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The Journal of Clinical Endocrinology and Metabolism|May 17, 2021
Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene DefectsSare Betul Kaygusuz, Esra Arslan Ates, Maria Lillina Vignola, et al.
European Journal of Endocrinology|March 2, 2022
Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high-normal testicular volumeEsra Arslan Ates, Mehmet Eltan, Bahadir Sahin, et al.
Turkish Journal of Medical Sciences|January 8, 2016
The value of FDG-PET/CT by using 3-dimensional stereotactic surface projection software analysis in the differential diagnosis of dementiaEsra Arslan, Özgül Ekmekçioğlu, Fatma Arzu Görtan, et al.
Human Genetics|July 16, 2013
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndromeEsther Pohl, Ayca Aykut, Filippo Beleggia, et al.
Archives of Endocrinology and Metabolism|January 14, 2022
When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus?Özlem Üstay, Tuğçe Apaydın, Onur Elbasan, et al.
Clinical Nuclear Medicine|January 25, 2024
Contribution of 68 Ga-DOTA-FAPI-04 PET/CT to Prostate Cancer Imaging : Complementary Role in PSMA-Negative CasesNurhan Ergül, Tevfik Fikret Çermik, Göksel Alçın, et al.
Revista Da Associacao Medica Brasileira (1992)|April 24, 2024
Predictors of recurrence in breast cancer patients with pathological partial responseFadime Didem Can Trabulus, Mehmet Ali Nazli, Esra Arslan, et al.
Journal of Human Genetics|May 29, 2021
Secondary findings in 622 Turkish clinical exome sequencing dataEsra Arslan Ateş, Ayberk Türkyilmaz, Özlem Yıldırım, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 9, 2026
A rare coexistence: tyrosinemia type III and Wolff-Parkinson-White syndromeEmel Yılmaz-Gümüş, Emine Genç, Damla Kocaman, et al.
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