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Journal Articles

Heterozygous Mutations of Clpb As a Newly Identified and Frequent Cause of Severe Congenital Neutropenia

Julia T Warren, MD PhD, Peeradol Wattanasirakul, David H Spencer, MD, Adam Locke, PhD, Vahagn Makaryan, MD, Audrey Anna Bolyard, RN, BS, Karl Welte, Julia Skokowa, MD PhD, David C. Dale, MD, Daniel C. Link, MD

Blood (2019) 134 (Supplement_1): 433.

https://doi.org/10.1182/blood-2019-129635

Published: 2019

Journal Articles

Regulation of Erythroid Heme Synthesis By the Mitochondrial Clpx Unfoldase

Catherine Rondelli, Aiden Danoff, Hector Bergonia, Samantha Gillis, Julia Free, John D. Phillips, PhD, Yvette Y Yien, PhD

Blood (2019) 134 (Supplement_1): 427.

https://doi.org/10.1182/blood-2019-132039

Published: 2019

Journal Articles

Hematological Disorders in Human Patients with Son Mutations

Lana Vukadin, Jung-Hyun Kim, PhD, Tara Bly Hackwelder, Nathan Ungerleider, PhD, Erik Flemington, Eun-Young Erin Ahn, PhD

Blood (2019) 134 (Supplement_1): 3709.

https://doi.org/10.1182/blood-2019-130616

Published: 2019

Journal Articles

Characterizing Dyskeratosis Congenita Caused By Parn Mutations in the Zebrafish

Anna Cordeiro, PhD, Adam P Deveau, MSc, Santhosh Dhanraj, PhD, Yigal Dror, MDFRCPC, Jason Berman, MD

Blood (2019) 134 (Supplement_1): 3744.

https://doi.org/10.1182/blood-2019-130147

Published: 2019

Journal Articles

Family Trio-Based Whole Genome Optical Mapping Identifies Candidate Structural Variations Predisposing Children to Acute Lymphoblastic Leukemia

Ute Fischer, PhD, Layal Yasin, PhD, Julia Täubner, PhD, Triantafyllia Brozou, MD, Arndt Borkhardt, MD

Blood (2019) 134 (Supplement_1): 5201.

https://doi.org/10.1182/blood-2019-130014

Published: 2019

Journal Articles

Electronic Health Record Tools to Promote Transition Readiness and Knowledge for Adolescents and Young Adults with Hemophilia

Jacob Parker, Clinical Informaticist, Katharine Farrow, RN, BSN, Rosalie Brooks, RN, Danielle Leonard, BS, Fernanda Cortez, Courtney D. Thornburg, MD

Blood (2019) 134 (Supplement_1): 4685.

https://doi.org/10.1182/blood-2019-124561

Published: 2019

Journal Articles

Phenotypes of Diamond Blackfan Anemia Patients with RPL35A Haploinsufficiency Due to 3q29 Deletion Compared with RPL35A Single Nucleotide Variants or Small Insertion/Deletions

Neelam Giri, MD, Matthew Gianferante, MD, Evangelia Atsidaftos, MA, MPH, Marcin W. Wlodarski, MD PhD, Paola Quarello, MD, Jana Volejnikova, MD, Polyxeni Delaporta, MD, Vijay G. Sankaran, MD PhD, Jason E. Farrar, MD, Maryam Hussain, MPH, Lisa J. McReynolds, MD PhD, Antonis Kattamis, Jeffrey M Lipton, MD PhD, Charlotte Niemeyer, MD, Dagmar Pospisilova, MD PhD, Ugo Ramenghi, MD, Sharon A. Savage, MD, Adrianna Vlachos, MD, Blanche P. Alter, MD MPH

Blood (2018) 132 (Supplement 1): 3854.

https://doi.org/10.1182/blood-2018-99-117171

Published: 2018

Journal Articles

Hemostatic Effect of the Combination of Factor VIII Concentrate with Tranexamic Acid (TXA) in the Prophylactic Setting in Severe Hemophilia a

Maissaa Janbain, MD, Nathalie Enjolras, PhD, Jean-Claude Bordet, Radu Bolbos, Cindy A. Leissinger, MD, Yesim Dargaud, MD PhD

Blood (2018) 132 (Supplement 1): 2490.

https://doi.org/10.1182/blood-2018-99-119407

Published: 2018

Journal Articles

Ruxolitinib and Steroid Refractory/Dependent Bronchiolitis Obliterans after Hematopoietic Cell Transplantation: A Steroid Sparing Agent That Also Resulted in Improved Lung Function in Children

Michelle Schoettler, MD, Meera Subramaniam, MD, Steven P. Margossian, MD PhD

Blood (2018) 132 (Supplement 1): 3407.

https://doi.org/10.1182/blood-2018-99-114971

Published: 2018

Journal Articles

Ten New Cases of Hermansky-Pudlak Syndrome in the Iberian Peninsula: Identification of Novel Genetic Variants in HPS3, HPS4, HPS6 and DTNBP1 Associated with Significant Clinical Complications

Blood (2018) 132 (Supplement 1): 1147.

https://doi.org/10.1182/blood-2018-99-112968

Published: 2018

Journal Articles

Macrophage Protease-Activated Receptor 2 Regulates Fetal Liver Hematopoiesis in Mice

Mona Saffarzadeh, PhD, Wolfram Ruf, MD

Blood (2018) 132 (Supplement 1): 134.

https://doi.org/10.1182/blood-2018-99-112829

Published: 2018

Journal Articles

Practice Patterns in the Use of MRI/MRA and Chronic Transfusion Therapy for Monitoring and Treatment of Stroke in Pediatric Patients with Sickle Cell Anemia

Alyssa M Schlenz, PhD, Martina Mueller, PhD, Shannon Phillips, PhD RN, Cathy Melvin, PhD MPH, Robert J. Adams, MD MS, Julie Kanter, MD

Blood (2018) 132 (Supplement 1): 4716.

https://doi.org/10.1182/blood-2018-99-116968

Published: 2018

Journal Articles

A Retrospective Assessment of Prevention and Treatment of Iron Deficiency Amongst Patients Requiring Peripartum Transfusion

Heather Vandermeulen, MD, Yulia Lin, MD FRCPC, Anne McLeod, MD, Jon Barrett, MD, Michelle Sholzberg, MDM, MSc, FRCPC, Jeannie Callum, MD

Blood (2018) 132 (Supplement 1): 1264.

https://doi.org/10.1182/blood-2018-99-115594

Published: 2018

Journal Articles

Developmental Outcomes of Children Exposed to Maternal Sickle Cell Disease (SCD)

Martha Brucato, PhD, Xiaobin Wang, MD ScD, Sophie Lanzkron, MD

Blood (2017) 130 (Supplement 1): 983.

https://doi.org/10.1182/blood.V130.Suppl_1.983.983

Published: 2017

Journal Articles

Adipocyte Induced Antagonism of ALL Growth Highlights a Novel Inhibitory Niche and Potential Therapeutic Opportunity

Nicholas Warrick, BSc, Farideh Miraki-Moud, PhD, A Aicher, Linda Ariza McNaughton, Pedro Casado-Izquierdo, Ai Nagano, PhD, Rebecca Carroll, Dominique Bonnet, PhD, John G. Gribben, MDDSc FMedSci, Bela Patel, MD

Blood (2017) 130 (Supplement 1): 371.

https://doi.org/10.1182/blood.V130.Suppl_1.371.371

Published: 2017

Journal Articles

Constitutional Ring Chromosome 21 Predisposes to Acute Lymphoblastic Leukaemia (ALL) with iAMP21

Claire Schwab, Eigil Kjeldsen, MD DMSc, Nyla A. Heerema, PhD, Andrew Carroll, PhD, Matthew Bashton, PhD, Sarra Ryan, PhD, Anthony V. Moorman, PhD, Stephen P. Hunger, MD, Mignon L. Loh, MD, Henrik Hasle, MD PhD, Christine J Harrison, PhD FRCPath

Blood (2017) 130 (Supplement 1): 3978.

https://doi.org/10.1182/blood.V130.Suppl_1.3978.3978

Published: 2017

Journal Articles

Copper Deficiency

Allison Close, MD, Lynn M. Malec, MD MSc

Blood (2017) 130 (Supplement 1): 4742.

https://doi.org/10.1182/blood.V130.Suppl_1.4742.4742

Published: 2017

Journal Articles

Co-Expression and Functional Interaction between CXCR4 and CD74 in Chronic Lymphocytic Leukemia

Tharshika Thavayogarajah, Dzmitry Sinitski, PhD, Jens P. Panse, MD, Idit Shachar, Professor, PhD, Tim H. Brümmendorf, MD, Jürgen Bernhagen, Professor, PhD, Steffen Koschmieder

Blood (2017) 130 (Supplement 1): 1724.

https://doi.org/10.1182/blood.V130.Suppl_1.1724.1724

Published: 2017

Journal Articles

A novel recombinant human thrombopoietin therapy for the management of immune thrombocytopenia in pregnancy

Zhangyuan Kong, Ping Qin, Shan Xiao, Hai Zhou, Hong Li, Renchi Yang, Xiaofan Liu, Jianmin Luo, Zhichun Li, Guochao Ji, Zhongguang Cui, Yusheng Bai, Yuxia Wu, Linlin Shao, Jun Peng, Jun Ma, Ming Hou

Blood (2017) 130 (9): 1097–1103.

https://doi.org/10.1182/blood-2017-01-761262

Published: 2017

Journal Articles

DNMT3A -Dependent DNA Methylation May Act As a Tumor Suppressor-Not a Tumor Promoter-during AML Progression

David Spencer, MDPhD, David Russler-Germain, Nichole M Helton, B.S., Tamara L Lamprecht, B.S., Marwan Shinawi, MD, Peter Westervelt, MD PhD, Jacqueline E. Payton, MD PhD, Robert S. Fulton, PhD, Richard K Wilson, PhD, Matthew J. Walter, MD, Daniel C. Link, MD, John F. DiPersio, MD, PhD, Timothy J. Ley, MD

Blood (2016) 128 (22): 1050.

https://doi.org/10.1182/blood.V128.22.1050.1050

Published: 2016

NARROW

Heterozygous Mutations of Clpb As a Newly Identified and Frequent Cause of Severe Congenital Neutropenia

Regulation of Erythroid Heme Synthesis By the Mitochondrial Clpx Unfoldase

Hematological Disorders in Human Patients with Son Mutations

Characterizing Dyskeratosis Congenita Caused By Parn Mutations in the Zebrafish

Family Trio-Based Whole Genome Optical Mapping Identifies Candidate Structural Variations Predisposing Children to Acute Lymphoblastic Leukemia

Electronic Health Record Tools to Promote Transition Readiness and Knowledge for Adolescents and Young Adults with Hemophilia

Phenotypes of Diamond Blackfan Anemia Patients with RPL35A Haploinsufficiency Due to 3q29 Deletion Compared with RPL35A Single Nucleotide Variants or Small Insertion/Deletions

Hemostatic Effect of the Combination of Factor VIII Concentrate with Tranexamic Acid (TXA) in the Prophylactic Setting in Severe Hemophilia a

Ruxolitinib and Steroid Refractory/Dependent Bronchiolitis Obliterans after Hematopoietic Cell Transplantation: A Steroid Sparing Agent That Also Resulted in Improved Lung Function in Children

Ten New Cases of Hermansky-Pudlak Syndrome in the Iberian Peninsula: Identification of Novel Genetic Variants in HPS3, HPS4, HPS6 and DTNBP1 Associated with Significant Clinical Complications

Macrophage Protease-Activated Receptor 2 Regulates Fetal Liver Hematopoiesis in Mice

Practice Patterns in the Use of MRI/MRA and Chronic Transfusion Therapy for Monitoring and Treatment of Stroke in Pediatric Patients with Sickle Cell Anemia

A Retrospective Assessment of Prevention and Treatment of Iron Deficiency Amongst Patients Requiring Peripartum Transfusion

Developmental Outcomes of Children Exposed to Maternal Sickle Cell Disease (SCD)

Adipocyte Induced Antagonism of ALL Growth Highlights a Novel Inhibitory Niche and Potential Therapeutic Opportunity

Constitutional Ring Chromosome 21 Predisposes to Acute Lymphoblastic Leukaemia (ALL) with iAMP21

Copper Deficiency

Co-Expression and Functional Interaction between CXCR4 and CD74 in Chronic Lymphocytic Leukemia

A novel recombinant human thrombopoietin therapy for the management of immune thrombocytopenia in pregnancy

DNMT3A -Dependent DNA Methylation May Act As a Tumor Suppressor-Not a Tumor Promoter-during AML Progression

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American Society of Hematology

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ASH Publications

American Society of Hematology

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