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Journal Abstract Search

213 related items for PubMed ID: 37710296

  • 1. Imerslund-Gräsbeck syndrome: a comprehensive review of reported cases.
    Kingma SDK, Neven J, Bael A, Meuwissen MEC, van den Akker M.
    Orphanet J Rare Dis; 2023 Sep 14; 18(1):291. PubMed ID: 37710296
    [Abstract] [Full Text] [Related]

  • 2. VIT. B12 DEFICIENCY IN CHILDREN (IMERSLUND-GRÄSBECK SYNDROME IN TWO PAIRS OF SIBLINGS).
    Krzemień G, Turczyn A, Szmigielska A, Roszkowska-Blaim M.
    Dev Period Med; 2015 Sep 14; 19(3 Pt 2):351-5. PubMed ID: 26958680
    [Abstract] [Full Text] [Related]

  • 3. Clinical and molecular characteristics of imerslund-gräsbeck syndrome: First report of a novel Frameshift variant in Exon 11 of AMN gene.
    Elshinawy M, Gao HH, Al-Nabhani DM, Al-Thihli KA.
    Int J Lab Hematol; 2021 Oct 14; 43(5):1009-1015. PubMed ID: 33491342
    [Abstract] [Full Text] [Related]

  • 4. Imerslund-Gräsbeck syndrome in a child with a novel compound heterozygous mutations in the AMN gene: a case report.
    Zhang D, Liu S, Xi B, Zhu Y, Chen Y, Zhang J, Liu A.
    Ital J Pediatr; 2024 Sep 27; 50(1):191. PubMed ID: 39334390
    [Abstract] [Full Text] [Related]

  • 5. Severe pancytopenia at the presentation of Imerslund-Gräsbeck syndrome in a 23-month-old Italian boy.
    Di Sario F, Piloni F, Gasparini F, Serpetti E, Bruschi B, Coccia P, Lionetti ME, Gatti S.
    Ital J Pediatr; 2024 Sep 18; 50(1):186. PubMed ID: 39294696
    [Abstract] [Full Text] [Related]

  • 6. Failure to thrive is an early symptom of the imerslund Gräsbeck syndrome.
    Wulffraat NM, De Schryver J, Bruin M, Pinxteren-Nagler E, van Dijken PJ.
    Am J Pediatr Hematol Oncol; 1994 May 18; 16(2):177-80. PubMed ID: 8166372
    [Abstract] [Full Text] [Related]

  • 7. Imerslund-Gräsbeck syndrome (selective vitamin B(12) malabsorption with proteinuria).
    Gräsbeck R.
    Orphanet J Rare Dis; 2006 May 19; 1():17. PubMed ID: 16722557
    [Abstract] [Full Text] [Related]

  • 8. Imerslund-Gräsbeck Syndrome in an Infant with a Novel Intronic Variant in the AMN Gene: A Case Report.
    Pacitto A, Prontera P, Stangoni G, Stefanelli M, Ceppi S, Cerri C, Gurdo G, Mencarelli A, Esposito S.
    Int J Mol Sci; 2019 Jan 27; 20(3):. PubMed ID: 30691194
    [Abstract] [Full Text] [Related]

  • 9. Imerslund-Gräsbeck Syndrome presenting with microangiopathic hemolytic anemia in a child.
    Gurlek Gokcebay D, Akpinar Tekgunduz S, Cavdarli B.
    Eur J Med Genet; 2020 Jun 27; 63(6):103880. PubMed ID: 32045704
    [Abstract] [Full Text] [Related]

  • 10. A child with Imerslund-Gräsbeck syndrome concealed by co-existing α-thalassaemia presenting with subacute combined degeneration of the spinal cord: a case report.
    Arunath V, Hoole TJ, Rathnasri A, Muthukumarana O, Kumarasiri IM, Liyanage ND, Costa Y, Mettananda S.
    BMC Pediatr; 2021 Jan 18; 21(1):41. PubMed ID: 33461510
    [Abstract] [Full Text] [Related]

  • 11. Reversal of severe neurological abnormalities after vitamin B12 replacement in the Imerslund-Grasbeck syndrome.
    Salameh MM, Banda RW, Mohdi AA.
    J Neurol; 1991 Sep 18; 238(6):349-50. PubMed ID: 1940989
    [Abstract] [Full Text] [Related]

  • 12. [IMERSLUND-GRÄSBECK SYNDROME CONGENITAL FORM OF VITAMIN B12 DEFICIENCY ANEMIA].
    Kvezereli-Kopadze M, Mtvarelidze Z.
    Georgian Med News; 2019 May 18; (290):45-48. PubMed ID: 31322513
    [Abstract] [Full Text] [Related]

  • 13. [Specific malabsorption of vitamin B12 proteinuria. Megaloblastic anemia of Imerslund-Najman-Grasbeck. Study of 4 cases].
    LAMY M, BESANCON F, LOVERDO A, AFIFI F.
    Arch Fr Pediatr; 1961 Oct 18; 18():1109-20. PubMed ID: 14461868
    [No Abstract] [Full Text] [Related]

  • 14. Imerslund syndrome with dolichocephaly.
    Ben-Ami M, Katzuni E, Koren A.
    Pediatr Hematol Oncol; 1990 Oct 18; 7(2):177-81. PubMed ID: 2169845
    [Abstract] [Full Text] [Related]

  • 15. Imerslund-Gräsbeck syndrome in an African patient.
    Stones DK, Ferreira M.
    J Trop Pediatr; 1999 Apr 18; 45(2):106-7. PubMed ID: 10341506
    [Abstract] [Full Text] [Related]

  • 16. An exon 53 frameshift mutation in CUBN abrogates cubam function and causes Imerslund-Gräsbeck syndrome in dogs.
    Fyfe JC, Hemker SL, Venta PJ, Fitzgerald CA, Outerbridge CA, Myers SL, Giger U.
    Mol Genet Metab; 2013 Aug 18; 109(4):390-6. PubMed ID: 23746554
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  • 19. Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.
    De Filippo G, Rendina D, Rocco V, Esposito T, Gianfrancesco F, Strazzullo P.
    Ital J Pediatr; 2013 Sep 17; 39():58. PubMed ID: 24044590
    [Abstract] [Full Text] [Related]

  • 20. A 17-Month-old Boy With Pancytopenia Caused by a Rare Genetic Defect of Vitamin B12 Malabsorption.
    Baker KM, Parikh NS, Salsbery KT, Shaw GR, Steiner RD, Oelstrom MJ, Manalang MA.
    J Pediatr Hematol Oncol; 2022 Mar 01; 44(2):e444-e446. PubMed ID: 34054045
    [Abstract] [Full Text] [Related]

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