Page 1 | Search Results | Blood | American Society of Hematology

1-9 of 9

Sort by

Sort Order Select

Journal Articles

A method for noninvasive prenatal diagnosis of monogenic autosomal recessive disorders

Anthony Cutts, Dimitrios V. Vavoulis, Mary Petrou, Frances Smith, Barnaby Clark, Shirley Henderson, Anna Schuh

Blood (2019) 134 (14): 1190–1193.

https://doi.org/10.1182/blood.2019002099

Published: 2019

Includes: Supplemental data

Journal Articles

Hydroxyurea Shows Clinical Benefit without Alteration of Fetal Hemoglobin, MCV, or Hemoglobin in Unselected Adult and Pediatric Patients with Sickle Cell Anemia

Crawford John Strunk, MD, Biree Andemariam, MD, Fredericka Sey, MB ChB, Fatimah Farooq, BS, Rebekah Urbonya, BS, Charles Antwi-Boasiako, PhD, Adetola A. Kassim, MD MS, Onike Rodrigues, MD, Connie M. Piccone, MD, Angela Rivers, MD PhD, Deepa Manwani, MD, Imma Tartaglione, MD, Laura Sainati, MD, Raffaella Colombatti, MDPhD, Andrew D. Campbell, MD

Blood (2015) 126 (23): 2187.

https://doi.org/10.1182/blood.V126.23.2187.2187

Published: 2015

Journal Articles

Earlier Antenatal Diagnosis of Hemoglobinopathies By Coelocentesis

Antonino Giambona, Gianfranca Damiani, Filippo Leto, Cristina Yakil, Cristina Passarello, Valentina Cigna, Giovanna Schillaci, Massimiliano Sacco, Rosario Di Maggio, Angela Vitrano, Aurelio Maggio

Blood (2015) 126 (23): 2133.

https://doi.org/10.1182/blood.V126.23.2133.2133

Published: 2015

Journal Articles

Differentiation of BM-HSCs Into FVIII Producing Hepatocytes: Approach to Haemophilia Treatment

Amal M. El-beshlawy, Professor, Hala Gabr, Prof, Dr, Rania Zayed, MD, Laila Hegaz, MD, Rania Fawzy, MSc, Magi Samir Abdelwahab, MD

Blood (2012) 120 (21): 4388.

https://doi.org/10.1182/blood.V120.21.4388.4388

Published: 2012

Journal Articles

Characterization of Chromosome 20q Deletions In Myeloproliferative Neoplasms Using Microarray Karyotyping and Next-Generation Sequencing

Roland Jäger, Tiina Berg, Ashot Harutyunyan, Thorsten Klampfl, Francesco Passamonti, Elisa Rumi, Daniela Pietra, Bettina Gisslinger, Damla Olcaydu, Miroslav Penka, Heinz Gisslinger, Mario Cazzola, Robert Kralovics

Blood (2010) 116 (21): 4099.

https://doi.org/10.1182/blood.V116.21.4099.4099

Published: 2010

Journal Articles

Identification of Somatically Acquired Gene Mutations In the Kineome and Exome In CLL

Xiaosong Zhang, MD, PhD, Meng Li, MD, PhD, Peter Ouillette, Luis Diaz, MD, Marcelo Reis, Victor Velculescu, MD, PhD, Kenneth Kinzler, PhD, Sami Malek, MD, Bert Vogelstein, MD

Blood (2010) 116 (21): 2410.

https://doi.org/10.1182/blood.V116.21.2410.2410

Published: 2010

Journal Articles

Phenotypic correction of von Willebrand disease type 3 blood-derived endothelial cells with lentiviral vectors expressing von Willebrand factor

Simon F. De Meyer, Karen Vanhoorelbeke, Marinee K. Chuah, Inge Pareyn, Veerle Gillijns, Robert P. Hebbel, Désiré Collen, Hans Deckmyn, Thierry VandenDriessche

Blood (2006) 107 (12): 4728–4736.

https://doi.org/10.1182/blood-2005-09-3605

Published: 2006

Journal Articles

Phenotypic Correction of von Willebrand Disease Type 3 Blood-Derived Endothelial Cells with Lentiviral Vectors Expressing von Willebrand Factor.

Simon F. De Meyer, Karen Vanhoorelbeke, PhD, Marinee K. Chuah, PhD, Inge Pareyn, Veerle Gillijns, Robert P. Hebbel, MD, Hans Deckmyn, PhD, Thierry Vandendriessche, PhD

Blood (2005) 106 (11): 5522.

https://doi.org/10.1182/blood.V106.11.5522.5522

Published: 2005

Journal Articles

Genetic Correction of p67 phox Deficient Chronic Granulomatous Disease Using Peripheral Blood Progenitor Cells as a Target for Retrovirus Mediated Gene Transfer

Wayne M. Weil, Gilda F. Linton, Narda Whiting-Theobald, Sarah J. Vowells, Steven P. Rafferty, Fei Li, Harry L. Malech

Blood (1997) 89 (5): 1754–1761.

https://doi.org/10.1182/blood.V89.5.1754

Published: 1997

NARROW

A method for noninvasive prenatal diagnosis of monogenic autosomal recessive disorders

Hydroxyurea Shows Clinical Benefit without Alteration of Fetal Hemoglobin, MCV, or Hemoglobin in Unselected Adult and Pediatric Patients with Sickle Cell Anemia

Earlier Antenatal Diagnosis of Hemoglobinopathies By Coelocentesis

Differentiation of BM-HSCs Into FVIII Producing Hepatocytes: Approach to Haemophilia Treatment

Characterization of Chromosome 20q Deletions In Myeloproliferative Neoplasms Using Microarray Karyotyping and Next-Generation Sequencing

Identification of Somatically Acquired Gene Mutations In the Kineome and Exome In CLL

Phenotypic correction of von Willebrand disease type 3 blood-derived endothelial cells with lentiviral vectors expressing von Willebrand factor

Phenotypic Correction of von Willebrand Disease Type 3 Blood-Derived Endothelial Cells with Lentiviral Vectors Expressing von Willebrand Factor.

Genetic Correction of p67 phox Deficient Chronic Granulomatous Disease Using Peripheral Blood Progenitor Cells as a Target for Retrovirus Mediated Gene Transfer

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only