Prof. Sultana MH Faradz, MD, PhD
Prof. Sultana MH Faradz, MD, PhD
Center for Biomedical Research, Faculty of Medicine, Diponegoro University, Indonesia
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Cited by
Cited by
Gonadoblastoma arising in undifferentiated gonadal tissue within dysgenetic gonads
M Cools, H Stoop, AMF Kersemaekers, SLS Drop, KP Wolffenbuttel, ...
The Journal of Clinical Endocrinology & Metabolism 91 (6), 2404-2413, 2006
Tumor risk in disorders of sex development
J Pleskacova, R Hersmus, JW Oosterhuis, BA Setyawati, SM Faradz, ...
Sexual Development 4 (4-5), 259-269, 2010
Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort
S Eggers, S Sadedin, JA Van Den Bergen, G Robevska, T Ohnesorg, ...
Genome Biology 17 (1), 243, 2016
Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures
A Utari, W Chonchaiya, SM Rivera, A Schneider, RJ Hagerman, ...
American journal on intellectual and developmental disabilities 115 (5), 433-443, 2010
Measurement of circulating levels of VEGF-A,-C, and-D and their receptors, VEGFR-1 and-2 in gastric adenocarcinoma
MS Al-Moundhri, A Al-Shukaili, M Al-Nabhani, B Al-Bahrani, IA Burney, ...
World journal of gastroenterology: WJG 14 (24), 3879, 2008
Systemic air embolism after transthoracic lung biopsy: a case report and review of literature
W Bou-Assaly, P Pernicano, E Hoeffner
World journal of radiology 2 (5), 193, 2010
Imbalance of angiopoietin-1 and angiopoetin-2 in severe dengue and relationship with thrombocytopenia, endothelial activation, and vascular stability
M Michels, AJAM van der Ven, K Djamiatun, R Fijnheer, PG de Groot, ...
The American journal of tropical medicine and hygiene 87 (5), 943-946, 2012
Immune‐mediated disorders among women carriers of fragile X premutation alleles
TI Winarni, W Chonchaiya, TA Sumekar, P Ashwood, GM Morales, ...
American journal of medical genetics Part A 158 (10), 2473-2481, 2012
Severe dengue is associated with consumption of von Willebrand factor and its cleaving enzyme ADAMTS-13
K Djamiatun, AJAM Van der Ven, PG de Groot, SMH Faradz, D Hapsari, ...
PLoS neglected tropical diseases 6 (5), 2012
SMAD2 Mutations Are Associated with Arterial Aneurysms and Dissections
D Micha, D Guo, Y Hilhorst‐Hofstee, F van Kooten, D Atmaja, E Overwater, ...
Human mutation 36 (12), 1145-1149, 2015
Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping
AM Siemiatkowska, K Arimadyo, LM Moruz, GDN Astuti, M de Castro-Miro, ...
Molecular vision 17, 3013, 2011
Short-term safety and efficacy of calcium montmorillonite clay (UPSN) in children
NJ Mitchell, J Kumi, M Aleser, SE Elmore, KA Rychlik, KE Zychowski, ...
The American journal of tropical medicine and hygiene 91 (4), 777-785, 2014
Increased PAI-1 plasma levels and risk of death from dengue: no association with the 4G/5G promoter polymorphism
ATA Mairuhu, TE Setiati, P Koraka, CE Hack, A Leyte, SMH Faradz, ...
Thrombosis journal 3 (1), 17, 2005
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark
GDN Astuti, M Bertelsen, MN Preising, M Ajmal, B Lorenz, SMH Faradz, ...
European Journal of Human Genetics 24 (7), 1071-1079, 2016
Body image and sexuality in Indonesian adults with a disorder of sex development (DSD)
A Ediati, AZ Juniarto, E Birnie, SLS Drop, SMH Faradz, AB Dessens
The Journal of Sex Research 52 (1), 15-29, 2015
Whole exome sequencing combined with linkage analysis identifies a novel 3 bp deletion in NR5A1
S Eggers, KR Smith, M Bahlo, LHJ Looijenga, SLS Drop, ZA Juniarto, ...
European Journal of Human Genetics 23 (4), 486-493, 2015
Gender development in Indonesian children, adolescents, and adults with disorders of sex development
A Ediati, AZ Juniarto, E Birnie, SLS Drop, SMH Faradz, AB Dessens
Archives of sexual behavior 44 (5), 1339-1361, 2015
A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient
ED Setijowati, FS Van Dijk, JM Cobben, RR Van Rijn, EA Sistermans, ...
European journal of medical genetics 55 (1), 17-21, 2012
High plasma mid-regional pro-adrenomedullin levels in children with severe dengue virus infections
M Michels, K Djamiatun, SMH Faradz, MMJF Koenders, Q de Mast, ...
Journal of clinical virology 50 (1), 8-12, 2011
Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa
MI Khan, RWJ Collin, K Arimadyo, S Micheal, M Azam, N Qureshi, ...
Molecular vision 16, 2753, 2010
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