Literature DB >> 6120287

Is the fragile X syndrome amenable to treatment?

J Lejeune.   

Abstract

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Year:  1982        PMID： 6120287     DOI： 10.1016/s0140-6736(82)90991-6

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  15 in total

1.  Fragile X syndrome: an important preventable cause of mental handicap.

Authors:  H G Kinnell
Journal:  Br Med J (Clin Res Ed)       Date:  1987-09-05

Review 2.  Brief report: low frequency of the fragile X syndrome among Japanese autistic subjects.

Authors:  O Hashimoto; Y Shimizu; Y Kawasaki
Journal:  J Autism Dev Disord       Date:  1993-03

3.  Folic acid blinded trial in identical twins with fragile X syndrome.

Authors:  D S Rosenblatt; E A Duschenes; F V Hellstrom; M S Golick; M J Vekemans; S F Zeesman; E Andermann
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

Review 4.  Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy.

Authors:  John A Tsiouris; W Ted Brown
Journal:  CNS Drugs       Date:  2004       Impact factor: 5.749

Review 5.  The fragile X syndrome: the patients and their chromosomes.

Authors:  M A De Arce; A Kearns
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

6.  Cognitive, behavioral, and adaptive functioning in fragile X and non-fragile X retarded men.

Authors:  E Dykens; J Leckman; R Paul; M Watson
Journal:  J Autism Dev Disord       Date:  1988-03

7.  Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28. Results of folic acid treatment on fra(X) expression.

Authors:  K B Nielsen; N Tommerup
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndrome.

Authors:  B W Popovich; D S Rosenblatt; B A Cooper; M Vekemans
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

9.  Fragile X chromosome: clinical and cytogenetic studies on cases from seven families.

Authors:  A McDermott; R Walters; R T Howell; A Gardner
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

10.  Mean corpuscular hemoglobin is increased in Martin-Bell syndrome.

Authors:  U Langenbeck; J Schmidtke; I Bartels; I Hansmann; H Knüppel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
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