Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Muhammad Gahan Satwiko"'
Autor:
Royhan Rozqie, Muhammad Gahan Satwiko, Dyah Wulan Anggrahini, Ahmad Hamim Sadewa, Gunadi, Anggoro Budi Hartopo, Hasanah Mumpuni, Lucia Kris Dinarti
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-6 (2022)
Abstract Background NKX2-5 variant in atrial septal defect patients has been reported. However, it is not yet been described in the Southeast Asian population. Here, we screened the NKX2-5 variants in patients with atrial septal defect (ASD) in the I
Externí odkaz:
https://doaj.org/article/b352742096744e59b7c92b4d8f4b693e
Autor:
Anggoro Budi Hartopo, Dyah Wulan Anggrahini, Muhammad Gahan Satwiko, Arditya Damarkusuma, Armalya Pritazahra, Muhammad Reyhan Hadwiono, Vera Christina Dewanto, Salvatore Di Somma, Noriaki Emoto, Lucia Kris Dinarti
Publikováno v:
Acta Medica Indonesiana, Vol 54, Iss 4 (2022)
Background: Atrial septal defect developed pulmonary hypertension (ASD-PH) at first diagnosis due to late presentation are common in Indonesia. Transthoracic echocardiogram (TTE) is a common tool to detect ASD-PH, before proceeding to invasive proced
Externí odkaz:
https://doaj.org/article/f8f60844b7fc480388151e610db259a4
Autor:
Lucia Kris Dinarti, Anggoro Budi Hartopo, Arditya Damar Kusuma, Muhammad Gahan Satwiko, Muhammad Reyhan Hadwiono, Aditya Doni Pradana, Dyah Wulan Anggrahini
Publikováno v:
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-11 (2020)
Abstract Backgrounds The COngenital HeARt Disease in adult and Pulmonary Hypertension (COHARD-PH) registry is the first registry for congenital heart disease (CHD) and CHD-related pulmonary hypertension (PH) in adults in Indonesia. The study aims to
Externí odkaz:
https://doaj.org/article/87538681f72440cf8c314e103c6f4433
Autor:
Aditya Doni Pradana, Anggoro Budi Hartopo, Muhammad Reyhan Hadwiono, Arditya Damar Kusuma, Lucia Kris Dinarti, Dyah Wulan Anggrahini, Muhammad Gahan Satwiko
Publikováno v:
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-11 (2020)
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders
Backgrounds The COngenital HeARt Disease in adult and Pulmonary Hypertension (COHARD-PH) registry is the first registry for congenital heart disease (CHD) and CHD-related pulmonary hypertension (PH) in adults in Indonesia. The study aims to describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e945360f03a74013170f4b1dec1020
http://link.springer.com/article/10.1186/s12872-020-01434-z
http://link.springer.com/article/10.1186/s12872-020-01434-z
Autor:
Royhan Rozqie, Muhammad Gahan Satwiko, Dyah Wulan Anggrahini, Ahmad Hamim Sadewa, null Gunadi, Anggoro Budi Hartopo, Hasanah Mumpuni, Lucia Kris Dinarti
Publikováno v:
BMC medical genomics. 15(1)
Background NKX2-5 variant in atrial septal defect patients has been reported. However, it is not yet been described in the Southeast Asian population. Here, we screened the NKX2-5 variants in patients with atrial septal defect (ASD) in the Indonesian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f452846ffcbb7c94a9519e5d89dadd98
https://pubmed.ncbi.nlm.nih.gov/35459168
https://pubmed.ncbi.nlm.nih.gov/35459168
Autor:
Fika Humaeda Assilmi, Lucia Kris Dinarti, Vera C Dewanto, Nu Pravitasari, Armalya Pritazahra, Dyah Wulan Anggrahini, Anggoro Budi Hartopo, Muhammad Gahan Satwiko, Alifia Salsabila, Detty Siti Nurdiati, Muhammad Reyhan Hadwiono, Erna Ashlihah Rochmat
Publikováno v:
Journal of Community Empowerment for Health; Vol 4, No 3 (2021)
Women adapt to pregnancy through multi-organ system physiologic changes, including cardiovascular adaptations. These changes affect those with pre-existing cardiovascular problems differently, and subsequently lead to higher probability of death caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17e678e0314117d7f536f3a298e03b7b
https://journal.ugm.ac.id/jcoemph/article/view/64970
https://journal.ugm.ac.id/jcoemph/article/view/64970
Autor:
Koji Ikeda, Noriaki Emoto, Berthold Hocher, Muhammad Gahan Satwiko, Keiko Yagi, Ken-ichi Hirata, Kazuhiko Nakayama
Publikováno v:
Biochemical and biophysical research communications. 465(3)
Pulmonary arterial hypertension (PAH) is a fatal disease that eventually results in right heart failure and death. Current pharmacologic therapies for PAH are limited, and there are no drugs that could completely cure PAH. Enhanced activity of endoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::283e7624e20a9073a7fda25d04b43354
https://pubmed.ncbi.nlm.nih.gov/26275708
https://pubmed.ncbi.nlm.nih.gov/26275708