Literature DB >> 28877561

A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion.

João L O Madeira1, Alexandre B C Souza1, Flavia S Cunha1, Rafael L Batista1, Nathalia L Gomes1, Andresa S Rodrigues1, Frederico Mennucci de Haidar Jorge2, Gerson Chadi2, Dagoberto Callegaro2, Berenice B Mendonca1, Elaine M F Costa1, Sorahia Domenice1.   

Abstract

Entities:  

Keywords:  Kennedy disease; X-linked muscular atrophy; androgen receptor gene; cardiomyopathy; testicular failure

Mesh：

Substances：

Year:  2017        PMID： 28877561     DOI： 10.1002/mus.25952

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN： 0148-639X            Impact factor:   3.217


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  3 in total

1.  Effect of leuprorelin in bulbar function of spinal and bulbar muscular atrophy patients: observational study for 1 year.

Authors:  Min-Gu Kang; Dae-Won Gwak; Hee-Jin Cho; Yu-Sun Min; Jin-Sung Park
Journal:  J Neurol       Date:  2021-03-06       Impact factor: 4.849

Review 2.  The Role of Sex and Sex Hormones in Neurodegenerative Diseases.

Authors:  Elisabetta Vegeto; Alessandro Villa; Sara Della Torre; Valeria Crippa; Paola Rusmini; Riccardo Cristofani; Mariarita Galbiati; Adriana Maggi; Angelo Poletti
Journal:  Endocr Rev       Date:  2020-04-01       Impact factor: 19.871

Review 3.  Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences.

Authors:  Terence Gall-Duncan; Nozomu Sato; Ryan K C Yuen; Christopher E Pearson
Journal:  Genome Res       Date:  2021-12-29       Impact factor: 9.438
  3 in total

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