Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rabia Miray Kışla, Ekinci"'
Autor:
Sibel Balcı, İlksen Demir, Mahir Serbes, Dilek Doğruel, Derya Ufuk Altıntaş, Rabia Miray Kışla Ekinci
Publikováno v:
Rheumatology, Vol 58, Iss 6, Pp 367-374 (2020)
Externí odkaz:
https://doaj.org/article/4e57622269c0486daeec638398f61b28
Autor:
Mustafa Yılmaz, Derya Ufuk Altıntaş, Sibel Balcı, Rabia Miray Kışla Ekinci, Dilek Doğruel, Mahir Serbes
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 4, Pp 1511-1514 (2019)
Juvenile dermatomyositis is a multisystemic autoimmune disease with uncertain etiology. Both innate immunity and adaptive immunity play a role on the pathogenesis of the disease. Selective immunoglobulin A deficiency is the most common primary immuno
Externí odkaz:
https://doaj.org/article/f793b647fe3a4006b0ddb9d9bd3cf5e9
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 3, Pp 186-191 (2019)
Aim:Primary Vesicoureteral reflux (VUR) is defined as retrograde urine flow from the bladder to the upper urinary system due to an insufficient valvular mechanism in the ureterovesical junction. We aimed to clarify factors affecting physical growth i
Externí odkaz:
https://doaj.org/article/fd95466e4f3d48ffa335938546c5a86c
Autor:
Rabia Miray Kışla Ekinci, Fatih Gürbüz, Sibel Balcı, Atıl Bişgin, Mehmet Taştan, Bilgin Yüksel, Mustafa Yılmaz
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 94-99 (2019)
Inactivating autosomal recessive mutations in fibroblast growth factor 23 (FGF23), klotho (KL) and polypeptide N-acetylgalactosaminotransferase 3 (GALNT3) genes lead to a rare disorder, hyperphosphatemic familial tumoral calcinosis (HFTC). Patients w
Externí odkaz:
https://doaj.org/article/a282db191c3c48caaded2a872b202157
Publikováno v:
Cukurova Medical Journal, Vol 43, Iss 1, Pp 235-240 (2018)
Mikst konnektif doku hastalığı birden fazla bağ doku hastalığına ait bulgular ile karakterize otoimmün bir hastalıktır. U1 RNP’ye karşı yüksek titre otoantikorlar ile karakterizedir. Hastaların %23’ünün çocukluk çağında bulgu
Externí odkaz:
https://doaj.org/article/c410e2fde0524d2085d9ee600d19973f
Autor:
Tuğba, Kurumoğlu İncekalan, Rabia Miray, Kışla Ekinci, Göksu Hande, Naz Şimdivar, Neşe Çetin, Doğan, Emine, Çiloğlu
Publikováno v:
Clinical Rheumatology. 41:2533-2540
To evaluate changes in the peripapillary, macular, and choroidal microvasculature in the eyes of patients with deficiency of adenosine deaminase 2 (DADA2) and no clinical signs of ocular involvement.The study included 12 eyes of 12 patients with DADA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::444a78d3379a5027392f90dd8b88ebbb
https://doi.org/10.1007/s10067-022-06194-z
https://doi.org/10.1007/s10067-022-06194-z
Publikováno v:
Indian journal of pediatrics. 89(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04cb6cafb8996887971e6b1007e172e0
https://pubmed.ncbi.nlm.nih.gov/35841516
https://pubmed.ncbi.nlm.nih.gov/35841516
Autor:
Dilek, Özcan, Mahir, Serbes, Rabia Miray Kışla, Ekinci, Sibel Balcı, Çetinkaya, Ayşe Şenay, Şaşihüseyinoğlu, Atıl, Bişgin, Derya Ufuk, Altıntaş
Publikováno v:
Allergologia et immunopathologia. 49(6)
Primary immunodeficiency diseases (PID) are the diseases characterized by a dysfunction of the immune system. Affected patients share a different phenotype such as chronic infections, allergy, autoimmunity, and autoinflammation.In all, 433 children w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b34a70c68c5c7c86c2652a339c233d0
https://pubmed.ncbi.nlm.nih.gov/34761650
https://pubmed.ncbi.nlm.nih.gov/34761650
Autor:
Rabia Miray Kışla Ekinci, Sibel Balcı, Ahmet Hakan Erol, Dilek Karagöz, Derya Ufuk Altıntaş, Atıl Bisgin
Publikováno v:
Archives of rheumatology. 36(4)
Objectives: In this study, we aimed to investigate the performance of Eurofever Registry and the Paediatric Rheumatology International Trials Organisation (PRINTO) classification criteria in pediatric patients with familial Mediterranean fever (FMF).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33a70fdf6ba40c2708ddf39930bdd35b
https://pubmed.ncbi.nlm.nih.gov/35382375
https://pubmed.ncbi.nlm.nih.gov/35382375
Autor:
Aysun Karabay-Bayazit, Engin Melek, Rabia Miray Kışla-Ekinci, Mustafa Yilmaz, Ali Anarat, Atil Bisgin, Bahriye Atmis
Publikováno v:
The Turkish Journal of Pediatrics. 61:444
Atmis B, Kisla-Ekinci RM, Melek E, Bisgin A, Yilmaz M, Anarat A, Karabay-Bayazit A. Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent. Turk J Pediatr 2019; 61: 444-448. Gitelman syndrome is a renal tubular salt-wasti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a27178fcfe1fc1aa29f718718ae93c31
https://doi.org/10.24953/turkjped.2019.03.021
https://doi.org/10.24953/turkjped.2019.03.021