Hemoglobin Fannin-Lubbock alpha 2 beta 2 119 (GH2) Gly replaced by Asp in Spain

Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains.

International journal of laboratory hematology·2014

Use of combined mass spectrometry methods for the characterization of a new variant of human hemoglobin: The double mutant hemoglobin villeparisis β77(EF1) His → Tyr, β 80 (EF4) Asn → Ser.

Journal of the American Society for Mass Spectrometry·2013

Foetal haemoglobin, erythrocytes containing foetal haemoglobin, and hematological features in congolese patients with sickle cell anaemia.

Anemia·2012

[The problem of sickle cell disease in Africa].

Medecine tropicale : revue du Corps de sante colonial·2011

Short insertion in a hemoglobin chain: Hb Esch, an unstable alpha1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68.

Blood cells, molecules & diseases·2003

[Good practices for the study of hemoglobin].

Annales de biologie clinique·2003

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Hemoglobin·2026

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Hemoglobin·2026

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Hemoglobin·2026

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Hemoglobin·2026

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Hemoglobin·2026

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

Hemoglobin·2026

An Unexpected Cause of Severe Steatohepatitis in a Young Male.

Gastroenterology·2026

High metanephrines with adrenal hemorrhage: a diagnostic dilemma.

JCEM case reports·2026

Timepoint-Specific Percentile Reference Curves for C-Reactive Protein and Erythrocyte Sedimentation Rate After Uncomplicated Primary Reverse Shoulder Arthroplasty: A Single-Center Cohort Study.

Diagnostics (Basel, Switzerland)·2026

Facts Do Not Organise Themselves: Whewell and the Conceptual Crisis in Medicine.

Journal of evaluation in clinical practice·2026

A parathyroid adenoma masquerading as an oesophageal cyst.

BMJ case reports·2026

Mounier-Kuhn syndrome incidentally diagnosed during the evaluation of atypical chest pain: CT findings and diagnostic challenges.

Radiology case reports·2026

Related Experiment Videos

Hemoglobin Fannin-Lubbock alpha 2 beta 2 119 (GH2) Gly replaced by Asp in Spain

Related Concept Videos

Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains.

Use of combined mass spectrometry methods for the characterization of a new variant of human hemoglobin: The double mutant hemoglobin villeparisis β77(EF1) His → Tyr, β 80 (EF4) Asn → Ser.

Foetal haemoglobin, erythrocytes containing foetal haemoglobin, and hematological features in congolese patients with sickle cell anaemia.

[The problem of sickle cell disease in Africa].

Short insertion in a hemoglobin chain: Hb Esch, an unstable alpha1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68.

[Good practices for the study of hemoglobin].

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

An Unexpected Cause of Severe Steatohepatitis in a Young Male.

High metanephrines with adrenal hemorrhage: a diagnostic dilemma.

Timepoint-Specific Percentile Reference Curves for C-Reactive Protein and Erythrocyte Sedimentation Rate After Uncomplicated Primary Reverse Shoulder Arthroplasty: A Single-Center Cohort Study.

Facts Do Not Organise Themselves: Whewell and the Conceptual Crisis in Medicine.

A parathyroid adenoma masquerading as an oesophageal cyst.

Mounier-Kuhn syndrome incidentally diagnosed during the evaluation of atypical chest pain: CT findings and diagnostic challenges.

Related Experiment Videos

Hemoglobin Fannin-Lubbock alpha 2 beta 2 119 (GH2) Gly replaced by Asp in Spain

Related Concept Videos

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