Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Yomna Farag"'
Autor:
Yasser El Miedany, Samia Salah, Hala M. Lotfy, Mohammed Hassan Abu-Zaid, Sally S. Mohamed, Sheren Esam Maher, Maha El Gaafary, Hala Abdulhady, Yomna Farag, Mervat Eissa, Ahmed Radwan, Basma M. Medhat, Dalia M. E. El Mikkawy, Waleed A. Hassan, Doaa Mosad Mosa, Ghada El Deriny, Mohamed Mortada, Naglaa S. Osman, Nermeen Ahmed Fouad, Youmna Ahmed Amer, Samah Ismail Nasef, Hend Abushady, Salwa Galal, Eiman Abd El-Latif, Dina Maria, Ahmed H. Shabana, Samar AbdAlhamed Tabra
Publikováno v:
Egyptian Rheumatology and Rehabilitation, Vol 50, Iss 1, Pp 1-17 (2023)
Abstract Background Kawasaki disease (KD) is an acute, self-limited febrile disease of unidentified cause that mostly affects children less than 5 years of age. This work aimed to provide an appropriate Egyptian evidence-based consensus on clinical p
Externí odkaz:
https://doaj.org/article/4d074ae11e854c089c9f2f4a9a1d6076
Publikováno v:
Journal of the Pakistan Medical Association, Vol 73, Iss 4 (2023)
Objectives: To assess the impact of cognitive therapy with the rehacom visual-motor module on the hand function in hemiplegic cerebral palsy children. Method: The randomised case-control study was conducted at Kafrelsheikh University, Egypt, from Sep
Externí odkaz:
https://doaj.org/article/f23d5271995e471896a2447ebe5cbced
Autor:
Yomna Farag, Shaimaa Sayed, Fatma Alzhraa Mostafa, Huda Marzouk, Raghda H. Mohamed, Rodina Sobhy
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-7 (2022)
Abstract Background Familial Mediterranean fever (FMF) is an autoinflammatory disease that can have conduction disturbances and cardiac rhythm disorders as manifestations of cardiac involvement. The aim of the study is to assess the susceptibility of
Externí odkaz:
https://doaj.org/article/1af5bdb5a55c41cd8eabc258027d6f76
Autor:
Basma M Medhat, Ahmed Elmaghraby, Yomna Farag, Huda Marzouk, Noha Mostafa, Iman Khalifa, AbdelAal Mohammed, Marwa Elkhalifa, Eman Hassan ElSayed Hassan, Waleed A Hassan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 33, Iss 1, Pp 90-105 (2022)
The study aimed to evaluate the association of demographic, clinical, and histopathologic characteristics with renal and disease outcomes. Persistent lack of partial or complete remission despite sequential induction therapy, chronic kidney disease (
Externí odkaz:
https://doaj.org/article/21197822c9e34d5c8a73d33c15708714
Publikováno v:
Egyptian Rheumatology and Rehabilitation, Vol 48, Iss 1, Pp 1-8 (2021)
Abstract Background Familial Mediterranean fever (FMF) is an autosomal recessive disorder affecting people in the region of the Mediterranean Sea. It is usually associated with mutation in Mediterranean fever (MEFV) gene that encodes the pyrin protei
Externí odkaz:
https://doaj.org/article/256f867a512a4fde8c12a331034f8d35
Publikováno v:
Egyptian Rheumatology and Rehabilitation, Vol 47, Iss 1, Pp 1-7 (2020)
Abstract Background Familial Mediterranean fever (FMF) is an autosomal recessive auto-inflammatory disease. Arthritis in early-onset FMF is a common finding. The aim of this study was to assess frequency of arthritis in 200 Egyptian children with FMF
Externí odkaz:
https://doaj.org/article/d638655fcb034da1b0716d74724f26a1
Autor:
Mohammed Hassan Abu-Zaid, Samia Salah, Hala M. Lotfy, Maha El Gaafary, Hala Abdulhady, Samar abd Alhamed Tabra, Hala Salah, Yomna Farag, Mervat Eissa, Sheren Esam Maher, Ahmed Radwan, Amira Tarek El-Shanawany, Basma M. Medhat, Dalia El Mikkawy, Doaa Mosad Mosa, Ghada El Deriny, Mohamed Mortada, Naglaa S. Osman, Nermeen Ahmed Fouad, Nourhan Elameen Elkaraly, Sally S. Mohamed, Waleed A. Hassan, Youmna A. Amer, Samah Ismail Nasef, Yasser El Miedany
Publikováno v:
Therapeutic Advances in Musculoskeletal Disease, Vol 13 (2021)
IgA vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the most common cause of systemic vasculitis in childhood. Given its potential life-threatening systemic complications, early and accurate diagnosis as well as management of IgAV
Externí odkaz:
https://doaj.org/article/73c2cdb72fd54f2e8da52a9a375af5db
Autor:
Hala M. Lofty, Huda Marzouk, Yomna Farag, Mohammad Nabih, Iman A. S. Khalifa, Noha Mostafa, Ahmed Salah, Laila Rashed, Kamal El Garf
Publikováno v:
International Journal of Rheumatology, Vol 2016 (2016)
Background and Objectives. SAA is an acute-phase reactant detected during an FMF attack or other inflammatory conditions. High SAA levels may increase the risk of amyloidosis. The aim of the study is to measure the serum amyloid A (SAA) level in a gr
Externí odkaz:
https://doaj.org/article/0fac8e8a6521475f91d5c89c0d394048
Publikováno v:
International journal of health sciences. :2812-2819
Background: Juvenile Systemic lupus erythematous is a chronic autoimmune inflammatory disease that causes damage to various organs such as kidneys, blood, musculoskeletal and nervous system. SLE is variable ranging From mild to severe with unpredicta
Akademický článek
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