Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stability

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

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

Revue d'epidemiologie et de sante publique·2018

Factors predictive of leg-ulcer healing in sickle cell disease: a multicentre, prospective cohort study.

The British journal of dermatology·2016

Maternal mortality among women with sickle-cell disease in France, 1996-2009.

European journal of obstetrics, gynecology, and reproductive biology·2015

Inhaled nitric oxide for acute chest syndrome in adult sickle cell patients: a randomized controlled study.

Intensive care medicine·2015

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

Case Report of Initial Manifestation of Hypogonadotropic Hypogonadism Based on Unoccluded Growth Plates in a 26-Year-Old Vietnamese Patient.

Cureus·2026

Clinical features of hereditary adrenocortical unresponsiveness to adrenocorticotropin (HAUA) in Japan: from a nationwide questionnaire based survey.

Endocrine journal·2026

Gastroduodenal Perforation Secondary to Heterotopic Pancreas in a Patient With Systemic Amyloidosis and End-Stage Renal Disease on Hemodialysis: A Case Report.

Cureus·2026

A Case of Convexity Meningioma Presenting With Acute Subdural Hematoma: A Case Report With a Pooled Analysis of 63 Reported Cases.

Cureus·2026

Hypothenar hammer syndrome: An expanded Kaji angiographic classification based on 91 cases.

Journal of plastic, reconstructive & aesthetic surgery : JPRAS·2026

Related Experiment Videos

Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stability

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.

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

Factors predictive of leg-ulcer healing in sickle cell disease: a multicentre, prospective cohort study.

Maternal mortality among women with sickle-cell disease in France, 1996-2009.

Inhaled nitric oxide for acute chest syndrome in adult sickle cell patients: a randomized controlled study.

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.

Case Report of Initial Manifestation of Hypogonadotropic Hypogonadism Based on Unoccluded Growth Plates in a 26-Year-Old Vietnamese Patient.

Clinical features of hereditary adrenocortical unresponsiveness to adrenocorticotropin (HAUA) in Japan: from a nationwide questionnaire based survey.

Gastroduodenal Perforation Secondary to Heterotopic Pancreas in a Patient With Systemic Amyloidosis and End-Stage Renal Disease on Hemodialysis: A Case Report.

A Case of Convexity Meningioma Presenting With Acute Subdural Hematoma: A Case Report With a Pooled Analysis of 63 Reported Cases.

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Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stability

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