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Journal Articles

Oryzocytosis: A Novel Morphological Variant of Hereditary Elliptocytosis Associated with a Novel Mutation in β-Spectrin ( SPTB c154 C>T p.Arg52Trp)

Alexander Glaros, MD, Manisha Gadgeel, MBBS, MS, Shruti Bagla, PhD, Steven Buck, MS, Roland Chu, MD, Yaddanapudi Ravindranath, MBBS, Brian Edwards, PhD, Asmita Vaishnav

Blood (2019) 134 (Supplement_1): 3509.

https://doi.org/10.1182/blood-2019-131219

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

Erythrocyte Rigidity Affects Blood Clot Contraction and Formation of Polyhedrocytes

Valerie Tutwiler, Rustem I. Litvinov, PhD, Chandrasekaran Nagaswami, J. Eric Russell, MD, Don L. Siegel, MD, PhD,, Carlos Hipolito Villa, MD PhD, Daniel Pan, PhD, Vladimir R Muzykantov, MD PhD, John W. Weisel

Blood (2016) 128 (22): 3814.

https://doi.org/10.1182/blood.V128.22.3814.3814

Published: 2016

Journal Articles

Genotype-Phenotype Correlations in Hereditary Elliptocytosis (HE) and Hereditary Pyropoikilocytosis (HPP)

Omar Niss, MD, Satheesh Chonat, MD, Karol Kerr, MD, Patrick T. McGann, MD MS, Marya Obaid Almansoori, MD, Maa-Ohui Quarmyne, MBChB MS, Kejian Zhang, MD MBA, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 3344.

https://doi.org/10.1182/blood.V126.23.3344.3344

Published: 2015

Journal Articles

A Comprehensive Next Generation Sequencing Gene Panel Focused on Unexplained Anemia

Frances Smith, David Brawand, Laura Steedman, Matthew Oakley, Christopher Wall, Peter Rushton, Margaret Allchurch, Keith Sibson, Claire Jane Hemmaway, MD, Swee Lay Thein, MD DSc, David C. Rees, FRCP, FRCPath, MA, MBBS, Barnaby E. Clark, PhD

Blood (2015) 126 (23): 946.

https://doi.org/10.1182/blood.V126.23.946.946

Published: 2015

Journal Articles

Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia

Paola Bianchi, PhD, Elisa Fermo, PhD, Jennifer C Eng, Jacob C Ulirsch, Cristina Vercellati, BSc, Paola Braidotti, MD, Gordon Hildick-Smith, Timothy J Satchwell, PhD, Stephanie Pellegrin, PhD, Alberto Zanella, MD, Wilma Barcellini, MD, Barry H. Paw, MD, PhD, Ashley Mark Toye, PhD, Vijay G Sankaran, MD PhD

Blood (2015) 126 (23): 272.

https://doi.org/10.1182/blood.V126.23.272.272

Published: 2015

Journal Articles

A mutation in the Gardos channel is associated with hereditary xerocytosis

Blood (2015) 126 (11): 1273–1280.

https://doi.org/10.1182/blood-2015-04-642496

Published: 2015

Journal Articles

A Family with Hereditary Elliptocytosis: Variable Clinical Severity Caused by Three Mutations in the α-Spectrin Gene,

Paul Hubert Frans Franck, PhD, Cobie Postma, Marjan Veuger, PhD, Pierre Wijermans, MD, Frans A Kuypers, PhD

Blood (2011) 118 (21): 3167.

https://doi.org/10.1182/blood.V118.21.3167.3167

Published: 2011

Journal Articles

A Case of Congenital Red Cell Pyruvate Kinase Deficiency Associated with Hereditary Spherocytosis

Cristina Vercellati, PhD, Anna Paola Maria Luisa Marcello, PhD, Elisa Fermo, PhD, Paola Bianchi, PhD, Carla Boschetti, Alessandra Iurlo, M.D., Alberto Zanella, M.D., Wilma Barcellini, MD

Blood (2011) 118 (21): 5272.

https://doi.org/10.1182/blood.V118.21.5272.5272

Published: 2011

Journal Articles

Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation

Marcela Salomao, Ke Chen, Jonathan Villalobos, Narla Mohandas, Xiuli An, Joel Anne Chasis

Blood (2010) 116 (2): 267–269.

https://doi.org/10.1182/blood-2010-02-264127

Published: 2010

Journal Articles

A Case Report of An Unusual Case of Myelodysplatic Syndrome in a 26 year old Female

Rami Y. Haddad, MD, FACP, Navneet Attri, MD, Yaser Kawar, MD

Blood (2008) 112 (11): 5103.

https://doi.org/10.1182/blood.V112.11.5103.5103

Published: 2008

Journal Articles

Coexistence of Congenital Red Cell Pyruvate Kinase Deficiency and Hereditary Stomatocytosis.

Anna P. Marcello, PhD, Cristina Vercellati, PhD, Elisa Fermo, PhD, Paola Bianchi, PhD, Wilma Barcellini, MD, Alberto Zanella, MD

Blood (2007) 110 (11): 1738.

https://doi.org/10.1182/blood.V110.11.1738.1738

Published: 2007

Journal Articles

Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice.

Raymond F. Robledo, PhD, Steven L. Ciciotte, MS, Babette Gwynn, MS, Kenneth E. Sahr, PhD, Diana M. Gilligan, MD, PhD, Luanne L. Peters, PhD

Blood (2007) 110 (11): 141.

https://doi.org/10.1182/blood.V110.11.141.141

Published: 2007

Journal Articles

Stubby elliptocytes are an invariable feature of leukoerythroblastosis

Michael Quigley, Ronald L. Linfesty, Kelly Bethel, Robert Sharpe

Blood (2007) 109 (6): 2666.

https://doi.org/10.1182/blood-2006-10-055020

Published: 2007

Journal Articles

Usefulness of Peripheral Blood Smears in Identifying the Causes of Anemia in Adults.

Peter McPhedran, MD, Robert B. Hall, MD

Blood (2005) 106 (11): 5565.

https://doi.org/10.1182/blood.V106.11.5565.5565

Published: 2005

Journal Articles

RBC Histogram Predictive of HE.

Carl Chakmakjian, Ed Rappaport

Blood (2005) 106 (11): 3706.

https://doi.org/10.1182/blood.V106.11.3706.3706

Published: 2005

Journal Articles

Two New Recessive Mouse Mutations Cause Severe Hemolytic Anemia and Reveal Unexpected Interactions in the C-Terminus of α-Spectrin.

Raymond F. Robledo, PhD, Amy J. Lambert, BS, Babette Gwynn, MS, Lucy B. Rowe, BA, Diana M. Gilligan, MD, Ph.D, Samuel E. Lux, MD, Luanne L. Peters, Ph.D

Blood (2005) 106 (11): 1662.

https://doi.org/10.1182/blood.V106.11.1662.1662

Published: 2005

Journal Articles

Marked Elliptocytosis in Myelodysplastic Syndromes (MDS) Is Associated to Deletion of Chromosome 20q.

Mansoina Baweja, MD, Alvaro Moreno-Aspitia, MD, David M. Menke, MD, Vivek Roy, MD, Abba Zubair, MD

Blood (2005) 106 (11): 4927.

https://doi.org/10.1182/blood.V106.11.4927.4927

Published: 2005

Journal Articles

HB Florida: A New Elongated C-Terminal β-Globin Variant Causing Dominant β-Thalassemia.

Maria F. Sonati, PhD, Beatriz I. Weinstein, PhD, Beatriz Erramouspe, Dulcineia M. Albuquerque, MSc, Elza M. Kimura, MSc, Denise M. Oliveira, Fernando F. Costa

Blood (2004) 104 (11): 3776.

https://doi.org/10.1182/blood.V104.11.3776.3776

Published: 2004

Journal Articles

Ability of Plasmodium falciparum to invade Southeast Asian ovalocytes varies between parasite lines

Alfred Cortés, Ariadna Benet, Brian M. Cooke, John W. Barnwell, John C. Reeder

Blood (2004) 104 (9): 2961–2966.

https://doi.org/10.1182/blood-2004-06-2136

Published: 2004

NARROW

Oryzocytosis: A Novel Morphological Variant of Hereditary Elliptocytosis Associated with a Novel Mutation in β-Spectrin ( SPTB c154 C>T p.Arg52Trp)

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

Erythrocyte Rigidity Affects Blood Clot Contraction and Formation of Polyhedrocytes

Genotype-Phenotype Correlations in Hereditary Elliptocytosis (HE) and Hereditary Pyropoikilocytosis (HPP)

A Comprehensive Next Generation Sequencing Gene Panel Focused on Unexplained Anemia

Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia

A mutation in the Gardos channel is associated with hereditary xerocytosis

A Family with Hereditary Elliptocytosis: Variable Clinical Severity Caused by Three Mutations in the α-Spectrin Gene,

A Case of Congenital Red Cell Pyruvate Kinase Deficiency Associated with Hereditary Spherocytosis

Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation

A Case Report of An Unusual Case of Myelodysplatic Syndrome in a 26 year old Female

Coexistence of Congenital Red Cell Pyruvate Kinase Deficiency and Hereditary Stomatocytosis.

Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice.

Stubby elliptocytes are an invariable feature of leukoerythroblastosis

Usefulness of Peripheral Blood Smears in Identifying the Causes of Anemia in Adults.

RBC Histogram Predictive of HE.

Two New Recessive Mouse Mutations Cause Severe Hemolytic Anemia and Reveal Unexpected Interactions in the C-Terminus of α-Spectrin.

Marked Elliptocytosis in Myelodysplastic Syndromes (MDS) Is Associated to Deletion of Chromosome 20q.

HB Florida: A New Elongated C-Terminal β-Globin Variant Causing Dominant β-Thalassemia.

Ability of Plasmodium falciparum to invade Southeast Asian ovalocytes varies between parasite lines

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American Society of Hematology

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American Society of Hematology

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