Marilu Fiegenbaum
Overview
Explore the profile of Marilu Fiegenbaum including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
52
Citations
420
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Rodrigues M, Mattos D, Almeida S, Fiegenbaum M
Hematol Transfus Cell Ther
. 2024 Sep;
46 Suppl 5:S246-S257.
PMID: 39242288
Background: Hemolytic disease of the fetus and newborn is a public health problem caused by maternal-fetal incompatibility; no prophylaxis is available for most alloantibodies that induce this disease. This study...
2.
Deconte D, Diniz B, Hartmann J, de Souza M, Zottis L, Gazzola Zen P, et al.
Int J Mol Sci
. 2024 Jul;
25(14).
PMID: 39063141
variants have been associated with a wide range of ciliopathies, mainly Joubert syndrome (JS, OMIM #616490) and short-rib thoracic dysplasia syndrome (SRTD, OMIM #616546). However, the hypothesis that this gene...
3.
Soares S, Aquino J, Petrolli F, de Oliveira T, Almeida S, Fiegenbaum M
Hematol Transfus Cell Ther
. 2022 Jun;
45(3):317-323.
PMID: 35715379
Introduction: To date, 340 antigen-organized 43 blood group systems are recognized, being ABO, Rh, Kell, Duffy, Kidd, MNS and Diego the most clinically relevant. The aim of this study was...
4.
Todendi P, Brand C, Silveira J, Burns R, Martinez J, Fiegenbaum M, et al.
Int J Environ Res Public Health
. 2021 Sep;
18(18).
PMID: 34574727
The human locus rs16835198 contributes positively to anthropometric phenotypes in children and adolescents. However, the role of specific components of physical fitness in this relationship is not known. The present...
5.
Rodrigues M, Hoher G, Waskow G, Hutz M, Lindenau J, Petzl-Erler M, et al.
Genet Mol Biol
. 2021 Apr;
44(2):e20200255.
PMID: 33877261
The study presents comparisons between blood group frequencies beyond ABO and Rh blood systems in Native American populations and previously published data from Brazilian blood donors. The frequencies of Diego...
6.
Alves A, de Moura A, Felipe Andreolla H, da Veiga A, Fiegenbaum M, Giovenardi M, et al.
Genet Mol Biol
. 2021 Apr;
44(2):e20190373.
PMID: 33821873
Any condition leading to chronic liver disease is a potential oncogenic agent for hepatocellular carcinoma (HCC). Alterations in the expression of antioxidant enzymes could alter the redox balance. Our aim...
7.
Deconte D, Correia E, Haubert G, de Souza V, Correia J, Maahs M, et al.
J Pediatr Genet
. 2021 Feb;
10(1):63-69.
PMID: 33552642
Cherubism is a rare genetic condition characterized by a bone nonneoplastic disease. We aimed to report a 6-year-old girl with cherubism presenting similar cases in the maternal family. However, her...
8.
Todendi P, Brand C, Silveira J, Gaya A, Agostinis-Sobrinho C, Fiegenbaum M, et al.
Scand J Med Sci Sports
. 2020 Dec;
31(4):894-902.
PMID: 33274504
Obesity is an important risk factor associated with non-communicable cardiometabolic diseases. Previous studies have indicated that children and adolescents with a predisposed genetic risk for obesity could benefit from an...
9.
Mousquer G, Peres A, Fiegenbaum M
Tuberculosis (Edinb)
. 2020 Nov;
126:102020.
PMID: 33246269
Tuberculosis (TB) and coronavirus disease 2019 (COVID-19) are currently the two main causes of death among infectious diseases. There is an increasing number of studies trying to elucidate the interactions...
10.
Deconte D, Kreusch T, Salvaro B, Perin W, Ferreira M, Kopacek C, et al.
J Pediatr Genet
. 2020 Aug;
9(4):263-269.
PMID: 32765931
Kenny-Caffey syndrome (KCS) is a rare genetic condition characterized by growth retardation, bone abnormalities, and hypoparathyroidism. Herein, we report an unusual case of a 10-year-old girl with Kenny-Caffey syndrome type...