A rare coexistence: tyrosinemia type III and Wolff-Parkinson-White syndrome
Yilmaz-Gumus, Emel; Genc, Emine; Kocaman, Damla; Saylan-Cevik, Berna; Polat, Hamza; Arslan-Ates, Esra; Yazkan-Akgul, Gozde; Saribas-Akmehmet, Sumeyye; Kilavuz, Sebile; Ozturk-Hismi, Burcu
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Save Suboptimal adoption of diabetes technology despite coverage and the impact on glycemic outcomes in children and adolescents with type 1 diabetes in Hong Kong
Poon, Sarah Wing-yiu; Chan, Kwong-tat; But, Betty Wai-man; Wong, Shirley Man-yee; Yam, Wing-in; Cheung, Pik-to; See, Wing-shan; Chan, Suk-yan; Yau, Ho-chung; Wong, Eunice Wai Yu; Wong, Lap Ming; Fu, Antony Chun-cheung; Kwan, Elaine Yin-wah; Tsui, Janez Heung-ching; Lai, Sin-ting; Lo, Priscilla Wai-chee; Lam, Yuen-yu; Yuen, Hoi-wing; Wong, Sammy Wai-chun; Chung, Jacky Ying-ki; Lee, Ching-yin; Tay, Ming-kut; Tung, Joanna Yuet-ling
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Save Childhood thiamine-responsive megaloblastic anemia and diabetes: a case series highlighting early diagnosis and management
Yilmaz, Ugur Cem; Bhriguvanshi, Arpita; Ozalp Kizilay, Deniz; Ozen, Samim; Darcan, Sukran; Dogan, Yusuf Can; Isik, Esra; Karadas, Nihal; Wood, Jamie R.; Libman, Ingrid; Goksen, Damla
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Save Hypertrophic cardiomyopathy as a novel phenotypic feature of NSUN3-related mitochondrial disease: a case report with review of the literature
Senol Ersak, Ayse; Cagiran, Tugce; Kocyigit, Aysen; Ciki, Kismet; Yildiz, Yilmaz; Aypar, Ebru; Ketenci Islek, Serap; Simsek Kiper, Pelin Ozlem; Haliloglu, Goknur; Dursun, Ali
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Save A novel CEP57 gene mutation in mosaic variegated aneuploidy syndrome 2: case report
Viudes, Cristina Pellicer; Manso Borras, Maria; Enrique Madrid, Susana; Diago Garcia, Berta; Maruenda Jimenez, Armando Carlos; Guzman Tena, Paula; Vazquez Alvarez, Maria Leticia; Canadas Olmo, Victoria; Guillamon, Dolores Tio; Edo Tena, Maria Amparo; Novella-Maestre, Edurne; Marin Reina, Purificacion
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