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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

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

An Unexpectedly High Frequency of Sptb Gene Mutation ( SPTB exon 29: c.6055T>C (p.Ser2019Pro; Spectrin Thai)) with a Single Origin in Thailand Suggesting a New Model of Red Blood Cell Trait Against Malarial Pressure

Supachai Ekwattanakit, PhD MD, Jiraporn Korchuenjit, BSc, Thidarat Suksangpleng, PhD, Suchada Riolueang, MSc, Tana Taechalertpaisarn, PhD, Parichat Prommana, MSc, Pakatip Silapamongkolkul, MD, Komgrid Charngkaew, MD, Sittiruk Roytrakul, PhD, Chairat Uthaipibull, PhD, Vip Viprakasit, MD DPhil

Blood (2018) 132 (Supplement 1): 2322.

https://doi.org/10.1182/blood-2018-99-110982

Published: 2018

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

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

GATA 1: pArg202Thr, a New GATA 1 Mutation Involved in a Severe Dyserythropoietic Phenotype

Serge Pissard, MDPhD, Chadia Mekki, PharmD, Serge Hovhannisyan, MD, Lydie M. Da Costa, MD PhD, Valentine Brousse, MD, Carole Conejero, Stephane Giraudier, MD PhD, Mariane De Montalembert

Blood (2014) 124 (21): 1343.

https://doi.org/10.1182/blood.V124.21.1343.1343

Published: 2014

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

Prenatal Fetal DNA Testing for Predicting HDFN, FNAIT, and RhIG Candidacy

C. Ellen van der Schoot, MD, PhD, Florentine Thurik, MD, Peter G. Scheffer, MD, PhD, Frithjofna Abbink, MSc, van der Ploeg P.B. Catharina, PhD, Barbera Veldhuisen, PhD, Masja de Haas, MD, PhD

Blood (2013) 122 (21): SCI-51.

https://doi.org/10.1182/blood.V122.21.SCI-51.SCI-51

Published: 2013

Journal Articles

A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis

Yaddanapudi Ravindranath, MD, Gerald Goyette, BS, Steven Buck, MS, Manisha Gadgeel, MD, Alan Dombkowski, Ph.D, Laurence A. Boxer, MD, Patrick G. Gallagher, MD, Robert M Johnson, Ph.D

Blood (2011) 118 (21): 2101.

https://doi.org/10.1182/blood.V118.21.2101.2101

Published: 2011

Journal Articles

Two Atypical Severe Cda Forms Presenting as Hydrops Foetalis Are Caused by Mutations in the SEC23B Gene.

Elisa Fermo, Paola Bianchi, Cristina Vercellati, Wilma Barcellini, Carla Boschetti, Anna Paola Marcello, Alberto Zanella

Blood (2009) 114 (22): 1981.

https://doi.org/10.1182/blood.V114.22.1981.1981

Published: 2009

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

Unrelated Donor Umbilical Cord Blood Transplant Following Intrauterine Transfusions for Treatment of Alpha Thalassemia Major.

Angela E. Rivers, MD, PhD, Douglas Richard, MD, Neil Harris, MD, David H.K. Chui, MD, William B. Slayton, MD, Keri Baacke, MD, Susan Lynn Staba, MD

Blood (2006) 108 (11): 5403.

https://doi.org/10.1182/blood.V108.11.5403.5403

Published: 2006

Journal Articles

Hemoglobin H Hydrops Fetalis Associated with Homozygous Hemoglobin Constant Spring. Case Report.

Monica V.E. Gallivan, MD, Emmanuel J. Vlastos, MD, Robin D. Hanson, MD, PhD, Maria P. Bettinoti, PhD, Steven A. Schonberg, PhD, Victoria M. Pratt, PhD, Ching-Nan Ou, PhD, Mario Mikula, MS, Matthew J. McGinniss, PhD, Weimin Sun, PhD, Charles M. Strom, MD, PhD

Blood (2005) 106 (11): 3821.

https://doi.org/10.1182/blood.V106.11.3821.3821

Published: 2005

Journal Articles

Hydrops fetalis–associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation

Angel F. Remacha, Isabel Badell, Núria Pujol-Moix, Juan Parra, Eduardo Muñiz-Diaz, Gemma Ginovart, M. Pilar Sardà, Angel Hernández, Elisenda Moliner, Montserrat Torrent

Blood (2002) 100 (1): 356–358.

https://doi.org/10.1182/blood-2001-12-0351

Published: 2002

Journal Articles

Survival of donor cells 25 years after intrauterine transfusion

Henk E. Viëtor, Eric Hallensleben, Simone P. M. J. van Bree, Ellen M. W. van der Meer, Suzanne E. J. Kaal, Jack Bennebroek-Gravenhorst, Humphrey H. H. Kanhai, Anneke Brand, Frans H. J. Claas

Blood (2000) 95 (8): 2709–2714.

https://doi.org/10.1182/blood.V95.8.2709

Published: 2000

Journal Articles

Intrauterine Transfusions Affect Fetal T-Cell Immunity

Henk E. Viëtor, Gail E. Hawes, Claudia van den Oever, Els van Beelen, Humphrey H.H. Kanhai, Anneke Brand, Peter J. Van den Elsen

Blood (1997) 90 (6): 2492–2501.

https://doi.org/10.1182/blood.V90.6.2492

Published: 1997

NARROW

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

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

An Unexpectedly High Frequency of Sptb Gene Mutation ( SPTB exon 29: c.6055T>C (p.Ser2019Pro; Spectrin Thai)) with a Single Origin in Thailand Suggesting a New Model of Red Blood Cell Trait Against Malarial Pressure

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

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

GATA 1: pArg202Thr, a New GATA 1 Mutation Involved in a Severe Dyserythropoietic Phenotype

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

Prenatal Fetal DNA Testing for Predicting HDFN, FNAIT, and RhIG Candidacy

A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis

Two Atypical Severe Cda Forms Presenting as Hydrops Foetalis Are Caused by Mutations in the SEC23B Gene.

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

Unrelated Donor Umbilical Cord Blood Transplant Following Intrauterine Transfusions for Treatment of Alpha Thalassemia Major.

Hemoglobin H Hydrops Fetalis Associated with Homozygous Hemoglobin Constant Spring. Case Report.

Hydrops fetalis–associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation

Survival of donor cells 25 years after intrauterine transfusion

Intrauterine Transfusions Affect Fetal T-Cell Immunity

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American Society of Hematology

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American Society of Hematology

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