Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Doaa Khater"'
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Background and ObjectiveThe optimal treatment protocol of intraabdominal testis is still a matter of debate and until now there are a lot of areas of controversy as regards this challenging subtype. The aim of this report is to document current pract
Externí odkaz:
https://doaj.org/article/f6c680eb94724d118926fff8d2d635fa
Autor:
Waleed Dawood, Dina Abdallah, Ashraf Soliman, Doaa Khater, Shaymaa Elsayed, Magdy Omar, Haytham Badawy
Publikováno v:
African Journal of Urology, Vol 26, Iss 1, Pp 1-5 (2020)
Abstract Background Surgery for clitoral reduction has been practised for over half a century. The aim of clitoral surgery is to achieve normal clitoral morphology without compromising sexual function. To achieve these purposes, many techniques were
Externí odkaz:
https://doaj.org/article/3b20fb41091743e698d02b2775907c17
Autor:
Nada Al-Marhoobi, Manar Maktoom, Mohamed Elshinawy, Hanan Nazir, Khalid Al Hashmi, Rashid Al-Abri, Khalil Macki, Abdulhakim Al-Rawas, Fatma AlBulushi, Yasser Wali, Doaa Khater
Publikováno v:
Oman Medical Journal, Vol 37, Iss 1, Pp e346-e346 (2022)
Objectives: Despite guidelines recommending no need for coagulation testing before surgeries when a history of bleeding is negative, surgeons still overuse it in this part of the world. We aim to measure unbiased estimates of hemostatic outcomes in e
Externí odkaz:
https://doaj.org/article/f62b615acd294443981da6195e26d47d
Publikováno v:
Oman Medical Journal, Vol 32, Iss 4, Pp 316-321 (2017)
Objectives: To identify the possible role of natural killer (NK) cells in the pathogenesis of type 1 diabetes mellitus (T1DM) through studying the expression of the KLRC3 gene, which encodes the NK cell activating receptor (NKG2E). Methods: This stud
Externí odkaz:
https://doaj.org/article/bc11c7a89b454afa90709e174d1963b2
Autor:
Vincenzo De Sanctis, Shahina Daar, Ashraf T Soliman, Heba Elsedfy, Doaa Khater, Salvatore Di Maio
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 21, Iss 4, Pp 636-637 (2017)
Externí odkaz:
https://doaj.org/article/7be16360e5d94ddb88dd71688e860658
Autor:
Reem, Abdwani, Muna, Al Saadoon, Sanjay, Jaju, Mohamed, Elshinawy, Asmaa, Almaimani, Yasser, Wali, Doaa, Khater
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e826-e832
The Ministry of Health in Oman and some of Gulf regions set the cut-off age of "transfer" from child health care to adult health care at 13 years of age. Within the existing health system in this part of the world, there is paucity of evidence on the
Autor:
Hussein Al-Kindi, Al-Shaima Al-Abri, Tabinda Naz, Doaa Khater, Saif Al-Yaarubi, Mohamed Al-Abri
Publikováno v:
Sleep and Breathing. 26:815-821
Sanjad Sakati syndrome (SSS) is a rare autosomal recessive genetic disorder caused by mutation in TBCE (tubulin folding cofactor E) gene. Reported cases were almost exclusively of Middle-Eastern and Arabian children of consanguineous parents. We repo
Autor:
Ashraf T, Soliman, Noor, Hamed, Vincenzo, De Sanctis, Mostafa, Elbaba, Fawzia, Alyafei, Nada, Alaaraj, Shayma, Ahmad, Maya, Itani, Fatima, Al-Naimi, Doaa, Khater
Publikováno v:
Acta bio-medica : Atenei Parmensis. 93(5)
Steroids are the main drugs used for the treatment of nephrotic syndrome (NS) in children. We investigated the steroid effect on linear growth and weight gain as well as the prevalence of different metabolic components and dysglycemia in children wit
Publikováno v:
Acta bio-medica : Atenei Parmensis. 93(4)
Sickle cell disease (SCD), caused by a mutation in the β-globin gene HBB, is widely distributed in malaria endemic regions. The prevalence of sickle cell trait and disease reaches up to 4.8-6% and 0.2% respectively, which is the highest among the Ar
Publikováno v:
Journal of pediatric hematology/oncology.
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, characterized by oculocutaneous albinism, a hemorrhagic diathesis secondary to storage pool-deficient platelets, and in some patients' pulmonary fibrosis, granulomatous colitis,