Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Magdy, A Ramadan"'
Autor:
Doaa Mohammed Youssef, Mohammad Nagib Abo Al Fotoh, Rabab Mohamed Elibehidy, Shreen Magdy Ahmad Ramadan, Ehab Mohammady Mohammad
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 2, Pp 250-254 (2015)
To evaluate the impact of nutritional knowledge following interventional educational sessions in chronic dialysis patients, we studied 40 children on chronic regular hemodialysis (HD) at the beginning and after six months of nutrition educational ses
Externí odkaz:
https://doaj.org/article/5733334ba06141a09b0162a7f7f17f11
Autor:
Shaymaa, Elsayed Abdel Meguid Ahmed, Ashraf, T Soliman, Magdy, A Ramadan, Ahmed, Elawwa, Ahmed, Mohamed Said Abugabal, Mohamed, Hassan Ahmed Emam, Vincenzo, De Sanctis
Publikováno v:
Acta Bio Medica : Atenei Parmensis
Background: Debate still exist about the safety of long-term use of prednisone (PD) versus hydrocortisone (HC) for treating children with congenital adrenal hyperplasia -21OH D (CAH). Despite recent developments in congenital adrenal hyperplasia -21O
Introduction Surgical site infection (SSI) is one of the most common healthcare-associated infections (HAIs). However, there is a lack of data available about SSI in children worldwide, especially from low-income and middle-income countries. This stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d6e0deacf8f618864ba5c9e804cf5b77
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103383
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103383
Publikováno v:
Journal of Tropical Pediatrics. 40:97-99
The amino acids citrulline, ornithine and arginine, total serum proteins, serum enzymes glutamic oxalacetic and glutamic pyruvic transaminases, blood ammonia and urea were measured in 20 marasmic children with manifest psychomotor changes, before and
Publikováno v:
Metabolism: clinical and experimental. 50(8)
Pycnodysostosis is a rare hereditary bone abnormality with an autosomal recessive mode of inheritance. We report the clinical, radiologic, and endocrine status of 8 children with this rare disease. All patients had the characteristic phenotype of the