Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Qurrota Ayuni Novia Putri"'
Autor:
Muhammad Faizi, Nur Rochmah, Yuni Hisbiyah, Rayi Kurnia Perwitasari, Qurrota Ayuni Novia Putri, Sukmawati Basuki, Anang Endaryanto, Soetjipto Soetjipto
Publikováno v:
Biomolecules & Biomedicine, Vol 23, Iss 4 (2023)
Thyroid dysfunction is the most common endocrine disorder in Down syndrome (DS) children. Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) is one of the immune regulatory genes that correlates with Hashimoto’s thyroiditis (HT). However, studies
Externí odkaz:
https://doaj.org/article/f7dc614a8cbc46a7a892937171828ca2
Autor:
Nur Rochmah, Farahdina Farahdina, Wika Yuli Deakandi, Qurrota Ayuni Novia Putri, Tyas Maslakhatien Nuzula, Katherine Fedora, Qorri ‘Aina, Muhammad Faizi
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 11:38-43
BACKGROUND: The COVID-19 pandemic determined a profound impact on the routine follow-up of type 1 diabetes (T1D) children. Telemedicine represents a critical tool to guarantee regular care for these patients in this form. AIM: The purpose of this stu
Autor:
Yuni Hisbiyah, Anang Endaryanto, Bagoes Setyoboedi, Nur Rochmah, Muhammad Faizi, Citrawati Dyah Kencono Wungu, Qurrota Ayuni Novia Putri
Publikováno v:
International journal of health sciences. :1395-1410
Deficiencies of Selenium (Se) is correlated with the risk and onset of autoimmune thyroid disease (AITD). The aim of this study was to determine the association between Se supplementation and AITD. Methods: Electronic data searches of 4 databases wer
Publikováno v:
International journal of health sciences. :434-438
We describe a case of a 9-day-old boy weighing 3800 grams and experiencing recurrent hypoglycemia and seizures was referred to the hospital. The patient's condition improved when the medical staff administered a dextrose bolus. The laboratory test re
Publikováno v:
International Journal Of Scientific Advances. 3
Osteogenesis Imperfecta (OI) or commonly referred to as brittle bone disease is a congenital connective tissue formation disorder characterized by bone fragility, osteopenia, skin disorders, blue sclera, dentinogenesis imperfecta (DI), and hearing lo
Publikováno v:
Proceedings of Surabaya International Physiology Seminar.