438 related articles for article (PubMed ID: 28653137)
1. Duchenne Muscular Dystrophy: A Practice Update.
Suthar R; Sankhyan N
Indian J Pediatr; 2018 Apr; 85(4):276-281. PubMed ID: 28653137
[TBL] [Abstract][Full Text] [Related]
2. [Clinical practice guidelines for Duchenne muscular dystrophy].
Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association ; Tan H; Liang D; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):258-262. PubMed ID: 32128741
[TBL] [Abstract][Full Text] [Related]
3. Clinical management of Duchenne muscular dystrophy: the state of the art.
Messina S; Vita GL
Neurol Sci; 2018 Nov; 39(11):1837-1845. PubMed ID: 30218397
[TBL] [Abstract][Full Text] [Related]
4. Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy.
Church JE; Trieu J; Chee A; Naim T; Gehrig SM; Lamon S; Angelini C; Russell AP; Lynch GS
Exp Physiol; 2014 Apr; 99(4):675-87. PubMed ID: 24443351
[TBL] [Abstract][Full Text] [Related]
5. [Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation].
Zhang C; Feng HY; Huang SL; Fang JP; Xiao LL; Yao XL; Chen C; Ye X; Zeng Y; Lu XL; Wen JM; Zhang WX; Li Z; Feng SW; Xu HG; Huang K; Zhou DH; Chen W; Xie YM; Xi J; Zhang M; Li Y; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):399-405. PubMed ID: 16086277
[TBL] [Abstract][Full Text] [Related]
6. Duane retraction syndrome in a patient with Duchenne muscular dystrophy.
Bosley TM; Salih MA; Alkhalidi H; Oystreck DT; El Khashab HY; Kondkar AA; Abu-Amero KK
Ophthalmic Genet; 2016 Sep; 37(3):276-80. PubMed ID: 26849454
[TBL] [Abstract][Full Text] [Related]
7. Gait deviations in Duchenne muscular dystrophy-Part 2. Statistical non-parametric mapping to analyze gait deviations in children with Duchenne muscular dystrophy.
Goudriaan M; Van den Hauwe M; Simon-Martinez C; Huenaerts C; Molenaers G; Goemans N; Desloovere K
Gait Posture; 2018 Jun; 63():159-164. PubMed ID: 29751322
[TBL] [Abstract][Full Text] [Related]
8. Clinical Manifestations and Overall Management Strategies for Duchenne Muscular Dystrophy.
Tsuda T
Methods Mol Biol; 2018; 1687():19-28. PubMed ID: 29067653
[TBL] [Abstract][Full Text] [Related]
9. Newborn screening for Duchenne muscular dystrophy-early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy.
Gruber D; Lloyd-Puryear M; Armstrong N; Scavina M; Tavakoli NP; Brower AM; Caggana M; Chung WK
Am J Med Genet C Semin Med Genet; 2022 Jun; 190(2):197-205. PubMed ID: 36152336
[TBL] [Abstract][Full Text] [Related]
10. Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification.
Wilson K; Faelan C; Patterson-Kane JC; Rudmann DG; Moore SA; Frank D; Charleston J; Tinsley J; Young GD; Milici AJ
Toxicol Pathol; 2017 Oct; 45(7):961-976. PubMed ID: 28974147
[TBL] [Abstract][Full Text] [Related]
11. Use of capillary Western immunoassay (Wes) for quantification of dystrophin levels in skeletal muscle of healthy controls and individuals with Becker and Duchenne muscular dystrophy.
Beekman C; Janson AA; Baghat A; van Deutekom JC; Datson NA
PLoS One; 2018; 13(4):e0195850. PubMed ID: 29641567
[TBL] [Abstract][Full Text] [Related]
12. Cardiomyopathy of Duchenne muscular dystrophy: current understanding and future directions.
Spurney CF
Muscle Nerve; 2011 Jul; 44(1):8-19. PubMed ID: 21674516
[TBL] [Abstract][Full Text] [Related]
13. Duchenne muscular dystrophy: an updated review of common available therapies.
Salmaninejad A; Valilou SF; Bayat H; Ebadi N; Daraei A; Yousefi M; Nesaei A; Mojarrad M
Int J Neurosci; 2018 Sep; 128(9):854-864. PubMed ID: 29351004
[TBL] [Abstract][Full Text] [Related]
14. Next Generation Sequencing approach to molecular diagnosis of Duchenne muscular dystrophy; identification of a novel mutation.
Ebrahimzadeh-Vesal R; Teymoori A; Azimi-Nezhad M; Hosseini FS
Gene; 2018 Feb; 644():1-3. PubMed ID: 29246534
[TBL] [Abstract][Full Text] [Related]
15. A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20.
Mata López S; Hammond JJ; Rigsby MB; Balog-Alvarez CJ; Kornegay JN; Nghiem PP
Skelet Muscle; 2018 May; 8(1):16. PubMed ID: 29843823
[TBL] [Abstract][Full Text] [Related]
16. Co-incidence of Turner syndrome and Duchenne muscular dystrophy - an important problem for the clinician.
Kaczorowska E; Zimowski J; Cichoń-Kotek M; Mrozińska A; Purzycka J; Wierzba J; Limon J; Lipska-Ziętkiewicz BS
Dev Period Med; 2016; 20(4):273-278. PubMed ID: 28216480
[TBL] [Abstract][Full Text] [Related]
17. DMD and West syndrome.
Cardas R; Iliescu C; Butoianu N; Seferian A; Gataullina S; Gargaun E; Nectoux J; Bienvenu T; Craiu D; Gidaro T; Servais L
Neuromuscul Disord; 2017 Oct; 27(10):911-913. PubMed ID: 28802771
[TBL] [Abstract][Full Text] [Related]
18. Human Umbilical Cord Mesenchymal Stem Cells in the Treatment of Duchenne Muscular Dystrophy: Safety and Feasibility Study in India.
Rajput BS; Chakrabarti SK; Dongare VS; Ramirez CM; Deb KD
J Stem Cells; 2015; 10(2):141-56. PubMed ID: 27125141
[TBL] [Abstract][Full Text] [Related]
19. Anesthesia and Duchenne or Becker muscular dystrophy: review of 117 anesthetic exposures.
Segura LG; Lorenz JD; Weingarten TN; Scavonetto F; Bojanić K; Selcen D; Sprung J
Paediatr Anaesth; 2013 Sep; 23(9):855-64. PubMed ID: 23919455
[TBL] [Abstract][Full Text] [Related]
20. Androgen receptor agonists increase lean mass, improve cardiopulmonary functions and extend survival in preclinical models of Duchenne muscular dystrophy.
Ponnusamy S; Sullivan RD; You D; Zafar N; He Yang C; Thiyagarajan T; Johnson DL; Barrett ML; Koehler NJ; Star M; Stephenson EJ; Bridges D; Cormier SA; Pfeffer LM; Narayanan R
Hum Mol Genet; 2017 Jul; 26(13):2526-2540. PubMed ID: 28453658
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]