Literature DB >> 14743650

Muscular dystrophy overview: genetics and diagnosis.

Katherine D Mathews1.   

Abstract

A specific genetic diagnosis can be reached for most children with muscular dystrophy. Advanced diagnostics, including genetic testing and analysis of nonmuscle tissues, such as skin and blood, often allow the diagnosis to be reached using minimally invasive procedures. These diagnostic advances accompany improved understanding of pathophysiology and pave the way for specific and curative treatments.

Entities:  

Mesh:

Year:  2003        PMID: 14743650     DOI: 10.1016/s0733-8619(03)00065-3

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  4 in total

Review 1.  The muscular dystrophies: from genes to therapies.

Authors:  Richard M Lovering; Neil C Porter; Robert J Bloch
Journal:  Phys Ther       Date:  2005-12

2.  Walker-Warburg Syndrome: A Case with multiple uncommon features.

Authors:  Hibba A Bedri; Babiker M Mustafa; Yosif M Jadallah
Journal:  Sudan J Paediatr       Date:  2011

Review 3.  Epigenetics and Human Disease.

Authors:  Huda Y Zoghbi; Arthur L Beaudet
Journal:  Cold Spring Harb Perspect Biol       Date:  2016-02-01       Impact factor: 10.005

4.  Genetic, chromosomal, and syndromic causes of neural tube defects.

Authors:  Mohammed Z Seidahmed; Omer B Abdelbasit; Meeralebbae M Shaheed; Khalid A Alhussein; Abeer M Miqdad; Abdulmohsen S Samadi; Mohammed I Khalil; Elham Al-Mardawi; Mustafa A Salih
Journal:  Saudi Med J       Date:  2014-12       Impact factor: 1.484

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.