Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Nadine Yazbeck"'
Publikováno v:
International Journal of Pediatrics, Vol 2024 (2024)
Conclusion: The present study shows that 32.6% of children aged 2–7 years in Lebanon suffer from constipation while only 51.7% of the recruited children’s physicians inquire about the child’s bowel movement during the well check visit. These nu
Externí odkaz:
https://doaj.org/article/fc4def3d42f44c87a2bd02e3ad8b6b33
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Mitochondrial DNA depletion syndrome type 3 is an emerging disorder linked to variants in the deoxyguanosine kinase gene, which encodes for mitochondrial maintenance. This autosomal recessive disorder is frequent in the Middle East and
Externí odkaz:
https://doaj.org/article/a89c4c557b3b468aa080432dc66b03e6
Autor:
Hiba Al Rifai, Hiba Shatila, Lara Nasreddine, Nadine Yazbeck, Tamar Kabakian-Khasholian, Leila Itani, Farah Naja
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0281865 (2023)
BackgroundRates of breastfeeding (BF) remain suboptimal despite overwhelming evidence for its benefits to the mother and child. Pediatricians play an important role in supporting breastfeeding (BF). In Lebanon, the rates of both exclusive and continu
Externí odkaz:
https://doaj.org/article/913d520c039048ad9671a4819c74072a
Publikováno v:
IDCases, Vol 19, Iss , Pp - (2020)
Background: We would like to raise awareness about the toxicities related to the added excipients present in the oral solution of Liponavir/ritonavir in particular alcohol and propylene glycol. Case presentation: In this case report, we describe an 1
Externí odkaz:
https://doaj.org/article/c2d1320faac244c68bb83a20adf324d0
Autor:
Yolla Youssef, Lena Naffaa, Sarah Chamseddine, Ahmad Zaghal, Mohammad Khalife, Nadine Yazbeck, Ghassan Dbaibo, Rima Hanna-Wakim
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 47, Iss , Pp - (2019)
Splenic abscess in the setting of salmonella infection is a rare entity, which has been reported during the course of typhoid fever. We describe the presentation of a healthy 11 year-old boy who had abdominal pain, incidental finding of splenic cyst
Externí odkaz:
https://doaj.org/article/187fd0355d93447682f07e42f32e5b66
Background Infants and children with congenital heart disease (CHD) are at higher risk of faltering growth and developing malnutrition. The aim of this study was to evaluate the prevalence of malnutrition and nutritional status of children with CHD p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dce7fac4f2d309a9a88ed46f94470138
https://doi.org/10.21203/rs.3.rs-2863304/v1
https://doi.org/10.21203/rs.3.rs-2863304/v1
Autor:
Chantal Farra, Johnny Awwad, Lama Hamadeh, Pierre Khoueiry, Zeina Halawi, Nadine Yazbeck, Rose Daher, Mirna Souaid, Layal Hamdar, Tony Yammine, Khalid Yunis
Publikováno v:
Annals of Human Genetics. 86:80-86
Cystic fibrosis is the most common life-limiting autosomal recessive disease in western countries with an incidence of 1:2500 in United States and 1:1000 in some European countries. Similar incidences were noted for the Middle East with variations fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43f5d6175d38c9b2ef9ea4dae24ca163
https://doi.org/10.1111/ahg.12450
https://doi.org/10.1111/ahg.12450
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cd671b125c9505e23b5e5632a2b1110
https://doi.org/10.7759/cureus.24384
https://doi.org/10.7759/cureus.24384
Autor:
Maria Valencia, Lara Tabet, Nadine Yazbeck, Alia Araj, Victor L. Ruiz-Perez, Khalil Charaffedine, Farah Fares, Rebecca Badra, Chantal Farra
Publikováno v:
Case Reports in Genetics, Vol 2015 (2015)
Background. Ellis-van Creveld (EvC) syndrome is a rare, autosomal recessive disorder characterized by short stature, short limbs, growth retardation, polydactyly, and ectodermal defects with cardiac anomalies occurring in around 60% of cases. EVC syn
Externí odkaz:
https://doaj.org/article/e2bfa111bef842338cd1fef004c9fe4e
Autor:
Scott B. Snapper, Veit Hornung, Hans Clevers, Moritz M. Gaidt, Nadine Yazbeck, Fabian Hauck, Rima Hanna-Wakim, Katja Lammens, Philip Bufler, Yue Li, Aleixo M. Muise, Maryam Ghalandary, Birgitta E. Michels, Anna S. Lehle, Henner F. Farin, Raffaele Conca, Thomas Magg, Batia Weiss, Yanshan Liu, Sibylle Koletzko, Atar Lev, Neil Warner, Olaf Groß, Daniel Kotlarz, Amos J. Simon, Christoph Walz, Christoph Klein, Sebastian Hollizeck, Benjamin Marquardt, Raz Somech, Dror S. Shouval, Meino Rohlfs
Publikováno v:
Gastroenterology, 156(1), 275-278. W.B. Saunders Ltd
Gastroenterology, 156(1), 275. W.B. Saunders Ltd
Gastroenterology, 156(1), 275. W.B. Saunders Ltd
Caspase-8 (CASP8) is a protease that initiates apoptosis and regulates inflammation and immune responses. We identified germline mutations in CASP8 in 3 unrelated patients with infant-onset inflammatory bowel disease: 2 patients were homozygous for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b79387687377a1d1cae56bce5fe90154
https://doi.org/10.1053/j.gastro.2018.09.041
https://doi.org/10.1053/j.gastro.2018.09.041