Juliana Teo

Sydney, NSW, Australia

Last Updated: 09/26/2026

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Found 13 publications

Mixed Autoimmune Hemolytic Anemia With Refractory Cold Agglutinin Syndrome in a Child Successfully Treated With Serial Whole Blood Exchange Transfusions and Immunosuppression.

Mixed Autoimmune Hemolytic Anemia With Refractory Cold Agglutinin Syndrome in a Child Successfully Treated With Serial Whole Blood Exchange Transfusions and Immunosuppression.

Journal: Journal of pediatric hematology/oncology

Published: June 17, 2025

Germline mutations in a G protein identify signaling cross-talk in T cells.

Germline mutations in a G protein identify signaling cross-talk in T cells.

Journal: Science (New York, N.Y.)

Published: September 19, 2024

Hematologic Manifestations in Primary Mitochondrial Diseases.

Hematologic Manifestations in Primary Mitochondrial Diseases.

Journal: Journal of pediatric hematology/oncology

Published: December 20, 2023

Sickle cell disease in Australia: a snapshot from the Australian Haemoglobinopathy Registry.

Sickle cell disease in Australia: a snapshot from the Australian Haemoglobinopathy Registry.

Journal: Internal medicine journal

Published: March 23, 2023

SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.

SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.

Journal: Human mutation

Published: January 26, 2021

A novel cause of DKC1-related bone marrow failure: Partial deletion of the 3' untranslated region.

A novel cause of DKC1-related bone marrow failure: Partial deletion of the 3' untranslated region.

Journal: EJHaem

Published: August 22, 2020

Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunity.

Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunity.

Journal: Nature immunology

Published: September 11, 2018

Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.

Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.

Journal: Blood

Published: August 02, 2018

Cardiac iron load and function in transfused patients treated with deferasirox (the MILE study).

Cardiac iron load and function in transfused patients treated with deferasirox (the MILE study).

Journal: European journal of haematology

Published: August 08, 2016

A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias.

A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias.

Journal: British journal of haematology

Published: February 22, 2016

LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure.

LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure.

Journal: JIMD reports

Published: July 29, 2015

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.

Journal: Blood

Published: September 11, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026