Viviana Varela

Buenos Aires, C, Argentina

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 8 publications

The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature.

The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature.

Journal: Hemoglobin

Published: December 19, 2018

Two novel unstable hemoglobin variants due to in-frame deletions of key amino acids in the β-globin chain.

Two novel unstable hemoglobin variants due to in-frame deletions of key amino acids in the β-globin chain.

Journal: European journal of haematology

Published: January 02, 2018

Regulation of the β-globin gene family expression, useful in the search for new therapeutic targets for hemoglobinopathies

Regulation of the β-globin gene family expression, useful in the search for new therapeutic targets for hemoglobinopathies

Journal: Medicina

Published: December 14, 2016

Multiple copy number variants in a pediatric patient with Hb H disease and intellectual disability.

Multiple copy number variants in a pediatric patient with Hb H disease and intellectual disability.

Journal: American journal of medical genetics. Part A

Published: October 01, 2015

Molecular bases of α-thalassemia in Argentina

Molecular bases of α-thalassemia in Argentina

Journal: Medicina

Published: April 29, 2015

Hb Wilde and Hb Patagonia: two novel elongated beta-globin variants causing dominant beta-thalassemia.

Hb Wilde and Hb Patagonia: two novel elongated beta-globin variants causing dominant beta-thalassemia.

Journal: European journal of haematology

Published: September 26, 2014

Coinheritance of a novel mutation on the HBA1 gene: c.187delG (p.W62fsX66) [codon 62 (-G) (α1)] with the α212 patchwork allele and Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T].

Coinheritance of a novel mutation on the HBA1 gene: c.187delG (p.W62fsX66) [codon 62 (-G) (α1)] with the α212 patchwork allele and Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T].

Journal: Hemoglobin

Published: June 29, 2013

Identification of a new HBA1 gene mutation (HBA1:c.301-2A>T) in cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser].

Identification of a new HBA1 gene mutation (HBA1:c.301-2A>T) in cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser].

Journal: Hemoglobin

Published: June 29, 2012

Showing 1-8 of 8

Last Updated: 09/26/2026