Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Osman Dönmez"'
Autor:
Ayşenur Paç Kısaarslan, Sümeyra Özdemir Çiçek, Ezgi D. Batu, Sezgin Şahin, Metin K. Gürgöze, Sibel Balcı Çetinkaya, Miray Kışla Ekinci, Bahriye Atmış, Kenan Barut, Amra Adrovic, Buket Esen Ağar, Nihal Şahin, Ferhat Demir, Esra Bağlan, Mehtap Akbalık Kara, Şenay Zırhlı Selçuk, Semanur Özdel, Elif Çomak, Betül Akkoyunlu, Gülçin Otar Yener, Deniz Gezgin Yıldırım, Kübra Öztürk, Mehmet Yıldız, Fatih Haşlak, Seher Şener, Hakan Kısaoğlu, Özge Baba, Zehra Kızıldağ, Rana İşgüder, Şengül Çağlayan, Raziye B. Güven Bilgin, Gülçin Aytaç, Burcu Bozkaya Yücel, Ayşe Tanatar, Hafize E. Sönmez, Mustafa Çakan, Aslıhan Kara, Ahmet T. Elmas, Beltinge Demircioğlu Kılıç, Nuray Aktay Ayaz, Belde Kasap, Banu Çelikel Acar, Ozan Ozkaya, Selçuk Yüksel, Sevcan Bakkaloğlu, Özlem Aydoğ, Güzide Aksu, Sema Akman, Osman Dönmez, Mehmet Bülbül, Mithat Büyükçelik, Yılmaz Tabel, Betül Sözeri, Mukaddes Kalyoncu, Yelda Bilginer, Muammer H. Poyrazoğlu, Erbil Ünsal, Özgür Kasapçopur, Seza Özen, Ruhan Düşünsel
Introduction: Neuropsychiatric (NP) involvement is a restricted area in juvenile-onset systemic lupus erythematosus (jSLE). Aim: To investigate the prevalence, demographic and clinical features, and outcomes of the neurological involvement in the Tur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb6b7220cf7a584661146dca57706bc6
https://doi.org/10.1016/j.jbspin.2023.105559
https://doi.org/10.1016/j.jbspin.2023.105559
Autor:
KEVSER ELMAS, Cansu Sivrikaya Yıldırım, Fatma Kocael, Bilge Demir, Hilal Özkan, Taner Özgür, Osman Dönmez, Melike Evim, Nilgün Köksal
Hemolytic disease of the fetus and newborn can cause hydrops and intrauterine death due to fetal anemia. Immunoglobulin and plasmapheresis have been used to defer blood transfusions to later gestational ages and treat fetal anemia in patients who wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::928633f9b84bc885e3322e90691e4b3b
https://doi.org/10.22541/au.165423618.86494953/v1
https://doi.org/10.22541/au.165423618.86494953/v1
Autor:
Ismail Dursun, Mehmet Taşdemir, Dilek Yılmaz, Ruhan Düşünsel, Engin Melek, Bağdagül Aksu, Yılmaz Tabel, Nur Canpolat, Sevcan A. Bakkaloglu, Mehtap Ezel Çelakil, Mustafa Koyun, Ayşe Seda Pınarbaşı, Osman Dönmez, Elif Çomak, Zeynep Yuruk Yildirim, Meral Torun Bayram, Meryem Benzer, Alper Soylu, Gül Özçelik, Ibrahim Gökce, Demet Tekcan, Elif Bahat, Neslihan Cicek, Seha Saygili
Publikováno v:
Pediatric Nephrology. 36:1195-1205
C3 glomerulopathy (C3G) is characterized by heterogeneous clinical presentation, outcome, and predominant C3 accumulation in glomeruli without significant IgG. There is scarce outcome data regarding childhood C3G. We describe clinical and pathologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2891221e7acd723369c7065857b4f4f9
https://doi.org/10.1007/s00467-020-04799-7
https://doi.org/10.1007/s00467-020-04799-7
Publikováno v:
Güncel Pediatri. 17:140-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f82bdc9885333b51fb33142aa9225adc
https://doi.org/10.4274/jcp.2019.0012
https://doi.org/10.4274/jcp.2019.0012
Autor:
Bagdagul Aksu, Alberto Caldas Afonso, Ipek Akil, Harika Alpay, Bahriye Atmis, Ozlem Aydog, Sevcan Bakkaloglu, Aysun Karabay Bayazıt, Meral Torun Bayram, Ilmay Bilge, Ipek Kaplan Bulut, Ayse Pinar Goksu Cetinkaya, Elif Comak, Belde Kasap Demir, Nida Dincel, Osman Donmez, Mehmet Akif Durmus, Hasan Dursun, Ruhan Dusunsel, Ali Duzova, Pelin Ertan, Asuman Gedikbasi, Nilufer Goknar, Sercin Guven, Duygu Hacihamdioglu, Augustina Jankauskiene, Mukaddes Kalyoncu, Salih Kavukcu, Bahriye Uzun Kenan, Nuran Kucuk, Bahar Kural, Mieczysław Litwin, Giovanni Montini, William Morello, Lukasz Obrycki, Beyhan Omer, Ebru Misirli Ozdemir, Nese Ozkayin, Dusan Paripovic, Cemile Pehlivanoglu, Seha Saygili, Franz Schaefer, Susanne Schaefer, Ferah Sonmez, Yilmaz Tabel, Nesrin Tas, Mehmet Tasdemir, Ana Teixeira, Demet Tekcan, Rezan Topaloglu, Sebahat Tulpar, Ozde Nisa Turkkan, Berfin Uysal, Metin Uysalol, Renata Vitkevic, Sevgi Yavuz, Sibel Yel, Tarik Yildirim, Zeynep Yuruk Yildirim, Nurdan Yildiz, Selcuk Yuksel, Eray Yurtseven, Alev Yilmaz
Publikováno v:
Frontiers in Urology, Vol 3 (2024)
BackgroundCongenital anomalies of the kidney and urinary tract (CAKUT) are defined as structural malformations of the kidney and/or urinary tract. Heat shock proteins (HSPs) are expressed in the kidney in response to cellular changes, such as thermal
Externí odkaz:
https://doaj.org/article/a80c88e2313546b599114335aabc3870
Publikováno v:
Journal of Hypertension and Management. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c1a8697ad6fe6e32df94a0118a7df90
https://doi.org/10.23937/2474-3690/1510027
https://doi.org/10.23937/2474-3690/1510027
Autor:
Cengiz Candan, Alev Yilmaz, Francesca Lugani, Kevin Kunzmann, Anna Niemirska, Franz Schaefer, Anette Melk, Jérôme Harambat, Sara Testa, Ali Anarat, Francesca Mencarelli, Betül Sözeri, Aysel Kiyak, Lucie Bessenay, Aysun Karabay Bayazit, Sibylle Tschumi, Harika Alpay, Hakan Erdogan, Amira Peco-Antic, Anke Doyon, Uwe Querfeld, Osman Dönmez, Klaus Arbeiter, Augustina Jankauskiene, Daniela Thurn-Valsassina, Ali Duzova, Dorota Drozdz, Alejandra Rosales, Nur Canpolat, Karolis Azukaitis
PubMedID: 28729033 Recent studies in adult chronic kidney disease (CKD) suggest that metabolic acidosis is associated with faster decline in estimated glomerular filtration rate (eGFR). Alkali therapies improve the course of kidney disease. Here we i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3fec3e4d131a81f848c9d53cc65fcae
https://ruj.uj.edu.pl/xmlui/handle/item/141089
https://ruj.uj.edu.pl/xmlui/handle/item/141089
Publikováno v:
Pediatrics International. 57:177-179
Congenital nephrotic syndrome (CNS) is a rare disease inherited as an autosomally recessive trait and defined as proteinuria manifesting at birth or in the first 3 months of life. The classical form is the Finnish type of CNS (CNF), which is caused b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7f588855b8d425eb2509e322fc1cadc
https://doi.org/10.1111/ped.12418
https://doi.org/10.1111/ped.12418
Publikováno v:
Türk Pediatri Arşivi. 45:380-383
Ozet Distal renal tubuler asidozlu hastalarda nefrokalsinoz sik bir bulgu olmasina ragmen bu hastalar genellikle normokalsemiktir Cocukluk caginda hiperkalseminin bir nedeni olarak distal renal tubuler asidoz nadir bir durumdur Bu yazimizda hiperkals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b75955e20445df213ddf311fe281f76
https://doi.org/10.4274/tpa.45.380
https://doi.org/10.4274/tpa.45.380
Autor:
Ozlem Erdogan, Fatoş Yalçınkaya, Nilgün Çakar, Salih Kavukçu, Elif Bahat, Ayfer Gür Güven, Rezan Topaloglu, Salim Caliskan, Osman Dönmez, Esra Baskin
Publikováno v:
Clinical and Experimental Nephrology. 15:108-113
The Turkish Renal Tubular Disorders Working Group aimed to form a patient registry database and gathered demographic, clinical, and laboratory data in various hereditary renal tubular disorders (HRTDs). A questionnaire comprising HRTDs was sent to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::144f33326c06a8f90ef4dd51cd542a0a
https://doi.org/10.1007/s10157-010-0367-z
https://doi.org/10.1007/s10157-010-0367-z