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

1-13 of 13

Sort by

Sort Order Select

Journal Articles

Use of Next Generation Sequencing Panel for Routine Diagnosis of Hereditary Hemolytic Anemias

Archana M Agarwal, MD, Jay L Patel, MD, Adam Clayton, PhD, Noel Scott Reading, PhD

Blood (2018) 132 (Supplement 1): 2325.

https://doi.org/10.1182/blood-2018-99-112589

Published: 2018

Journal Articles

UGT1A1 Polymorphism and Mortality Outcome after Allogeneic Stem Cell Transplantation with Busulfan Based Regimen

Patrizia Chiusolo, Angelo Minucci, Metafuni Elisabetta, Sabrina Giammarco, MD PhD, Monica Rossi, Gessica Minnella, Cecilia Zuppi, Andrea Urbani, Andrea Bacigalupo, MD, Ettore Capoluongo, Simona Sica, MD

Blood (2017) 130 (Supplement 1): 3218.

https://doi.org/10.1182/blood.V130.Suppl_1.3218.3218

Published: 2017

Journal Articles

Using a Next Generation Sequencing Panel to Discover the Obscure Causes of Hereditary Hemolytic Anemias

Archana M Agarwal, MD, N. Scott Reading, PhD, Kimberly Frizzell, PhD, Wei Shen, PhD, Shelly Sorrells, PhD, Mohamed E Salama, MD, Josef T. Prchal, MD, Hassan M. Yaish, Jay L Patel, MD, Robert D. Christensen, MD

Blood (2016) 128 (22): 2433.

https://doi.org/10.1182/blood.V128.22.2433.2433

Published: 2016

Journal Articles

The Association of Gilbert's Syndrome with Hyperbilirubinaemia Occurring on Any of Imatinib, Dasatinib and Nilotinib in Patients with Chronic Myeloid Leukaemia (CML)

Jeeyune Bahk, BSc, Simone Claudiani, MD, Richard M Szydlo, BSc, PhD, Sarmad Toma, BSc, Faisal Abdillah, BSc, Sandra Hing, BSc, Simona Deplano, MDPhD, Dragana Milojkovic, Jane F Apperley, MD, Letizia Foroni, MD PhD

Blood (2015) 126 (23): 2795.

https://doi.org/10.1182/blood.V126.23.2795.2795

Published: 2015

Journal Articles

Cation Leak in Red Blood Cells of Patients with Wiskott-Aldrich Syndrome Leads to Non-Immunologic Hemolysis

Robert A. Sokolic, MD, Satheesh Chonat, MD, Mary Risinger, RN, Michael Eckhaus, DVM, Elizabeth Garabedian, RN, MSLS, Katherine R. Calvo, MD, PhD, Irina Maric, MD, Theodosia A. Kalfa, MD PhD, Fabio Candotti, MD

Blood (2014) 124 (21): 1338.

https://doi.org/10.1182/blood.V124.21.1338.1338

Published: 2014

Journal Articles

Polymorphism of UGT1A1 and Frequency of Hyperbilirubinemia in Patients with Chronic Myeloid Leukemia Treated By Nilotinib

Anastasia Bykova, MD, Adhamjon Abdullaev, MD PhD, Galina Gusarova, MD PhD, Ekaterina Chelysheva, MD PhD, Svetlana Treglazova, MD, Svetlana Smirnova, MD, Anna G. Turkina, MD PhD

Blood (2014) 124 (21): 5538.

https://doi.org/10.1182/blood.V124.21.5538.5538

Published: 2014

Journal Articles

Long-Term Results and Adverse Events Of Second Line Nilotinib Therapy After Imatinib Failure In Patients With Chronic Myeloid Leukemia In Chronic Phase In Clinical Practice

Anastasia Bykova, MD, Galina Gusarova, MD, PhD, Ekaterina Yu. Chelysheva, MD, PhD, Anna G. Turkina, MD, PhD,

Blood (2013) 122 (21): 5181.

https://doi.org/10.1182/blood.V122.21.5181.5181

Published: 2013

Journal Articles

Phenobarbital for Long-Term Management of Marked Hyperbilirubinemia.

A. Majid Shojania, MD

Blood (2009) 114 (22): 5089.

https://doi.org/10.1182/blood.V114.22.5089.5089

Published: 2009

Journal Articles

Pyrimidine 5′ Nucleotidase-1 (P5N-1) Deficiency Associated with 4 Novel Mutations in 5 New Turkish Families: Genotype-Phenotype Analysis.

Gunay Balta, PhD, Aytemiz Gurgey, MD, Fatma Gumruk, MD, Yahya Buyukasik, MD, Meral Beksac, MD, Cigdem Altay, MD

Blood (2006) 108 (11): 3743.

https://doi.org/10.1182/blood.V108.11.3743.3743

Published: 2006

Journal Articles

Pyrimidine 5′ Nucleotidase Deficiency: Clinical and Molecular Characterization of Two New Italian Patients.

Elisa Fermo, PhD, Anna Marcello, PhD, Paola Bianchi, PhD, Simona Viglio, Laurent R. Chiarelli, Giovanna Valentini, Alberto Zanella, MD

Blood (2005) 106 (11): 3711.

https://doi.org/10.1182/blood.V106.11.3711.3711

Published: 2005

Journal Articles

Three New Mutations of Glucose-6-Phosphate Isomerase Associated with Chronic Hemolytic Anemia.

Cristina Vercellati, Elisa Fermo, Anna Marcello, Mariagabriella Mariani, Paola Bianchi, Wilma Barcellini, Saverio Ladogana, Alessandro De Fanti, Alberto Zanella

Blood (2004) 104 (11): 3673.

https://doi.org/10.1182/blood.V104.11.3673.3673

Published: 2004

Journal Articles

Ethnic Differences in Polymorphisms and Haplotypes within the UGT1A Gene Complex.

Jeeranut Sawattep, Thad A. Howard, MS, Noppawan P. Morales, PhD, Yupin Sanvaridna, PhD, Pranee Fucharoen, PhD, Suthat Fucharoen, MD, PhD, Russell E. Ware, MD, PhD

Blood (2004) 104 (11): 3777.

https://doi.org/10.1182/blood.V104.11.3777.3777

Published: 2004

Journal Articles

Coinheritance of Gilbert Syndrome Increases the Risk for Developing Gallstones in Patients With Hereditary Spherocytosis: Presented in part at the 40th Annual Meeting of the American Society of Hematology, Miami Beach, FL, December 4-8, 1998 and published in Blood 92:470a, 1998 (abstr, suppl 1) .

Emanuele Miraglia del Giudice, Silverio Perrotta, Bruno Nobili, Claudia Specchia, Giovanna d’Urzo, Achille Iolascon

Blood (1999) 94 (7): 2259–2262.

https://doi.org/10.1182/blood.V94.7.2259.419k42_2259_2262

Published: 1999

NARROW

Use of Next Generation Sequencing Panel for Routine Diagnosis of Hereditary Hemolytic Anemias

UGT1A1 Polymorphism and Mortality Outcome after Allogeneic Stem Cell Transplantation with Busulfan Based Regimen

Using a Next Generation Sequencing Panel to Discover the Obscure Causes of Hereditary Hemolytic Anemias

The Association of Gilbert's Syndrome with Hyperbilirubinaemia Occurring on Any of Imatinib, Dasatinib and Nilotinib in Patients with Chronic Myeloid Leukaemia (CML)

Cation Leak in Red Blood Cells of Patients with Wiskott-Aldrich Syndrome Leads to Non-Immunologic Hemolysis

Polymorphism of UGT1A1 and Frequency of Hyperbilirubinemia in Patients with Chronic Myeloid Leukemia Treated By Nilotinib

Long-Term Results and Adverse Events Of Second Line Nilotinib Therapy After Imatinib Failure In Patients With Chronic Myeloid Leukemia In Chronic Phase In Clinical Practice

Phenobarbital for Long-Term Management of Marked Hyperbilirubinemia.

Pyrimidine 5′ Nucleotidase-1 (P5N-1) Deficiency Associated with 4 Novel Mutations in 5 New Turkish Families: Genotype-Phenotype Analysis.

Pyrimidine 5′ Nucleotidase Deficiency: Clinical and Molecular Characterization of Two New Italian Patients.

Three New Mutations of Glucose-6-Phosphate Isomerase Associated with Chronic Hemolytic Anemia.

Ethnic Differences in Polymorphisms and Haplotypes within the UGT1A Gene Complex.

Coinheritance of Gilbert Syndrome Increases the Risk for Developing Gallstones in Patients With Hereditary Spherocytosis: Presented in part at the 40th Annual Meeting of the American Society of Hematology, Miami Beach, FL, December 4-8, 1998 and published in Blood 92:470a, 1998 (abstr, suppl 1) .

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only