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Journal Articles

Clinical and Cytogenomic Features of Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21) in the Context of Constitutional Ring Chromosome 21

Tatiana Tvrdik, PhD MSc, Kristian T. Schafernak, MD MPH, Jeffrey R Jacobsen, MD, Reha Toydemir, MD PhD, Alexandra M Walsh, MD, Bo Hong, MD

Blood (2019) 134 (Supplement_1): 5208.

https://doi.org/10.1182/blood-2019-123766

Published: 2019

Journal Articles

Congenital Dyserythropoietic Anemia Type I Due to Biallelic CDAN1 mutations: Report from the Congenital Dyserythropoietic Anemia Registry (CDAR)

Omar Niss, MD, Robert B. Lorsbach, MD PhD, David K. Buchbinder, MD MSHS, Satheesh Chonat, MD, Morgan L. McLemore, MD, Timothy McCavit, MD, Jeffrey H Schwartz, MD, Jessica Meznarich, MD, Katie Seu, Wenying Zhang, MD PhD, Theodosia A. Kalfa, MD PhD

Blood (2019) 134 (Supplement_1): 3521.

https://doi.org/10.1182/blood-2019-128975

Published: 2019

Journal Articles

Large Genomic Deletions in Shwachman-Diamond Syndrome

Lisa J. McReynolds, MD PhD, Kristine Jones, BS, Kedest Teshome, BS, Alyssa Kennedy, MD PhD, Akiko Shimamura, MD PhD, Neelam Giri, MD, Blanche P. Alter, MD MPH, Sharon A. Savage, MD

Blood (2018) 132 (Supplement 1): 2586.

https://doi.org/10.1182/blood-2018-99-118495

Published: 2018

Journal Articles

Rare Case of Adult Onset DOCK8 Mutated Hyper Ige Syndrome

Damien Hansra, MD, Maureen Cioffi-Lavina, MD, Hugo Granada, MD, Brendan McIntyre, Cory Patrick, Sean Keniff

Blood (2017) 130 (Supplement 1): 4825.

https://doi.org/10.1182/blood.V130.Suppl_1.4825.4825

Published: 2017

Journal Articles

Polymorphonuclears Display a New Type of Abnormal Cytologic Granules (Chediak Higashi-Like) in a Very Rare Syndrome Linked to a Biallelic Defect of WDR81

Marion Eveillard, PharmD, PhD, Myriam Chevalier, Thomas Besnard, Benjamin Cogne, Alice Kuster, Stephane Bezieau, Marie C Bene, PharmSciD, PhD, Claire Beneteau

Blood (2016) 128 (22): 1331.

https://doi.org/10.1182/blood.V128.22.1331.1331

Published: 2016

Journal Articles

Rac1, but Not Rac2, Mediates Osteoclast Gain-of-Function Induced by Nf1 Haploinsufficiency.

Shi Chen, Jincheng Yan, Yingze Zhang, Yan Li, Xiaohong Li, Jin Yuan, Selina Eskwick, Todd D. Nebesio, Alexander Robling, Rebecca J. Chan, FengChun Yang

Blood (2007) 110 (11): 237.

https://doi.org/10.1182/blood.V110.11.237.237

Published: 2007

Journal Articles

Imatinib and Pregnancy.

S. Pye, Jorge Cortes, G. Rosti, P. Ault, T. Oliveto, R. Pilot, Hagop M. Kantarjian, Alan Hatfield, J. Apperley

Blood (2006) 108 (11): 431.

https://doi.org/10.1182/blood.V108.11.431.431

Published: 2006

Journal Articles

Hyperactivation of p21 ras and PI3-K Cooperate To Alter Murine and Human NF1 Haploinsufficient Osteoclast Functions.

Shi Chen, MD, Alexander Robling, Ph.D., Xiaohong Li, Jin Yuan, Janet Hock, Ph.D., David A. Ingram, M.D., D. Wade Clapp, M.D., Fengchun Yang, MD, PhD

Blood (2006) 108 (11): 675.

https://doi.org/10.1182/blood.V108.11.675.675

Published: 2006

Journal Articles

Efficacy of Aprotinin in Reducing Blood Loss in Paediatric Patients Undergoing Major Spinal Surgery.

Hayley M. Greenfield, MRCP, Vesna Colovic, MRCP, Maged I. Gharib, MRCPath, Sarah Rushman, MRCP, Davendra K. Patel, MRCP, Andrew M. Will, FRCP, Robert W.M. Walker, MRCP

Blood (2004) 104 (11): 2716.

https://doi.org/10.1182/blood.V104.11.2716.2716

Published: 2004

Journal Articles

The Use of Recombinant Activated Factor VII for Controlling Bleeding in Pediatric Patients Undergoing Invasive Surgeries.

Ampaiwan Chuansumrit, MD, Sumate Teeraratkul, MD, Sukasom Attanawanich, MD, Pracha Nantnarumit, MD, Suradej Hongeng, MD, Suthep Wanitkun, MD, Junya Jirapradittha, MD, Mali Rungreungvanich, MD, Taweesak Janwityanujit, MD, Teerachai Chantarojanasiri, MD

Blood (2004) 104 (11): 4011.

https://doi.org/10.1182/blood.V104.11.4011.4011

Published: 2004

NARROW

Clinical and Cytogenomic Features of Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21) in the Context of Constitutional Ring Chromosome 21

Congenital Dyserythropoietic Anemia Type I Due to Biallelic CDAN1 mutations: Report from the Congenital Dyserythropoietic Anemia Registry (CDAR)

Large Genomic Deletions in Shwachman-Diamond Syndrome

Rare Case of Adult Onset DOCK8 Mutated Hyper Ige Syndrome

Polymorphonuclears Display a New Type of Abnormal Cytologic Granules (Chediak Higashi-Like) in a Very Rare Syndrome Linked to a Biallelic Defect of WDR81

Rac1, but Not Rac2, Mediates Osteoclast Gain-of-Function Induced by Nf1 Haploinsufficiency.

Imatinib and Pregnancy.

Hyperactivation of p21 ras and PI3-K Cooperate To Alter Murine and Human NF1 Haploinsufficient Osteoclast Functions.

Efficacy of Aprotinin in Reducing Blood Loss in Paediatric Patients Undergoing Major Spinal Surgery.

The Use of Recombinant Activated Factor VII for Controlling Bleeding in Pediatric Patients Undergoing Invasive Surgeries.

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American Society of Hematology

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American Society of Hematology

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