Tatjana Kilo
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 11 publications
Sitosterolemia-An Underdiagnosed and Heterogeneous Lipid Disorder. A Case Series From a Tertiary Care Centre in Australia.
Journal: Journal of paediatrics and child health
Published: July 07, 2024
Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy.
Journal: European journal of human genetics : EJHG
Published: January 03, 2024
COVID-19-associated rhabdomyolysis in a paediatric patient with sickle cell trait.
Journal: Journal of paediatrics and child health
Published: November 07, 2021
A novel cause of DKC1-related bone marrow failure: Partial deletion of the 3' untranslated region.
Journal: EJHaem
Published: August 22, 2020
Telomere Length Measurement by Molecular Combing.
Journal: Frontiers in cell and developmental biology
Published: February 14, 2020
Safety and effectiveness of stoss therapy in children with vitamin D deficiency.
Journal: Journal of paediatrics and child health
Published: June 29, 2018
Goldilocks meets heparin dosing-enough but not too much.
Journal: The Journal of thoracic and cardiovascular surgery
Published: March 02, 2018
Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding.
Journal: Journal of thrombosis and haemostasis : JTH
Published: June 29, 2017
York platelet syndrome is a CRAC channelopathy due to gain-of-function mutations in STIM1.
Journal: Molecular genetics and metabolism
Published: December 15, 2014
Persistent MRD before and after allogeneic BMT predicts relapse in children with acute lymphoblastic leukaemia.
Journal: British journal of haematology
Published: July 14, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026