All Relations between Muscular Diseases and dmd

Reference Sentence Publish Date Extraction Date Species
Wen-Chin Weng, Jung-Chih Chen, Chia-Yen Lee, Chia-Wei Lin, Wang-Tso Lee, Jeng-Yi Shieh, Chia-Chen Wang, Ching-Cheng Chuan. Cross-section and feasibility study on the non-invasive evaluation of muscle hemodynamic responses in Duchenne muscular dystrophy by using a near-infrared diffuse optical technique. Biomedical optics express vol 9 issue 10 2020 30319901 duchenne muscular dystrophy (dmd) is an x-linked debilitating muscular disease that may decrease nitric oxide (no) production and lead to functional muscular ischemia. 2020-10-01 2023-01-26 human
Irene Persiconi, Francesca Cosmi, Noemi Antonella Guadagno, Giuseppe Lupo, Maria Egle De Stefan. Dystrophin Is Required for the Proper Timing in Retinal Histogenesis: A Thorough Investigation on the Frontiers in neuroscience vol 14 issue 2020 32982660 dystrophin is required for the proper timing in retinal histogenesis: a thorough investigation on the duchenne muscular dystrophy (dmd) is a lethal x-linked muscular disease caused by defective expression of the cytoskeletal protein dystrophin (dp427). 2020-10-01 2023-01-26 Not clear
Dimitrios Tsika. Urinary Dimethylamine (DMA) and Its Precursor Asymmetric Dimethylarginine (ADMA) in Clinical Medicine, in the Context of Nitric Oxide (NO) and Beyond. Journal of clinical medicine vol 9 issue 6 2020 32545708 discussed diseases mainly include those relating to the renal and cardiovascular systems such as peripheral arterial occlusive disease, coronary artery disease, chronic kidney disease, rheumatoid arthritis, becker muscular disease, duchenne muscular disease (dmd), attention deficit hyperactivity disorder (adhd), and type i diabetes. 2020-09-28 2023-01-26 human
Salvo Danilo Lombardo, Emanuela Mazzon, Katia Mangano, Maria Sofia Basile, Eugenio Cavalli, Santa Mammana, Paolo Fagone, Ferdinando Nicoletti, Maria Cristina Petrali. Transcriptomic Analysis Reveals Involvement of the Macrophage Migration Inhibitory Factor Gene Network in Duchenne Muscular Dystrophy. Genes vol 10 issue 11 2020 31752120 duchenne muscular dystrophy (dmd) is a progressive hereditary muscular disease with x-linked recessive inheritance, that leads patients to premature death. 2020-05-05 2023-01-26 Not clear
Takuya Hiraide, Tsutomu Ogata, Seiji Watanabe, Mitsuko Nakashima, Tokiko Fukuda, Hirotomo Saits. Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases. Brain & development vol 41 issue 5 2019 30723005 coexistence of a cav3 mutation and a dmd deletion in a family with complex muscular diseases. 2019-07-26 2023-01-26 Not clear
Takuya Hiraide, Tsutomu Ogata, Seiji Watanabe, Mitsuko Nakashima, Tokiko Fukuda, Hirotomo Saits. Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases. Brain & development vol 41 issue 5 2019 30723005 we revealed the coexistence of the cav3 mutation and the dmd deletion in a family with complex muscular diseases and confirmed the usefulness of wes for elucidating such etiology. 2019-07-26 2023-01-26 Not clear
Tetsushi Yamamoto, Hiroyuki Awano, Zhujun Zhang, Mio Sakuma, Shoko Kitaaki, Masaaki Matsumoto, Masashi Nagai, Itsuko Sato, Takamitsu Imanishi, Nobuhide Hayashi, Masafumi Matsuo, Kazumoto Iijima, Jun Saegus. Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions. Circulation. Genomic and precision medicine vol 11 issue 1 2019 29874176 duchenne muscular dystrophy (dmd), the most common inherited muscular disease in childhood, is caused by dystrophin deficiency because of mutations in the 2019-03-07 2023-01-26 Not clear
Dilayla K DE Abreu, Janaina M Monteiro, Carolina C Souza, Rafael G Karam, Renata A Fernandes, Thais B Lessa, Jos\\xc3\\xa9 J Fagliari, Maria Angelica Miglino, Carlos Eduardo Ambrosi. Immunophenotyping lymphocyte and acute phase proteins in canine X-linked muscular dystrophy. Anais da Academia Brasileira de Ciencias vol 90 issue 3 2019 30304229 duchenne muscular dystrophy (dmd) is the most common x-linked muscular disease affecting humans. 2019-01-08 2023-01-26 Not clear
Carola Saure, Carolina Caminiti, Julieta Weglinski, Fernanda de Castro Perez, Soledad Monge. Energy expenditure, body composition, and prevalence of metabolic disorders in patients with Duchenne muscular dystrophy. Diabetes & metabolic syndrome vol 12 issue 2 2018 28869151 duchenne muscular dystrophy (dmd) is a severe muscular disease characterized by progressive loss of functional muscle mass followed by changes in body composition. 2018-09-24 2023-01-26 Not clear
Jillian Davis, Emily Samuels, Lucille Mullin. Nutrition Considerations in Duchenne Muscular Dystrophy. Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition vol 30 issue 4 2016 25977513 duchenne muscular dystrophy (dmd) is a serious degenerative muscular disease affecting males. 2016-05-04 2023-01-25 Not clear
Fran\\xc3\\xa7ois-Xavier Goudot, Karim Wahbi, Linda A\\xc3\\xafssou, Emmanuel Sorbets, Val\\xc3\\xa9rie Siam-Tsieu, Bruno Eymard, Christine Themar Noel, Jean-Yves Devaux, Odile Dessault, Denis Duboc, Christophe Meun. Reduced inotropic reserve is predictive of further degradation in left ventricular ejection fraction in patients with Duchenne muscular dystrophy. European journal of heart failure vol 17 issue 2 2015 25823361 duchenne muscular dystrophy (dmd), an inherited x-linked muscular disease, is associated with dilated cardiomyopathy that is responsible for death in 40% of patients. 2015-12-15 2023-01-25 Not clear
Emma Tabe Eko Niba, Van Khanh Tran, Le Anh Tuan-Pham, Dung Chi Vu, Ngoc Khanh Nguyen, Van Thanh Ta, Thinh Huy Tran, Tomoko Lee, Yasuhiro Takeshima, Masafumi Matsu. Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene. Clinica chimica acta; international journal of clinical chemistry vol 436 issue 2015 24892813 duchenne muscular dystrophy (dmd) is the most common inherited muscular disease and caused by mutations in the dmd gene on the x-chromosome. 2015-08-27 2023-01-25 Not clear
Valentina Saccone, Silvia Consalvi, Lorenzo Giordani, Chiara Mozzetta, Iros Barozzi, Martina Sandon\\xc3\\xa1, Tammy Ryan, Agustin Rojas-Mu\\xc3\\xb1oz, Luca Madaro, Pasquale Fasanaro, Giovanna Borsellino, Marco De Bardi, Gianmaria Frig\\xc3\\xa8, Alberto Termanini, Xin Sun, Janet Rossant, Benoit G Bruneau, Mark Mercola, Saverio Minucci, Pier Lorenzo Pur. HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic muscles. Genes & development vol 28 issue 8 2014 24682306 whether faps support muscle regeneration or promote fibro-adipogenic degeneration is emerging as a key determinant in the pathogenesis of muscular diseases, including duchenne muscular dystrophy (dmd). 2014-05-29 2023-01-25 mouse
Yoichi Negishi, Nobuhito Hamano, Hitomi Shiono, Saki Akiyama, Yoko Endo-Takahashi, Ryo Suzuki, Kazuo Maruyama, Yukihiko Aramak. [Development of an ultrasound-mediated nucleic acid delivery system for treating muscular dystrophies]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan vol 132 issue 12 2014 23208045 duchenne muscular dystrophy (dmd) is a fatal, x-linked muscular disease that occurs in 1 out of every 3500 males. 2014-04-03 2023-01-25 Not clear
Thi Hoai Thu Tran, Zhujun Zhang, Mariko Yagi, Tomoko Lee, Hiroyuki Awano, Atsushi Nishida, Takeshi Okinaga, Yasuhiro Takeshima, Masafumi Matsu. Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28. Journal of human genetics vol 58 issue 1 2013 23223008 duchenne muscular dystrophy (dmd) is the most common inherited muscular disease and is characterized by progressive muscle wasting. 2013-11-14 2023-01-25 Not clear
Hideya Mizuno, Akinori Nakamura, Yoshitsugu Aoki, Naoki Ito, Soichiro Kishi, Kazuhiro Yamamoto, Masayuki Sekiguchi, Shin'ichi Takeda, Kazuo Hashid. Identification of muscle-specific microRNAs in serum of muscular dystrophy animal models: promising novel blood-based markers for muscular dystrophy. PloS one vol 6 issue 3 2011 21479190 creatine kinase (ck) is generally used as a blood-based biomarker for muscular disease including dmd, but it is not always reliable since it is easily affected by stress to the body, such as exercise. 2011-07-26 2023-01-25 dog
Mirella Meregalli, Andrea Farini, Yvan Torrent. Combining stem cells and exon skipping strategy to treat muscular dystrophy. Expert opinion on biological therapy vol 8 issue 8 2008 18613758 mutations in the dystrophin gene cause hereditary muscular diseases such as becker muscular dystrophy (bmd) and duchenne muscular dystrophy (dmd), the most severe form. 2008-08-28 2023-01-25 Not clear
Janusz G Zimowski, Elzbieta Fidzianska, Mariola Holding, Jacek Zaremb. [Carrier detection in Duchenne/Becker muscular dystrophy in the families in which the DNA of the affected person is not available]. Medycyna wieku rozwojowego vol 10 issue 1 Pt 2 2007 17028400 duchenne muscular dystrophy (dmd) is a severe, progressive, x-linked muscular disease, which affects 1 in 3500 male newborns. 2007-03-21 2023-01-24 human
Boaz Weisz, Anna L David, Lisa G Gregory, Dany Perocheau, Ali Ruthe, Simon N Waddington, Mike Themis, Terry Cook, Charles Coutelle, Charles H Rodeck, Donald M Peeble. Targeting the respiratory muscles of fetal sheep for prenatal gene therapy for Duchenne muscular dystrophy. American journal of obstetrics and gynecology vol 193 issue 3 Pt 2 2005 16157120 duchenne muscular dystrophy (dmd) is a lethal degenerative muscular disease. 2005-10-26 2023-01-24 Not clear
Kiichiro Matsumura, Di Zhong, Fumiaki Saito, Ken Arai, Katsuhito Adachi, Hisaomi Kawai, Itsuro Higuchi, Ichizo Nishino, Teruo Shimiz. Proteolysis of beta-dystroglycan in muscular diseases. Neuromuscular disorders : NMD vol 15 issue 5 2005 15833425 in this study, we investigated the proteolysis of beta-dystroglycan in the biopsied skeletal muscles of various human muscular diseases, including sarcoglycanopathy, duchenne muscular dystrophy (dmd), becker muscular dystrophy, fukuyama congenital muscular dystrophy, miyoshi myopathy, lgmd2a, facioscapulohumeral muscular dystrophy, myotonic dystrophy and dermatomyositis/polymyositis. 2005-06-17 2023-01-24 human