A new unstable hemoglobin variant with low oxygen affinity: Hb Ilmenau [beta41 (C7)Phe-->Cys]

Safety of prostaglandins in the peripartum period in case of sickle-cell disease: A multicenter cohort study.

Pregnancy (Hoboken, N.J.)·2026

Perioperative management of adult sickle cell disease patients requiring cardiac surgery: A 25-year experience in a referral center.

Anaesthesia, critical care & pain medicine·2026

A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype.

Journal of pediatric hematology/oncology·2026

A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell Anemia.

American journal of hematology·2026

Plasma proteome signatures are predictive of mortality in sickle cell disease.

Blood advances·2026

Genetic Contribution to Asthma Informs Acute Chest Syndrome Pathophysiology and Risk Stratification.

American journal of hematology·2026

A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China.

Hemoglobin·2026

Pain Assessment and Management in Patients with Beta-Thalassemia Major: A Systematic Review.

Hemoglobin·2026

Beta Thalassemia Carrier Detection in Individuals with Borderline Normal Hemoglobin A2 Levels.

Hemoglobin·2026

Incidence and Laboratory Differentiation of Hb S/D-Punjab and Hb S/Korle-Bu in Newborn Screening in Minas Gerais, Brazil: A 10-Year Prospective Study.

Hemoglobin·2026

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn).

Hemoglobin·2026

Gender Pattern of Thyroid Dysfunction Among Patients with Beta-Thalassemia Intermedia: A Cross-Sectional Study from Yasuj, Iran.

Hemoglobin·2026

Risk factors for poor prognosis in patients with acute ischaemic stroke: a retrospective study.

Acta cardiologica·2026

A Phase IIa, Double Blind, Randomized, Placebo Controlled, Parallel, Multicentre, Proof-of-Concept Study to Evaluate the Efficacy and Safety of Desidustat Oral Tablet for Treatment of Sickle Cell Disease.

European journal of haematology·2026

Associations of hereditary angioedema attacks with intestinal permeability and inflammatory cytokines.

Frontiers in immunology·2026

Development and Validation of a Nomogram Based on Red Blood Cell and Reticulocyte Parameters for Differentiating Thalassemia Trait From Iron Deficiency Anemia.

Journal of clinical laboratory analysis·2026

Primary Anastomosis Versus Hartmann's Procedure in Acute Care Surgery: Evidence, Indications, and Barriers to Adoption.

The American surgeon·2026

Related Experiment Videos

A new unstable hemoglobin variant with low oxygen affinity: Hb Ilmenau [beta41 (C7)Phe-->Cys]

Related Concept Videos

Safety of prostaglandins in the peripartum period in case of sickle-cell disease: A multicenter cohort study.

Perioperative management of adult sickle cell disease patients requiring cardiac surgery: A 25-year experience in a referral center.

A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype.

A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell Anemia.

Plasma proteome signatures are predictive of mortality in sickle cell disease.

Genetic Contribution to Asthma Informs Acute Chest Syndrome Pathophysiology and Risk Stratification.

A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China.

Pain Assessment and Management in Patients with Beta-Thalassemia Major: A Systematic Review.

Beta Thalassemia Carrier Detection in Individuals with Borderline Normal Hemoglobin A2 Levels.

Incidence and Laboratory Differentiation of Hb S/D-Punjab and Hb S/Korle-Bu in Newborn Screening in Minas Gerais, Brazil: A 10-Year Prospective Study.

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn).

Gender Pattern of Thyroid Dysfunction Among Patients with Beta-Thalassemia Intermedia: A Cross-Sectional Study from Yasuj, Iran.

Risk factors for poor prognosis in patients with acute ischaemic stroke: a retrospective study.

A Phase IIa, Double Blind, Randomized, Placebo Controlled, Parallel, Multicentre, Proof-of-Concept Study to Evaluate the Efficacy and Safety of Desidustat Oral Tablet for Treatment of Sickle Cell Disease.

Associations of hereditary angioedema attacks with intestinal permeability and inflammatory cytokines.

Development and Validation of a Nomogram Based on Red Blood Cell and Reticulocyte Parameters for Differentiating Thalassemia Trait From Iron Deficiency Anemia.

Primary Anastomosis Versus Hartmann's Procedure in Acute Care Surgery: Evidence, Indications, and Barriers to Adoption.

Related Experiment Videos

A new unstable hemoglobin variant with low oxygen affinity: Hb Ilmenau [beta41 (C7)Phe-->Cys]

Related Concept Videos

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