Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gulden Gokcay"'
Autor:
Abdurrahman Akgun, Gulden Gokcay, Neslihan Onenli Mungan, Hatice Serap Sivri, Hasan Tezer, Cigdem Aktuglu Zeybek, Fatih Ezgu
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
This expert-opinion-based document was prepared by a group of specialists in pediatric inherited metabolic diseases and infectious diseases including administrative board members of Turkish Society for Pediatric Nutrition and Metabolism to provide gu
Externí odkaz:
https://doaj.org/article/1910dd11ee834a16b3614b54a8b92b29
Autor:
Berna Seker Yilmaz, Julien Baruteau, Nur Arslan, Halil Ibrahim Aydin, Magalie Barth, Ayse Ergul Bozaci, Anais Brassier, Ebru Canda, Aline Cano, Efstathia Chronopoulou, Grainne M. Connolly, Lena Damaj, Charlotte Dawson, Dries Dobbelaere, Claire Douillard, Fatma Tuba Eminoglu, Sahin Erdol, Melike Ersoy, Sherry Fang, François Feillet, Gulden Gokcay, Emine Goksoy, Magali Gorce, Asli Inci, Banu Kadioglu, Fatih Kardas, Cigdem Seher Kasapkara, Gonca Kilic Yildirim, Deniz Kor, Melis Kose, Cecilia Marelli, Helen Mundy, Siobhan O’Sullivan, Burcu Ozturk Hismi, Radha Ramachandran, Agathe Roubertie, Mehtap Sanlilar, Manuel Schiff, Srividya Sreekantam, Karolina M. Stepien, Ozlem Uzun Unal, Yilmaz Yildiz, Tanyel Zubarioglu, Paul Gissen
Publikováno v:
Life, Vol 12, Iss 11, p 1721 (2022)
X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle defect. The disease severity ranges from asymptomatic carrier state to severe neonatal presentation with hyperammonaemic encephalopathy. We audited the diagnosis and
Externí odkaz:
https://doaj.org/article/800ce92a6de9427e948d1938b211e04c
Autor:
Hans Demmelmair, Anita MacDonald, Urania Kotzaeridou, Peter Burgard, Domingo Gonzalez-Lamuno, Elvira Verduci, Melike Ersoy, Gulden Gokcay, Behiye Alyanak, Eva Reischl, Wolfgang Müller-Felber, Fabienne Lara Faber, Uschi Handel, Sabrina Paci, Berthold Koletzko
Publikováno v:
Nutrients, Vol 10, Iss 12, p 1944 (2018)
Children with phenylketonuria (PKU) follow a protein restricted diet with negligible amounts of docosahexaenoic acid (DHA). Low DHA intakes might explain subtle neurological deficits in PKU. We studied whether a DHA supply modified plasma DHA and neu
Externí odkaz:
https://doaj.org/article/d18bed7101184b83992e1f3c8c9a3493
Autor:
Seda Susgun, Yesim Kesim, Dovlat Khalilov, Nermin Gorkem Sirin, Hasim Gezegen, Baris Salman, Emrah Yucesan, Gulden Gokcay, Huseyin Kutay Korbeyli, Mehmet Cihan Balci, Sibel Aylin Ugur Iseri, Betul Baykan, Nerses Bebek
Publikováno v:
Neurological Sciences.
Autor:
Pilar Giraldo, Gulden Gokcay, Isabela Batsu, Julie Kissell, Maria G. Perichon, Guillermo I. Drelichman
Publikováno v:
Molecular Genetics and Metabolism. 138:107113
Autor:
John Mitchell, Paul Harmatz, Laila Selim, Iman Gamal El Din, Neslihan Mungan, Fatma Bulut, Christina Lampe, Christina L. Grant, Carlos R. Ferreira, Ratna D. Puri, Sunita Bijarnia-Mahay, Nur Arslan, Norberto Guelbert, Maha S. Zaki, Seema Kapoor, Andreas Hahn, Bo Magnusson, Erik Sundberg, Seza Ozen, Ezgi D. Batu, Maja Di Rocco, Gulden Gokcay, Kathleen Crosby, Alexander Solyom
Publikováno v:
Molecular Genetics and Metabolism. 135:S83-S84
Autor:
John Mitchell, Paul Harmatz, Laila Selim, Iman Gamal El Din, Neslihan Mungan, Fatma Bulut, Christina Lampe, Christina L. Grant, Carlos R. Ferreira, Ratna D. Puri, Sunita Bijarnia-Mahay, Noberto Guelbert, Nur Arslan, Maha S. Zaki, Seema Kapoor, Andreas Hahn, Bo Magnusson, Erik Sundberg, Seza Ozen, Ezgi D. Batu, Maja Di Rocco, Gulden Gokcay, Kathleen Crosby, Alexander Solyom
Publikováno v:
Molecular Genetics and Metabolism. 135:S84