Literature DB >> 17495152

Neurological disorders. The mystery of the missing smile.

Greg Miller.   

Abstract

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Year:  2007        PMID： 17495152     DOI： 10.1126/science.316.5826.826

Source DB:  PubMed          Journal:  Science        ISSN： 0036-8075            Impact factor:   47.728


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  12 in total

1.  Identification of STAC3 variants in non-Native American families with overlapping features of Carey-Fineman-Ziter syndrome and Moebius syndrome.

Authors:  Aida Telegrafi; Bryn D Webb; Sarah M Robbins; Carlos E Speck-Martins; David FitzPatrick; Leah Fleming; Richard Redett; Andreas Dufke; Gunnar Houge; Jeske J T van Harssel; Alain Verloes; Angela Robles; Irini Manoli; Elizabeth C Engle; Ethylin W Jabs; David Valle; John Carey; Julie E Hoover-Fong; Nara L M Sobreira
Journal:  Am J Med Genet A       Date:  2017-08-04       Impact factor: 2.802

2.  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

Review 3.  The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.

Authors:  Carolyn P Graeber; David G Hunter; Elizabeth C Engle
Journal:  Semin Ophthalmol       Date:  2013 Sep-Nov       Impact factor: 1.975

4.  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

5.  Peptide sharing between influenza A H1N1 hemagglutinin and human axon guidance proteins.

Authors:  Guglielmo Lucchese; Giovanni Capone; Darja Kanduc
Journal:  Schizophr Bull       Date:  2013-01-31       Impact factor: 9.306

6.  HOXA1 mutations are not a common cause of Möbius syndrome.

Authors:  Jessica K Rankin; Caroline Andrews; Wai-Man Chan; Elizabeth C Engle
Journal:  J AAPOS       Date:  2010-02       Impact factor: 1.220

7.  Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometry.

Authors:  Neda Sadeghi; Elizabeth Hutchinson; Carol Van Ryzin; Edmond J FitzGibbon; John A Butman; Bryn D Webb; Flavia Facio; Brian P Brooks; Francis S Collins; Ethylin Wang Jabs; Elizabeth C Engle; Irini Manoli; Carlo Pierpaoli
Journal:  Brain Commun       Date:  2020-02-14

8.  Prostaglandin E2 alters Wnt-dependent migration and proliferation in neuroectodermal stem cells: implications for autism spectrum disorders.

Authors:  Christine T Wong; Eizaaz Ahmad; Hongyan Li; Dorota A Crawford
Journal:  Cell Commun Signal       Date:  2014-03-23       Impact factor: 5.712

9.  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.  Moebius syndrome: clinical features, diagnosis, management and early intervention.

Authors:  Odoardo Picciolini; Matteo Porro; Elisa Cattaneo; Silvia Castelletti; Giuseppe Masera; Fabio Mosca; Maria Francesca Bedeschi
Journal:  Ital J Pediatr       Date:  2016-06-03       Impact factor: 2.638
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