Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Mohamed A Elmonem"'
Autor:
Rasha Helmy, Rasha Selim Mahmoud, Mohamed A. Elmonem, Sally Emadeldin, Neveen Abd Elmonem Soliman
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-10 (2024)
Abstract Background Cystinosis is an autosomal recessive lysosomal storage disorder caused by cystine crystals accumulation within lysosomes resulting in multi-organ dysfunction. Infantile nephropathic cystinosis is the most common phenotype of the d
Externí odkaz:
https://doaj.org/article/c8cba388e6e44574807b96410376457e
Autor:
Benedicte Eneman, Mohamed A Elmonem, Lambertus P van den Heuvel, Laleh Khodaparast, Ladan Khodaparast, Chris van Geet, Kathleen Freson, Elena Levtchenko
Publikováno v:
PLoS ONE, Vol 12, Iss 7, p e0182100 (2017)
Pituitary adenylate cyclase-activating polypeptide (PACAP) is an inhibitor of megakaryopoiesis and platelet function. Recently, PACAP deficiency was observed in children with nephrotic syndrome (NS), associated with increased platelet count and aggre
Externí odkaz:
https://doaj.org/article/0a13a61eb08a455b8542f1f2ec999d81
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Alkaptonuria (AKU) is a rare autosomal recessive metabolic disorder caused by pathogenic variants in the homogentisate 1,2-dioxygenase (HGD) gene. This leads to a deficient HGD enzyme with the consequent accumulation of homogentisic acid (HG
Externí odkaz:
https://doaj.org/article/ab9cb2c2a02a46ea89e293af1b1cbdfd
Autor:
Amira Ahmed Gad, Radwa Shamma, Mohamed A. Elmonem, Nora E. Badawi, Lubna Fawaz, Mona Mamdouh Hassan
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 71, Iss 1, Pp 1-7 (2023)
Abstract Background Short stature is one of the main causes of children referral to pediatric endocrinologists. Common etiologies include idiopathic growth hormone deficiency (IGHD), small for gestational age (SGA), and idiopathic short stature (ISS)
Externí odkaz:
https://doaj.org/article/c7f50c6cb5b4408eaaf999424db59fcf
Autor:
Noha A. Yassin, Salma Z. El-Houchi, Sarah F. Abd El-Shafy, Noha S. Soliman, Mohamed A. Elmonem, Nehal El-Koofy
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 70, Iss 1, Pp 1-6 (2022)
Abstract Background Hepatitis A is the most common form of acute viral hepatitis in developing countries. In children < 6 years of age, most infections are asymptomatic, and if illness does occur, it is usually anicteric. This study aimed to determin
Externí odkaz:
https://doaj.org/article/cd8237c6417344e28ad2bc30a3989c27
Autor:
Neveen A. Soliman, Mohamed A. Elmonem, Safaa M. Abdelrahman, Marwa M. Nabhan, Yosra A. Fahmy, Andrea Cogal, Peter C. Harris, Dawn S. Milliner
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Primary hyperoxaluria (PH) is an autosomal recessive disorder of oxalate metabolism caused by pathogenic variants in either of three genes (AGXT, GRHPR or HOGA1). The study aimed at characterizing the clinical phenotypes as well as the genot
Externí odkaz:
https://doaj.org/article/dcb32cde93ad4e1ab60666323adc7bfa
Publikováno v:
Clinical and Experimental Pediatrics, Vol 65, Iss 8, Pp 410-416 (2022)
Background Dyslipidemia is a major health problem among children and adolescents worldwide due to its significant association with cardiovascular disease. Primary dyslipidemias are commonly familial syndromes that can be completely asymptomatic. Purp
Externí odkaz:
https://doaj.org/article/20685d3f855a478ebf7082dc3e614c3f
Autor:
Mohammed K. Afifi, Ahmed S. Kenawy, Heba H. El Demellawy, Amany A. Azouz, Torki Al-Otaibi, Osama Gheith, Mohamed Abd ElMonem, Mohamed S. AbdElhalim, Raghda R. S. Hussein
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-7 (2021)
Abstract Background Osteoporosis and osteopenia occur frequently in renal transplant recipients due to long-term use of immune-suppressants including corticosteroids. Previous treatment options like bisphosphonates had acceptable but rather unsatisfa
Externí odkaz:
https://doaj.org/article/43a3a8f01b2a442087716d99e6b0b46f
Autor:
Nehal M. El-koofy, Yasmeen A. Abdo, Dina El-Fayoumi, Amanne F. Esmael, Mohamed. A. Elmonem, Zahraa Ezzeldin
Publikováno v:
Lipids in Health and Disease, Vol 20, Iss 1, Pp 1-8 (2021)
Abstract Background Neonatal severe hypertriglyceridemia is rarely reported in the literature and there is no consensus for hypertriglyceridemia management at this age group. Methods The index case is a 4-week-old male infant with severe hypertriglyc
Externí odkaz:
https://doaj.org/article/11d0c60b509d4a8abba327d0ac97ec11
Autor:
Mohamed S. AbdElhalim, Ahmed S. Kenawy, Heba H. El Demellawy, Amany A. Azouz, Sarah S. Alghanem, Torki Al-Otaibi, Osama Gheith, Mohamed Abd ElMonem, Mohammed K. Afifi, Raghda R. S. Hussein
Publikováno v:
Kidney Research and Clinical Practice, Vol 39, Iss 4, Pp 479-486 (2020)
Background : The absorption rates of mycophenolate mofetil (MMF) and enteric-coated mycophenolate sodium (EC-MPS) may be influenced by the concomitant use of omeprazole. Methods : One hundred kidney transplant patients were recruited during their out
Externí odkaz:
https://doaj.org/article/7e2899e0b9724c9b94979efb5372259f