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Journal Abstract Search

201 related items for PubMed ID: 4045602

  • 1. Diabetes mellitus, thiamine-dependent megaloblastic anemia, and sensorineural deafness associated with deficient alpha-ketoglutarate dehydrogenase activity.
    Abboud MR, Alexander D, Najjar SS.
    J Pediatr; 1985 Oct; 107(4):537-41. PubMed ID: 4045602
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  • 2. Thiamine responsive megaloblastic anemia: a novel SLC19A2 compound heterozygous mutation in two siblings.
    Mozzillo E, Melis D, Falco M, Fattorusso V, Taurisano R, Flanagan SE, Ellard S, Franzese A.
    Pediatr Diabetes; 2013 Aug; 14(5):384-7. PubMed ID: 23289844
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  • 5. Identification of four SLC19A2 mutations in four Chinese thiamine responsive megaloblastic anemia patients without diabetes.
    Liu G, Yang F, Han B, Liu J, Nie G.
    Blood Cells Mol Dis; 2014 Apr; 52(4):203-4. PubMed ID: 24355766
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  • 6. Recurrent psychiatric manifestations in thiamine-responsive megaloblastic anemia syndrome due to a novel mutation c.63_71 delACCGCTC in the gene SLC19A2.
    Wood MC, Tsiouris JA, Velinov M.
    Psychiatry Clin Neurosci; 2014 Jun; 68(6):487. PubMed ID: 24520986
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  • 12. Thiamine-responsive megaloblastic anemia syndrome with atrial standstill: a case report.
    Aycan Z, Baş VN, Cetinkaya S, Ağladioğlu SY, Kendirci HN, Senocak F.
    J Pediatr Hematol Oncol; 2011 Mar; 33(2):144-7. PubMed ID: 21285901
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  • 13. Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity.
    Raz T, Barrett T, Szargel R, Mandel H, Neufeld EJ, Nosaka K, Viana MB, Cohen N.
    Hum Genet; 1998 Oct; 103(4):455-61. PubMed ID: 9856490
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  • 14. Thiamine-responsive megaloblastic anemia syndrome: long term follow-up.
    Borgna-Pignatti C, Azzalli M, Pedretti S.
    J Pediatr; 2009 Aug; 155(2):295-7. PubMed ID: 19619756
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  • 20. Thiamine-responsive megaloblastic anemia syndrome.
    Bay A, Keskin M, Hizli S, Uygun H, Dai A, Gumruk F.
    Int J Hematol; 2010 Oct; 92(3):524-6. PubMed ID: 20835854
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