Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Syafrizal Aji Pamungkas"'
Publikováno v:
Medicine in Microecology, Vol 20, Iss , Pp 100103- (2024)
Objective: To evaluate the diagnostic performance of the polyclonal antibody generated from the subunit surface protein of MRSA for MRSA detection. Methods: The MRSA clinical isolates were identified by the cefoxitin disc diffusion test and confirmed
Externí odkaz:
https://doaj.org/article/b632eda8527443bb9bc7af9cb3b2eadf
Autor:
Yuliono Trika Nur Hasan, Zulvikar Syambani Ulhaq, Muhammad A’raaf Sirojan Kusuma, Maharani Oryza Sativa, Azka Faradiba Anjani Hulayya, Badariyatud Dini, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, Lina Puspita Hutasoit
Publikováno v:
Revista Médica Clínica Las Condes, Vol 34, Iss 3, Pp 187-194 (2023)
Purpose: To evaluate the short-term effects of intravitreal ranibizumab (IVR) injection on visual and structural changes in diabetic macular edema (DME). Patients and methods: A retrospective study including 108 eyes of 74 patients with DME in which
Externí odkaz:
https://doaj.org/article/a4878ba896fa4f6a92e782e5c1f9b60b
Autor:
Zulvikar Syambani Ulhaq, Ferry Nur Nasyroh, Amalia Nur Aisa, Achmad Arief Hidayatullah, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, Achmad Rilyadi Sholeh, Gita Vita Soraya
Publikováno v:
American Journal of Medicine Open, Vol 10, Iss , Pp 100054- (2023)
Objective: Online and blended learning methods have experienced rapid growth in higher education due to the COVID-19 pandemic. Our study aimed to compare students’ academic performance between online and blended Clinical Skill Laboratories (CSL) le
Externí odkaz:
https://doaj.org/article/412c0db0a6a643fb986843d4faffd08c
Autor:
Ditya Arisanti, Zulvikar Syambani Ulhaq, Ferdi Kurniawan, Syifaus Shodry, Ratu Belqys Rosadeila Putri, Sarah Herawangsa, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, Beni Wicaksono, Nurul Endah Hartati, Lely Retno Wulandari
Publikováno v:
Global Pediatrics, Vol 4, Iss , Pp 100048- (2023)
Objective: Pediatric glaucoma is a rare disease that is potentially more severe than adult glaucoma because it is more challenging to diagnose and more difficult to treat. The segmented retinal layer has been shown to have excellent capability in ass
Externí odkaz:
https://doaj.org/article/23c602fb517c4bbd8d23762be7e1bc25
Autor:
Zulvikar Syambani Ulhaq, Yuliono Trika Nur Hasan, Nanang Khulafa’ur Rosyidin, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, Gita Vita Soraya
Publikováno v:
Journal of Diabetes & Metabolic Disorders. 22:801-815
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed72ce3c77abd30bd168dda390204bcc
https://doi.org/10.1007/s40200-023-01204-6
https://doi.org/10.1007/s40200-023-01204-6
Autor:
Zulvikar Syambani Ulhaq, Dian Kesumapramudya Nurputra, Gita Vita Soraya, Siti Kurniawati, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, William Ka Fai Tse
Publikováno v:
Clinical geneticsREFERENCES. 103(2)
Treacher Collins syndrome (TCS, OMIM: 154500) is a rare congenital craniofacial disorder that is caused by variants in the genes TCOF1, POLR1D, POLR1C, and POLR1B. Studies on the association between phenotypic variability and their relative variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::852f17142d08aa4ddb82fa2acb099a76
https://pubmed.ncbi.nlm.nih.gov/36203321
https://pubmed.ncbi.nlm.nih.gov/36203321
Autor:
Zulvikar Syambani Ulhaq, Gita Vita Soraya, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, Ditya Arisanti, Badariyatud Dini, Lina Fitria Astari, Yuliono Trika Nur Hasan, Prida Ayudianti, Muhammad A’raaf Sirojan Kusuma, Syifaus Shodry, Sarah Herawangsa, Dian Kesumapramudya Nurputra, Sri Idaiani, William Ka Fai Tse
Publikováno v:
The Cleft Palate-Craniofacial Journal. :105566562211361
Objective Genetic variants in EFTUD2 were proven to influence variable phenotypic expressivity in mandibulofacial dysostosis Guion-Almeida type (MFDGA) or mandibulofacial dysostosis with microcephaly (MFDM). Yet, the association between the severity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000fe20a07b27104f77e1ad0e2677284
https://doi.org/10.1177/10556656221136177
https://doi.org/10.1177/10556656221136177
Autor:
Zulvikar Syambani Ulhaq, Gita Vita Soraya, Lola Ayu Istifiani, Syafrizal Aji Pamungkas, William Ka Fai Tse
Publikováno v:
The Cleft Palate-Craniofacial Journal. :105566562210891
Nager syndrome (NS) is a rare disease marked with craniofacial and preaxial limb anomalies. In this report, we summarized the current evidence to determine a possible genotype–phenotype association among NS individuals. Twenty-four articles compris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c2636edd0261bb82e3e26a82a4f9322
https://doi.org/10.1177/10556656221089156
https://doi.org/10.1177/10556656221089156