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Journal Articles

Coarse basophilic stippling in lead poisoning

Nelson C. N. Chan, K. P. Chan

Blood (2017) 129 (24): 3270.

https://doi.org/10.1182/blood-2017-03-773499

Published: 2017

Journal Articles

Munoz J, Guo Y. Basophilic stippling: a lead to the diagnosis. Blood . 2011;118(20): 5370 .

Blood (2014) 123 (2): 302.

https://doi.org/10.1182/blood-2013-11-540237

Published: 2014

Journal Articles

Hemoglobin Agenogi in Argentina: Case Report

Ana Paula Martin, Sr., Patricia Martha Gargallo, Irma Margarita Bragos, Bioquimica, Alejandro Abbate, Mara Jorgelina Ojeda, Verónica Susana Montero

Blood (2012) 120 (21): 4776.

https://doi.org/10.1182/blood.V120.21.4776.4776

Published: 2012

Journal Articles

Beta Thalassemia Trait: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Susanna Barella, MD, Ramon Simon-Lopez, MD, Nicola Di Gaetano, BS, PhD, Renzo Galanello, MD

Blood (2012) 120 (21): 5186.

https://doi.org/10.1182/blood.V120.21.5186.5186

Published: 2012

Journal Articles

Novel Haemoglobin Variant [β42 Phe → Cys]: Hb Little Venice

Jack Bartram, MBBCh, MRCPCH, John Old, PhD, Lorry Phelan, Mark Layton, MD, Josu de la Fuente, PhD, FRCP, MRCPCH, FRCPath

Blood (2012) 120 (21): 1013.

https://doi.org/10.1182/blood.V120.21.1013.1013

Published: 2012

Journal Articles

Basophilic stippling: a lead to the diagnosis

Javier Munoz, Yue Guo

Blood (2011) 118 (20): 5370.

https://doi.org/10.1182/blood-2010-12-320911

Published: 2011

Journal Articles

Congenital Erythropoietic Porphyria Due to Co-Inheritance of GATA1 and UROS Gene Mutations

Zeynep Karakas, MD, Chiara Refaldi, Valentina Brancaleoni, Ismail Kurt, MD, Elena Di Pierro, PhD, Maria Domenica Cappellini, MD

Blood (2010) 116 (21): 3208.

https://doi.org/10.1182/blood.V116.21.3208.3208

Published: 2010

Journal Articles

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

Kavita Natarajan, Niren Patel, MBBS, Lina Zhuang, MD, Harris Carmichael, Elizabeth Manaloor, MD, Abdullah Kutlar, MD, Ferdane Kutlar, MD

Blood (2010) 116 (21): 4814.

https://doi.org/10.1182/blood.V116.21.4814.4814

Published: 2010

Journal Articles

A Comprehensive Report of Blood Cell Morphology for Neonates with Down's Syndrome In the UK: A Report From the Children with Down's Syndrome Study

Rebecca James, Tom Johnston, Tracy Lightfoot, Dan Painter, Pat Ansell, Eve Roman, Sally Kinsey

Blood (2010) 116 (21): 80.

https://doi.org/10.1182/blood.V116.21.80.80

Published: 2010

Journal Articles

BAND 3CEINGE (Gly796Arg) Mutation Causes Dehydrated Hereditary Stomatocytosis (DHS) with Dyserythropoietic Phenotype

Luigia De Falco, Lucia De Franceschi, Frank Borgese, Carmelo Piscopo, Maria Rosaria Esposito, Rosa Anna Avvisati, Pietro Izzo, Helene Guizouarn, Andrea Biondani, Achille Iolascon, MD, PhD

Blood (2008) 112 (11): 2874.

https://doi.org/10.1182/blood.V112.11.2874.2874

Published: 2008

Journal Articles

Trisomy 21 Expands the Megakaryocyte-Erythroid Progenitor Compartment in Human Fetal Liver-Implications for Down Syndrome AMKL.

Oliver Tunstall-Pedoe, MB, Josu de la Fuente, MB, Phillip R. Bennett, MB, PhD, Nicholas M. Fisk, MB, PhD, Paresh Vyas, MB, PhD, Irene A.G. Roberts, MD

Blood (2006) 108 (11): 563.

https://doi.org/10.1182/blood.V108.11.563.563

Published: 2006

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

Ten Year-Old Male with Hemoglobin Lufkin/Beta-Zero Thalassemia Compound Heterozygote Who Exhibited Beta-Thalassemia Major Characteristics.

Ahna M. Blutreich, MD, Peihong Shu, MD, Jeremy S. Bragdon, MD, Paul J. Kurtin, MD, James D. Hoyer, MD, Gungor Karayalcin, MD

Blood (2005) 106 (11): 3815.

https://doi.org/10.1182/blood.V106.11.3815.3815

Published: 2005

Journal Articles

Hemoglobin Ville-Marie: A New β-Globin Variant (del480C) Causing Oxydative Hemolysis.

Celine Devaux, MD, Pierre Chagnon, PhD, Claude Belisle, M.Sc., Denis Soulieres, MD, M.Sc., Lambert Busque, MD

Blood (2005) 106 (11): 3783.

https://doi.org/10.1182/blood.V106.11.3783.3783

Published: 2005

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

Functional Analysis of Two Mutants of Pyrimidine 5′ Nucleotidase Causing Nonspherocytic Hemolytic Anemia.

Laurent Chiarelli, Andrea Mattevi, Alessandro Galizzi, Elisa Fermo, Paola Bianchi, Alberto Zanella, Giovanna Valentini

Blood (2004) 104 (11): 1592.

https://doi.org/10.1182/blood.V104.11.1592.1592

Published: 2004

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

Chronic Aluminum Toxicity Due to Intravenous Substance Abuse Managed with Deferoxamine Chelation Therapy: Case Report.

Gayatri M. Sreenivasan, MD, Raymund L.M. Yong, MD, Dan Holmes, MD

Blood (2004) 104 (11): 3695.

https://doi.org/10.1182/blood.V104.11.3695.3695

Published: 2004

Journal Articles

Molecular characterization of Turkish patients with pyrimidine 5′ nucleotidase-I deficiency

Gunay Balta, Fatma Gumruk, Nurten Akarsu, Aytemiz Gurgey, Cigdem Altay

Blood (2003) 102 (5): 1900–1903.

https://doi.org/10.1182/blood-2003-02-0628

Published: 2003

Journal Articles

Genetic basis of hemolytic anemia caused by pyrimidine 5′ nucleotidase deficiency

Anthony M. Marinaki, Emilia Escuredo, John A. Duley, H. Anne Simmonds, Adolfo Amici, Valeria Naponelli, Giulio Magni, Martin Seip, Isaac Ben-Bassat, Eric H. Harley, Swee Lay Thein, David C. Rees

Blood (2001) 97 (11): 3327–3332.

https://doi.org/10.1182/blood.V97.11.3327

Published: 2001

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Coarse basophilic stippling in lead poisoning

Munoz J, Guo Y. Basophilic stippling: a lead to the diagnosis. Blood . 2011;118(20): 5370 .

Hemoglobin Agenogi in Argentina: Case Report

Beta Thalassemia Trait: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Novel Haemoglobin Variant [β42 Phe → Cys]: Hb Little Venice

Basophilic stippling: a lead to the diagnosis

Congenital Erythropoietic Porphyria Due to Co-Inheritance of GATA1 and UROS Gene Mutations

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

A Comprehensive Report of Blood Cell Morphology for Neonates with Down's Syndrome In the UK: A Report From the Children with Down's Syndrome Study

BAND 3CEINGE (Gly796Arg) Mutation Causes Dehydrated Hereditary Stomatocytosis (DHS) with Dyserythropoietic Phenotype

Trisomy 21 Expands the Megakaryocyte-Erythroid Progenitor Compartment in Human Fetal Liver-Implications for Down Syndrome AMKL.

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

Ten Year-Old Male with Hemoglobin Lufkin/Beta-Zero Thalassemia Compound Heterozygote Who Exhibited Beta-Thalassemia Major Characteristics.

Hemoglobin Ville-Marie: A New β-Globin Variant (del480C) Causing Oxydative Hemolysis.

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

Functional Analysis of Two Mutants of Pyrimidine 5′ Nucleotidase Causing Nonspherocytic Hemolytic Anemia.

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

Chronic Aluminum Toxicity Due to Intravenous Substance Abuse Managed with Deferoxamine Chelation Therapy: Case Report.

Molecular characterization of Turkish patients with pyrimidine 5′ nucleotidase-I deficiency

Genetic basis of hemolytic anemia caused by pyrimidine 5′ nucleotidase deficiency

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