Literature DB >> 9641152

Autosomal dominant hypertension with brachydactyly: an enigmatic form of monogenic hypertension.

H Schuster1.   

Abstract

Entities:  

Mesh：

Year:  1998        PMID： 9641152     DOI： 10.1093/ndt/13.6.1337

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  4 in total

1.  A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

Authors:  S Baulac; I Gourfinkel-An; F Picard; M Rosenberg-Bourgin; J F Prud'homme; M Baulac; A Brice; E LeGuern
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

Review 2.  "Treasure your exceptions": recent advances in molecular genetics of glomerular disease.

Authors:  Andrzej Ciechanowicz; Andrzej Brodkiewicz; Agnieszka Bińczak-Kuleta; Miłosz Parczewski; Stanłisaw Czekalski
Journal:  J Appl Genet       Date:  2008       Impact factor: 3.240

Review 3.  Brachydactyly E: isolated or as a feature of a syndrome.

Authors:  Arrate Pereda; Intza Garin; Maria Garcia-Barcina; Blanca Gener; Elena Beristain; Ane Miren Ibañez; Guiomar Perez de Nanclares
Journal:  Orphanet J Rare Dis       Date:  2013-09-12       Impact factor: 4.123

Review 4.  Progress in the molecular mechanisms of genetic epilepsies using patient-induced pluripotent stem cells.

Authors:  Ruijiao Zhou; Guohui Jiang; Xin Tian; Xuefeng Wang
Journal:  Epilepsia Open       Date:  2018-07-08
  4 in total

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