Hb Olympia [beta 20 (B2) Val----MeT] in a Swedish family

Analyses of registry data of patients with anti-GBM and antineutrophil cytoplasmatic antibody-associated (ANCA) vasculitis treated with or without therapeutic apheresis.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis·2021

Analysis of extracorporeal photopheresis within the frame of the WAA register.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis·2021

European dermatology forum - updated guidelines on the use of extracorporeal photopheresis 2020 - part 1.

Journal of the European Academy of Dermatology and Venereology : JEADV·2020

European dermatology forum: Updated guidelines on the use of extracorporeal photopheresis 2020 - Part 2.

Journal of the European Academy of Dermatology and Venereology : JEADV·2020

Evaluation of health and quality of life in apheresis patients - data from the WAA register.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis·2019

Effects of age, gender and menstrual cycle on platelet function assessed by impedance aggregometry.

Platelets·2018

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

Hemoglobin·2026

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Hemoglobin·2026

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Hemoglobin·2026

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Hemoglobin·2026

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Hemoglobin·2026

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

Hemoglobin·2026

Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.

Hormone research in paediatrics·2026

Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.

Frontiers in behavioral neuroscience·2026

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series.

Clinical case reports·2026

The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).

Wellcome open research·2026

The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).

Wellcome open research·2026

Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.

The Journal of molecular diagnostics : JMD·2026

Related Experiment Videos

Hb Olympia [beta 20 (B2) Val----MeT] in a Swedish family

Related Concept Videos

Analyses of registry data of patients with anti-GBM and antineutrophil cytoplasmatic antibody-associated (ANCA) vasculitis treated with or without therapeutic apheresis.

Analysis of extracorporeal photopheresis within the frame of the WAA register.

European dermatology forum - updated guidelines on the use of extracorporeal photopheresis 2020 - part 1.

European dermatology forum: Updated guidelines on the use of extracorporeal photopheresis 2020 - Part 2.

Evaluation of health and quality of life in apheresis patients - data from the WAA register.

Effects of age, gender and menstrual cycle on platelet function assessed by impedance aggregometry.

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

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

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

Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.

Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series.

The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).

The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).

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Related Experiment Videos

Hb Olympia [beta 20 (B2) Val----MeT] in a Swedish family

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