Symptomatic dystrophinopathies in female children-Reference-Cited by-同舟云学术

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Symptomatic dystrophinopathies in female children

Published:2011-03 Issue:3 Volume:21 Page:172-177
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Seemann Natashia,Selby Kathy,McAdam Laura,Biggar Doug,Kolski Hanna,Goobie Sharan,Yoon Grace,Campbell Craig

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference32 articles.

1. Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study;Hoogerwaard;Lancet,1999

2. Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy;Hoogerwaard;Neurology,2005

3. Psuedo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene;Romero;Neuromuscul Disord,2001

4. Muscle pain as only presenting symptom in a girl with dystrophinopathy;Ceulemans;Pediatr Neurol,2008

5. Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy;Palmucci;Eur Neurol,1999

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A rare complex structural variant of novel intragenic inversion combined with reciprocal translocation t(X;1)(p21.2;p13.3) in Duchenne muscular dystrophy;Neuromuscular Disorders;2024-06

2. DUCHENNE MUSKÜLER DİSTROFİ TAŞIYICI KADINLARDA GÖRÜLEN SEMPTOMLAR: GELENEKSEL DERLEME;Gazi Sağlık Bilimleri Dergisi;2023-08-25

3. Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy;Genes;2023-01-14

4. Dystrophinopathies;Current Clinical Neurology;2023

5. Long‐term outcomes for females with early‐onset dystrophinopathy;Developmental Medicine & Child Neurology;2022-12-23

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