Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Iffa Mutmainah"'
Autor:
Iffa Mutmainah, Willy Nillesen, Farmaditya Mundhofir, Tri Winarni, Ineke van der Burgt, Helger Yntema, Sultana Faradz
Publikováno v:
Paediatrica Indonesiana, Vol 56, Iss 1, Pp 62-6 (2016)
Noonan syndrome (NS; OMIM#163950) is a relatively common autosomal dominant disorder with a worldwide prevalence of approximately 1:1,000 to 1:2,500. The syndrome is characterized by distinctive facial features, congenital heart defects (CHD), and sh
Externí odkaz:
https://doaj.org/article/c7bed8e85e94444dbb56a52b582962bd
Autor:
Mahrani, Pukovisa Prawirohardjo, Nurfanida Librianty, Uti Nilam Sari, Gadistya Novitri Adinda, Fitriana Nur Rahmawati, Hana Khairina Putri Faisal, Sarah Shafa Marwadhani, Adi Kurniawan, Paramita Khairan, Iffa Mutmainah
Publikováno v:
Journal Of The Indonesian Medical Association. 70:173-181
Tujuan: COVID-19 adalah suatu penyakit infeksi yang baru ditemukan sejak Desember 2019 yang kemudian diumumkan oleh WHO sebagai pandemi global. Gambaran radiologi pada COVID-19 cukup bervariasi, namun yang paling sering ditemukan adalah ground-glass
Autor:
Willy M. Nillesen, Helger G. Yntema, Iffa Mutmainah, Tri Indah Winarni, Sultana M.H. Faradz, Ineke van der Burgt, Farmaditya Ep Mundhofir
Publikováno v:
Paediatrica Indonesiana, Vol 56, Iss 1, Pp 62-6 (2016)
Noonan syndrome (NS; OMIM#163950) is a relatively common autosomal dominant disorder with a worldwide prevalence of approximately 1:1,000 to 1:2,500. The syndrome is characterized by distinctive facial features, congenital heart defects (CHD), and sh