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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

Deciphering the Causal Diagnosis of Hydrops Fetalis or Unexplained Fetal Anemia Using Targeted Next Generation and Exome Sequencing

Julie Galimand, Helene Bourdeau, Odile Fenneteau, Sophie Dreux, Nathalie Couque, PharmD, Severine Drunat, PharmD, PhD, Serge Pissard, PhD, Thierry Leblanc, MD, Anne Lambilliotte, MD, Catherine Thong Vanh, Caroline Alby, jelena-Hélène martinovic-Bouriel, Chloé Quelin, Mohandas Narla, DSc, Anne Cortey, Lydie Da Costa

Blood (2019) 134 (Supplement_1): 3519.

https://doi.org/10.1182/blood-2019-127432

Published: 2019

Journal Articles

Is There a Role for Titre Monitoring in Kell Alloimmunized Pregnancies?

Evangelia Vlachodimtropoulou Koumoutsea, MBBS,PhDBSc, Maciej W Garbowski, MD PhD, Gareth Seaward, MD, Rory Windrim, MD, Johannes Keunen, Edmond Kelly, MB, BCh, BAO, DCH, FRCPC, FAAP, Tim VanMieghem, MD PhD, Nadine Shehata, MDFRCPC,MSc, Greg Ryan, MD

Blood (2019) 134 (Supplement_1): 1174.

https://doi.org/10.1182/blood-2019-125144

Published: 2019

Journal Articles

Evaluation of Phenotype-Genotype Correlation in Two Common PIEZO1 Mutations p.R2456H and p.L2495_E2495dup

Mary Risinger, PhD, Vandy Black, MDMSc, Loan Hsieh, MD, Renee C. Prins, MD, Jill Menell, MD, Mohamad Badawi, MD, Cynthia Rutherford, MD, Karen L. Bride, MD PhD, Omar Niss, MD, Charles T. Quinn, MD, Katie Giger Seu, PhD, Wenying Zhang, MDPhD, Theodosia A. Kalfa, MD PhD

Blood (2018) 132 (Supplement 1): 1040.

https://doi.org/10.1182/blood-2018-99-117299

Published: 2018

Journal Articles

Dysregulated Transcriptional Upregulation of Cell-Cycle Regulators By KLF1 Mutation E325K Induces Cell-Cycle Arrest in Erythroid Cells Differentiated from the Congenital Dyserythropoietic Anemia (CDA)-Patient Specific Induced Pluripotent Stem Cells

Hiroshi Kohara, PhD, Taiju Utsugisawa, MD PhD, Hiromi Ogura, MD PhD, Ai Sugawara, B.Sc., Ogawa Yoshie, M.Sc., Chika Sakamoto, M.Sc., Hitoshi Kanno, MDPhD, Kenzaburo Tani, MD PhD

Blood (2017) 130 (Supplement 1): 2197.

https://doi.org/10.1182/blood.V130.Suppl_1.2197.2197

Published: 2017

Journal Articles

Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes

Marcin W. Wlodarski, MD PhD, Lydie M. Da Costa, MD PhD, Marie-Francoise O'-Donohue, Marc Gastou, Ina Hainmann, Enikoe Amina Szvetnik, Thierry Leblanc, MD, Marc Bierings, MD PhD, Nathalie Montel-Lehry, Hannah Tamary, MD, Charlotte M. Niemeyer, MD, Pierre-Emmanuel Gleizes, Alyson W. MacInnes

Blood (2017) 130 (Supplement 1): 1172.

https://doi.org/10.1182/blood.V130.Suppl_1.1172.1172

Published: 2017

Journal Articles

Serum Ferritin Underestimates Liver Iron Concentration in Patients with Homozygous Alpha-0 Thalassemia

Ali Amid, MD, Shiyi Chen, Uma Athale, Karen Charpentier, Manuela Merelles-Pulcini, Isaac Odame, Melanie Ann Kirby-Allen

Blood (2017) 130 (Supplement 1): 3504.

https://doi.org/10.1182/blood.V130.Suppl_1.3504.3504

Published: 2017

Journal Articles

An international registry of survivors with Hb Bart's hydrops fetalis syndrome

Duantida Songdej, Christian Babbs, Douglas R. Higgs

Blood (2017) 129 (10): 1251–1259.

https://doi.org/10.1182/blood-2016-08-697110

Published: 2017

Includes: Supplemental data

Journal Articles

Generation and Functional Analysis of Congenital Dyserythropoietic Anemia (CDA) Patient-Specific Induced Pluripotent Stem Cells

Hiroshi Kohara, PhD, Hiromi Ogura, MD PhD, Takako Aoki, MLS, Chika Sakamoto, Yoshie Ogawa, Shohei Miyamoto, PhD, Hitoshi Kanno, MD PhD, Kenzaburo Tani, MD PhD

Blood (2016) 128 (22): 2426.

https://doi.org/10.1182/blood.V128.22.2426.2426

Published: 2016

Journal Articles

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

Satheesh Chonat, MD, Mary Risinger, Neha Dagaonkar, Tamara Maghathe, Jennifer Rothman, MD, Jessica Connor, Karen Kalinyak, MD, Amber H Begtrup, PhD, Kejian Zhang, MD MBA, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 941.

https://doi.org/10.1182/blood.V126.23.941.941

Published: 2015

Journal Articles

A New and Extensive α 0 Deletion in a Brazilian Patient with Hb H Disease

Natália Oliveira Mota, Master Student, Elza Miyuki Kimura, B.Sc., Roberta Dorta Ferreira, Dulcineia Albuquerque, PhD, Daniela Maria Ribeiro, Magnun Santos, Fernando F Costa, MD, PhD, Maria Fatima Sonati, PhD

Blood (2015) 126 (23): 2160.

https://doi.org/10.1182/blood.V126.23.2160.2160

Published: 2015

Journal Articles

Introduction of a Treatment Approach for Chronic Myeloid Leukemia and Pregnancy Considering Leukemic Burden and Pregnancy Terms

Ekaterina Chelysheva, Anna Turkina, Prof., MD, Evgenia Polushkina, Roman G. Shmakov, MD

Blood (2015) 126 (23): 5144.

https://doi.org/10.1182/blood.V126.23.5144.5144

Published: 2015

Journal Articles

Congenital Dyserythropoietic Anemia Type 1: A New Variant Pathogenic CDAN1 Mutation

Jenny McDaniel, MD, Stuart Cramer, D.O.

Blood (2015) 126 (23): 4551.

https://doi.org/10.1182/blood.V126.23.4551.4551

Published: 2015

Journal Articles

KLF1 -null neonates display hydrops fetalis and a deranged erythroid transcriptome

Graham W. Magor, Michael R. Tallack, Kevin R. Gillinder, Charles C. Bell, Naomi McCallum, Bronwyn Williams, Andrew C. Perkins

Blood (2015) 125 (15): 2405–2417.

https://doi.org/10.1182/blood-2014-08-590968

Published: 2015

Includes: Supplemental data

Journal Articles

KLF1 Null Neonates Display Hydrops Fetalis and a Deranged Erythroid Transcriptome

Andrew C Perkins, MDPhD, Graham Magor, BSc, Michael R Tallack, BSc PhD, Kevin R Gillinder, BSc PhD, Charles Bell, BSc, Bronwyn Williams, MBBS,FRACP,FRCPA

Blood (2014) 124 (21): 2700.

https://doi.org/10.1182/blood.V124.21.2700.2700

Published: 2014

Journal Articles

Red Blood Cell Alloimmunization and Hemolytic Disease of the Fetus and Newborn: New Approaches Using Animal Models

Jeanne E. Hendrickson, MD

Blood (2013) 122 (21): SCI-49.

https://doi.org/10.1182/blood.V122.21.SCI-49.SCI-49

Published: 2013

Journal Articles

Alfa Thalassemia Intermedia (HbH disease): How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Susanna Barella, MD, Ramon Simon-Lopez, MD, Nicola Di Gaetano, BS, PhD, Renzo Galanello, MD

Blood (2012) 120 (21): 5180.

https://doi.org/10.1182/blood.V120.21.5180.5180

Published: 2012

Journal Articles

An Unusual Presentation of Congenital Dyserythropoietic Anemia Type II (CDAII) Associated with Severe Anemia in a Patient with a Novel Mutation of the SEC23B Gene

Melanie A Villanueva, DO, Carol J Saunders, Ph.D, David Zwick, MD, Laurie Smith, MD, PhD, Darrell Dinwiddie, PhD, Emily Farrow, PhD, Neil Miller, BA, Stephen Kingsmore, M.B., Ch.B., B.A.O., D.Sc., Keith J. August, M.D., M.Sc.

Blood (2012) 120 (21): 990.

https://doi.org/10.1182/blood.V120.21.990.990

Published: 2012

Journal Articles

Significance of Low Levels of Glucose-6-Phosphate Dehydrogenase Levels in Pregnancy

Rangaswamy Chintapatla, MD, Hrvoje Melinscak, MD, Mala Varma, MD

Blood (2012) 120 (21): 5165.

https://doi.org/10.1182/blood.V120.21.5165.5165

Published: 2012

Journal Articles

Circulating mitotic figures in CMV-associated hydrops fetalis

Ronald Jackups, Mitra Mehrad

Blood (2012) 119 (14): 3201.

https://doi.org/10.1182/blood-2011-06-364778

Published: 2012

NARROW

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

Deciphering the Causal Diagnosis of Hydrops Fetalis or Unexplained Fetal Anemia Using Targeted Next Generation and Exome Sequencing

Is There a Role for Titre Monitoring in Kell Alloimmunized Pregnancies?

Evaluation of Phenotype-Genotype Correlation in Two Common PIEZO1 Mutations p.R2456H and p.L2495_E2495dup

Dysregulated Transcriptional Upregulation of Cell-Cycle Regulators By KLF1 Mutation E325K Induces Cell-Cycle Arrest in Erythroid Cells Differentiated from the Congenital Dyserythropoietic Anemia (CDA)-Patient Specific Induced Pluripotent Stem Cells

Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes

Serum Ferritin Underestimates Liver Iron Concentration in Patients with Homozygous Alpha-0 Thalassemia

An international registry of survivors with Hb Bart's hydrops fetalis syndrome

Generation and Functional Analysis of Congenital Dyserythropoietic Anemia (CDA) Patient-Specific Induced Pluripotent Stem Cells

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

A New and Extensive α 0 Deletion in a Brazilian Patient with Hb H Disease

Introduction of a Treatment Approach for Chronic Myeloid Leukemia and Pregnancy Considering Leukemic Burden and Pregnancy Terms

Congenital Dyserythropoietic Anemia Type 1: A New Variant Pathogenic CDAN1 Mutation

KLF1 -null neonates display hydrops fetalis and a deranged erythroid transcriptome

KLF1 Null Neonates Display Hydrops Fetalis and a Deranged Erythroid Transcriptome

Red Blood Cell Alloimmunization and Hemolytic Disease of the Fetus and Newborn: New Approaches Using Animal Models

Alfa Thalassemia Intermedia (HbH disease): How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

An Unusual Presentation of Congenital Dyserythropoietic Anemia Type II (CDAII) Associated with Severe Anemia in a Patient with a Novel Mutation of the SEC23B Gene

Significance of Low Levels of Glucose-6-Phosphate Dehydrogenase Levels in Pregnancy

Circulating mitotic figures in CMV-associated hydrops fetalis

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American Society of Hematology

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American Society of Hematology

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