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dr. Yulia Ariani, Sp.A(K)

Primaya Hospital Bekasi Barat

HariWaktu

Senin

07:45-08:00

Selasa

07:45-08:00

Rabu

07:45-08:00

Kamis

07:45-08:00

Jumat

07:45-08:00

Sabtu

10:00-10:30

dr. Yulia Ariani, Sp.A(K) sebagai Dokter Spesialis Anak yang berpraktik di Primaya Hospital Bekasi Barat. dr Yulia Ariani menempuh pendidikan Kedokteran Spesialis Anak – Universitas Indonesia.

Adapun pelayanan medis yang dapat beliau berikan yakni Konsultasi kesehatan anak menyeluruh. dr. Yulia juga merupakan anggota dari Ikatan Dokter Anak Indonesia (IDI).

Pendidikan

- Medical doctor, Faculty of medicine, Universitas Indonesia, 1990 -1996

- Pediatrician, Department of Clidh Health, Cipto Mangunkusumo Hospital Jakarta, 2002 -2008

- Course on Genetic epidemiology and statistic genetics, Leuven University, Belgium, 2006

- Medical Genetic course, Diponegoro University -Radboud University, 2011

- Workshop on Molecular and cytogenetics analysis, 2011

- Course on cytogenetics and microarray, UMC Utrecht, Netherlands, 2011

- Course on microarray, UMC Utrecht, Netherlands, 2014

- Course on NGS, UMC Nijmegen, Netherlands, 2014

- Course on radiologic examination of Inborn error of metabolism patients, Manchester, UK, 2014

- Fellow of Pediatric Nutrition and Metabolic Diseases, FMUI, Jakarta, Indonesia, 2016-2019

- Master Class of MPS, Singapore, 2016

- Course on Clinical genetics, Hong Kong, 2016

- The 1st summit on Genetics and Genomic medicine, National Human Genome Research Institute (NHGRI), National Institutes of Health (NIH), Bethesda, Washington, USA, 2016

- Clinical attachment on inborn metabolic diseases, Department of Pediatric, University Medical Center Groningen, Netherlands, 2018

- Doctoral program of Biomedical science FMUI, Jakarta, Indonesia, 2013-2019

Sub Spesialisasi

Konsultan Nutrisi dan Penyakit Metabolik Anak

Pengalaman Kerja

- Medical team of Center of Excellence for Indonesian Rare Diseases, RSCM-FKUI

- Senior staff of Human Genetic Center IMERI FKUI

- Dokter Spesialis Anak di Primaya Hospital Bekasi Barat

- Dokter Spesialis Anak Konsultan di RSU Bunda Menteng Jakarta Pusat

Publikasi

- Secondary nephrotic syndrome due to Hodgkin lymphoma, 1st author, National Congress oh Child Health, Bandung, Indonesia, 2004

- Profile of tetanus patients in pediatric ward Cipto Mangunkusumo Hospital, Jakarta in 1995-2000, 1st author, National Congress oh Child Health, Bandung, Indonesia, 2004

- Diagnosis and treatment of supra ventricular tachycardia in children, 1st author, Annual Meeting of Child Heath, Yogyakarta, Indonesia, 2007

- Diagnosis and treatment of secondary nephritic syndrome due to Hodgkin lymphoma, 1st author, Sari Pediatri Journal, Indonesia, 2006

- Besarnya kontribusi 4eneti 4enetic dan lingkungan terhadap variasi Indeks Massa Tubuh pada keluarga dengan proban obes: sebuah penelitian pendahuluan melalui pendekatan 4enetic4c dengan menggunakan program SAGE, 1st author, Thesis, 2007

- Genetic and environmental contributions to body mass index variability of the obese proband's family. A preliminary study with biometrical approach using SAGE software, 1st author, National Obesity Symposium VII, Jakarta, 2009

- Genetic and environmental contributions to body mass index variability of the obese proband's family. A preliminary study with biometrical approach using SAGE software, 1st author, Annual Meeting of Child Health First winner of Young Researcher Award, 2010

- Konseling 4enetic:antara kebutuhan dan keterbatasan (editorial), 1st author, Majalah Kedokteran Indonesia, 2010

- Identification of new mutation on NPHS1 genes in congenital nephrotic syndrome patient, 1st author, Asia Pacific Conference on Human Genetics, Kuala Lumpur, 2012

- Role of Genetic and Environment on body mass variability in obese children, 1st author, Asia Pacific Conference on Human Genetics, Kuala Lumpur, 2012

- Evaluation on level of knowledge and skills of third year medical students to do prenatal counseling, 1st author, Majalah Kedokteran Indonesia, 2012

- Loss of heterozigosity in child with multiple congenital anomaly, 1st author, Ann Transl Med. 2015 Sep; 3(Suppl 2): AB170, 2015

- Developing diagnostic strategy of multiple congenital anomalies in Indonesia, 2nd author, Ann Transl Med. 2015 Sep; 3(Suppl 2): AB016., 2015

- DNA-array profiles of 8 children with multiple congenital anomalies, 1st author, The 1st Asian Researcher Symposium, 2016, Indonesia, 2016

- Identification of a Novel Variant in Exon 5 of Galactosamine (N-Acetyl)-6-Sulfatase (GALNS) Gene in Mucopolysaccharidosis IVA Patients in Indonesia. Ariani Y, Priambodo R, Sjarif DR., J Natural Sc Biol Med. 2019.

- Mutation Analysis of Exon 8 of the Iduronate-2-Sulfatase Gene in Mucopolysaccharidosis Type II Patients in Indonesia.

- Identification of A Deletion Variant in Exon 9 of Iduronate 2-Sulfatase Gene in Patients with Type II. Ariani Y, Priambodo R, Hafifah CN, Sjarif DR. J Natural Sc Biol Med. 2019.

- Profile of Iduronate 2-Sulphatase (IDS) gene variants from Indonesian Mucopolysaccharidosis type II Patients: A Preliminary Study, Ariani Y, Priambodo R, Hafifah CN, Sjarif DR, 13th Asia Pacific Conference on Human Genetics, Manila, Philippine. 2019

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