BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 20835854)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Thiamine-responsive megaloblastic anemia or Rogers syndrome: A literature review].
    Lu H; Lu H; Vaucher J; Tran C; Vollenweider P; Castioni J
    Rev Med Interne; 2019 Jan; 40(1):20-27. PubMed ID: 30031565
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?
    Akın L; Kurtoğlu S; Kendirci M; Akın MA; Karakükçü M
    J Clin Res Pediatr Endocrinol; 2011; 3(1):36-9. PubMed ID: 21448333
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Thiamine-responsive megaloblastic anemia (TRMA) in an Austrian boy with compound heterozygous SLC19A2 mutations.
    Pichler H; Zeitlhofer P; Dworzak MN; Diakos C; Haas OA; Kager L
    Eur J Pediatr; 2012 Nov; 171(11):1711-5. PubMed ID: 22576805
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia.
    Setoodeh A; Haghighi A; Saleh-Gohari N; Ellard S; Haghighi A
    Gene; 2013 May; 519(2):295-7. PubMed ID: 23454484
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thiamine-responsive megaloblastic anemia syndrome: a novel mutation.
    Yilmaz Agladioglu S; Aycan Z; Bas VN; Peltek Kendirci HN; Onder A
    Genet Couns; 2012; 23(2):149-56. PubMed ID: 22876572
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cochlear implant and thiamine-responsive megaloblastic anemia syndrome.
    Hagr AA
    Ann Saudi Med; 2014; 34(1):78-80. PubMed ID: 24658560
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case report.
    Li X; Cheng Q; Ding Y; Li Q; Yao R; Wang J; Wang X
    BMC Pediatr; 2019 Jul; 19(1):233. PubMed ID: 31296181
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An Adult Case of Thiamine-Sensitive Megaloblastic Anemia Syndrome Accidentally Diagnosed Myelodysplastic Syndrome.
    Kutlucan A
    J Coll Physicians Surg Pak; 2019 Jun; 29(6):S13-S15. PubMed ID: 31142407
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Leber's congenital amaurosis as the retinal degenerative phenotype in thiamine responsive megaloblastic anemia: a case report.
    Srikrupa NN; Meenakshi S; Arokiasamy T; Murali K; Soumittra N
    Ophthalmic Genet; 2014 Jun; 35(2):119-24. PubMed ID: 23638917
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thiamine Responsive Megaloblastic Anaemia, Diabetes Mellitus and Sensorineural Hearing Loss in a Child.
    Khurshid A; Fatimah S; Altaf C; Malik HS; Sajjad Z; Khadim MT
    J Coll Physicians Surg Pak; 2018 Sep; 28(9):S169-S171. PubMed ID: 30173687
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.
    Katipoğlu N; Karapinar TH; Demir K; Aydin Köker S; Nalbantoğlu Ö; Ay Y; Korkmaz HA; Oymak Y; Yıldız M; Tunç S; Hazan F; Vergin C; Ozkan B
    Arch Argent Pediatr; 2017 Jun; 115(3):e153-e156. PubMed ID: 28504500
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Thiamine-responsive megaloblastic anemia syndrome with Ebstein anomaly: a case report.
    Akbari MT; Zare Karizi S; Mirfakhraie R; Keikhaei B
    Eur J Pediatr; 2014 Dec; 173(12):1663-5. PubMed ID: 24357267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pancytopenia in an adult patient with thiamine-responsive megaloblastic anaemia.
    Moulin V; Grandoni F; Castioni J; Lu H
    BMJ Case Rep; 2018 Jun; 2018():. PubMed ID: 29903777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Novel Mutation of SLC19A2 in a Chinese Zhuang Ethnic Family with Thiamine-Responsive Megaloblastic Anemia.
    Xian X; Liao L; Shu W; Li H; Qin Y; Yan J; Luo J; Lin FQ
    Cell Physiol Biochem; 2018; 47(5):1989-1997. PubMed ID: 29969779
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Thiamine responsive megaloblastic anemia in three Indian children.
    Raju K N Gowda V; Shivananda GM; Sankhyan N
    Indian J Pediatr; 2011 Jul; 78(7):888-9. PubMed ID: 21340725
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.
    Odaman-Al I; Gezdirici A; Yıldız M; Ersoy G; Aydoğan G; Şalcıoğlu Z; Tahtakesen TN; Önal H; Küçükemre-Aydın B
    Turk J Pediatr; 2019; 61(2):257-260. PubMed ID: 31951336
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G.
    Pomahačová R; Zamboryová J; Sýkora J; Paterová P; Fiklík K; Votava T; Černá Z; Jehlička P; Lád V; Šubrt I; Dort J; Dortová E
    Pediatr Diabetes; 2017 Dec; 18(8):844-847. PubMed ID: 28004468
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.