Literature DB >> 9105971

Brief report: cognitive and behavioral profiles in persons with Smith-Magenis syndrome.

E M Dykens1, B M Finucane, C Gayley.   

Abstract

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Year:  1997        PMID： 9105971     DOI： 10.1023/a:1025800126086

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN： 0162-3257


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  9 in total

1.  Interstitial deletion of (17)(p11.2p11.2) in nine patients.

Authors:  A C Smith; L McGavran; J Robinson; G Waldstein; J Macfarlane; J Zonona; J Reiss; M Lahr; L Allen; E Magenis
Journal:  Am J Med Genet       Date:  1986-07

2.  The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome.

Authors:  B M Finucane; D Konar; B Haas-Givler; M B Kurtz; C I Scott
Journal:  Dev Med Child Neurol       Date:  1994-01       Impact factor: 5.449

3.  K-ABC profiles in children with fragile X syndrome, Down syndrome, and nonspecific mental retardation.

Authors:  R M Hodapp; J F Leckman; E M Dykens; S S Sparrow; D G Zelinsky; S I Ort
Journal:  Am J Ment Retard       Date:  1992-07

4.  Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome.

Authors:  B M Finucane; E R Jaeger; M B Kurtz; M Weinstein; C I Scott
Journal:  Am J Med Genet       Date:  1993-02-15

5.  Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2 p11.2) (Smith-Magenis syndrome).

Authors:  A F Colley; M A Leversha; L E Voullaire; J G Rogers
Journal:  J Paediatr Child Health       Date:  1990-02       Impact factor: 1.954

6.  Profiles, correlates, and trajectories of intelligence in Prader-Willi syndrome.

Authors:  E M Dykens; R M Hodapp; K Walsh; L J Nash
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1992-11       Impact factor: 8.829

7.  Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.

Authors:  R F Stratton; W B Dobyns; F Greenberg; J B DeSana; C Moore; G Fidone; G H Runge; P Feldman; G S Sekhon; R M Pauli
Journal:  Am J Med Genet       Date:  1986-07

Review 8.  Measuring behavioral phenotypes: provocations from the "new genetics".

Authors:  E M Dykens
Journal:  Am J Ment Retard       Date:  1995-03

9.  Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Authors:  F Greenberg; V Guzzetta; R Montes de Oca-Luna; R E Magenis; A C Smith; S F Richter; I Kondo; W B Dobyns; P I Patel; J R Lupski
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025
  9 in total
  19 in total

1.  Brief Report: Contrasting Profiles of Everyday Executive Functioning in Smith-Magenis Syndrome and Down Syndrome.

Authors:  Lucy Wilde; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2017-08

2.  An indirect examination of the function of problem behavior associated with fragile X syndrome and Smith-Magenis syndrome.

Authors:  Paul Langthorne; Peter McGill
Journal:  J Autism Dev Disord       Date:  2012-02

3.  Differences in Social Motivation in Children with Smith-Magenis Syndrome and Down Syndrome.

Authors:  Lucy Wilde; Anna Mitchell; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2016-06

4.  Adaptive and maladaptive behavior in children with Smith-Magenis Syndrome.

Authors:  Staci C Martin; Pamela L Wolters; Ann C M Smith
Journal:  J Autism Dev Disord       Date:  2006-05

5.  Autism spectrum features in Smith-Magenis syndrome.

Authors:  Gonzalo Laje; Rebecca Morse; William Richter; Jonathan Ball; Maryland Pao; Ann C M Smith
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-11-15       Impact factor: 3.908

6.  Pharmacological treatment of disruptive behavior in Smith-Magenis syndrome.

Authors:  Gonzalo Laje; Rebecca Bernert; Rebecca Morse; Maryland Pao; Ann C M Smith
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-11-15       Impact factor: 3.908

7.  [Speech impairment and the Smith-Magenis syndrome].

Authors:  C Bergmann; S Morlot; M Ptok
Journal:  HNO       Date:  2007-08       Impact factor: 1.284

8.  DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome.

Authors:  L Potocki; K S Chen; T Koeuth; J Killian; S T Iannaccone; S K Shapira; C D Kashork; A S Spikes; L G Shaffer; J R Lupski
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

9.  The prevalence and phenomenology of repetitive behavior in genetic syndromes.

Authors:  Joanna Moss; Chris Oliver; Kate Arron; Cheryl Burbidge; Katy Berg
Journal:  J Autism Dev Disord       Date:  2008-11-27

10.  Neurodevelopment of children under 3 years of age with Smith-Magenis syndrome.

Authors:  Pamela L Wolters; Andrea L Gropman; Staci C Martin; Michaele R Smith; Hanna L Hildenbrand; Carmen C Brewer; Ann C M Smith
Journal:  Pediatr Neurol       Date:  2009-10       Impact factor: 3.372
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