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Journal Articles

Acquired 1p Uniparental Disomy Is Associated with Biallelic MPL W515L Mutation in RARS-T.

Hadrian Szpurka, MSc, PhD, Lukasz P Gondek, MD, Sanjay R Mohan, MD, Eric D Hsi, MD, Karl S Theil, MD, Mikkael A Sekeres, MD, MS, Jaroslaw P Maciejewski, MD, PhD

Blood (2008) 112 (11): 1643.

https://doi.org/10.1182/blood.V112.11.1643.1643

Published: 2008

Journal Articles

Proteinase-3 Deficiency Contributes to Thrombotic Risk in PNH

Anna M. Jankowska, MSc, Hadrian Szpurka, MSc, PhD, Andrew E. Schade, MD, PhD, Sanjay R. Mohan, MD, Jaroslaw P. Maciejewski, MD, PhD

Blood (2008) 112 (11): 406.

https://doi.org/10.1182/blood.V112.11.406.406

Published: 2008

Journal Articles

Dysfunction of Lipid Raft Microdomains and Defective Apoptotic Signal Transduction in PNH.

Hadrian Szpurka, MSc, Andrew E. Schade, MD, PhD, Mahrukh K. Ganapathi, PhD, Jaroslaw P. Maciejewski, MD, PhD

Blood (2006) 108 (11): 122.

https://doi.org/10.1182/blood.V108.11.122.122

Published: 2006

Journal Articles

Hemochromatois-Associated Gene Mutations in Patients with Myelodysplastic Syndromes with Refractory Anemia and Ringed Sideroblasts.

Zachary P. Nearman, BS, Bianca Serio, MD, Hadrian Szpurka, MSc, Ilka Warshawsky, MD,PhD, Alan Lichtin, MD, Mikkael A. Sekeres, MD, MS, Jaroslaw P. Maciejewski, MD, PhD

Blood (2006) 108 (11): 1541.

https://doi.org/10.1182/blood.V108.11.1541.1541

Published: 2006

Journal Articles

Presence of JAK2 Mutations in MDS/MPD-u WHO Classified Patients and Not Other Forms of MDS Suggests Their Derivation from Classical Myeloproliferative Syndrome.

Hadrian Szpurka, MSc, Ramon Tiu, MD, Eric Hsi, MD, Alan E. Lichtin, MD, Mikkael A. Sekeres, MD, MS, Karl S. Theil, MD, Jaroslaw P. Maciejewski, MD, PhD

Blood (2005) 106 (11): 369.

https://doi.org/10.1182/blood.V106.11.369.369

Published: 2005

Journal Articles

Increased Frequency of Polymorphisms in XRCC3 and OGG1 Genes in Patients with MDS.

Hadrian Szpurka, MSc, Abdo Haddad, MD, Soumit Basu, MD, PhD, Mikkael Sekeres, MD, MSc, Jaroslaw P. Maciejewski, MD, PhD

Blood (2005) 106 (11): 3445.

https://doi.org/10.1182/blood.V106.11.3445.3445

Published: 2005

NARROW

Acquired 1p Uniparental Disomy Is Associated with Biallelic MPL W515L Mutation in RARS-T.

Proteinase-3 Deficiency Contributes to Thrombotic Risk in PNH

Dysfunction of Lipid Raft Microdomains and Defective Apoptotic Signal Transduction in PNH.

Hemochromatois-Associated Gene Mutations in Patients with Myelodysplastic Syndromes with Refractory Anemia and Ringed Sideroblasts.

Presence of JAK2 Mutations in MDS/MPD-u WHO Classified Patients and Not Other Forms of MDS Suggests Their Derivation from Classical Myeloproliferative Syndrome.

Increased Frequency of Polymorphisms in XRCC3 and OGG1 Genes in Patients with MDS.

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ASH Publications

American Society of Hematology

Acquired 1p Uniparental Disomy Is Associated with Biallelic MPL W515L Mutation in RARS-T.

Proteinase-3 Deficiency Contributes to Thrombotic Risk in PNH

Dysfunction of Lipid Raft Microdomains and Defective Apoptotic Signal Transduction in PNH.

Hemochromatois-Associated Gene Mutations in Patients with Myelodysplastic Syndromes with Refractory Anemia and Ringed Sideroblasts.

Presence of JAK2 Mutations in MDS/MPD-u WHO Classified Patients and Not Other Forms of MDS Suggests Their Derivation from Classical Myeloproliferative Syndrome.

Increased Frequency of Polymorphisms in XRCC3 and OGG1 Genes in Patients with MDS.

Email alerts

ASH Publications

American Society of Hematology

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