✦ LIBER ✦

Cerebral Specialization for Speech Perception and Movement Organization in Adults with Down's Syndrome

✍ Scribed by Elliott, Digby; Weeks, Daniel J.

Book ID: 122665738
Publisher: Masson, Italy (now Elsevier Masson)
Year: 1993
Tongue: English
Weight: 761 KB
Volume: 29
Category: Article
ISSN: 0010-9452
DOI: 10.1016/S0010-9452(13)80215-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Cerebral Specialization for Speech Produ

Cerebral Specialization for Speech Production in Persons with Down Syndrome

✍ Matthew Heath; Digby Elliott 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 157 KB

Cerebral specialization and verbal-motor

Cerebral specialization and verbal-motor integration in adults with and without Down syndrome

✍ Timothy N Welsh; Digby Elliott; Dominic A Simon 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 219 KB

Comparison of rating scales for the diag

Comparison of rating scales for the diagnosis of dementia in adults with Down’s syndrome

✍ S. Deb; J. Braganza 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 84 KB

The modified CAMDEX informant interview

The modified CAMDEX informant interview is a valid and reliable tool for use in the diagnosis of dementia in adults with Down's syndrome

✍ S. L. Ball; A. J. Holland; F. A. Huppert; P. Treppner; P. Watson; J. Hon 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 112 KB

Review of donepezil, rivastigmine, galan

Review of donepezil, rivastigmine, galantamine and memantine for the treatment of dementia in Alzheimer's disease in adults with Down syndrome: implications for the intellectual disability population

✍ V. P. Prasher 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 74 KB 👁 2 views

## Abstract The management of dementia in Alzheimer's disease has dramatically changed since the development of anti‐dementia drugs. However, there is limited information available regarding the bio‐medical aspects of the differing drugs; particularly relating to adults with intellectual disability

Homozygosity for a missense mutation in

Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders

✍ Clare N Lynex; Ian M Carr; Jack P Leek; Rajgopal Achuthan; Simon Mitchell; Eamon 📂 Article 📅 2004 🏛 BioMed Central 🌐 English ⚖ 553 KB