Biallelic Variants in MNS1 Are Associated with Laterality Defects and Respiratory Involvement.

Autor: Hjeij R; Department of General Pediatrics, University Hospital Muenster, 48149 Muenster, Germany., Leslie J; Institute of Biomedical and Clinical Science, RILD Wellcome Wolfson Centre, University of Exeter Medical School, Royal Devon University Healthcare NHS Foundation Trust, Exeter EX2 5DW, UK., Rizk H; Department of Pediatrics, Faculty of Medicine, University of Mansoura, Mansoura 35516, Egypt., Dworniczak B; Department of General Pediatrics, University Hospital Muenster, 48149 Muenster, Germany., Olbrich H; Department of General Pediatrics, University Hospital Muenster, 48149 Muenster, Germany., Raidt J; Department of General Pediatrics, University Hospital Muenster, 48149 Muenster, Germany., Bode SFN; Department of Pediatrics, University Hospital Ulm, 89075 Ulm, Germany., Gardham A; North West Thames Regional Genetic Service, North West London Hospitals, London HA1 2UJ, UK., Stals K; Exeter Genomics Laboratory (NHS South West Genomic Laboratory Hub), Royal Devon University Healthcare NHS Foundation Trust, Exeter EX2 5DW, UK., Al-Haggar M; Genetics Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt., Osman E; Department of Pediatrics, Faculty of Medicine, University of Mansoura, Mansoura 35516, Egypt., Crosby A; Institute of Biomedical and Clinical Science, RILD Wellcome Wolfson Centre, University of Exeter Medical School, Royal Devon University Healthcare NHS Foundation Trust, Exeter EX2 5DW, UK., Eldesoky T; Department of Pediatrics, Faculty of Medicine, University of Mansoura, Mansoura 35516, Egypt., Baple E; Institute of Biomedical and Clinical Science, RILD Wellcome Wolfson Centre, University of Exeter Medical School, Royal Devon University Healthcare NHS Foundation Trust, Exeter EX2 5DW, UK.; Peninsula Clinical Genetics Service, Royal Devon & Exeter Hospital (Heavitree), Exeter EX1 2ED, UK., Omran H; Department of General Pediatrics, University Hospital Muenster, 48149 Muenster, Germany.

Publikováno v: Cells [Cells] 2024 Jun 11; Vol. 13 (12). Date of Electronic Publication: 2024 Jun 11.

Recurrence pattern of non-syndromic familial congenital heart diseases among a large cohort of families from Egypt.

Autor: Rakha S; Pediatric Cardiology Unit, Pediatrics department, Faculty of Medicine, Mansoura University , El Gomhouria Street, 35516, Mansoura, Dakahlia Governorate, Egypt. drshimaarhaka@mans.edu.eg., Mohy-Eldeen R; Resident of Pediatrics, Mansoura University Children Hospital, Mansoura University, Mansoura, Egypt., Al-Haggar M; Genetics Unit, Pediatrics department, Faculty of Medicine, Mansoura University, Mansoura, Egypt., El-Bayoumi MA; Intensive care Unit, Pediatrics department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.

Publikováno v: BMC pediatrics [BMC Pediatr] 2022 Oct 19; Vol. 22 (1), pp. 607. Date of Electronic Publication: 2022 Oct 19.

Regulatory T Cells in Pediatric Lupus Nephritis

Autor: Derbala S.A Derbala S.A, Al-haggar M Al-haggar M, Zahran F Zahran F

Publikováno v: Indian Journal of Applied Research. 3:1-3

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a5ac4494eae5de24ca2997a7f2cf13f4
https://doi.org/10.15373/2249555x/oct2013/91

Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma.

Autor: Al-Haggar M; Genetics Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt., Osman E; Pulmonology Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt., Eid AR; Genetics Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt., Barakat T; Genetics Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt., El-Morsi S; Pediatrics Department, Faculty of Medicine, Mansoura University Children's Hospital, Mansoura, Egypt.

Publikováno v: Journal of pediatric genetics [J Pediatr Genet] 2020 Sep; Vol. 9 (3), pp. 164-170. Date of Electronic Publication: 2020 Feb 03.

Prevalence and CCR3-T51C genotype–phenotype correlation of bronchial asthma among basic education school children: an observational study.

Autor: Zedan, Magdy¹ (AUTHOR) magdyzedan1250@gmail.com, Elwassefy, Mona² (AUTHOR), Zareif, Ismail El³ (AUTHOR), ElTahan, Hossam³ (AUTHOR), Wahba, Yahya⁴ (AUTHOR)

Publikováno v: Egyptian Pediatric Association Gazette. 9/6/2024, Vol. 72 Issue 1, p1-11. 11p.