✦ LIBER ✦

Polyuria and polydipsia in a young child: diagnostic considerations and identification of novel mutation causing familial neurohypophyseal diabetes insipidus

✍ Scribed by Matthew D. Stephen, Raymond G. Fenwick, Patrick G. Brosnan

Book ID: 120757199
Publisher: Springer US
Year: 2010
Tongue: English
Weight: 206 KB
Volume: 15
Category: Article
ISSN: 1386-341X
DOI: 10.1007/s11102-010-0230-y

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Clinical and molecular analysis of a Chi

Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin–neurophysin II gene

✍ Luo, Yongfeng; Wang, Binbin; Qiu, Yu; Zhang, Chuan; Jin, Chengluo; Zhao, Yakun; 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 268 KB

Identification of novel GCK and HNF1A/TC

Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY)

✍ Dalia Toaima; Andrea Näke; Jutta Wendenburg; Kirsten Praedicow; Julia Rohayem; K 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 74 KB 👁 2 views

Maturity-onset diabetes of the young is a genetically heterogenous autosomal dominant form of diabetes mellitus, characterized by an early age at onset and a primary defect in beta-cell function. Forty families with a clinical presentation suggestive of MODY were screened for the most common MODY su