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Academic Journal

Leveraging Multi-Omics Approaches and Advanced Technologies to Unravel the Molecular Complexities, Modifiers, and Precision Medicine Strategies for Hemoglobin H Disease.

  • Authors : Pahelkar A; SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Mumbai, Maharashtra, India.; Sharma D

Subjects: Precision Medicine*/Precision Medicine*/Precision Medicine*/methods ; Genomics*/Genomics*/Genomics*/methods ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics

  • Source: European journal of haematology [Eur J Haematol] 2024 Dec; Vol. 113 (6), pp. 738-744. Date of Electronic Publication: 2024 Oct 09.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1600-0609

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Academic Journal

Disease burden, management strategies, and unmet needs in α-thalassemia due to hemoglobin H disease.

  • Authors : Lal A; University of California-San Francisco School of Medicine, Pediatric Hematology, Oakland, California, USA.; Viprakasit V

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/therapy ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/complications

  • Source: American journal of hematology [Am J Hematol] 2024 Nov; Vol. 99 (11), pp. 2164-2177. Date of Electronic Publication: 2024 Jul 22.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence.

  • Authors : Jajodia E; Molecular Genetics, Unipath Specialty Laboratory, Ahmedabad, Gujarat, India.; Menghani H

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/complications ; Phenotype*

  • Source: Annals of hematology [Ann Hematol] 2024 Sep; Vol. 103 (9), pp. 3805-3810. Date of Electronic Publication: 2024 Jul 11.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A case report on congenital hypothyroidism and alpha thalassemia in children with anemia and muscle damage as the main manifestation.

  • Authors : Zhang Y; Department of Child Rehabilitation, Dali Bai Autonomous Prefecture People's Hospital, Dali, Yunnan, China.; Li X

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/complications ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/diagnosis ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/complications

  • Source: Medicine [Medicine (Baltimore)] 2024 Aug 16; Vol. 103 (33), pp. e39446.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN:

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Report

Suppression of Hb Bart's to improve tissue oxygenation and fetal development in homozygous alpha-thalassemia.

  • Authors : Lugthart G; Leiden University Medical Center (LUMC) Willem-Alexander Children's Hospital, Pediatric Hematology and HSCT, Leiden, The Netherlands.; Verweij EJT

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/therapy ; Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics

  • Source: American journal of hematology [Am J Hematol] 2024 Aug; Vol. 99 (8), pp. 1613-1615. Date of Electronic Publication: 2024 Apr 24.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Report

A novel α 0 -thalassemia deletion in a Brazilian child with Hb H disease: -- Mococa .

  • Authors : Soler AM; Laboratorio de Genética Molecular Humana, Departamento de Ciencias Biológicas, Centro Universitario Regional (CENUR) Litoral Norte. Universidad de la República (UdelaR), Salto, Uruguay.; Pedroso GA

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; Sequence Deletion*; Humans

  • Source: International journal of laboratory hematology [Int J Lab Hematol] 2024 Aug; Vol. 46 (4), pp. 747-750. Date of Electronic Publication: 2024 Apr 03.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Epidemiology of clinically significant forms of alpha- and beta-thalassemia: A global map of evidence and gaps.

  • Authors : Musallam KM; Thalassemia Center, Burjeel Medical City, Abu Dhabi, United Arab Emirates.; Lombard L

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/epidemiology ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/epidemiology ; Hemoglobins, Abnormal*

  • Source: American journal of hematology [Am J Hematol] 2023 Sep; Vol. 98 (9), pp. 1436-1451. Date of Electronic Publication: 2023 Jun 26.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Additional value of red blood cell parameters in predicting uncommon α-thalassemia; experience from 10 years of α-globin gene sequencing and copy number variation analysis.

  • Authors : Fjeld B; Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.; Faculty of Medicine, University of Oslo, Oslo, Norway.

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/diagnosis ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; Hemoglobinopathies*

  • Source: International journal of laboratory hematology [Int J Lab Hematol] 2023 Apr; Vol. 45 (2), pp. 250-259. Date of Electronic Publication: 2022 Dec 26.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Severity scoring system to guide transfusion management in pediatric non-deletional HbH.

  • Authors : Songdej D; Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.; Tandhansakul M

Subjects: alpha-Thalassemia*; Child ; Humans

  • Source: Pediatrics international : official journal of the Japan Pediatric Society [Pediatr Int] 2023 Jan-Dec; Vol. 65 (1), pp. e15568.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 100886002 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Reduction of extramedullary erythropoiesis and amelioration of anemia in a β-thalassemia patient treated with thalidomide.

  • Authors : Pinto VM; Centro della Microcitemia, delle Anemie Congenite e dei Disordini del Metabolismo del Ferro, Ente Ospedaliero Ospedali Galliera, Genoa, Italy.; Romano N

Subjects: beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/complications ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/drug therapy ; Hematopoiesis, Extramedullary*

  • Source: American journal of hematology [Am J Hematol] 2024 Mar; Vol. 99 (3), pp. 463-464. Date of Electronic Publication: 2023 Dec 26.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  146 results for ""Thalassemia blood""