ProfileOfResearchers

TÃTULO: Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study
AUTORES: Verploegen, Maartje F. A.; Vargas Poussou, Rosa; Walsh, Stephen B.; Alpay, Harika; Amouzegar, Atefeh; Ariceta, Gema; Atmis, Bahriye; Bacchetta, Justine; Barany, Peter; Baron, Stephanie; Bayrakci, Umut Selda; Belge, Hendrica; Besouw, Martine; Blanchard, Anne; Bokenkamp, Arend; Boyer, Olivia; Burgmaier, Kathrin; Calo, Lorenzo A.; Decramer, Stephane; Devuyst, Olivier; van Dyck, Maria; Ferraro, Pietro Manuel; Fila, Marc; Francisco, Telma; Ghiggeri, Gian Marco; Gondra, Leire; Guarino, Stefano; Hooman, Nakysa; Hoorn, Ewout J.; Houillier, Pascal; Kamperis, Konstantinos; Kari, Jameela A.; Konrad, Martin; Levtchenko, Elena; Lucchetti, Laura; Lugani, Francesca; Marzuillo, Pierluigi; Mohidin, Barian; Neuhaus, Thomas J.; Osman, Abdaldafae; Papizh, Svetlana; Perello, Manel; Rookmaaker, Maarten B.; Conti, Valerie Said; Santos, Fernando; Sawaf, Ghalia; Serdaroglu, Erkin; Szczepanska, Maria; Taroni, Francesca; Topaloglu, Rezan; Trepiccione, Francesco; Vidal, Enrico; Wan, Elizabeth R.; Weber, Lutz; Yildirim, Zeynep Yuruk; Yuksel, Selcuk; Zlatanova, Galia; Bockenhauer, Detlef; Emma, Francesco; Nijenhuis, Tom; ...Mais
PUBLICAÇÃO: 2022, FONTE: NEPHROLOGY DIALYSIS TRANSPLANTATION

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TÃTULO: Growth Patterns After Kidney Transplantation in European Children Over the Past 25 Years: An ESPN/ERA-EDTA Registry Study
AUTORES: Marjolein Bonthuis; Jaap W Groothoff; Gema Ariceta; Sergey Baiko; Nina Battelino; Anna Bjerre; Karlien Cransberg; Gabriel Kolvek; Heather Maxwell; Polina Miteva; Maria S Molchanova; Thomas J Neuhaus; Lars Pape; Gyorgy Reusz; Caroline Rousset Rouviere; Ana Rita Sandes; Rezan Topaloglu; Maria Van Dyck; Elisa Ylinen; Ilona Zagozdzon; Kitty J Jager; Jerome Harambat; ...Mais
PUBLICAÇÃO: 2020, FONTE: TRANSPLANTATION, VOLUME: 104, NÚMERO: 1

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TÃTULO: Infants with congenital nephrotic syndrome have comparable outcomes to infants with other renal diseases
AUTORES: Stephanie Dufek; Elisa Ylinen; Agnes Trautmann; Harika Alpay; Gema Ariceta; Christoph Aufricht; Justine Bacchetta; Sevcan Bakkaloglu; Aysun Bayazit; Salim Caliskan; Maria do Sameiro Faria; Ismail Dursun; Mesiha Ekim; Augustina Jankauskiene; Guenter Klaus; Fabio Paglialonga; Andrea Pasini; Nikoleta Printza; Valerie Said Conti; Claus Peter Schmitt; Constantinos Stefanidis; Enrico Verrina; Enrico Vidal; Hazel Webb; Argyroula Zampetoglou; Alberto Edefonti; Tuula Holtta; Rukshana Shroff; ...Mais
PUBLICAÇÃO: 2019, FONTE: PEDIATRIC NEPHROLOGY, VOLUME: 34, NÚMERO: 4

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TÃTULO: Management of children with congenital nephrotic syndrome: challenging treatment paradigms
AUTORES: Stephanie Dufek; Tuula Holtta; Agnes Trautmann; Elisa Ylinen; Harika Alpay; Gema Ariceta; Christoph Aufricht; Justine Bacchetta; Sevcan A Bakkaloglu; Aysun Bayazit; Rumeysa Yasemin Cicek; Ismail Dursun; Ali Duzova; Mesiha Ekim; Daniela Iancu; Augustina Jankauskiene; Guenter Klaus; Fabio Paglialonga; Andrea Pasini; Nikoleta Printza; Valerie Said Conti; Maria do Sameiro Faria; Claus Peter Schmitt; Constantinos J Stefanidis; Enrico Verrina; Enrico Vidal; Karel Vondrak; Hazel Webb; Argyroula Zampetoglou; Detlef Bockenhauer; Alberto Edefonti; Rukshana Shroff; ...Mais
PUBLICAÇÃO: 2019, FONTE: NEPHROLOGY DIALYSIS TRANSPLANTATION, VOLUME: 34, NÚMERO: 8

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TÃTULO: Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)(2)D serum levels are associated with PHEX mutation type Full Text
AUTORES: Marcos Morey; Lidia Castro Feijoo; Jesus Barreiro; Paloma Cabanas; Manuel Pombo; Marta Gil; Ignacio Bernabeu; Jose M Diaz Grande; Lourdes Rey Cordo; Gema Ariceta; Itxaso Rica; Jose Nieto; Ramon Vilalta; Loreto Martorell; Jaime Vila Cots; Fernando Aleixandre; Ana Fontalba; Leandro Soriano Guillen; Jose M Garcia Sagredo; Sixto Garcia Minaur; Berta Rodriguez; Saioa Juaristi; Carmen Garcia Pardos; Antonio Martinez Peinado; Jose M Millan; Ana Medeira; Oana Moldovan; Angeles Fernandez; Lourdes Loidi; ...Mais
PUBLICAÇÃO: 2011, FONTE: BMC MEDICAL GENETICS, VOLUME: 12, NÚMERO: 1

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