Resultados de procura - Cengiz Candan
- Mostrando 1 - 4 Resultados de 4
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1
Cardiovascular Phenotypes in Children with CKD: The 4C Study por Franz Schaefer, Anke Doyon, Karolis Ažukaitis, Aysun Karabay Bayazıt, Nur Canpolat, Ali Düzova, Anna Niemirska, Betül Sözeri, Daniela Thurn, Ali Anarat, Bruno Ranchin, Mieczysław Litwin, Salim Çalışkan, Cengiz Candan, Esra Baskın, Ebru Yılmaz, Sevgı Mır, Marietta Kirchner, Anja Sander, Dieter Haffner, Anette Melk, Elke Wühl, Rukshana Shroff, Uwe Querfeld
Publicado 2016Artigo -
2
Metabolic acidosis is common and associates with disease progression in children with chronic kidney disease por Jérôme Harambat, Kevin Kunzmann, Karolis Ažukaitis, Aysun Karabay Bayazıt, Nur Canpolat, Anke Doyon, Ali Düzova, Anna Niemirska, Betül Sözeri, Daniela Thurn‐Valsassina, Ali Anarat, Lucie Bessenay, Cengiz Candan, Amira Peco‐Antić, Alev Yılmaz, Sibylle Tschumi, Sara Testa, Augustina Jankauskiené, Hakan Erdoğan, Alejandra Rosales, Harika Alpay, Francesca Lugani, Klaus Arbeiter, Francesca Mencarelli, Aysel Kıyak, Osman Dönmez, Dorota Drożdż, Anette Melk, Uwe Querfeld, Franz Schaefer
Publicado 2017Artigo -
3
Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children por Karolis Ažukaitis, Wenjun Ju, Marietta Kirchner, Viji Nair, Michelle R. Smith, Zhiyin Fang, Daniela Thurn‐Valsassina, Aysun Karabay Bayazıt, Anna Niemirska, Nur Canpolat, İpek Kaplan Bulut, Fatoş Yalçınkaya, Dušan Paripović, Jérôme Harambat, Nilgün Çakar, Harika Alpay, Francesca Lugani, Francesca Mencarelli, Mahmut Çivilibal, Hakan Erdoğan, Jutta Gellermann, Enrico Vidal, Yılmaz Tabel, Charlotte Gimpel, Pelin Ertan, Önder Yavaşcan, Anette Melk, Uwe Querfeld, Elke Wühl, Matthias Kretzler, Franz Schaefer, Klaus Arbeiter, Alejandra Rosales, Ladislav Dušek, Ariane Zaloszyc, Uwe Querfeld, Jutta Gellermann, Max C. Liebau, Lutz T. Weber, Evelin Muschiol, Rainer Büscher, Jun Oh, Anette Melk, Daniela Thurn-Valassina, Dieter Haffner, Franz Schaefer, Charlotte Gimpel, Ulrike John, Simone Wygoda, Nikola Jeck, Marianne Wigger, Sara Testa, Luisa Murer, Chiara Matteucci, Augustina Jankauskiené, Karolis Ažukaitis, Dorota Drożdż, Francesca Lugani, Aleksandra Żurowska, Marcin Zaniew, Mieczysław Litwin, Anna Nimierska, Ana Teixeira, Amira Peco‐Antić, Dušan Paripović, Guido F. Laube, Ali Anarat, Aysun Karabay Bayazıt, Ali Düzova, Yelda Bilginer, Salim Çalışkan, Nur Canpolat, Mahmut Çivilibal, Sevgı Mır, Betül Sözeri, Brigitta Kranz, Francesca Mencarelli, Barry C. Dorn, Fatoş Yalçınkaya, Esra Baskın, Nilgün Çakar, Oğuz Söylemezoğlu, Sevinç Emre, Cengiz Candan, Aysel Kıyak, Gül Özçelik, Harika Alpay, Rukshana Shroff, Bruno Rachin, Jérôme Harambat, Maria Szczepańska, Hakan Erdoğan, Osman Dönmez, Ayşe Balat, Nejat Aksu, Yılmaz Tabel, Pelin Ertan, Ebru Yılmaz, Ali Anarat, Ayşı̇n Bakkaloğlu
Publicado 2019Artigo -
4
Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants por Kathrin Burgmaier, Leonie Violetta Brinker, Florian Erger, Bodo B. Beck, Marcus R. Benz, Carsten Bergmann, Olivia Boyer, Laure Collard, Claudia Dafinger, Marc Fila, Claudia Kowalewska, Bärbel Lange-Sperandio, Laura Massella, Antonio Mastrangelo, Djalila Mekahli, Monika Miklaszewska, Nadina Ortiz-Bruechle, Ludwig Patzer, Larisa Prikhodina, Bruno Ranchin, Nadejda Ranguelov, Raphael Schild, Tomáš Seeman, Lale Sever, Przemysław Sikora, Maria Szczepańska, Ana Teixeira, Julia Thumfart, Barbara Uetz, Lutz T. Weber, Elke Wühl, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau, Loai Eid, Klaus Arbeiter, Nathalie Godefroid, Jacques Lombet, Aurélie De Mul, Markus Feldkoetter, Jakub Zieg, Franziska Grundmann, Matthias Galiano, Bjoern Buchholz, Anja Buescher, Karsten Häffner, Oliver Groß, Ludwig Patzer, Jun Oh, Dieter Haffner, Wanja M. Bernhardt, Susanne Schaefer, Simone Wygoda, Jan Halbritter, Ute Derichs, Günter Klaus, Felix Lechner, Sabine Ponsel, Jens König, Hagen Staude, Donald Wurm, Martin Bald, Michaela Geßner, Neveen A. Soliman, Gema Ariceta, Juan David González-Rodríguez, Francisco de la Cerda Ojeda, Jérôme Harambat, Denis Morin, Claire Dossier, Guillaume Dorval, Rukshana Shroff, Stella Stabouli, Nakysa Hooman, Francesca Mencarelli, William Morello, Germana Longo, Francesco Emma, Augustina Jankauskiené, Katarzyna Taranta‐Janusz, Ilona Zagożdżon, Katarzyna Zachwieja, Małgorzata Stańczyk, Beata Bieniaś, Mieczysław Litwin, Aurelia Morawiec‐Knysak, Alberto Caldas Afonso, Oliver Dunand, Andreea Liana Răchişan, Gordana Miloševski‐Lomić, Svetlana Papizh, Rina Rus, Houweyda Jilani, Bahriye Atmış, Ali Düzova, Alper Soylu, Cengiz Candan, Salim Çalışkan, Alev Yılmaz
Publicado 2021Artigo
Ferramentas de procura:
Materias Relacionadas
Internal medicine
Medicine
Kidney disease
Disease
Endocrinology
Acidosis
Autosomal Recessive Polycystic Kidney Disease
Autosomal dominant polycystic kidney disease
Biology
Blood pressure
Cardiology
Carotid arteries
Comorbidity
Epidermal growth factor
Gene
Genetics
Genotype
Intensive care medicine
Intima-media thickness
Kidney
Left ventricular hypertrophy
Mathematics
Metabolic acidosis
Missense mutation
PKD1
Pathology
Percentile
Phenotype
Physiology
Prospective cohort study