Hemoglobin Ube-2 (alpha 68 Asn----Asp) observed in a Turkish family

Serum zinc levels and zinc binding capacity in thalassemia.

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)·2002

Recombinant human growth hormone treatment in children with thalassemia major.

Pediatrics international : official journal of the Japan Pediatric Society·2000

Studies on the chronic oral toxicity of an analgesic drug combination consisting of acetylsalicylic acid, paracetamol and caffeine in rats including an electron microscopical evaluation of kidneys.

Arzneimittel-Forschung·1996

Immunocytochemical localization of GABA immunoreactivity in dentate granule cells of normal and kindled rats.

Neuroscience letters·1996

Kindling induces a lasting, regionally selective increase of kynurenic acid in the nucleus accumbens.

Brain research·1996

L-deprenyl (selegiline) exerts anticonvulsant effects against different seizure types in mice.

The Journal of pharmacology and experimental therapeutics·1996

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-Thalassemia Major and Intermedia Patients: 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

Adult-Onset Alagille Syndrome Presenting With Recurrent Cholestasis: A Rare Genetic Diagnosis Confirmed by Whole Exome Sequencing.

Cureus·2026

Genomic meta-analyses of binge-eating behavior and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.

Nature. Mental health·2026

The genome sequence of the Bluebell moth, Eana incanana (Stephens, 1852) (Lepidoptera: Tortricidae).

Wellcome open research·2026

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences.

Nature communications·2026

Accelerated Aging Fontan Phenotype Is Associated With Systemic Right Ventricles and Adverse Hemodynamics.

Journal of the American Heart Association·2026

Related Experiment Videos

Hemoglobin Ube-2 (alpha 68 Asn----Asp) observed in a Turkish family

Related Concept Videos

Serum zinc levels and zinc binding capacity in thalassemia.

Recombinant human growth hormone treatment in children with thalassemia major.

Studies on the chronic oral toxicity of an analgesic drug combination consisting of acetylsalicylic acid, paracetamol and caffeine in rats including an electron microscopical evaluation of kidneys.

Immunocytochemical localization of GABA immunoreactivity in dentate granule cells of normal and kindled rats.

Kindling induces a lasting, regionally selective increase of kynurenic acid in the nucleus accumbens.

L-deprenyl (selegiline) exerts anticonvulsant effects against different seizure types in mice.

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-Thalassemia Major and Intermedia Patients: 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.

Adult-Onset Alagille Syndrome Presenting With Recurrent Cholestasis: A Rare Genetic Diagnosis Confirmed by Whole Exome Sequencing.

Genomic meta-analyses of binge-eating behavior and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.

The genome sequence of the Bluebell moth, Eana incanana (Stephens, 1852) (Lepidoptera: Tortricidae).

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences.

Accelerated Aging Fontan Phenotype Is Associated With Systemic Right Ventricles and Adverse Hemodynamics.

Related Experiment Videos

Hemoglobin Ube-2 (alpha 68 Asn----Asp) observed in a Turkish family

Related Concept Videos

Related Articles