Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hanaa M. El-Karaksy"'
Publikováno v:
Journal of the Egyptian Ophthalmological Society, Vol 109, Iss 3, Pp 117-121 (2016)
Objectives The aim of this study was to report the prevalence of interferon (IFN)-associated retinopathy and other serious ocular complications in a prospectively studied group of children with chronic hepatitis C virus (HCV) receiving pegylated IFN
Externí odkaz:
https://doaj.org/article/fd0e7c4f5d22436292be5106342d241b
Publikováno v:
Journal of the Egyptian Ophthalmological Society, Vol 109, Iss 3, Pp 98-104 (2016)
Background Neonatal and infantile cholestasis can be associated with ocular findings that might aid in the diagnosis of diseases such as Alagille syndrome (AGS) and Niemann–Pick disease (NPD). Aim We aimed to investigate the frequency of ocular man
Externí odkaz:
https://doaj.org/article/9b0872d15d5847378c73351da49be478
Autor:
Noha A.E. Yasin, Shereen Abdel Alem, Engy A. Mogahed, Hadeel Gamal Eldeen, Ahmed Nagy, Hala Abdullatif, Hanaa M. El-Karaksy, Mona S. El-Raziky
Publikováno v:
The Journal of Pediatrics. 233:126-131
To assess the degree of liver stiffness using transient elastography in Egyptian children infected with hepatitis C virus (HCV) at baseline and 1 year after achievement of sustained virologic response (SVR) with direct acting antivirals.This prospect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81d3275f62e39c1a682cc163692977a1
https://doi.org/10.1016/j.jpeds.2021.02.012
https://doi.org/10.1016/j.jpeds.2021.02.012
Autor:
Nehal M El-Koofy, Ghada M Anwar, Mona S El-Raziky, Ahmad M El-Hennawy, Fatma M El-Mougy, Hanaa M El-Karaksy, Fetouh M Hassanin, Heba M Helmy
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 18, Iss 1, Pp 44-49 (2012)
Background/Aim: To study the prevalence of metabolic syndrome (MS), insulin resistance (IR) and non-alcoholic fatty liver disease (NAFLD) in overweight/obese children with clinical hepatomegaly and/or raised alanine aminotransferase (ALT). Patients a
Externí odkaz:
https://doaj.org/article/dc54849e65584e26a02b3e19d54628b4
Autor:
Mortada H El-Shabrawi, Hanaa M El-Karaksy, Sawsan H Okahsa, Naglaa M Kamal, Gamal El-Batran, Khaled A Badr
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 18, Iss 1, Pp 26-33 (2012)
Background/Aim: We aim to investigate the safety of outpatient blind percutaneous liver biopsy (BPLB) in infants and children with chronic liver disease (CLD). Patients and Methods: BPLB was performed as an outpatient procedure using the aspiration M
Externí odkaz:
https://doaj.org/article/2c97f14d3b0c4ae993372001aba4eba5
Autor:
Hanaa M El-Karaksy, Nehal M El-Koofy, Ghada M Anwar, Fatma M El-Mougy, Ahmed El-Hennawy, Mona E Fahmy
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 17, Iss 1, Pp 40-46 (2011)
Background/Aim: Pediatric non-alcoholic fatty liver disease (NAFLD) is a global problem which has been increasingly recognized with the dramatic rise in pediatric obesity. The aim of the present study was to identify the clinical, sonographic, and bi
Externí odkaz:
https://doaj.org/article/a03ca9330fd24c4289abad4d0f633d17
Autor:
Nehal M El-Koofy, Hanaa M El-Karaksy, Iman M Mandour, Ghada M Anwar, Mona S El-Raziky, Ahmad M El-Hennawy
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 17, Iss 4, Pp 265-270 (2011)
Background/Aim : Polymorphisms in the promoter of microsomal triglyceride transfer protein (MTP) lead to decreased MTP transcription, less export of triglyceride from hepatocytes, and greater intracellular triglyceride accumulation. Therefore, functi
Externí odkaz:
https://doaj.org/article/a51224848de34e3d8303a1f7ef5d8a1e
Publikováno v:
South African Journal of Child Health. 14:104
Hereditary tyrosinaemia type 1 (HT1) is a rare inherited genetic disorder attributed to deficiency of the enzyme fumarylacetoacetate hydrolase (FAH). HT1 may present with diarrhoea in its acute form. We report on a 2.5-year-old Egyptian girl diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f98e9e2629e628b179b80005bb43e3
https://doi.org/10.7196/sajch.2020.v14i2.01661
https://doi.org/10.7196/sajch.2020.v14i2.01661
Publikováno v:
Pediatric Gastroenterology, Hepatology & Nutrition
Purpose The outcome predictors of Kasai portoenterostomy (KPE) for biliary atresia (BA) are controversial. This study aimed to identify possible short-term outcome predictors of KPE for BA in infants. Methods This retrospective study included infants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e6e1c0e61080258c34b51276d021cfe
https://doi.org/10.5223/pghn.2020.23.3.266
https://doi.org/10.5223/pghn.2020.23.3.266
Publikováno v:
AACE Clinical Case Reports.
Background: Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare autosomal recessive disorder characterized by cardinal triad features of megaloblastic anemia, sensorineural deafness and diabetes mellitus. TRMA manifestation is caused b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c84b5834a36b2ff7f6bc44c2b6e0666e
https://doi.org/10.4158/ep171821.cr
https://doi.org/10.4158/ep171821.cr