UB Paderborn / Katalog / Suche / in CDI

Challenges and Opportunities of Precision Medicine in Sickle Cell Disease: Novel European Approach by GenoMed4All Consortium and ERN‐EuroBloodNet

HemaSphere, 2023-03, Vol.7 (3), p.e844-n/a

2023

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Combining microfluidics with machine learning algorithms for RBC classification in rare hereditary hemolytic anemia

Scientific reports, 2021-06, Vol.11 (1), p.13553-13553, Article 13553

2021

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New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II

International journal of molecular sciences, 2023-06, Vol.24 (12), p.9935

2023

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Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene

British journal of haematology, 2012-11, Vol.159 (4), p.492-495

2012

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Use of intravenous iron in the current clinical practice

Medicina clinica, 2018-03, Vol.150 (5), p.188

Beneitez Pastor, David

2018

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Respuesta

Medicina clínica, 2018-04, Vol.150 (8), p.328-328

Beneitez Pastor, David

2018

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Uso del hierro intravenoso en la clínica actual

Medicina clínica, 2018-03, Vol.150 (5), p.188-190

Beneitez Pastor, David

2018

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Reply

Medicina clinica, 2018-04, Vol.150 (8), p.328

Beneitez Pastor, David

2018

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Reply

Medicina clínica (English ed.), 2018-04, Vol.150 (8), p.328

Beneitez Pastor, David

2018

Volltextzugriff (PDF)

Use of intravenous iron in the current clinical practice

Medicina clínica (English ed.), 2018-03, Vol.150 (5), p.188-190

Beneitez Pastor, David

2018

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Mitapivat versus Placebo for Pyruvate Kinase Deficiency

The New England journal of medicine, 2022-04, Vol.386 (15), p.1432-1442

2022

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New Cases and Mutations in ISEC23B/I Gene Causing Congenital Dyserythropoietic Anemia Type II

International journal of molecular sciences, 2023-06, Vol.24 (12)

2023

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ERN-EuroBloodNet European Registry of Patients Affected by Red Blood Cell Disorders and COVID-19

Blood, 2021-11, Vol.138 (Supplement 1), p.4058-4058

2021

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Addition of danicopan to ravulizumab or eculizumab in patients with paroxysmal nocturnal haemoglobinuria and clinically significant extravascular haemolysis (ALPHA): a double-blind, randomised, phase 3 trial

The Lancet. Haematology, 2023-12, Vol.10 (12), p.e955-e965

2023

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Hematological and Molecular Characteristics of Hb Sarrebourg [β131(H9)Gln→Arg (CAG→CGG)] Found in a Spanish Family

Hemoglobin, 2007-01, Vol.31 (2), p.183-185

2007

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International sentinel site surveillance of patients with transfusional hemosiderosis treated with deferasirox in actual practice setting

Hematology (Luxembourg), 2019-01, Vol.24 (1), p.238-246

2019

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Identification and characterization of the first SLC 11 A 2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC 11 A 2 gene

British journal of haematology, 2012-11, Vol.159 (4), p.492-495

2012

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50 años del programa de cribado neonatal en Cataluña

Revista española de salud pública, 2020 (94)

2020

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50 years of the Neonatal Screening Program in Catalonia.

Revista espanola de salud publica, 2020-12, Vol.94

2020

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Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene

British journal of haematology, 2012, Vol.159 (4), p.492-495

2012

Volltextzugriff (PDF)

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Challenges and Opportunities of Precision Medicine in Sickle Cell Disease: Novel European Approach by GenoMed4All Consortium and ERN‐EuroBloodNet

Combining microfluidics with machine learning algorithms for RBC classification in rare hereditary hemolytic anemia

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II

Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-thalassemia

Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene

Use of intravenous iron in the current clinical practice

Respuesta

Uso del hierro intravenoso en la clínica actual

Reply

Reply

Use of intravenous iron in the current clinical practice

Mitapivat versus Placebo for Pyruvate Kinase Deficiency

New Cases and Mutations in ISEC23B/I Gene Causing Congenital Dyserythropoietic Anemia Type II

ERN-EuroBloodNet European Registry of Patients Affected by Red Blood Cell Disorders and COVID-19

Addition of danicopan to ravulizumab or eculizumab in patients with paroxysmal nocturnal haemoglobinuria and clinically significant extravascular haemolysis (ALPHA): a double-blind, randomised, phase 3 trial

Hematological and Molecular Characteristics of Hb Sarrebourg [β131(H9)Gln→Arg (CAG→CGG)] Found in a Spanish Family

International sentinel site surveillance of patients with transfusional hemosiderosis treated with deferasirox in actual practice setting

Identification and characterization of the first SLC 11 A 2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC 11 A 2 gene

50 años del programa de cribado neonatal en Cataluña

Correction to: Spanish registry of hemoglobinopathies and rare anemias (REHem- AR): demographics, complications, and management of patients with β-thalassemia

50 years of the Neonatal Screening Program in Catalonia.

Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene

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