Steven J Steinberg
Overview
Explore the profile of Steven J Steinberg including associated specialties, affiliations and a list of published articles.
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25
Citations
780
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0
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Recent Articles
1.
Moser A, Liu Y, Shi X, Schrifl U, Hiebler S, Fatemi A, et al.
J Cell Biochem
. 2021 May;
122(10):1337-1349.
PMID: 34056752
X-linked adrenoleukodystrophy (XALD) is a genetic neurologic disorder with multiple phenotypic presentations and limited therapeutic options. The childhood cerebral phenotype (CCALD), a fatal demyelinating disorder affecting about 35% of patients,...
2.
De Biase I, Tortorelli S, Kratz L, Steinberg S, Cusmano-Ozog K, Braverman N
Genet Med
. 2019 Dec;
22(4):686-697.
PMID: 31822849
Peroxisomal disorders are a clinically and genetically heterogeneous group of diseases caused by defects in peroxisomal biogenesis or function, usually impairing several metabolic pathways. Peroxisomal disorders are rare; however, the...
3.
Falkenberg K, Braverman N, Moser A, Steinberg S, Klouwer F, Schluter A, et al.
Am J Hum Genet
. 2017 Dec;
101(6):965-976.
PMID: 29220678
Zellweger spectrum disorders (ZSDs) are autosomal-recessive disorders that are caused by defects in peroxisome biogenesis due to bi-allelic mutations in any of 13 different PEX genes. Here, we identified seven...
4.
Arnold B, Schiff K, Ercumen A, Benjamin-Chung J, Steele J, Griffith J, et al.
Am J Epidemiol
. 2017 May;
186(7):866-875.
PMID: 28498895
Rainstorms increase levels of fecal indicator bacteria in urban coastal waters, but it is unknown whether exposure to seawater after rainstorms increases rates of acute illness. Our objective was to...
5.
Braverman N, Raymond G, Rizzo W, Moser A, Wilkinson M, Stone E, et al.
Mol Genet Metab
. 2016 Jan;
117(3):313-21.
PMID: 26750748
Peroxisome biogenesis disorders in the Zellweger spectrum (PBD-ZSD) are a heterogeneous group of genetic disorders caused by mutations in PEX genes responsible for normal peroxisome assembly and functions. As a...
6.
Wang X, Yik W, Zhang P, Lu W, Huang N, Kim B, et al.
Stem Cell Res Ther
. 2015 Aug;
6:158.
PMID: 26319495
Introduction: Zellweger spectrum disorder (PBD-ZSD) is a disease continuum caused by mutations in a subset of PEX genes required for normal peroxisome assembly and function. They highlight the importance of...
7.
Mints Y, Yarmohammadi H, Khurram I, Hoyt H, Hansford R, Zimmerman S, et al.
Clin Med Insights Cardiol
. 2015 May;
9:39-45.
PMID: 26005361
Aims: Recent studies have shown that several genetic variants near the PITX2 locus on chromosome 4q25 are associated with atrial fibrillation (AF). However, the mechanism that mediates this association remains...
8.
Tran C, Hewson S, Steinberg S, Mercimek-Mahmutoglu S
Pediatr Neurol
. 2014 Aug;
51(2):262-5.
PMID: 25079577
Background: Zellweger spectrum disorder is an autosomal recessively inherited multisystem disorder caused by one of the 13 different PEX gene defects resulting in defective peroxisomal assembly and multiple peroxisomal enzyme...
9.
Hiebler S, Masuda T, Hacia J, Moser A, Faust P, Liu A, et al.
Mol Genet Metab
. 2014 Feb;
111(4):522-532.
PMID: 24503136
Zellweger spectrum disorder (ZSD) is a disease continuum that results from inherited defects in PEX genes essential for normal peroxisome assembly. These autosomal recessive disorders impact brain development and also...
10.
Wang X, Yik W, Zhang P, Lu W, Dranchak P, Shibata D, et al.
Stem Cell Res Ther
. 2012 Oct;
3(5):39.
PMID: 23036268
Introduction: X-linked adrenoleukodystrophy (X-ALD) is a complex disorder with variable expressivity that affects the nervous, adrenocortical and male reproductive systems. Although ABCD1 mutations are known to provide the genetic basis...