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

Journal Abstract Search


197 related items for PubMed ID: 9809815

  • 41. Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.
    Pogoriler J, O'Neill AF, Voss SD, Shamberger RC, Perez-Atayde AR.
    Pediatr Dev Pathol; 2018; 21(1):84-90. PubMed ID: 28382841
    [Abstract] [Full Text] [Related]

  • 42. Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient.
    Sharari S, Aouida M, Mohammed I, Haris B, Bhat AA, Hawari I, Nisar S, Pavlovski I, Biswas KH, Syed N, Maacha S, Grivel JC, Saifaldeen M, Ericsson J, Hussain K.
    Front Endocrinol (Lausanne); 2022; 13():841788. PubMed ID: 35663312
    [Abstract] [Full Text] [Related]

  • 43. Acquired growth hormone deficiency in Fanconi-Bickel syndrome.
    Scully KJ, Wolfsdorf J, Dedekian M.
    BMJ Case Rep; 2021 Nov 02; 14(11):. PubMed ID: 34728514
    [Abstract] [Full Text] [Related]

  • 44. Evidence for a Genotype-Phenotype Correlation in Patients with Pathogenic GLUT2 (SLC2A2) Variants.
    Grünert SC, Schumann A, Baronio F, Tsiakas K, Murko S, Spiekerkoetter U, Santer R.
    Genes (Basel); 2021 Nov 10; 12(11):. PubMed ID: 34828390
    [Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46. Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome.
    Setoodeh A, Rabbani A.
    Acta Med Iran; 2012 Nov 10; 50(12):836-8. PubMed ID: 23456528
    [Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48. Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature.
    Xiong LJ, Jiang ML, Du LN, Yuan L, Xie XL.
    World J Clin Cases; 2020 Nov 06; 8(21):5467-5473. PubMed ID: 33269285
    [Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50. A novel mutation (N32K) of GLUT2 gene in a Japanese patient with Fanconi-Bickel syndrome.
    Matsuura T, Tamura T, Chinen Y, Ohta T.
    Clin Genet; 2002 Sep 06; 62(3):255-6. PubMed ID: 12220445
    [No Abstract] [Full Text] [Related]

  • 51. Clinical and biochemical signs in Fleckvieh cattle with genetically confirmed Fanconi-Bickel syndrome (cattle homozygous for Fleckvieh haplotype 2).
    Burgstaller J, Url A, Pausch H, Schwarzenbacher H, Egerbacher M, Wittek T.
    Berl Munch Tierarztl Wochenschr; 2016 Sep 06; 129(3-4):132-7. PubMed ID: 27169150
    [Abstract] [Full Text] [Related]

  • 52. Catch-up growth in Fanconi-Bickel syndrome with uncooked cornstarch.
    Lee PJ, Van't Hoff WG, Leonard JV.
    J Inherit Metab Dis; 1995 Sep 06; 18(2):153-6. PubMed ID: 7564233
    [No Abstract] [Full Text] [Related]

  • 53.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 54. Fanconi-Bickel syndrome.
    Karande S, Kumbhare N, Kulkarni M.
    Indian Pediatr; 2007 Mar 06; 44(3):223-5. PubMed ID: 17413201
    [Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56. [The Fanconi-Bickel syndrome: one more case].
    Ruffa G, Ferrando M, Sbolgi P, Bartolozzi G, Lavia N.
    Minerva Pediatr; 1992 Jun 06; 44(6):313-8. PubMed ID: 1635533
    [Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi-Bickel Syndrome.
    Sharari S, Kabeer B, Mohammed I, Haris B, Pavlovski I, Hawari I, Bhat AA, Toufiq M, Tomei S, Mathew R, Syed N, Nisar S, Maacha S, Grivel JC, Chaussabel D, Ericsson J, Hussain K.
    Biomedicines; 2022 Aug 29; 10(9):. PubMed ID: 36140215
    [Abstract] [Full Text] [Related]

  • 59. Glucose transporters: structure, function and consequences of deficiency.
    Brown GK.
    J Inherit Metab Dis; 2000 May 29; 23(3):237-46. PubMed ID: 10863940
    [Abstract] [Full Text] [Related]

  • 60. Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature.
    Hadipour F, Sarkheil P, Noruzinia M, Hadipour Z, Baghdadi T, Shafeghati Y.
    Indian J Hum Genet; 2013 Jan 29; 19(1):84-6. PubMed ID: 23901198
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 10.