Hb Roubaix [alpha55(E4)Val-->Leu]: a new neutral hemoglobin variant involving the alpha1 gene

Deciphering Pain Experience in Adult Patients With Sickle Cell Disease: A Network Analysis of Pain-Related Factors in a Single French Sickle Cell Centre.

European journal of pain (London, England)·2025

Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study.

European journal of obstetrics, gynecology, and reproductive biology·2023

Transient liver injury and severe neonatal cholestasis in infant with glucose-6-phosphate dehydrogenase deficiency due to a new mutation.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2019

Multiple-resistance to ivermectin and benzimidazole of a Haemonchus contortus population in a sheep flock from mainland France, first report.

Veterinary parasitology, regional studies and reports·2019

Neurofilament light chain levels in pregnant multiple sclerosis patients: a prospective cohort study.

European journal of neurology·2019

[Prevention of genetic diseases : the return of the family practitioner ?]

Revue d'epidemiologie et de sante publique·2018

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

Hemoglobin·2026

An Unusual Presentation of Erythrocytosis Resulting in the Identification of a Novel Unstable Hemoglobin Variant: Hb Koskullskulle HBB: C.311T > C (p.Phe104Ser).

Hemoglobin·2026

Hematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients.

Hemoglobin·2026

The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection.

Hemoglobin·2026

Tailoring Genetic Approaches for Easier Detection of Anti-3.7 Alpha-Globin Gene Triplication in the Iranian Population.

Hemoglobin·2026

Microcytic Anemia with Low HbA2 and Normal HbA: Two Cases of Rare Thalassemia.

Hemoglobin·2026

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

Blue rubber bleb nevus syndrome as an uncommon cause of gastrointestinal overt bleeding: a diagnostic and therapeutic challenge.

Revista espanola de enfermedades digestivas·2026

Spontaneous Rupture of Multifocal Hepatic Artery Pseudoaneurysms in Systemic Lupus Erythematosus: A Rare Vasculopathic Emergency With Aberrant Hepatic Arterial Anatomy.

Cureus·2026

Undiagnosed von Willebrand Disease Presenting as Delayed Hematoma after Total Hip Arthroplasty: A Case Report.

Journal of orthopaedic case reports·2026

Prevalence and Real-World Clinical Outcomes of Hydroxyurea Resistance and Intolerance in Polycythemia Vera and Essential Thrombocythemia: A Single-Centre Experience.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion·2026

Interaction of an α-globin Gene Triplication with Other Forms of Thalassemia or Hemoglobinopathy in Northern Thailand.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion·2026

Related Experiment Videos

Hb Roubaix [alpha55(E4)Val-->Leu]: a new neutral hemoglobin variant involving the alpha1 gene

Related Concept Videos

Deciphering Pain Experience in Adult Patients With Sickle Cell Disease: A Network Analysis of Pain-Related Factors in a Single French Sickle Cell Centre.

Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study.

Transient liver injury and severe neonatal cholestasis in infant with glucose-6-phosphate dehydrogenase deficiency due to a new mutation.

Multiple-resistance to ivermectin and benzimidazole of a Haemonchus contortus population in a sheep flock from mainland France, first report.

Neurofilament light chain levels in pregnant multiple sclerosis patients: a prospective cohort study.

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Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

An Unusual Presentation of Erythrocytosis Resulting in the Identification of a Novel Unstable Hemoglobin Variant: Hb Koskullskulle HBB: C.311T > C (p.Phe104Ser).

Hematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients.

The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection.

Tailoring Genetic Approaches for Easier Detection of Anti-3.7 Alpha-Globin Gene Triplication in the Iranian Population.

Microcytic Anemia with Low HbA2 and Normal HbA: Two Cases of Rare Thalassemia.

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

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Spontaneous Rupture of Multifocal Hepatic Artery Pseudoaneurysms in Systemic Lupus Erythematosus: A Rare Vasculopathic Emergency With Aberrant Hepatic Arterial Anatomy.

Undiagnosed von Willebrand Disease Presenting as Delayed Hematoma after Total Hip Arthroplasty: A Case Report.

Prevalence and Real-World Clinical Outcomes of Hydroxyurea Resistance and Intolerance in Polycythemia Vera and Essential Thrombocythemia: A Single-Centre Experience.

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Hb Roubaix [alpha55(E4)Val-->Leu]: a new neutral hemoglobin variant involving the alpha1 gene

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