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Journal Articles

Inversion of Chromosome 12 and Translocations of 12q13-q15 In Primary Myelofibrosis (PMF) Are Associated with Disease Progression and a Poor Prognosis

Vesna Najfeld, PhD, Joseph Tripodi, Nathaniel Wisch, MD, Amory Novoselac, MD, Heike L. Pahl, PhD, Ronald Hoffman, MD

Blood (2010) 116 (21): 4110.

https://doi.org/10.1182/blood.V116.21.4110.4110

Published: 2010

Journal Articles

Pivotal role of mast cells in pruritogenesis in patients with myeloproliferative disorders

Takefumi Ishii, Jiapeng Wang, Wei Zhang, John Mascarenhas, Ronald Hoffman, Ying Dai, Nathaniel Wisch, Mingjiang Xu

Blood (2009) 113 (23): 5942–5950.

https://doi.org/10.1182/blood-2008-09-179416

Published: 2009

Journal Articles

The Relationship Between Chromosomally Abnormal Hematopoiesis and the JAK2V617F Allele Burden in Patients (pts) with Ph-Negative Chronic Myeloproliferative Disorders (Ph-neg MPD)

Xialoli Wang, MD, Ph.D., Amanda Leblanc, Steven Gruenstein, MD, Mingjiang Xu, Ph.D., Nathaniel Wisch, MD, Ronald Hoffman, MD, Vesna Najfeld, Ph.D

Blood (2008) 112 (11): 3106.

https://doi.org/10.1182/blood.V112.11.3106.3106

Published: 2008

Journal Articles

Mast Cells Are Involved by the Malignant Process and Play An Important Role in the Pruritogenesis in Patients with Myeloproliferative Disorders

Takefumi Ishii, M.D., Ph.D., Jiapeng Wang, Wei Zhang, John Mascarenhas, M.D., Ying Dai, Vesna Najfeld, Ph.D, Ronald Hoffman, M.D., Nathaniel Wisch, M.D., Mingjiang Xu, M.D., Ph.D.

Blood (2008) 112 (11): 3729.

https://doi.org/10.1182/blood.V112.11.3729.3729

Published: 2008

Journal Articles

Familial Hypohaptoglobinemia : A Genetically Determined Trait Segregating from Glucose-6-Phosphate Dehydrogenase Deficiency

ARLAN GOTTLIEB, M.D., NATHANIEL WISCH, M.D., JOHN ROSS, Ph.D.

Blood (1963) 21 (2): 129–140.

https://doi.org/10.1182/blood.V21.2.129.129

Published: 1963

NARROW

Inversion of Chromosome 12 and Translocations of 12q13-q15 In Primary Myelofibrosis (PMF) Are Associated with Disease Progression and a Poor Prognosis

Pivotal role of mast cells in pruritogenesis in patients with myeloproliferative disorders

The Relationship Between Chromosomally Abnormal Hematopoiesis and the JAK2V617F Allele Burden in Patients (pts) with Ph-Negative Chronic Myeloproliferative Disorders (Ph-neg MPD)

Mast Cells Are Involved by the Malignant Process and Play An Important Role in the Pruritogenesis in Patients with Myeloproliferative Disorders

Familial Hypohaptoglobinemia : A Genetically Determined Trait Segregating from Glucose-6-Phosphate Dehydrogenase Deficiency

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ASH Publications

American Society of Hematology

Inversion of Chromosome 12 and Translocations of 12q13-q15 In Primary Myelofibrosis (PMF) Are Associated with Disease Progression and a Poor Prognosis

Pivotal role of mast cells in pruritogenesis in patients with myeloproliferative disorders

The Relationship Between Chromosomally Abnormal Hematopoiesis and the JAK2V617F Allele Burden in Patients (pts) with Ph-Negative Chronic Myeloproliferative Disorders (Ph-neg MPD)

Mast Cells Are Involved by the Malignant Process and Play An Important Role in the Pruritogenesis in Patients with Myeloproliferative Disorders

Familial Hypohaptoglobinemia : A Genetically Determined Trait Segregating from Glucose-6-Phosphate Dehydrogenase Deficiency

Email alerts

ASH Publications

American Society of Hematology

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