Zobrazeno 1 - 2
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pro vyhledávání: '"Hiba Karimeldin Mohamed"'
Autor:
Karimeldin Mohamed Ali Salih, Atif Ahmed Saad, Widad Mohamed Eldouch, Hiba Karimeldin Mohamed, Jaber Alfaifi, Mohamed O Andarawi, Ayman A. Elshayeb
Background Sickle cell Anemia and/or Disease (SCA/SCD) is an autosomal recessive disease leading to abnormal hemoglobin with global prevalence in general and tribal burden in sub-Saharan Africa particularly. Methods Recent patients’ assessments wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9aa90444b5aa623b08c6ef0a9b65e4a6
https://doi.org/10.21203/rs.3.rs-2107299/v1
https://doi.org/10.21203/rs.3.rs-2107299/v1
Autor:
Karimeldin Mohamed Ali Salih, Mohammed Abbas, Muddathir H Hamad, Hiba Karimeldin Mohamed, Sarar Mohamed
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:394-396
Introduction: Childhood enuresis is a stressful condition for both family members and patients. Different strategies can be offered to manage this condition with variable success rates. Data on the treatment of enuresis are scarce Sudan. We compared