Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosis

Adaptive genetic changes related to haemoglobin concentration in native high-altitude Tibetans.

Experimental physiology·2015

End-tidal carbon monoxide as an indicator of the hemolytic rate.

Blood cells, molecules & diseases·2015

Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study.

Leukemia·2013

Lessons to better understanding of hypoxia sensing. Acquired and congenital mutations resulting in polycythemia.

Advances in experimental medicine and biology·2002

Non-anemic homozygous beta(o) thalassemia in an African-American family: association of high fetal hemoglobin levels with beta thalassemia alleles.

American journal of hematology·2001

Genetic heterogeneity of primary familial and congenital polycythemia.

American journal of hematology·2001

A new reporter strategy reveals a subset of nonmigratory hematopoietic stem cells located in a dynamic bone marrow niche.

Blood·2026

A randomized phase 2 study combining midostaurin, low-dose cytarabine and venetoclax in newly diagnosed AML ≥60 years.

Blood·2026

Cases of High-Titer Inhibitor Formation After AAV Gene Therapy for Hemophilia A.

Blood·2026

Genomic and clinical landscape of RAS mutations in acute myeloid leukemia.

Blood·2026

Molecular Consequences and Targeting of PPM1D Overexpression in Myeloproliferative Neoplasms.

Blood·2026

Ambient oxygen disrupts amino acid homeostasis and impairs human hematopoietic stem and progenitor cell engraftment.

Blood·2026

Microbiological aetiology of paediatric ventilator-associated pneumonia and risk factors for carbapenem-resistant acinetobacter and Pseudomonas in a tertiary-care hospital in Thailand.

Infection prevention in practice·2026

Effects of standardized parenteral nutrition on electrolyte balance: an observational study in preterm neonates.

Frontiers in nutrition·2026

Cochlear Implantation in a Child With Arnold-Chiari Syndrome, Severe Inner Ear Malformations, and Cochlear Nerve Hypoplasia: A Case Report.

The American journal of case reports·2026

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Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosis

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Adaptive genetic changes related to haemoglobin concentration in native high-altitude Tibetans.

End-tidal carbon monoxide as an indicator of the hemolytic rate.

Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study.

Lessons to better understanding of hypoxia sensing. Acquired and congenital mutations resulting in polycythemia.

Non-anemic homozygous beta(o) thalassemia in an African-American family: association of high fetal hemoglobin levels with beta thalassemia alleles.

Genetic heterogeneity of primary familial and congenital polycythemia.

A new reporter strategy reveals a subset of nonmigratory hematopoietic stem cells located in a dynamic bone marrow niche.

A randomized phase 2 study combining midostaurin, low-dose cytarabine and venetoclax in newly diagnosed AML ≥60 years.

Cases of High-Titer Inhibitor Formation After AAV Gene Therapy for Hemophilia A.

Genomic and clinical landscape of RAS mutations in acute myeloid leukemia.

Molecular Consequences and Targeting of PPM1D Overexpression in Myeloproliferative Neoplasms.

Ambient oxygen disrupts amino acid homeostasis and impairs human hematopoietic stem and progenitor cell engraftment.

Microbiological aetiology of paediatric ventilator-associated pneumonia and risk factors for carbapenem-resistant acinetobacter and Pseudomonas in a tertiary-care hospital in Thailand.

Effects of standardized parenteral nutrition on electrolyte balance: an observational study in preterm neonates.

Cochlear Implantation in a Child With Arnold-Chiari Syndrome, Severe Inner Ear Malformations, and Cochlear Nerve Hypoplasia: A Case Report.

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Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosis

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