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ICSH recommendations for identification, diagnostic value, and quantitation of schistocytes

International journal of laboratory hematology, 2012-04, Vol.34 (2), p.107-116

2012

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Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders

International journal of laboratory hematology, 2018-02, Vol.40 (1), p.94-102

2018

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ICSH Guideline for worldwide point-of-care testing in haematology with special reference to the complete blood count

International journal of laboratory hematology, 2008-04, Vol.30 (2), p.105-116

2008

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P1551: CONFORMATIONAL STUDY OF PYRUVATE KINASE DEFICIENT VARIANTS WITH HEMOLYTIC ANEMIA. THE RELATIONSHIPS BETWEEN THE LOSS OF ENZYME FUNCTION AND STRUCTURAL DISRUPTION

HemaSphere, 2022-06, Vol.6 (Suppl), p.1432-1433

2022

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PB2248: CONCOMITANT HEREDITARY SPHEROCYTOSIS AND PYRUVATE KINASE DEFICIENCY IN A SPANISH FAMILY WITH CHRONIC HEMOLYTIC ANEMIA. CONTRIBUTION OF LASER EKTACYTOMETRY TO CLINICAL DIAGNOSIS

HemaSphere, 2022-06, Vol.6 (Suppl), p.2118-2119

2022

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P1550: NEW GENERATION EKTACYTOMETRY STUDY OF RED BLOOD CELLS RHEOLOGICAL PARAMETERS IN HEMOGLOBINOPATHIES

HemaSphere, 2022-06, Vol.6 (Suppl), p.1431-1432

2022

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P1542: COMORBIDITIES AND COMPLICATIONS ACROSS GENOTYPES IN ADULT PATIENTS WITH PYRUVATE KINASE DEFICIENCY: ANALYSIS FROM THE PEAK REGISTRY

HemaSphere, 2022-06, Vol.6 (Suppl), p.1423-1424

2022

Volltextzugriff (PDF)

P1562: CHARACTERIZING IRON OVERLOAD BY AGE IN PATIENTS DIAGNOSED WITH PYRUVATE KINASE DEFICIENCY – A DESCRIPTIVE ANALYSIS FROM THE PEAK REGISTRY

HemaSphere, 2022-06, Vol.6 (Suppl), p.1443-1444

2022

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Neonatal haemoglobinopathy screening in Spain

Journal of clinical pathology, 2009-01, Vol.62 (1), p.22-25

2009

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Detection of circulating neoplastic cells by reverse-transcriptase polymerase chain reaction in malignant melanoma: association with clinical stage and prognosis

Journal of clinical oncology, 1996-07, Vol.14 (7), p.2091-2097

1996

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Machine learning microfluidic based platform: Integration of Lab-on-Chip devices and data analysis algorithms for red blood cell plasticity evaluation in Pyruvate Kinase Disease monitoring

Sensors and actuators. A. Physical., 2023-03, Vol.351, p.114187, Article 114187

2023

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Concise review: how do red blood cells born, live, and die?

Annals of hematology, 2021-10, Vol.100 (10), p.2425-2433

2021

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New haplotype for the Glu104Asp mutation in triose‐phosphate isomerase deficiency and prenatal diagnosis in a Spanish family

Journal of inherited metabolic disease, 2005-01, Vol.28 (5), p.807-809

2005

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Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase A

Blood, 1989-11, Vol.74 (7), p.2550-2555

1989

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New e-health services for the European Network for Rare and Congenital Anaemias (e-ENERCA)

Orphanet journal of rare diseases, 2014-11, Vol.9 (9042), p.P9-P9, Article P9

2014

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Red cell membrane Na+ transport systems in hereditary spherocytosis : relevance to understanding the increased Na+ permeability

Annals of hematology, 2001-09, Vol.80 (9), p.535-539

2001

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Presence of adenosine deaminase on the surface of mononuclear blood cells: immunochemical localization using light and electron microscopy

The journal of histochemistry and cytochemistry, 1991-08, Vol.39 (8), p.1001-1008

1991

Volltextzugriff (PDF)

Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

Haematologica (Roma), 2007-11, Vol.92 (11), p.e102-e105

2007

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Chronic myeloid leukemia of thrombocythemic onset : a CML subtype with distinct hematological and molecular features ?

Leukemia, 1996-07, Vol.10 (7), p.1241-1243

1996

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European expert network on rare communicable diseases and other rare diseases linked to mobility and globalisation focused on health care provision (EURaDMoG): a feasibility study

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-291, Article 291

2020

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Co-existence of hereditary spherocytosis and a new red cell pyruvate kinase variant: PK mallorca

Haematologica (Roma), 2000-03, Vol.85 (3), p.227

2000

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Surface expression of adenosine deaminase in mitogen‐stimulated lymphocytes

Clinical and experimental immunology, 1993-08, Vol.93 (2), p.286-291

1993

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Increased susceptibility of microcytic red blood cells to in vitro oxidative stress

European journal of haematology, 1995-11, Vol.55 (5), p.327-331

1995

Volltextzugriff (PDF)

mTOR inhibition and erythropoiesis: microcytosis or anaemia?

Nephrology, dialysis, transplantation, 2012-02, Vol.27 (2), p.537-541

2012

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Malignant transformation and life expectancy in monoclonal gammopathy of undetermined significance

British journal of haematology, 1992-07, Vol.81 (3), p.391-394

1992

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ICSH recommendations for identification, diagnostic value, and quantitation of schistocytes

Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders

ICSH Guideline for worldwide point-of-care testing in haematology with special reference to the complete blood count

P1551: CONFORMATIONAL STUDY OF PYRUVATE KINASE DEFICIENT VARIANTS WITH HEMOLYTIC ANEMIA. THE RELATIONSHIPS BETWEEN THE LOSS OF ENZYME FUNCTION AND STRUCTURAL DISRUPTION

PB2248: CONCOMITANT HEREDITARY SPHEROCYTOSIS AND PYRUVATE KINASE DEFICIENCY IN A SPANISH FAMILY WITH CHRONIC HEMOLYTIC ANEMIA. CONTRIBUTION OF LASER EKTACYTOMETRY TO CLINICAL DIAGNOSIS

P1550: NEW GENERATION EKTACYTOMETRY STUDY OF RED BLOOD CELLS RHEOLOGICAL PARAMETERS IN HEMOGLOBINOPATHIES

P1542: COMORBIDITIES AND COMPLICATIONS ACROSS GENOTYPES IN ADULT PATIENTS WITH PYRUVATE KINASE DEFICIENCY: ANALYSIS FROM THE PEAK REGISTRY

P1562: CHARACTERIZING IRON OVERLOAD BY AGE IN PATIENTS DIAGNOSED WITH PYRUVATE KINASE DEFICIENCY – A DESCRIPTIVE ANALYSIS FROM THE PEAK REGISTRY

Neonatal haemoglobinopathy screening in Spain

Detection of circulating neoplastic cells by reverse-transcriptase polymerase chain reaction in malignant melanoma: association with clinical stage and prognosis

Machine learning microfluidic based platform: Integration of Lab-on-Chip devices and data analysis algorithms for red blood cell plasticity evaluation in Pyruvate Kinase Disease monitoring

Concise review: how do red blood cells born, live, and die?

New haplotype for the Glu104Asp mutation in triose‐phosphate isomerase deficiency and prenatal diagnosis in a Spanish family

Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase A

New e-health services for the European Network for Rare and Congenital Anaemias (e-ENERCA)

Red cell membrane Na+ transport systems in hereditary spherocytosis : relevance to understanding the increased Na+ permeability

Presence of adenosine deaminase on the surface of mononuclear blood cells: immunochemical localization using light and electron microscopy

Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

Chronic myeloid leukemia of thrombocythemic onset : a CML subtype with distinct hematological and molecular features ?

European expert network on rare communicable diseases and other rare diseases linked to mobility and globalisation focused on health care provision (EURaDMoG): a feasibility study

Co-existence of hereditary spherocytosis and a new red cell pyruvate kinase variant: PK mallorca

Surface expression of adenosine deaminase in mitogen‐stimulated lymphocytes

Increased susceptibility of microcytic red blood cells to in vitro oxidative stress

mTOR inhibition and erythropoiesis: microcytosis or anaemia?

Malignant transformation and life expectancy in monoclonal gammopathy of undetermined significance

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