Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Mona El-Ghamrawy"'
Autor:
Bahia Moustafa, Neveen A. Soliman, Ihab Shaheen, Ahmed Badr, Fatma M. Atia, Mohamed K. El Hatw, Engy Adel Mogahed, Mona EL-Ghamrawy, Khaled El Khashab, Noha Shaheen, Mohamad G. Shouman, Abeer Selim, Magdy El-Sharkawy, Tarek Abd El Azeem, Mohamad Esmat, Manal Salman, Bedeir Ali-El-Dein, Mona Abdel Rahim, Muhamed A. El-Hadedy, Moatasem Elsayed Ghoneim, Mai S. Korkor, Tarek E. I. Omar, Yasser Amer, Ashraf Abdel Baky, On Behalf of Egyptian Pediatric Clinical Practice Guideline Committee
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-21 (2024)
Abstract Background Pediatric kidney transplantation is unique when compared to adults. They need optimum post-transplant care to achieve longer graft and patient survival. Infections, rejection, recurrence, malignancy, bone problems, hypertension, a
Externí odkaz:
https://doaj.org/article/67fcc01f830c402d994d7da723758f31
Autor:
Mona El-Ghamrawy, Neveen A. Soliman
Publikováno v:
Journal of Rare Diseases, Vol 3, Iss 1, Pp 1-12 (2024)
Abstract Nephropathic cystinosis (NC) is a rare autosomal recessive lysosomal storage disease characterized by defective lysosomal efflux of cystine due to variations in the CTNS gene encoding the lysosomal cystine transporter, cystinosin. This leads
Externí odkaz:
https://doaj.org/article/17cd10a02a6c4dff9ae2194479bbc43b
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 68, Iss 1, Pp 1-7 (2020)
Abstract Background Sickle cell disease (SCD) is a disorder characterized by a heterogeneous clinical outcome. Interleukin-1β (IL-1β) and interleukin-6 (IL-6) are important mediators of inflammatory response. Genetic modifiers that alter cytokine l
Externí odkaz:
https://doaj.org/article/0f33796981014067bfb401834844f7cc
Autor:
Manal Michel Wilson, Hanan Al-Wakeel, Fadwa Said, Mona El-Ghamrawy, Mary Assaad, Amal El-Beshlawy
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 129-133 (2015)
Background: HFE gene mutations have been shown to be responsible for hereditary hemochromatosis. Their effect on iron load in β-thalassemia patients and carriers remains controversial. Objectives: We aimed to determine the prevalence of HFE gene mut
Externí odkaz:
https://doaj.org/article/ac4cb00064414e3e9fa56a15d7ee05d7
Publikováno v:
HemaSphere, Vol 7, p e7135519 (2023)
Externí odkaz:
https://doaj.org/article/40bd50a1414c4bfa9a467ed58b1ad470
Autor:
Mona El-Ghamrawy, Nesrine El-Gharbawi, Gehan Shahin, Alaa Abdelhady, Rasha Sayed, Nehal Diaa, Irene Bishai
Publikováno v:
International Journal of Hematology. 117:856-862
Background Primary immune thrombocytopenia (ITP) is a common autoimmune disorder. Secretion of TNF-α, TNF-β and IFN-γ plays a major role in the pathogenesis of ITP. Objective This cross-sectional study aimed to detect TNF-α (−308 G/A) and TNF-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::178e1910a78d31c6929b90b4b10f3b3a
https://doi.org/10.1007/s12185-023-03551-9
https://doi.org/10.1007/s12185-023-03551-9
Publikováno v:
Indian Journal of Hematology and Blood Transfusion.
Non-transfusion dependent thalassemia (NTDT) refers to a group of thalassemic disorders who do not need regular transfusions for survival, however it may be needed in certain conditions. Metformin was reported as a potential fetal hemoglobin (HbF) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f9cb7cfa934c7c91203fdc3a21f3498
https://doi.org/10.1007/s12288-023-01662-1
https://doi.org/10.1007/s12288-023-01662-1
Autor:
Mahmoud Mahrous, Niveen Salama, Hadeel M. Seif, Farzana Pashankar, Lyn Balsamo, Ilham Youssry, Mona El-Ghamrawy
Publikováno v:
International Journal of Hematology. 115:399-405
Little is known about cognitive impairment in patients with sickle cell disease in Africa. This study aimed to assess cognitive impairment and identify possible risk factors in patients with sickle cell disease in Egypt. This study was conducted at C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5c50df92baf34a69baf8f3aafa9d474
https://doi.org/10.1007/s12185-021-03260-1
https://doi.org/10.1007/s12185-021-03260-1
Publikováno v:
Hemoglobin. 44:418-422
Transcranial Doppler (TCD) screening is an established tool to identify children with sickle cell disease at high risk of stroke. Our objective was to study TCD velocities among sickle cell disease patients while in a steady state. This cross-section
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fc665a96c85cb9442108378a724fccb
https://doi.org/10.1080/03630269.2020.1843483
https://doi.org/10.1080/03630269.2020.1843483
Autor:
Marwa Abd El-hady, Mona El-Ghamrawy, Angie M. S. Tousson, Nada B. Mohamed, Mervat M. Khorshied, Marianne E. Yassa, Erini Mikhaeil
Publikováno v:
Annals of Hematology. 99:2279-2288
Sickle cell disease (SCD) is a monogenic disease characterized by multisystem morbidity and highly variable clinical course. Inter-individual variability in hemoglobin F (HbF) levels is one of the main modifiers that account for the clinical heteroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df1c50e4bb01664ac540d65fec16bb6f
https://doi.org/10.1007/s00277-020-04187-z
https://doi.org/10.1007/s00277-020-04187-z