Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Manal AbdelGawad"'
Autor:
Mohamed Abdelmalak Abokandil, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdelhady, Mohamed Mansy, Mostafa Kotb
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Progressive familial intrahepatic cholestasis is an autosomal recessive genetic disorder that manifests primarily with jaundice and pruritus and can progresses from persistent cholestasis to cirrhosis and late childhood liver fail
Externí odkaz:
https://doaj.org/article/2e15d55f344e426f8a2be85c6f75fc31
Autor:
Mohamed A Yassin, Ashraf T Soliman, Vincenzo De Sanctis, Mohamed Osman Abdelrahman, Elsaid M Aziz Bedair, Manal AbdelGawad
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 18, Iss 4, Pp 546-551 (2014)
Introduction: Osteoporosis represents the second most common cause of endocrinopathy in patients with beta thalassemia major (BTM). Some drugs proved effective to reduce vertebral and non-vertebral fracture risk. Denosumab is a fully human monoclonal
Externí odkaz:
https://doaj.org/article/6663a683c1304ce0b315677da4c9599d
Publikováno v:
Acta Scientific Gastrointestinal Disorders. 2:03-07
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d90a4316e0a37ef99cc7cb1b60ce8015
https://doi.org/10.31080/asgis.2019.02.0069
https://doi.org/10.31080/asgis.2019.02.0069
Publikováno v:
Journal of Hepatology. 70:e208
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::590741cd248a0c4a7f1a2d4117652686
https://doi.org/10.1016/s0618-8278(19)30388-3
https://doi.org/10.1016/s0618-8278(19)30388-3