Literature DB >> 7304406

Early cardiac manifestations of Marfan's syndrome in the newborn.

Z Lababidi, C Monzon.   

Abstract

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Year:  1981        PMID： 7304406     DOI： 10.1016/0002-8703(81)90051-x

Source DB:  PubMed          Journal:  Am Heart J        ISSN： 0002-8703            Impact factor:   4.749


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  9 in total

1.  Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.

Authors:  M Wang; P Kishnani; M Decker-Phillips; S G Kahler; Y T Chen; M Godfrey
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

2.  Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndrome.

Authors:  M Godfrey; M Raghunath; J Cisler; C L Bevins; A DePaepe; M Di Rocco; J Gregoritch; K Imaizumi; P Kaplan; Y Kuroki
Journal:  Am J Pathol       Date:  1995-06       Impact factor: 4.307

3.  Megalocornea. Clinical and genetic aspects.

Authors:  F M Meire
Journal:  Doc Ophthalmol       Date:  1994       Impact factor: 2.379

4.  The Marfan syndrome--analysis of growth and cardiovascular manifestation.

Authors:  U Vetter; R Mayerhofer; D Lang; G von Bernuth; M B Ranke; A A Schmaltz
Journal:  Eur J Pediatr       Date:  1990-04       Impact factor: 3.183

Review 5.  Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders.

Authors:  D M Milewicz
Journal:  Tex Heart Inst J       Date:  1994

6.  Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency.

Authors:  I M Buntinx; P J Willems; S E Spitaels; P J Van Reempst; A M De Paepe; J E Dumon
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

7.  Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype.

Authors:  D Bonneau; J L Huret; G Godeau; D Couet; M Putterman; J Tanzer; P Babin; M Larrègue
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

8.  An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathy.

Authors:  P Tamminga; F G Jennekens; P G Barth; P Fleury; H van den Berg; J W Oorthuys
Journal:  Eur J Pediatr       Date:  1985-01       Impact factor: 3.183

9.  Severe neonatal Marfan syndrome resulting from a de novo 3-bp insertion into the fibrillin gene on chromosome 15.

Authors:  D M Milewicz; M Duvic
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025
  9 in total

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