Zobrazeno 1 - 10 of 105 pro vyhledávání: '"Sultana M.H Faradz"'
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Akademický článek
Pengaruh Kadar Timbal dalam Darah terhadap Peningkatan Kadar Superoxide Dismutase (SOD) pada Preeklampsia
Autor: Besari Adi Pramono, Sultana M.H Faradz, Suhartono Suhartono, Noor Pramono
Publikováno v: JAI (Jurnal Anestesiologi Indonesia), Vol 14, Iss 3, Pp 184-191 (2022)
Latar Belakang: Angka kematian ibu (AKI) adalah masalah yang masih menjadi perhatian khusus di Indonesia. Preeklampsia adalah suatu komplikasi dalam kehamilan yang menjadi salah satu penyebab utama mortalitas ibu dan janin di seluruh dunia. Preeklamp
Externí odkaz: https://doaj.org/article/ce30713a7e5b4f9bbf9c1eae0f9f4914
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3
Akademický článek
A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots
Autor: Vivienne J. Tan, Mulias Lian, Sultana M.H. Faradz, Tri I. Winarni, Samuel S. Chong
Publikováno v: Frontiers in Genetics, Vol 9 (2018)
Background:FMR1 CGG trinucleotide repeat hyper-expansions are observed in 99% of individuals with fragile X mental retardation syndrome (FXS). We evaluated the reliability of a rapid single-step gender-neutral molecular screen for FXS when performed
Externí odkaz: https://doaj.org/article/b8553475975040d183396233778a1543
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4
Distribusi Kelainan Kromosom Sindrom Down dan Usia Ibu saat Melahirkan di SLB Negeri Semarang
Autor: Sultana M.H. Faradz, Vidyaningtyas Bothi Andrianti
Publikováno v: Jurnal Pengabdian Kedokteran Indonesia. 2:54-62
Latar belakang: Sindrom Down merupakan penyebab umum dari 25-30% retardasi mental di dunia. Studi sitogenetik menunjukkan bahwa 94% dari kasus Sindrom Down adalah trisomi yang disebabkan oleh nondisjunction, 3,5% translokasi dan 2,5% mosaik. Nondisju
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bdbb6c4e2cb770eb4081c9d09ad1d5e4
https://doi.org/10.33096/jpki.v2i2.152
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5
The Evaluation of Parental Acceptance Towards Children with Sex Chromosomal Disorders of Sex Development Using A Mixed-Method
Autor: Tri Indah Winarni, Sultana M.H. Faradz, Iit Fitrianingrum, Annastasia Ediati
Publikováno v: Journal of Biomedicine and Translational Research, Vol 7, Iss 1, Pp 14-21 (2021)
Background: Sex chromosomal Disorder of sex development (DSD) is an atypical abnormality of external genitalia which is mismatched with its sex chromosome traits. The condition of children with DSD affects the dynamics in the family. Parents’ react
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b694bdd989f344676e727c66df7aade
https://ejournal2.undip.ac.id/index.php/jbtr/article/view/10710
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6
Gangguan Perilaku pada Anak Perempuan dengan Hiperplasia Adrenal Kongenital: Persepsi Orang Tua
Autor: Sultana M.H. Faradz, Nida Hanifah, Annastasia Ediati, Mahayu Dewi Ariani, Agustini Utari
Publikováno v: Sari Pediatri, Vol 22, Iss 2, Pp 65-70 (2020)
Latar belakang. Paparan androgen sejak prenatal diduga berdampak pada banyak aspek perkembangan anak perempuan dengan Hiperplasia Adrenal Kongenital (HAK). Namun, data mengenai gangguan emosi atau gangguan perilaku pada anak dengan HAK di Indonesia m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec4f7a18096681127e4a922e72dd5ba
https://saripediatri.org/index.php/sari-pediatri/article/view/1764
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7
Unraveling of Diagnosis Odyssey in A Girl with Primary Amenorrhea: A case report
Autor: Ni Made Indri Dwi Susanti, Nurin Aisyiyah Listyasari, Inu Mulyantoro, Dik Puspasari, Sultana M.H. Faradz
Publikováno v: Journal of Biomedicine and Translational Research, Vol 6, Iss 1, Pp 19-22 (2020)
Background:Primary amenorrhea may result from congenital abnormalities in the development of the gonads, genital tract, or external genitalia or from a disturbance within the hypothalamic-pituitary-ovarian axis. Gonadal dysgenesis is a disorder of se
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1e4111e369dfe54bf0e6c089cf1f4e2
https://doi.org/10.14710/jbtr.v6i1.6218
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8
Differences in thrombin and plasmin generation potential between East African and Western European adults: The role of genetic and non-genetic factors
Autor: Godfrey S. Temba, Nadira Vadaq, Jun Wan, Vesla Kullaya, Dana Huskens, Tal Pecht, Martin Jaeger, Collins K. Boahen, Vasiliki Matzaraki, Wieteke Broeders, Leo A.B. Joosten, Sultana M.H. Faradz, Gibson Kibiki, Saskia Middeldorp, Duccio Cavalieri, Paolo Lionetti, Philip G. de Groot, Joachim L. Schultze, Mihai G. Netea, Vinod Kumar, Bas de Laat, Blandina T. Mmbaga, Andre J. van der Ven, Mark Roest, Quirijn de Mast
Publikováno v: Journal of thrombosis and haemostasis 20(5), 1089-1105 (2022). doi:10.1111/jth.15657
Journal of Thrombosis and Haemostasis, 20, 5, pp. 1089-1105
Journal of Thrombosis and Haemostasis, 20(5), 1089-1105. Wiley
Journal of Thrombosis and Haemostasis, 20, 1089-1105
Journal of thrombosis and haemostasis, 20(5), 1089-1105. Wiley-Blackwell
Contains fulltext : 251902.pdf (Publisher’s version ) (Open Access) BACKGROUND: Geographic variability in coagulation across populations and their determinants are poorly understood. OBJECTIVE: To compare thrombin (TG) and plasmin (PG) generation p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c42789ae0052d54f8fafb1c368bb2ff2
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