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The frequency of hypothyroidism and its relationship with HCV positivity in patients with thalassemia major in southern Iran. Haghpanah S, Jelodari S, Karamifar H, Saki F, Rahimi R, De Sanctis V, Dehbozorgian J, Karimi M. Acta Biomed. 2018 Mar 27; 89(1):55-60. Epub 2018 Mar 27.
A pilot trial of deferiprone in pantothenate kinase-associated neurodegeneration patients. Rohani M, Razmeh S, Shahidi GA, Alizadeh E, Orooji M. Neurol Int. 2017 Dec 11; 9(4):7279. Epub 2018 Feb 15.
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease. Hussein N, Weng SF, Kai J, Kleijnen J, Qureshi N. Cochrane Database Syst Rev. 2018 Mar 14; 3:CD010849. Epub 2018 Mar 14.
Hydroxyurea responses in clinically varied beta, HbE-beta thalassaemia and sickle cell anaemia patients of Eastern India. Chatterjee T, Chakravarty A, Chakravarty S. Ann Hematol. 2018 May; 97(5):893-898. Epub 2018 Feb 17.
Pathogenesis of chronic rhinosinusitis in patients affected by β-thalassemia major and sickle cell anaemia post allogenic bone marrow transplant. Martino F, Di Mauro R, Paciaroni K, Gaziev J, Alfieri C, Greco L, Floris R, Di Girolamo S, Di Girolamo M. Int J Pediatr Otorhinolaryngol. 2018 Mar; 106:35-40. Epub 2018 Jan 6.
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The Effect of Iron Chelation Therapy on Overall Survival in Sickle Cell Disease and β-Thalassemia: A Systematic Review. Ballas SK, Zeidan AM, Duong VH, DeVeaux M, Heeney MM. Am J Hematol. 2018 Apr 10; . Epub 2018 Apr 10.
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease. Hussein N, Weng SF, Kai J, Kleijnen J, Qureshi N. Cochrane Database Syst Rev. 2018 Mar 14; 3:CD010849. Epub 2018 Mar 14.
The prevalence of hepatitis C virus infection in thalassemia patients in Iran from 2000 to 2017: a systematic review and meta-analysis. Behzadifar M, Gorji HA, Bragazzi NL. Arch Virol. 2018 May; 163(5):1131-1140. Epub 2018 Feb 6.
Artemisinin Therapy for Malaria in Hemoglobinopathies: A Systematic Review. Sugiarto SR, Moore BR, Makani J, Davis TME. Clin Infect Dis. 2018 Feb 10; 66(5):799-804.
Hydroxyurea for lifelong transfusion-dependent β-thalassemia: A meta-analysis. Algiraigri AH, Wright NAM, Paolucci EO, Kassam A. Pediatr Hematol Oncol. 2017 Nov; 34(8):435-448. Epub 2018 Jan 16.
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Medical Genetics Topic: All Diagnosis Differential Diagnosis Clinical Description Management Genetic Counseling Molecular Genetics Genetic Testing
Prenatal screening for genetic disorders: Suggested guidelines for the Indian Scenario. Phadke SR, Puri RD, Ranganath P. Indian J Med Res. 2017 Dec; 146(6):689-699.
Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children. Traivaree C, Boonyawat B, Monsereenusorn C, Rujkijyanont P, Photia A. Appl Clin Genet. 2018; 11:23-30. Epub 2018 Apr 3.
Coinheritance of Sicilian (δβ)<sup>0</sup>-Thalassemia and Two Rare Hemoglobin Variants: A Complex Case of Hemoglobinopathy. Eftekhari H, Pilehchian Langroudi M, Banihashemi A, Azizi M, Kamangar RY, Akhavan-Niaki H. Indian J Clin Biochem. 2018 Apr; 33(2):231-234. Epub 2017 Jul 5.
Geographical distribution of β-globin gene mutations in Syria. Murad H, Moasses F, Dabboul A, Mukhalalaty Y, Bakoor AO, Al-Achkar W, Jarjour RA. Hematology. 2018 Apr 11; :1-8. Epub 2018 Apr 11.
Genetics of Iranian Alpha-Thalassemia Patients: A Comprehensive Original Study. Keikhaei B, Slehi-Fard P, Shariati G, Khosravi A. Biochem Genet. 2018 Apr 7; . Epub 2018 Apr 7.
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