1161/01.str.28.9.1749
https://doi.org/10.1161/01.str.28.9.1749
Autor:
Aytemiz Gurgey, Nihat Bilginturan, S. S. K. Dişkapi, Çiĝdem Altay, Nursen Yordam, Sadi Vidinlisan
Publikováno v:
Pediatric Hematology and Oncology. 12:83-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e11458eb45e0dbccaea432f6e2069bc
https://doi.org/10.3109/08880019509029533
https://doi.org/10.3109/08880019509029533
Autor:
Nihat Bilginturan, Herbert Schuster, Okan Toka, Hakan R. Toka, Hermann Haller, Thomas F. Wienker, Falko Skrabal, Sylvia Bähring, Özgür Öztekin, Friedrich C. Luft, Andreas Busjahn
A cross-over medication trial for patients with autosomal dominant hypertension with brachydactyly. We examined a family with autosomal-dominant hypertension and brachydactyly from northeastern Turkey. The hypertension was defined as severe, resultin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95116af87971bbd930e399cb45cfc69
http://hdl.handle.net/11655/14215
http://hdl.handle.net/11655/14215
Autor:
Albrecht Hempel, Thomas F. Wienker, Hakan R. Toka, Nihat Bilginturan, Andreas Busjahn, Herbert Schuster, Sylvia Bähring, Okan Toka, Friedrich C. Luft, Eva Jeschke, Wolfgang Oelkers, Christoph Tahlhammer, Jürgen Kunze, Hermann Haller
Publikováno v:
Scopus-Elsevier
We examined a Turkish kindred with a unique form of autosomal dominant hypertension that cosegregates 100% with brachydactyly and maps to chromosome 12p. Affected adults were 10 to 15 cm shorter than unaffected people; however, their body mass index
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83c81c113dab10ea87b87f34e9dd9f4c
https://pubmed.ncbi.nlm.nih.gov/8952601
https://pubmed.ncbi.nlm.nih.gov/8952601
Autor:
Sylvia Bähring, Friedrich C. Luft, Okan Toka, Dennis Gilbert, Nihat Bilginturan, Jurg Ott, Adam Lowe, Herbert Schuster, Heidemarie Neitzel, Hermann Haller, Thomas F. Wienker, Eva Jeschke, Hakan R. Toka
Publikováno v:
Scopus-Elsevier
Finding genes that cause human hypertension is not straightforward, since the determinants of blood pressure in primary hypertension are multifactorial1. One approach to identifying relevant genes is to elucidate rare forms of monogenic hypertension.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c30c2ce4ff857454eba46260d8525ed
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030140024&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030140024&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
Objective : To discuss the relevance of rare monogenic forms of hypertension to the diagnosis, pathogenesis and treatment of essential hypertension. Study selection : Three monogenic forms of hypertension have been identified that are inherited as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4396f4c59f19aed16f828453a8d0087
http://www.scopus.com/inward/record.url?eid=2-s2.0-0029562454&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0029562454&partnerID=MN8TOARS
Autor:
Nihat Bilginturan, Sinasi Özsoylu
Publikováno v:
The Journal of Pediatrics. 114:508-509
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8354883c8f69ab86e0d4d2422607a32e
https://doi.org/10.1016/s0022-3476(89)80591-8
https://doi.org/10.1016/s0022-3476(89)80591-8
Autor:
Nihat Bilginturan, John F. Crigler
Publikováno v:
The Journal of Pediatrics. 67:966
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34eba74e02ac1fbfc882b398ca7bbde8
https://doi.org/10.1016/s0022-3476(65)81916-3
https://doi.org/10.1016/s0022-3476(65)81916-3