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38 in total

Review 1. Neuronal migration disorders in humans and in mouse models--an overview.

Authors: A J Copp; B N Harding
Journal: Epilepsy Res Date: 1999-09 Impact factor: 3.045

2. Syndromes of bilateral symmetrical polymicrogyria.

Authors: A J Barkovich; R Hevner; R Guerrini
Journal: AJNR Am J Neuroradiol Date: 1999 Nov-Dec Impact factor: 3.825

Review 3. Therapeutic choices in the locomotor management of the child with cerebral palsy--more luck than judgement?

Authors: J H Patrick; A P Roberts; G F Cole
Journal: Arch Dis Child Date: 2001-10 Impact factor: 3.791

4. Cortical dysplasia: a possible substrate for brain tumors.

Authors: Shiyong Liu; Chunqing Zhang; Haifeng Shu; Didier Wion; Hui Yang
Journal: Future Oncol Date: 2012-03 Impact factor: 3.404

5. Middle interhemispheric variant of holoprosencephaly associated with diffuse polymicrogyria.

Authors: Jun-Ichi Takanashi; A James Barkovich; Nancy J Clegg; Mauricio R Delgado
Journal: AJNR Am J Neuroradiol Date: 2003-03 Impact factor: 3.825

6. Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum.

Authors: A B Ekici; D Hilfinger; M Jatzwauk; C T Thiel; D Wenzel; I Lorenz; E Boltshauser; T W Goecke; G Staatz; D J Morris-Rosendahl; H Sticht; U Hehr; A Reis; A Rauch
Journal: Mol Syndromol Date: 2010-09-14

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

Review 1. Neuronal migration disorders in humans and in mouse models--an overview.

2. Syndromes of bilateral symmetrical polymicrogyria.

Review 3. Therapeutic choices in the locomotor management of the child with cerebral palsy--more luck than judgement?

4. Cortical dysplasia: a possible substrate for brain tumors.

5. Middle interhemispheric variant of holoprosencephaly associated with diffuse polymicrogyria.

6. Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum.

Review 7. Genetics of the polymicrogyria syndromes.

Review 8. Genetic malformations of cortical development.

9. Does asymptomatic septal agenesis exist? A review of 34 cases.

Review 10. Neurodevelopmental liabilities in epilepsy.