Rezultati pretrage - Francisco de la Cerda Ojeda
- Prikaz rezultata 1 – 2 od 2
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1
Severe and malignant hypertension are common in primary atypical hemolytic uremic syndrome od Teresa Cavero, Emilia Arjona, Karina Soto, Fernando Caravaca‐Fontán, Cristina Rabasco, Luis Eduardo Bravo, Francisco de la Cerda Ojeda, Nàdia Martín, Miquel Blasco, Ana Ávila, Ana Huerta, Virginia Cabello, Ana Jarque, Concepción Alcázar, Xavier Fulladosa, Javier Carbayo, S Anaya, Carmen Cobelo, Natàlia Ramos, Elena Iglesias, José Baltar, Rocío Martínez-Gallardo, Lourdes Pérez, Enrique Morales, Roberto González, Manuel Macía, Juliana Draibe, Luis Pallardó, Luís F. Quintana, Mario Espinosa, Xoana Barros, Fernando Pereira, Mercedes Cao, Juan Antonio Moreno, Santiago Rodrı́guez de Córdoba, Manuel Praga
Izdano 2019Artigo -
2
Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants od 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
Izdano 2021Artigo
Alati za pretragu:
Povezani predmeti
Disease
Internal medicine
Medicine
Antibody
Atypical hemolytic uremic syndrome
Autosomal Recessive Polycystic Kidney Disease
Autosomal dominant polycystic kidney disease
Biology
Complement system
Eculizumab
Gastroenterology
Gene
Genetics
Genotype
Immunology
Missense mutation
PKD1
Pathology
Phenotype
Plasmapheresis
Thrombotic microangiopathy