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1 . Academic Journal
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development
저자
by
Abali, Saygin
;
Abali, Zehra Yavas
;
Akin, Leyla
;
Almaraz, Maricruz
;
Audí, Laura
, et al.
소스
In
eBioMedicine
January 2024 99
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7 . Academic Journal
A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B
저자
by
Campbell, Devon
;
Reyes, Monica
;
Kaygusuz, Sare Betul
;
Abali, Saygın
;
Guran, Tulay
, et al.
소스
In
Bone
April 2022 157
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7 . Academic Journal
Interdisiplinary and intraobserver reliability of the Greulich-Pyle method among Turkish children
저자
by
Sariyilmaz, Kerim
;
Abali, Saygin
;
Ziroglu, Nezih
;
Cingoz, Tunca
;
Ozkunt, Okan
, et al.
소스
Journal of Pediatric Endocrinology and Metabolism
. 36(12):1181-1185
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7 . Academic Journal
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature.
저자
by
Kirkgoz, Tarik
;
Abali, Saygin
;
Seker, Askin
;
Gurpinar Tosun, Busra
;
Eltan, Mehmet
, et al.
소스
Hormone Research in Paediatrics
. 2023, Vol. 96 Issue 5, p527-537. 11p.
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7 . Academic Journal
Application of complementary and alternative medicine in epileptic children at a tertiary pediatric neurology center in Turkey
저자
by
Ekici, Barış
;
Tatlı, Burak
;
Abalı, Saygın
;
Aydınlı, Nur
;
Özmen, Meral
.
소스
In
European Journal of Integrative Medicine
March 2012 4(1):e71-e75
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7 . Academic Journal
Preterm ovarian hyperstimulation syndrome mimicking clitoromegaly
저자
by
Ay, Zeynep Alize
;
Abali, Saygin
;
Korkmaz, Ayse
;
Beken, Serdar
.
소스
In
Pediatrics & Neonatology
November 2023 64(6):690-691
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6 . Academic Journal
Clinical Features of Children and Adolescents at the Onset of Diabetes: A Single-center Experience.
저자
by
Abalı, Saygın
;
Akın, Yasemin
.
소스
Medical Journal of Bakirkoy
. Mar2023, Vol. 19 Issue 1, p22-30. 9p.
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4 . Academic Journal
Early postnatal metabolic profile in neonates with critical CHDs.
저자
by
Guvenc, Osman
;
Beken, Serdar
;
Abali, Saygin
;
Saral, Neslihan Yildirim
;
Yalcin, Gizem
, et al.
소스
Cardiology in the Young; Mar2023, Vol. 33 Issue 3, p349-353, 5p
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7 . Academic Journal
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
저자
by
Eltan, Mehmet
;
Yavas Abali, Zehra
;
Turkyilmaz, Ayberk
;
Gokce, Ibrahim
;
Abali, Saygın
, et al.
소스
Calcified Tissue International
. Apr2022, Vol. 110 Issue 4, p441-450. 10p.
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7 . Report
Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia
저자
by
Abali, Saygin
;
Yavas Abali, Zehra
;
Yararbas, Kanay
;
Semiz, Serap
.
소스
Journal of Pediatric Endocrinology and Metabolism
. 34(9):1201-1205
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