A Brehm
Overview
Explore the profile of A Brehm including associated specialties, affiliations and a list of published articles.
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Articles
63
Citations
2381
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Recent Articles
1.
Gusmao L, Antao-Sousa S, Faustino M, Abovich M, Aguirre D, Alghafri R, et al.
Forensic Sci Int Genet
. 2025 Feb;
76:103232.
PMID: 39893847
The analysis of STRs located on the X chromosome has been one of the strategies used to address complex kinship cases. Its usefulness is, however, limited by the low availability...
2.
Brehm A, Nguyen K, Blackham K, Psychogios M
AJNR Am J Neuroradiol
. 2022 Oct;
43(11):1621-1626.
PMID: 36202555
Background And Purpose: Patients with acute ischemic stroke are increasingly triaged with one-stop management approaches, resulting in baseline imaging with a flat detector CT scanner. This study aimed to estimate...
3.
Maurer C, Dobrocky T, Joachimski F, Neuberger U, Demerath T, Brehm A, et al.
AJNR Am J Neuroradiol
. 2020 Feb;
41(3):464-468.
PMID: 32029470
Background And Purpose: Large intracranial vessel occlusion due to calcified emboli is a rare cause of major stroke. We assessed the prevalence, imaging appearance, the effectiveness of mechanical thrombectomy, and...
4.
Brehm A, Tsogkas I, Maier I, Eisenberg H, Yang P, Liu J, et al.
AJNR Am J Neuroradiol
. 2019 Jul;
40(8):1330-1334.
PMID: 31296523
Background And Purpose: In-hospital time delays lead to a relevant deterioration of neurologic outcomes in patients with stroke with large-vessel occlusions. At the moment, CT perfusion is relevant in the...
5.
Roetzer K, Uyanik G, Brehm A, Zwerina J, Zandieh S, Czech T, et al.
Bone
. 2017 Dec;
107:154-160.
PMID: 29208525
The Wnt signalling pathway is a critical regulator of bone mass and quality. Several heterozygous mutations in the LRP5 gene, a Wnt co-receptor, causing high bone mass (LRP5-HBM) have been...
6.
Spinola H, Lemos A, Couto A, Parreira B, Soares M, Dutra I, et al.
Int J Immunogenet
. 2017 Aug;
44(6):305-313.
PMID: 28834219
This study confirms for Madeira Island (Portugal) population the Type 1 Diabetes (T1D) susceptible and protective Human leucocyte antigens (HLA) markers previously reported in other populations and adds some local...
7.
Feist E, Brehm A, Kallinich T, Kruger E
Z Rheumatol
. 2017 Jan;
76(4):328-334.
PMID: 28124745
Functional disorders of the proteasome can have a severe impact on the innate immune system. Characterized by an autosomal recessive mode of inheritance, this novel type of interferonopathy is considered...
8.
Spinola H, Lemos A, Couto A, Parreira B, Soares M, Dutra I, et al.
Int J Immunogenet
. 2016 Dec;
44(1):27-31.
PMID: 28032448
This study shows, for the first time, high-resolution allele frequencies of HLA-DQA1 loci in Madeira Island (Portugal) and allows us to better understand and refine present knowledge on DQB1 variation,...
9.
Pereira A, Palma Dos Reis R, Rodrigues R, Sousa A, Gomes S, Borges S, et al.
Physiol Genomics
. 2016 Sep;
48(11):810-815.
PMID: 27614204
Recent genetic studies have revealed an association between polymorphisms at the ADAMTS7 gene locus and coronary artery disease (CAD) risk. Functional studies have shown that a CAD-associated polymorphism (rs3825807) affects...
10.
Effects of pioglitazone versus glimepiride exposure on hepatocellular fat content in type 2 diabetes
Phielix E, Brehm A, Bernroider E, Krssak M, Anderwald C, Krebs M, et al.
Diabetes Obes Metab
. 2013 Apr;
15(10):915-22.
PMID: 23574533
Aims: Thiazoledinediones decrease blood glucose by their insulin-sensitizing properties. Here, we examined whether pioglitazone plus nateglinide (PIO) interferes with hepatocellular lipid (HCL) content and/or improves insulin sensitivity in well-controlled non-obese...