𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cortisol levels in Prader–Willi syndrome support changes and routine care

✍ Scribed by Merlin G. Butler; Duane T. Brandau; Mariana Theodoro; Uttam Garg


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
36 KB
Volume
149A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Comparison of leptin protein levels in P
✍ Butler, Merlin G.; Moore, Jason; Morawiecki, Andrew; Nicolson, Margery 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 26 KB 👁 2 views

Prader-Willi syndrome (PWS) is characterized by early childhood obesity, mental deficiency, hypogonadism, hypotonia, hypopigmentation, short stature, small hands and feet, and a characteristic face. It is the most common genetic cause of obesity and obesity is the most significant health problem for

Carnitine and coenzyme Q10 levels in ind
✍ Jennifer L. Miller; Christy H. Lynn; Jonathan Shuster; Daniel J. Driscoll 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 100 KB 👁 2 views

## Abstract Carnitine deficiency or coenzyme Q10 (CoQ10) deficiency may present with hypotonia, poor growth, easy fatigability, and apnea. This constellation of findings can also be seen in individuals with Prader–Willi syndrome (PWS). Animal studies indicate that increased fat mass due to obesity