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Rumah Sakit Nasional Diponegoro melayani BPJS Kesehatan

dr. Agustini Utari MSi Med, Sp.AK » Profil Dokter

dr. Agustini Utari MSi Med, Sp.AK

Dokter Spesialis Anak

______________________

Pendidikan

S1 : FK UNDIP, 1991-1997
S2 : 1. Magister Ilmu Biomedik, FK UNDIP, 2003-2007
2. Magister Ilmu Biomedik, konsentrasi konseling genetik, FK UNDIP, 2008-2009, join research dengan MIND (Medical              Investigation for Neurodevelopmental Disorder) Institute, UC Davis, USA
S3:
Spesialis I : Spesialis Ilmu Kesehatan Anak, FK UNDIP, 2003-2007
Spesialis II : Konsultan Endokrin Anak, FK UI, Jakarta 2014-2015

Pengalaman Profesional

Kepala Puskesmas Wolojita , 1998-2000
Kepala Puskesmas Kota Ende, 2001-2002

Penelitian

“Congenital Adrenal Hyperplasia (CAH) : Diagnostic Approach using High Resolution Melting Technique and Comprehensif Management “ (Co PI), 2012, Sumber dana : Dikti
“ The Effect of Low Glycaemic Index Intervention to Adiponectin and insulin resistance in Obese Adolescent “, 2012, Sumber dana : Hibah FK UNDIP
“ Strategi Peningkatan Compliance Penderita Hiperplasia Adrenal Kongenital : Pendekatan komprehensif pada pasien dan keluarga” (on going study), 2015-2016, Sumber dana : Dikti
“ Pengembangan Teknik High Resolution Melting untuk biomarker mutasi gen androgen reseptor (AR gene) pada individu dengan 46, XY DSD, 2015-2016 (on going study), Sumber dana : DIPA Undip
“ Analisis Profil Hormonal pada Indovidu dengan Untreated Congenital Adrenal Hyperplasia”, 2016, Sumber dana : FK Undip.

Publikasi
International Journals:

  1. Chonchaiya W, Utari A, Pereira GM, Tassone F, Hessl D, Hagerman R. Broad Clinical involvement in family affected by fragile X premutation. J Dev Behav Pediatr 30: 2009.
  2. Utari A, Adams E, Berry-Kravis E, Chavez A, Scaggs F, Ngotran L, et al. Aging in Fragile X Syndrome. J Neurodevelop Disord (2010) 2:70–76
  3. Utari A, Chonchaiya W, Schneider A, Rivera SM, Faradz SMH, Hagerman RJ. Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcomes measure. AJIDD 2010; 115 (5).
  4. Chonchaiya W, Nguyen DV, Au J, Campos L, Berry-Kravis EM, Lohse K, Mu K, Utari A, et al. Clinical Involvement in daughters of men with fragile X- tremor ataxia syndrome. Clinical Genetic 2010 ; 78 : 38-46.
  5. Winarni TI, Utari A, Mundhofir FEP, Tong T, Durbin-Johnson B, Faradz SMH, Tassone F. Identification of Expanded Alleles of the FMR1 gene among High Risk Population in Indonesia using blood spot screening. Genetic Testing and Molecular Biomarkers, 2012, vol 16 (3): 162-166. DOI : 10.1089/gtmb.2011.0089.
  6. Winarni TI, Utari A, Mundhofir FE, Hagerman RJ, Faradz SMH. Fragile X syndrome: clinical, cytogenetics and molecular screening among autism spectrum disorder children in Indonesia. Clin Genet 2013. DOI : 10.1111/cge.12095.
  7. Mexitalia M, Yamauchi T, Utari A, Sjarif D, Subagio HW, Soemantri A, Takafumi I. The Role of uncoupling protein 2 and 3 genes polymorphism and energy expenditure in Indonesian Obese Children. J Pediatr Endocrinol Metab. 2013 ;26 (5-6) : 441-447. doi: 10.1515/jpem-2012-0311.
  8. Soetadji A, Suhartono, Kartini A, Budiyono, Hardaningsih G, Utari A. Aortic elasticity profile of children living in area of chronic organophosphate exposure: a preliminary study. Procedia Environmental Scinece 23 (2015) : 11-16.

National Journals

  1. Mexitalia M, Utari A, Sakundarno M, Yamauchi T, Subagio HW, Soemantri A. Sindroma metabolik pada remaja obesitas (Metabolic Syndrome in Obese Adolescense ). M Med Indones 2009; 43 (6). 2.
  2. Soetadji A, Utari A, Pratiwi R, Mexitalia M, Sbagjo HW. Hubungan kadar lipid darah dan hsCRP pada anak obesitas (The correlation between lipid profile and hsCRP on obese children). Med Hosp 2014; vol 2(3) : 162-66.