✦ LIBER ✦

Anatomical and Electrophysiological Manifestations in a Patient with Congenital Corpus Callosum Agenesis

✍ Scribed by Yi-Ting Hsu,Jeng-Ren Duann,Chun-Ming Chen,Yu-Wan Yang,Chon-Haw Tsai…

Book ID: 126353340
Publisher: Springer
Year: 2012
Tongue: English
Weight: 368 KB
Volume: 26
Category: Article
ISSN: 0896-0267
DOI: 10.1007/s10548-012-0247-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Neurophysiological investigation of cong

Neurophysiological investigation of congenital mirror movements in a patient with agenesis of the corpus callosum

✍ Jean-François Lepage; Vincent Beaulé; Myriam Srour; Guy Rouleau; Alvaro Pascual- 📂 Article 📅 2012 🏛 Elsevier 🌐 English ⚖ 221 KB

Disturbances of spatial perception in a

Disturbances of spatial perception in a patient with agenesis of the corpus callosum

✍ J.D. Meerwaldt 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 222 KB

Total agenesis of the corpus callosum in

Total agenesis of the corpus callosum in a patient with childhood-onset schizophrenia

✍ S.M. Dursun; J.E. Hallak; J.A. Crippa; A.W. Zuardi; P. McGuire; J.F. Deakin 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 260 KB

Case study: A patient with agenesis of t

Case study: A patient with agenesis of the corpus callosum with minimal associated neuropsychological impairment

✍ Brescian, Natalie E.; Curiel, Rosie E.; Gass, Carlton S. 📂 Article 📅 2013 🏛 Taylor and Francis Group 🌐 English ⚖ 261 KB

Transient and permanent neuroimaging abn

Transient and permanent neuroimaging abnormalities due to partial status epilepticus in a patient with corpus callosum agenesis

✍ Safouris, Apostolos; Popa, Irina; Divano, Luisa; Preseau, Thierry; Dardiotis, Ef 📂 Article 📅 2014 🏛 Springer 🌐 English ⚖ 433 KB

Patient with an Xp21 contiguous gene del

Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosum

✍ Baranzini, Sergio E.; del Rey, Graciela; Nigro, Nora; Szijan, Irene; Chamoles, N 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 761 KB

The so-called Xp21 contiguous deletion syndrome or complex glycerol kinase deficiency (GKD) usually presents with classical Duchenne muscular dystrophy (DMD) or a milder dystrophic myopathy, adrenal hypoplasia, and GKD. A number of syndromic and nonsyndromic cases of agenesis of the corpus callosum