Abdul Salam M Sofro
Overview
Explore the profile of Abdul Salam M Sofro including associated specialties, affiliations and a list of published articles.
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8
Citations
68
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0
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Recent Articles
1.
Ioannidis A, Blanco-Portillo J, Sandoval K, Hagelberg E, Barberena-Jonas C, Hill A, et al.
Nature
. 2021 Sep;
597(7877):522-526.
PMID: 34552258
Polynesia was settled in a series of extraordinary voyages across an ocean spanning one third of the Earth, but the sequences of islands settled remain unknown and their timings disputed....
2.
Yuliwulandari R, Prayuni K, Razari I, Susilowati R, Zulhamidah Y, Soedarsono S, et al.
Pharmacogenomics
. 2021 Jan;
22(3):157-163.
PMID: 33399479
Owing to the high resistance rate of tuberculosis (TB) to isoniazid, which is metabolized by -acetyltransferase 2 (NAT2), we investigated the associations between variants and multidrug-resistant (MDR)-TB. The acetylator status...
3.
Yuliwulandari R, Prayuni K, Susilowati R, Sofro A, Tokunaga K, Shin J
Pharmacogenomics
. 2019 Nov;
20(18):1303-1311.
PMID: 31699005
We investigated the contribution of NAT2 variants and acetylator status to anti-tuberculosis drug-induced liver injury (AT-DILI) severity. 100 patients with clinically severe AT-DILI and 210 non-AT-DILI controls were subjected to...
4.
Rujito L, Basalamah M, Siswandari W, Setyono J, Wulandari G, Mulatsih S, et al.
Hematol Oncol Stem Cell Ther
. 2016 Mar;
9(2):55-63.
PMID: 27009595
Objective/background: Thalassemia is a monogenic hematologic disease that has the highest prevalence globally. In addition, there is complexity of the genetic background associated with a variety of phenotypes presented among...
5.
Rujito L, Sasongko T, Mulatsih S, Sofro A
Hemoglobin
. 2015 Aug;
39(6):452-3.
PMID: 26291969
No abstract available.
6.
Rujito L, Basalamah M, Mulatsih S, Sofro A
Hemoglobin
. 2015 Aug;
39(5):330-3.
PMID: 26291967
Thalassemia is the most prevalent genetic blood disorder worldwide, and particularly prevalent in Indonesia. The purpose of this study was to determine the spectrum of β-thalassemia (β-thal) mutations found in...
7.
Rujito L, Mulatsih S, Sofro A
N Am J Med Sci
. 2015 Jun;
7(5):194-8.
PMID: 26110130
Background: Thalassemia is a collection of genetic impairments in beta and alpha genes causing various states of anemia. Severe types of the disease need lifelong transfusions, leading to oxidant-antioxidant disturbance...
8.
Sadewa A, Sunarti , Sutomo R, Hayashi C, Lee M, Ayaki H, et al.
Kobe J Med Sci
. 2003 Feb;
48(5-6):137-44.
PMID: 12594357
The presence of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene has been regarded as a genetic risk factor for coronary artery diseases and neural tube defects. Although the...