Martina Sukova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 18 publications

TCF3::HLF Fusion Gene in a Pediatric B-Cell Lymphoblastic Lymphoma With Multifocal Osteolytic Lesions: Expanding the Clinical and Molecular Landscape.

TCF3::HLF Fusion Gene in a Pediatric B-Cell Lymphoblastic Lymphoma With Multifocal Osteolytic Lesions: Expanding the Clinical and Molecular Landscape.

Journal: Pediatric blood & cancer

Published: October 29, 2025

Epigenetic risk stratification in juvenile myelomonocytic leukemia by targeted methylation analysis of the BMP4 locus.

Epigenetic risk stratification in juvenile myelomonocytic leukemia by targeted methylation analysis of the BMP4 locus.

Journal: Clinical epigenetics

Published: June 02, 2025

Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiency.

Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiency.

Journal: Blood cancer journal

Published: December 13, 2024

Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factor.

Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factor.

Journal: Haematologica

Published: June 27, 2024

Proliferative glomerulonephritis with monoclonal IgG deposits in an adolescent successfully treated with daratumumab.

Proliferative glomerulonephritis with monoclonal IgG deposits in an adolescent successfully treated with daratumumab.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 25, 2024

Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria.

Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria.

Journal: Journal of pediatric hematology/oncology

Published: June 04, 2023

Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome.

Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome.

Journal: Haematologica

Published: May 25, 2023

Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic.

Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic.

Journal: Italian journal of pediatrics

Published: May 27, 2022

Hydrops fetalis and failure of hematopoietic stem cell transplantation - A long route to the diagnosis of SPTA1-associated hereditary spherocytosis.

Hydrops fetalis and failure of hematopoietic stem cell transplantation - A long route to the diagnosis of SPTA1-associated hereditary spherocytosis.

Journal: Blood cells, molecules & diseases

Published: January 04, 2022

TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins.

TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins.

Journal: American journal of hematology

Published: December 23, 2021

Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions.

Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions.

Journal: Blood cells, molecules & diseases

Published: August 30, 2019

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.

Journal: Haematologica

Published: October 15, 2015

Showing 1-12 of 18

Last Updated: 09/26/2026