J. Prchal

发表

Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection

J. Harley, A. Carroll, Prchal Jf, 1980 .

Genetic Adaptation to Extreme Hypoxia. Study of High-Altitude Pulmonary Edema in a Three Generations of Chinese Han Family

T. Simonson, Ying-zhong Yang, R. Ge, 2013 .

Association of G6PD202A,376G with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia

M. Gladwin, G. Kato, O. Castro, 2010, British journal of haematology.

Developmental changes in iron metabolism and erythropoiesis in mice with human gain‐of‐function erythropoietin receptor

K. Kapralova, V. Divoky, Jihyun Song, 2022, American journal of hematology.

Polymorphisms in African-Americans

E. Beutler, Wanda Kuhl, A. Kay, 2006 .

Perspective: Pivotal translational hematology and therapeutic insights in chronic myeloid hematopoietic stem cell malignancies

R. Bejar, T. Brümmendorf, T. Barbui, 2022, Hematological oncology.

Non‐anemic homozygous βo thalassemia in an African‐American family: Association of high fetal hemoglobin levels with β thalassemia alleles

M. Mrug, V. Divoky, D. Thornley‐Brown, 2001 .

Splenectomy for hematologic disease.

J. Carpenter, H. L. Laws, M. Conrad, 1979, Surgery, gynecology & obstetrics.

Tissue factor activity is increased in neutrophils from JAK2 V617F‐mutated essential thrombocythemia and polycythemia vera patients

R. Pawlinski, N. Key, Soo Jin Kim, 2021, American journal of hematology.

Hemolytic anemia, recurrent metabolic acidosis, and incomplete albinism associated with glutathione synthetase deficiency.

W. Crist, J. Prchal, M. Roper, 1983, Blood.

Sickle cell acute chest syndrome associated with parvovirus B19 infection: Case series and review

J. Prchal, R. Player, E. Lowenthal, 1996, American journal of hematology.

Possible association of 3′ UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency

N. S. Reading, M. Sirdah, J. Prchal, 2017, Hematology.

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

J. Prchal, E. Lowenthal, 1995, Blood.

β‐Thalassemia Due to Intronic LINE‐1 Insertion in the β‐Globin Gene (HBB): Molecular Mechanisms Underlying Reduced Transcript Levels of the β‐GlobinL1 Allele

J. Issa, V. Divoky, J. Prchal, 2013, Human mutation.

Novel compound VHL heterozygosity (VHL T124A/L188V) associated with congenital polycythaemia

L. Lanikova, F. Lorenzo, Chunzhang Yang, 2013, British journal of haematology.

Recommendations for diagnosis and treatment of methemoglobinemia

A. Iolascon, A. Kulozik, R. Russo, 2021, American journal of hematology.

Clinical utility of next‐generation sequencing in the diagnosis of hereditary haemolytic anaemias

S. Perkins, M. Salama, H. Yaish, 2016, British journal of haematology.

Extramedullary blast transformation in the central nervous system in idiopathic myelofibrosis

C. W. Scott, J. Prchal, H. Barnes, 1981, American journal of hematology.

Triosephosphate isomerase deficiency: Repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families

J. Prchal, E. Beutler, R. Berkow, 1995, American journal of hematology.

P1005: A PHASE 1, OPEN-LABEL, DOSE-ESCALATION STUDY OF SELINEXOR PLUS RUXOLITINIB IN PATIENTS WITH TREATMENT-NAÏVE MYELOFIBROSIS

S. Tantravahi, K. Chamoun, A. Kishtagari, 2022, HemaSphere.

A randomized phase 3 trial of interferon-α vs hydroxyurea in polycythemia vera and essential thrombocythemia

A. Mead, J. Tripodi, V. Najfeld, 2022, Blood.

Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestry.

Timothy M. Bahr, R. Christensen, A. Agarwal, 2021, Blood cells, molecules & diseases.

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

L. Jorde, C. Huff, T. Simonson, 2015, Experimental physiology.

Successful treatment of thrombotic thrombocytopenia purpura by vincristine

M. Schreeder, J. Prchal, 1983, American journal of hematology.

Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of Methemoglobinemia

A. Iolascon, A. Kulozik, R. Russo, 2021, HemaSphere.

Concomitant JAK2 V617F‐positive polycythemia vera and B‐cell chronic lymphocytic leukemia in three patients originating from two separate hematopoietic stem cells

J. Jelinek, M. Jarošová, K. Indrák, 2013, American journal of hematology.

Biomarkers of erythropoiesis response to intravenous iron in a crossover pilot study in unexplained anemia of the elderly.

H. Cohen, A. Artz, J. Yoo, 2023, Hematology.

Increased blood reactive oxygen species and hepcidin in obstructive sleep apnea precludes expected erythrocytosis

C. Lundby, T. Ganz, K. Indrák, 2023, American journal of hematology.

Novel, de novo, beta‐globin variant with decreased oxygen affinity (HBB:c.317T>A, “Hemoglobin St. George”) in a healthy child with low oxygen saturations and anemia

F. Kuypers, R. Christensen, A. Agarwal, 2021, American journal of hematology/oncology.

Aberrant expression of microRNA in polycythemia vera

J. Prchal, A. Bashirullah, J. Prchal, 2008, Haematologica.

Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis.

B. Julian, J. Prchal, T. Stopka, 1998, Journal of the American Society of Nephrology : JASN.

Red Cells Red Cell Membrane Disorders

H. Bonkovsky, E. Beutler, P. Gallagher, 2005 .

The CYB5R3c.350C>G and G6PD A alleles modify severity of anemia in malaria and sickle cell disease

M. Gladwin, G. Kato, R. Machado, 2020, American journal of hematology.

Increased transferrin protects from thrombosis in Chuvash erythrocytosis

T. Ganz, V. Gordeuk, Xu Zhang, 2023, American journal of hematology.

Novel germline JAK2R715T mutation causing PV‐like erythrocytosis in 3 generations. Amelioration by Ropeg‐Interferon

L. Lanikova, S. Constantinescu, J. Prchal, 2024, American journal of hematology.