These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

244 related items for PubMed ID: 31322513

  • 1. [IMERSLUND-GRÄSBECK SYNDROME CONGENITAL FORM OF VITAMIN B12 DEFICIENCY ANEMIA].
    Kvezereli-Kopadze M, Mtvarelidze Z.
    Georgian Med News; 2019 May; (290):45-48. PubMed ID: 31322513
    [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 May; 19(3 Pt 2):351-5. PubMed ID: 26958680
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No 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. 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]

  • 6. 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]

  • 7. 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 19; 43(5):1009-1015. PubMed ID: 33491342
    [Abstract] [Full Text] [Related]

  • 8. [Imerslund-Najman-Grasbeck anemia. Apropos of a case].
    Ben Meriem C, Pousse H, Bourgeay-Causse M, Amri F, Besbes A, Belkhir A, Sfar MT, Jrad T.
    Pediatrie; 1993 Oct 19; 48(10):693-5. PubMed ID: 8015868
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 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. Megaloblastic anemia and benign proteinuria: Clues to the diagnosis of Imerslund-Gräsbeck syndrome.
    Luo X, Wang J, Lin Z, Zhao J, Cao K, Liu J.
    Pediatr Blood Cancer; 2024 Jan 18; 71(1):e30731. PubMed ID: 37855200
    [No Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. [Imerslund-Gräsbeck syndrome: megaloblastic anaemia with proteinuria].
    Aparicio López C, de Lucas Collantes C, Jimenez F, Antón Martín P.
    An Pediatr (Barc); 2014 Feb 18; 80(2):e62-3. PubMed ID: 24103239
    [No Abstract] [Full Text] [Related]

  • 14. Molecular study of proteinuria in patients treated with B₁₂ supplements: do not forget megaloblastic anemia type 1.
    Levin-Iaina N, Dinour D, Morduchowicz G, Ganon L, Holtzman EJ.
    Nephron Clin Pract; 2011 Feb 18; 118(2):c67-71. PubMed ID: 21150213
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B(12) absorption?
    Boina Abdallah A, Ogier de Baulny H, Kozyraki R, Passemard S, Fenneteau O, Lebon S, Rigal O, Mesples B, Yacouben K, Giraudier S, Benoist JF, Schiff M.
    Mol Genet Metab; 2012 Sep 14; 107(1-2):66-71. PubMed ID: 22854512
    [Abstract] [Full Text] [Related]

  • 17. Imerslund-Grasbeck syndrome in a cross-breed dog.
    Sancho IM, Holmes A, Adamantos S.
    J Small Anim Pract; 2021 Aug 14; 62(8):709-711. PubMed ID: 33022748
    [Abstract] [Full Text] [Related]

  • 18. Imerslund-Gräsbeck syndrome in an African patient.
    Stones DK, Ferreira M.
    J Trop Pediatr; 1999 Apr 14; 45(2):106-7. PubMed ID: 10341506
    [Abstract] [Full Text] [Related]

  • 19. [Megaloblastic anaemia in childhood due to vitamin B12 deficiency, report of 3 cases of congenital selective vitamin B12 malabsorption (author's tranls)].
    Bienzle U, Olischläger A, Leupold D, Kohne E, Harnisch R, Kleihauer E.
    Klin Padiatr; 1976 Mar 14; 188(2):97-103. PubMed ID: 944359
    [Abstract] [Full Text] [Related]

  • 20. [Selective vitamin B 12 malabsorption in a 19-year-old patient].
    Walser A, Eigenmann H, Gut A.
    Schweiz Med Wochenschr; 1989 Jul 29; 119(30):1053-6. PubMed ID: 2552572
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.