Serum protein biomarker signature of Duchenne muscular dystrophy by Paul Dowling, Elisa Negroni, Capucine Trollet, Margit Zweyer, Dieter Swandulla, Kay Ohlendieck

Subjects: “…Dystrophinopathy…”
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Dystrophinopathy in the paravertebral muscle of adolescent idiopathic scoliosis: a prospective case-control study in China by Junyu Li, Danfeng Zheng, Zekun Li, Jiaxi Li, Zexi Yang, Xiang Zhang, Yingshuang Zhang, Miao Yu

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Manifesting Pediatric Carrier of Isolated Dystrophinopathy with Initial Presentation of Myalgia and Persistent HyperCKemia by Chien-Hua Wang, Wen-Chen Liang, Yi-Ning Su, Wen-Chieh Lee, Ching-Chyuan Su, Yuh-Jyh Jong

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Duchenne muscular dystrophy with Kocher-Debre-Semelaigne syndrome: a double jeopardy by Arumugom Archana, Pediredla Karunakar, Vaishnavi Sreenivasan, Reena Gulati

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Cardiac MRI in Duchenne and Becker Muscular Dystrophy by Manu Santhappan Girija, Deepak Menon, Kiran Polavarapu, Veeramani Preethish-Kumar, Seena Vengalil, Saraswati Nashi, Madassu Keertipriya, Mainak Bardhan, Priya Treesa Thomas, Valasani Ravi Kiran, Vikas Nishadham, Arun Sadasivan, Akshata Huddar, Gopi Krishnan Unnikrishnan, Ashita Barthur, Atchayaram Nalini

Subjects: “…dystrophinopathy…”
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Muscular dystrophy associated with the DMD gene in women by E. O. Vorontsova, A. V. Zinina, O. A. Shchagina

Subjects: “…dystrophinopathy…”
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Patient demographics, clinical characteristics and genetic mutations of DMD and BMD patients in Qatar Epidemiological and genetic profile of Duchenne muscular dystrophy and Becker... by Mohammad Sawahreh, Fatima Al-Maadid, Khalid Omer Ibrahim, Tawfeg Ben Omran, Mahmoud Fawzi Osman

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Genomic insights into Duchene muscular dystrophy: Analysis of 1250 patients reveals 30% novel genetic patterns and 6 novel variants by Khalda Amr, Nagia Fahmy, Ghada El-Kamah

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Multicentric Study on the Diagnostic of Neuromuscular Diseases in Children with High Creatinine Phosphokinase Levels by Cláudia Monteiro, Cristina Garrido, Ângela Pereira, Andreia Dias, Mariana Costa, Catarina Magalhães, Manuela Ferreira, Miguel Costa, Manuela Santos

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Peripheral blood transcriptome profiling enables monitoring disease progression in dystrophic mice and patients by Mirko Signorelli, Mitra Ebrahimpoor, Olga Veth, Kristina Hettne, Nisha Verwey, Raquel García‐Rodríguez, Christa L Tanganyika‐deWinter, Luz B Lopez Hernandez, Rosa Escobar Cedillo, Benjamín Gómez Díaz, Olafur T Magnusson, Hailiang Mei, Roula Tsonaka, Annemieke Aartsma‐Rus, Pietro Spitali

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Genotype-phenotype correlation of neurodevelopmental disorders in patients with dystrophinopathies by Fabrício M. Soares, Bruna F. Rosa, Gabriela M. Giordani, Daniele L. Rocha, Ana Carolina Brusius-Facchin, Michele M. Becker, Jonas Alex M. Saute

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Comparative analysis of phenotypes features in two common genetic variants of limb-girdle muscular dystrophy by I. V. Sharkova, E. L. Dadali, I. V. Ugarov, O. P. Ryzhkova, A. V. Polyakov

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