Conducting a medical examination in the COVID-19 era: an Egyptian experience.

Autor: Gado AS; Department of Gastroenterology, Misr International Hospital, Giza, Egypt., Khater RA; Department of Medicine, Cairo University, Giza, Egypt.

Publikováno v: The Egyptian journal of internal medicine [Egypt J Intern Med] 2021; Vol. 33 (1), pp. 9. Date of Electronic Publication: 2021 Mar 01.

Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene.

Autor: Baskin B; Division of Molecular Genetics, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, 555 University Avenue, Toronto, Ont., Canada. berivan.baskin@sickkids.ca, Banwell B, Khater RA, Hawkins C, Ray PN

Publikováno v: Neuromuscular disorders : NMD [Neuromuscul Disord] 2009 Mar; Vol. 19 (3), pp. 189-92. Date of Electronic Publication: 2009 Feb 18.

Covid 19 And Its Impact On Medical Education: "Anniversary Reaction" From College Of Medicine And Health Sciences, National University, Oman.

Autor: Raj, Arockia Philip

Publikováno v: Journal of Positive School Psychology; 2022, Vol. 6 Issue 6, p922-927, 6p

RNAseq analysis for the diagnosis of muscular dystrophy.

Autor: Gonorazky, Hernan^1,2,3, Liang, Minggao^2,4, Cummings, Beryl^5,6, Lek, Monkol^5,6, Micallef, Johann², Hawkins, Cynthia⁷, Basran, Raveen⁷, Cohn, Ronald^2,3,4, Wilson, Michael D.^2,4, MacArthur, Daniel^5,6, Marshall, Christian R.⁷, Ray, Peter N.^2,4,7, Dowling, James J.^1,2,3,4

Publikováno v: Annals of Clinical & Translational Neurology. Jan2016, Vol. 3 Issue 1, p55-60. 6p.

Faulty RNA splicing: consequences and therapeutic opportunities in brain and muscle disorders.

Autor: Pagliarini, Vittoria, La Rosa, Piergiorgio, Sette, Claudio

Publikováno v: Human Genetics; Sep2017, Vol. 136 Issue 9, p1215-1235, 21p