✦ LIBER ✦

Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome

✍ Scribed by E. Spaggiari; R. Salati; P. Nicolini; R. Borgatti; U. Pozzoli; F. Polenghi

Book ID: 111564956
Publisher: Springer Netherlands
Year: 1999
Tongue: English
Weight: 73 KB
Volume: 23
Category: Article
ISSN: 0165-5701
DOI: 10.1023/a:1026560721525

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Bardet-Biedl syndrome type 3 in an Irani

Bardet-Biedl syndrome type 3 in an Iranian family: Clinical study and confirmation of disease localization

✍ Ghadami, Mohsen ;Tomita, Hiro-Aki ;Najafi, Mohammad-Taghi ;Damavandi, Elia ;Fara 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 176 KB 👁 2 views

Clinical and genetic characterization of

Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis

✍ M'hamdi, O.; Redin, C.; Stoetzel, C.; Ouertani, I.; Chaabouni, M.; Maazoul, F.; 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 English ⚖ 548 KB

First description of obstructive sleep a

First description of obstructive sleep apnea and its clinical consequences on quality of life in Bardet–Biedl syndrome

✍ Domenico Viggiano; Carlo Santoriello; Alfonso Ferretti; Gabriele Malgieri; Franc 📂 Article 📅 2008 🏛 Elsevier 🌐 English ⚖ 178 KB

Clinical and genetic epidemiology of Bar

Clinical and genetic epidemiology of Bardet–Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study

✍ Susan J. Moore; Jane S. Green; Yanli Fan; Ashvinder K. Bhogal; Elizabeth Dicks; 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 230 KB 👁 2 views

Bardet-Biedl syndrome (BBS) and Laurence-Moon syndrome (LMS) have a similar phenotype, which includes retinal dystrophy, obesity, and hypogenitalism. They are differentiated by the presence of spasticity and the absence of polydactyly in LMS. The aims of this study were to describe the epidemiology

Clinical evidence of decreased olfaction

Clinical evidence of decreased olfaction in Bardet–Biedl syndrome caused by a deletion in the BBS4 Gene

✍ Alessandro Iannaccone; Kirk Mykytyn; Antonio M. Persico; Charles C. Searby; Alfo 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 82 KB 👁 2 views

Clinical and electrophysiological findin

Clinical and electrophysiological findings in two cases of Miller Fisher syndrome

✍ F. Sartucci; G. Tognoni; B. Rossi; M. Manetti; C. Giraldi 📂 Article 📅 1990 🏛 Springer Milan 🌐 English ⚖ 301 KB