Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Yahya, Wahba"'
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-11 (2024)
Abstract Background Bronchial asthma (BA) is a chronic inflammatory disorder identified by different endotypes and phenotypes. Chemokine receptor 3 (CCR3) is one of the essential chemokine receptors that have a crucial role in asthma development by a
Externí odkaz:
https://doaj.org/article/fd30ab0173fa46758e644fff6b8b82fb
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-9 (2022)
Abstract Background Mutations in the neuronal sodium voltage-gated channel, alpha subunit 1 (SCN1A) gene have been associated with epilepsy. We investigated the SCN1A-A3184G polymorphism among Egyptian children and adolescents with non-lesional epile
Externí odkaz:
https://doaj.org/article/a5679f9d5b5643e9b34dcf81d24fba39
Publikováno v:
Middle East Fertility Society Journal, Vol 27, Iss 1, Pp 1-5 (2022)
Abstract Background Chromosomal abnormalities represent an important cause of human infertility. Little is known about the prevalence of chromosomal abnormalities among Egyptian couples with infertility. We estimated the cytogenetic profiles and seme
Externí odkaz:
https://doaj.org/article/7f558de29cf44c5b922df4ae885bcfbc
Publikováno v:
Anales de Pediatría, Vol 95, Iss 6, Pp 406-412 (2021)
Resumen: Introducción: El síndrome nefrótico (SN) primario es una glomerulopatía común en la edad pediátrica. Se evaluaron los genotipos y frecuencias alélicas del polimorfismo rs5370 del gen EDN1 en niños con SN primario. Pacientes y método
Externí odkaz:
https://doaj.org/article/80b516dbc38941f48012dea1bff3caaa
Publikováno v:
Anales de Pediatría (English Edition), Vol 95, Iss 6, Pp 406-412 (2021)
Introduction: Primary nephrotic syndrome (NS) is a common glomerular disease in children. We assessed the genotypes and frequency of the rs5370 allelic variant of the EDN1 gene in children with primary NS. Patients and methods: We conducted a case-co
Externí odkaz:
https://doaj.org/article/bfc81de8e83f44989c303ab361861592
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 70, Iss 2, Pp 208-214 (2021)
Background Asthma is known to be a heterogeneous disease that forms a problem in asthma management. Symptom-based asthma phenotyping with endotyping of the proposed phenotype is a trial to solve this problem. Asthma phenotypes and endotypes facilitat
Externí odkaz:
https://doaj.org/article/0adf4a786edc474f894e02023fcf038e
Publikováno v:
Central European Journal of Immunology, Vol 43, Iss 3, Pp 248-254 (2018)
Down syndrome (DS) is the commonest genetic disorder and more liable for recurrent infections. We aimed to determine the differences in lymphocyte subgroups between DS children and the healthy population and to study the pattern and likelihood for re
Externí odkaz:
https://doaj.org/article/b55fca0037d145db8461253ec0284e5a
Publikováno v:
Egyptian Journal of Critical Care Medicine, Vol 5, Iss 3, Pp 87-91 (2017)
Background: The role of oral hygiene in the intensive care unit is indisputable. Several studies were carried out in different pediatric intensive care units using different oral hygiene regimes. Chlorhexidine preparations are widely used in oral car
Externí odkaz:
https://doaj.org/article/98e423f42cc2413fb28568d634f963ff
Publikováno v:
Annals of Saudi Medicine, Vol 37, Iss 5, Pp 386-392 (2017)
BACKGROUND: The pattern and risk factors for congenital heart diseases (CHD) in children with Down syndrome (DS) vary over time. OBJECTIVES: To update knowledge of the prevalence, types, trends and associated factors for CHD in children with DS in th
Externí odkaz:
https://doaj.org/article/080af424a2d245d480b543b842839c20
Autor:
Mohammad Al-Haggar, Ashraf Bakr, Yahya Wahba, Paul J Coucke, Fatma El-Hussini, Mona Hafez, Riham Eid, Abdel-Rahman Eid, Amr Sarhan, Ali Shaltout, Ayman Hammad, Sohier Yahia, Ahmad El-Rifaie, Dina Abdel-Hadi
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 1, Pp 141-148 (2017)
Marfan syndrome (MFS), the founding member of connective tissue disorder, is an autosomal dominant disease; it is caused by a deficiency of the microfibrillar protein fibrillin-1 (FBN1) and characterized by involvement of three main systems; skeletal
Externí odkaz:
https://doaj.org/article/1243858dedaa4cd682a50f0b8764c30f