Literature DB >> 17572338

Congenital cranial dysinnervation disorders and more.

Elias I Traboulsi.   

Abstract

Entities:  

Mesh：

Year:  2007        PMID： 17572338     DOI： 10.1016/j.jaapos.2007.04.007

Source DB:  PubMed          Journal:  J AAPOS        ISSN： 1091-8531            Impact factor:   1.220


× No keyword cloud information.
  10 in total

1.  HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.

Authors:  Bryn D Webb; Sherin Shaaban; Harald Gaspar; Luis F Cunha; Christian R Schubert; Ke Hao; Caroline D Robson; Wai-Man Chan; Caroline Andrews; Sarah MacKinnon; Darren T Oystreck; David G Hunter; Anthony J Iacovelli; Xiaoqian Ye; Anne Camminady; Elizabeth C Engle; Ethylin Wang Jabs
Journal:  Am J Hum Genet       Date:  2012-07-05       Impact factor: 11.025

2.  Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes.

Authors:  Janet C Rucker; Bryn D Webb; Tamiesha Frempong; Harald Gaspar; Thomas P Naidich; Ethylin Wang Jabs
Journal:  Brain       Date:  2014-02-21       Impact factor: 13.501

Review 3.  Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs).

Authors:  A A Assaf
Journal:  Eye (Lond)       Date:  2011-07-01       Impact factor: 3.775

4.  Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomalies.

Authors:  Shaimaa Abdelsattar Mohammad; Tougan Taha Abdelaziz; Mohamed I Gadelhak; Hanan H Afifi; Ghada M H Abdel-Salam
Journal:  Neuroradiology       Date:  2018-08-03       Impact factor: 2.804

5.  A congenital cranial dysinnervation disorder: Möbius' syndrome.

Authors:  Hatice Mutlu Albayrak; Nuriye Tarakçı; Hüseyin Altunhan; Rahmi Örs; Hüseyin Çaksen
Journal:  Turk Pediatri Ars       Date:  2017-09-01

6.  Computer-assisted diagnosis of monocular elevation deficiency.

Authors:  Siegfried Priglinger; Matthias Rohleder; Simone Reitböck; Claudia Priglinger; Thomas Kaltofen
Journal:  Int Ophthalmol       Date:  2013-06-05       Impact factor: 2.031

Review 7.  Fourth cranial nerve palsy and Brown syndrome: two interrelated congenital cranial dysinnervation disorders?

Authors:  Pierre-François Kaeser; Michael C Brodsky
Journal:  Curr Neurol Neurosci Rep       Date:  2013-06       Impact factor: 5.081

8.  Plexin A3 and plexin A4 convey semaphorin signals during facial nerve development.

Authors:  Quenten Schwarz; Kathryn E Waimey; Matthew Golding; Hyota Takamatsu; Atsushi Kumanogoh; Hajime Fujisawa; Hwai-Jong Cheng; Christiana Ruhrberg
Journal:  Dev Biol       Date:  2008-09-03       Impact factor: 3.582

9.  Brain Abnormalities in Congenital Fibrosis of the Extraocular Muscles Type 1: A Multimodal MRI Imaging Study.

Authors:  Wen Miao; Fengyuan Man; Shaoqin Wu; Bin Lv; Zhenchang Wang; Junfang Xian; Bernhard A Sabel; Huiguang He; Yonghong Jiao
Journal:  PLoS One       Date:  2015-07-17       Impact factor: 3.240

10.  Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies.

Authors:  Tanya Lehky; Reversa Joseph; Camilo Toro; Tianxia Wu; Carol Van Ryzin; Andrea Gropman; Flavia M Facio; Bryn D Webb; Ethylin W Jabs; Brenda S Barry; Elizabeth C Engle; Francis S Collins; Irini Manoli
Journal:  Muscle Nerve       Date:  2021-01-19       Impact factor: 3.217
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.