Literature DB >> 5300597

[On a unusual brain atrophy syndrome in hyperammonemia in childhood].

A Rett.   

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Year:  1966        PMID: 5300597

Source DB:  PubMed          Journal:  Wien Med Wochenschr        ISSN: 0043-5341


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  197 in total

Review 1.  Recent insights into hyperventilation from the study of Rett syndrome.

Authors:  A M Kerr; P O Julu
Journal:  Arch Dis Child       Date:  1999-04       Impact factor: 3.791

2.  Methylation-dependent silencing at the H19 imprinting control region by MeCP2.

Authors:  Robert A Drewell; Carolyn J Goddard; Jean O Thomas; M Azim Surani
Journal:  Nucleic Acids Res       Date:  2002-03-01       Impact factor: 16.971

Review 3.  Child and adolescent psychiatry: past scientific achievements and challenges for the future.

Authors:  Michael Rutter
Journal:  Eur Child Adolesc Psychiatry       Date:  2010-05-11       Impact factor: 4.785

Review 4.  Complexities of Rett syndrome and MeCP2.

Authors:  Rodney C Samaco; Jeffrey L Neul
Journal:  J Neurosci       Date:  2011-06-01       Impact factor: 6.167

5.  Neurophysiological observations on corticospinal projections to the upper limb in subjects with Rett syndrome.

Authors:  J A Eyre; A M Kerr; S Miller; M C O'Sullivan; V Ramesh
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-10       Impact factor: 10.154

Review 6.  The role of MeCP2 in CNS development and function.

Authors:  Elisa S Na; Lisa M Monteggia
Journal:  Horm Behav       Date:  2010-05-31       Impact factor: 3.587

7.  Two sisters with Rett syndrome.

Authors:  C A Haenggeli; J Moura-Serra; C D DeLozier-Blanchet
Journal:  J Autism Dev Disord       Date:  1990-03

8.  A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing.

Authors:  Steven W Long; Jenny Y Y Ooi; Peter M Yau; Peter L Jones
Journal:  Biosci Rep       Date:  2011-10       Impact factor: 3.840

Review 9.  Brief report: systematic review of Rett syndrome in males.

Authors:  Brian Reichow; Annie George-Puskar; Tara Lutz; Isaac C Smith; Fred R Volkmar
Journal:  J Autism Dev Disord       Date:  2015-10

10.  A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.

Authors:  N C Schanen; E J Dahle; F Capozzoli; V A Holm; H Y Zoghbi; U Francke
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

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