Literature DB >> 26130973

Clinical Images: Postterm Newborn with Lissencephaly Presented with Seizure: Case Report and Review of Literature.

Mustafa Alhasan1, Mansour Mathkour2, James M Milburn1.   

Abstract

Entities:  

Year:  2015        PMID： 26130973      PMCID： PMC4482552     

Source DB:  PubMed          Journal:  Ochsner J        ISSN： 1524-5012


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  8 in total

1.  X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings.

Authors:  Dominique Bonneau; Annick Toutain; Annie Laquerrière; Stéphane Marret; Pascale Saugier-Veber; Marie-Anne Barthez; Sophie Radi; Valérie Biran-Mucignat; Diana Rodriguez; Antoinette Gélot
Journal:  Ann Neurol       Date:  2002-03       Impact factor: 10.422

2.  Lissencephaly, abnormal genitalia and refractory epilepsy: case report of XLAG syndrome.

Authors:  Mônica Jaques Spinosa; Paulo Breno Noronha Liberalesso; Simone Carreiro Vieira; Alaídes Susana Fojo Olmos; Alfredo Löhr
Journal:  Arq Neuropsiquiatr       Date:  2006-12       Impact factor: 1.420

3.  Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria).

Authors:  M Ozmen; Y Yilmaz; M Calişkan; O Minareci; N Aydinli
Journal:  Turk J Pediatr       Date:  2000 Jul-Sep       Impact factor: 0.552

Review 4.  X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.

Authors:  W B Dobyns; E Berry-Kravis; N J Havernick; K R Holden; D Viskochil
Journal:  Am J Med Genet       Date:  1999-10-08

Review 5.  [Genetic and clinical aspects of lissencephaly].

Authors:  A Verloes; M Elmaleh; M Gonzales; A Laquerrière; P Gressens
Journal:  Rev Neurol (Paris)       Date:  2007-05       Impact factor: 2.607

6.  Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene.

Authors:  H Hartmann; G Uyanik; C Gross; U Hehr; T Lücke; M Arslan-Kirchner; B Antosch; A M Das; J Winkler
Journal:  Neuropediatrics       Date:  2004-06       Impact factor: 1.947

7.  ARX mutations in X-linked lissencephaly with abnormal genitalia.

Authors:  G Uyanik; L Aigner; P Martin; C Gross; D Neumann; H Marschner-Schäfer; U Hehr; J Winkler
Journal:  Neurology       Date:  2003-07-22       Impact factor: 9.910

8.  Epidemiology of lissencephaly type I.

Authors:  J F de Rijk-van Andel; W F Arts; A Hofman; A Staal; M F Niermeijer
Journal:  Neuroepidemiology       Date:  1991       Impact factor: 3.282
  8 in total
  1 in total

Review 1.  CRISPR Gene-Editing Models Geared Toward Therapy for Hereditary and Developmental Neurological Disorders.

Authors:  Poh Kuan Wong; Fook Choe Cheah; Saiful Effendi Syafruddin; M Aiman Mohtar; Norazrina Azmi; Pei Yuen Ng; Eng Wee Chua
Journal:  Front Pediatr       Date:  2021-03-11       Impact factor: 3.418
  1 in total

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