Academic Journal

Successful Treatment With Evocalcet Against Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Identified by AP2S1 Gene Mutation (p.Arg15Leu)

التفاصيل البيبلوغرافية
العنوان: Successful Treatment With Evocalcet Against Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Identified by AP2S1 Gene Mutation (p.Arg15Leu)
المؤلفون: Ai Chida, Yutaka Hasegawa, Toshie Segawa, Daisuke Yamabe, Hirotaka Yan, Yusuke Chiba, Hiraku Chiba, Hirofumi Kinno, Tomoyasu Oda, Yoshihiko Takahashi, Koji Nata, Yasushi Ishigaki
المصدر: Case Reports in Endocrinology, Vol 2025 (2025)
بيانات النشر: Wiley, 2025.
سنة النشر: 2025
المجموعة: LCC:Diseases of the endocrine glands. Clinical endocrinology
مصطلحات موضوعية: Diseases of the endocrine glands. Clinical endocrinology, RC648-665
الوصف: Conclusion: Evocalcet may be a promising therapeutic candidate for symptomatic FHH3.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2090-651X
Relation: https://doaj.org/toc/2090-651X
DOI: 10.1155/crie/9514578
URL الوصول: https://doaj.org/article/5e502893f22c4b439af62c5bc4e39bfe
رقم الانضمام: edsdoj.5e502893f22c4b439af62c5bc4e39bfe
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2090651X
DOI:10.1155/crie/9514578