Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Farmaditya EP Mundhofir"'
Publikováno v:
Journal of Biomedicine and Translational Research, Vol 2, Iss 1, Pp 10-16 (2016)
Background: Intellectual disability (ID) is a major public health problem because the defect, treatment and rehabilitation require long life both medical and socio-economic assessment. Fragile X syndrome (FXS) is the most common cause of inherited X-
Externí odkaz:
https://doaj.org/article/24a9366f7fc547978857edd3a0e90d35
Autor:
Farmaditya EP Mundhofir, Rahajeng N Tunjungputri, Willy M Nillesen, Bregje WM van Bon, Martina Ruiterkamp-Versteeg, Tri I Winarni, Ben CJ Hamel, Helger G Yntema, Sultana MH Faradz
Publikováno v:
Paediatrica Indonesiana, Vol 53, Iss 2, Pp 83-8 (2013)
Background Intellectual disability (ID) often coincides with an abnormal head circumference (HC). Since the HC is a reflection of brain size, abnormalities in HC may be a sign of a brain anomaly. Although microcephaly is often secondary to ID, heredi
Externí odkaz:
https://doaj.org/article/89de7237e44e4e4caed5d86fdbca8bd4
Autor:
Rina Purnamasari, Muflihatul Muniroh, Novi Kusumaningrum, Farmaditya EP Mundhofir, Renni Yuniati
Publikováno v:
Jurnal Aisyah : Jurnal Ilmu Kesehatan. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f30a46bc1a74dae720b5b8fddd7ff38c
https://doi.org/10.30604/jika.v8i1.1502
https://doi.org/10.30604/jika.v8i1.1502
Autor:
Reza Dian Pratama, M. Ali Sobirin, Rizky Aditya Fardhani, Bahrudin, Farmaditya Ep Mundhofir, Yuriz Bakhtiar, Nani Maharani
Publikováno v:
Bioscientia Medicina: Journal of Biomedicine and Translational Research, Vol 5, Iss 10, Pp 968-975 (2021)
Background: Atherosclerosis is the main cause of ischemic heart disease which leads to death for people aged more than 40 years old. Genistein is an important isoflavone compound which may protect the blood vessels from endothelial injury. This resea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbbd2c11c6e4297fa3580bcf49b67e37
https://www.bioscmed.com/index.php/bsm/article/view/414
https://www.bioscmed.com/index.php/bsm/article/view/414
Autor:
Tri Nur Kristina, Farmaditya Ep Mundhofir, Renni Yuniati, Arti Rachmawati, Innelya Innelya, Matthew Brian Khrisna, K Heri Nugroho Hario Seno, Harold Jefferson Matthew Charlex, Alfi Rahmatika
Publikováno v:
Journal of Experimental Pharmacology
Renni Yuniati,1 Innelya Innelya,2 Arti Rachmawati,2 Harold Jefferson Matthew Charlex,2 Alfi Rahmatika,2 Matthew Brian Khrisna,1 Farmaditya EP Mundhofir,3 K Heri Nugroho Hario Seno,4 Tri Nur Kristina5 1Dermatology and Venereology Department, Faculty o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94580a81fb82319ec1edf30bc06dffac
http://europepmc.org/articles/PMC8374851
http://europepmc.org/articles/PMC8374851
Autor:
Etisa Adi Murbawani, Muflihatul Muniroh, Fronthea Swastawati, Farmaditya Ep Mundhofir, Yora Nindita, Sepsina Reski, Endang Mahati
Publikováno v:
International Journal of Pharmacy and Pharmaceutical Sciences. :18-22
Objective: This study aimed to evaluate the effect of catfish (Pangasius hypophthalmus) oil on hs-CRP and transthyretin levels of undernourished Wistar rats. Methods: Thirty male Wistar rats were divided into five equal groups. Healthy control (KN) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::496ded29547c4ff6ffcec2031eff0d8f
https://doi.org/10.22159/ijpps.2021v13i5.40357
https://doi.org/10.22159/ijpps.2021v13i5.40357
Publikováno v:
Frontiers in Pharmacology. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13f04599deb031451187385f4c4cf8c3
Publikováno v:
Journal of Biomedicine and Translational Research, Vol 2, Iss 1, Pp 10-16 (2016)
Background: Intellectual disability (ID) is a major public health problem because the defect, treatment and rehabilitation require long life both medical and socio-economic assessment. Fragile X syndrome (FXS) is the most common cause of inherited X-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13f5fcbb2ee3e7b27d52d5d3f12cc319
http://ejournal2.undip.ac.id/index.php/jbtr/article/view/536
http://ejournal2.undip.ac.id/index.php/jbtr/article/view/536
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c762b4ebb70977a11f15309bda4b4a6
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/81
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/81
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 17:1539-1546
Specific patterns of t he hereditary breast and ovarian cancer (HBOC) syndrome are related to mutations in the BRCA1 gene. One hundred unrelated breast cancer patients were interviewed to obtain clinical symptoms and signs, pedigree and familial hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fb471f7e5df52d475b6192633332756
https://doi.org/10.7314/apjcp.2016.17.3.1539
https://doi.org/10.7314/apjcp.2016.17.3.1539