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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

Whole Exome Sequencing Identifies a Novel Variant in the Pklr Gene Which Worsen the Anemia Status in a Congenital Dyserthropoietic Anemia Patient

Ching-Tien Peng, MD PhD

Blood (2018) 132 (Supplement 1): 4880.

https://doi.org/10.1182/blood-2018-99-112743

Published: 2018

Journal Articles

Identification of a Digenic Inheritance of Pklr and KLF1 Mutations Resulting in Hemolytic Anemia in a Neonate from a Study of Genotype-Phenotype Correlation of Globin, Pklr and KLF1 in Thai Patients with Pyruvate Kinase (PK) Deficiency

Supachai Ekwattanakit, BSc, PhD MD, Suchada Riolueang, M.Sc., Kalaya Tachavanich, Hitoshi Kanno, MDPhD, Vip Viprakasit, MD DPhil, Thidarat Suksangpleng, PhD, Vorravarn S Tanphaichitr

Blood (2017) 130 (Supplement 1): 3477.

https://doi.org/10.1182/blood.V130.Suppl_1.3477.3477

Published: 2017

Journal Articles

Umbilical Cord Blood Hemogram: What Is the Effect of Maternal Anemia?

Rithika Rajendran, MBBS, Febe Renjitha Suman, MD, Reddy Salmon Sudheer Raj, MSc MLT, Paidipamula Rajesh Kanna, MSc MLT, Naga Raju Borra, MSc MLT

Blood (2015) 126 (23): 4536.

https://doi.org/10.1182/blood.V126.23.4536.4536

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

Non-Invasive Protocol For The Screening, Diagnosis and Treatment Of Hemolytic Perinatal

Nancy Rodriguez, Pilar Noguerol, Lutgardo García, Hada Macher, Magdalena Carmona, MD, Jesús Martín, Jose Antonio Pérez Simon

Blood (2013) 122 (21): 2405.

https://doi.org/10.1182/blood.V122.21.2405.2405

Published: 2013

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

Alloantibodies to a paternally derived RBC KEL antigen lead to hemolytic disease of the fetus/newborn in a murine model

Sean R. Stowell, Kate L. Henry, Nicole H. Smith, Krystalyn E. Hudson, Greg R. Halverson, Jaekeun C. Park, Ashley M. Bennett, Kathryn R. Girard-Pierce, C. Maridith Arthur, Silvia T. Bunting, James C. Zimring, Jeanne E. Hendrickson

Blood (2013) 122 (8): 1494–1504.

https://doi.org/10.1182/blood-2013-03-488874

Published: 2013

Journal Articles

Tropomodulin3-Null Mice Are Embryonic Lethal with Anemia and Impaired Definitive Erythropoiesis in the Fetal Liver

Roberta B. Nowak, B.S., Andrea Bacconi, Ph.D., Zhenhua Sui, Ph.D., Nancy E. Kim, B.S., Velia M. Fowler, PhD

Blood (2011) 118 (21): 1036.

https://doi.org/10.1182/blood.V118.21.1036.1036

Published: 2011

Journal Articles

ISWI Chromatin Remodeling ATPase Smarca5 (Snf2h) Is Required for Murine Erythroid Development and Globin Gene Regulation

Juraj Kokavec, Romit Majumdar, PhD, Martina Kapalova, Nikola Curik, Filipp Savvulidi, Emanuel Necas, Arthur I. Skoultchi, PhD, Tomas Stopka, MD, PhD

Blood (2010) 116 (21): 2062.

https://doi.org/10.1182/blood.V116.21.2062.2062

Published: 2010

Journal Articles

Early Intravenous Immunoglobulin (IVIG) Therapy and Non Invasive Fetal Monitoring in Rh Alloimmunization (AI) and Pregnancy

Santhosh Ambika, M.D, Glenn Wong, D.O, Amandeep Salhotra, M.D, Maria Falzon, M.D, Lucy Bayer- Zwirello, M.D., Rekha Parameswaran, MD

Blood (2008) 112 (11): 4069.

https://doi.org/10.1182/blood.V112.11.4069.4069

Published: 2008

Journal Articles

Anti-Glycophorin C Induces a Loss of Mitochondrial Membrane Potential but Fails To Activate Apoptotic Caspases.

Gregory A. Denomme, PhD, Jonathan Micieli, Jenny Shu, Dan Wang, PhD, Bernard J. Fernandes, MD

Blood (2007) 110 (11): 4097.

https://doi.org/10.1182/blood.V110.11.4097.4097

Published: 2007

Journal Articles

Pbx1 Regulates the Self-Renewal of Long-Term Hematopoietic Stem Cells by Maintaining Their Quiescence.

Francesca Ficara, PhD, Mark J. Murphy, Ph.D., Min Lin, Ph.D, Michael L. Cleary, M.D.

Blood (2007) 110 (11): 94.

https://doi.org/10.1182/blood.V110.11.94.94

Published: 2007

Journal Articles

A global role for EKLF in definitive and primitive erythropoiesis

Denise Hodge, Elise Coghill, Janelle Keys, Tina Maguire, Belinda Hartmann, Alasdair McDowall, Mitchell Weiss, Sean Grimmond, Andrew Perkins

Blood (2006) 107 (8): 3359–3370.

https://doi.org/10.1182/blood-2005-07-2888

Published: 2006

Journal Articles

The Transcription Factor Pbx1 Is Required for the Development of Double Positive Thymic T Cells.

Mrinmoy Sanyal, PhD, James W. Tung, PhD, Sussan Dejbakhsh-Jones, PhD, Samuel Strober, MD, Leonore A. Herzenberg, PhD, Michael L. Cleary, MD

Blood (2004) 104 (11): 2771.

https://doi.org/10.1182/blood.V104.11.2771.2771

Published: 2004

Journal Articles

Targeted disruption of the activating transcription factor 4 gene results in severe fetal anemia in mice

Howard C. Masuoka, Tim M. Townes

Blood (2002) 99 (3): 736–745.

https://doi.org/10.1182/blood.V99.3.736

Published: 2002

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?

Whole Exome Sequencing Identifies a Novel Variant in the Pklr Gene Which Worsen the Anemia Status in a Congenital Dyserthropoietic Anemia Patient

Identification of a Digenic Inheritance of Pklr and KLF1 Mutations Resulting in Hemolytic Anemia in a Neonate from a Study of Genotype-Phenotype Correlation of Globin, Pklr and KLF1 in Thai Patients with Pyruvate Kinase (PK) Deficiency

Umbilical Cord Blood Hemogram: What Is the Effect of Maternal Anemia?

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

Non-Invasive Protocol For The Screening, Diagnosis and Treatment Of Hemolytic Perinatal

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

Alloantibodies to a paternally derived RBC KEL antigen lead to hemolytic disease of the fetus/newborn in a murine model

Tropomodulin3-Null Mice Are Embryonic Lethal with Anemia and Impaired Definitive Erythropoiesis in the Fetal Liver

ISWI Chromatin Remodeling ATPase Smarca5 (Snf2h) Is Required for Murine Erythroid Development and Globin Gene Regulation

Early Intravenous Immunoglobulin (IVIG) Therapy and Non Invasive Fetal Monitoring in Rh Alloimmunization (AI) and Pregnancy

Anti-Glycophorin C Induces a Loss of Mitochondrial Membrane Potential but Fails To Activate Apoptotic Caspases.

Pbx1 Regulates the Self-Renewal of Long-Term Hematopoietic Stem Cells by Maintaining Their Quiescence.

A global role for EKLF in definitive and primitive erythropoiesis

The Transcription Factor Pbx1 Is Required for the Development of Double Positive Thymic T Cells.

Targeted disruption of the activating transcription factor 4 gene results in severe fetal anemia in mice

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American Society of Hematology

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ASH Publications

American Society of Hematology

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