✦ LIBER ✦

Incoercible topiramate-related vomiting in a patient with epilepsy and mental retardation

✍ Scribed by S. Striano; E. Marano; P. Striano; L. Bilo

Publisher: Springer Milan
Year: 2001
Tongue: English
Weight: 27 KB
Volume: 22
Category: Article
ISSN: 1590-1874
DOI: 10.1007/s100720100014

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Rhombencephalosynapsis in a patient with

Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms

✍ Pasquale Striano; Giovanni Morana; Marianna Pezzella; Tommaso Bellini; Andrea Ro 📂 Article 📅 2010 🏛 Springer Milan 🌐 English ⚖ 201 KB

Localization-related epilepsy mimiking e

✍ Seiji Kimura; Kaori Adachi 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 993 KB

Temozolomide treatment does not affect t

Temozolomide treatment does not affect topiramate and oxcarbazepine plasma concentrations in chronically treated patients with brain tumor-related epilepsy

✍ Marta Maschio; Fiorenzo Albani; Bruno Jandolo; Alessia Zarabla; Manuela Contin; 📂 Article 📅 2008 🏛 Springer US 🌐 English ⚖ 150 KB

A microduplication of CBP in a patient w

A microduplication of CBP in a patient with mental retardation and a congenital heart defect

✍ Bernard Thienpont; Jeroen Breckpot; Maureen Holvoet; Joris R. Vermeesch; Koen De 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 219 KB 👁 3 views

Familial paroxysmal exercise-induced dys

Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance

✍ T. Perniola; L. Margari; M.G. de Iaco; A. Presicci; P. Ventura; E. Ferrannini; G 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 177 KB

## Abstract Only few sporadic and familial cases of paroxysmal exercise‐induced dyskinesia (PED) have been described in literature. PED associated with familial epilepsy has been rarely reported. We describe a family in which six members in different generations were affected by a long‐lasting PED,

Chromosome 19p13.3 deletion in a patient

Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems

✍ Adam J. de Smith; Mieke M. van Haelst; Richard J. Ellis; Susan E. Holder; Stewar 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB 👁 3 views

FIG. 1. Patient aged 11 years. Note high forehead, frontal upsweep, upslanting palpebral fissures, and small nose and mouth.