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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 8165754)

  • 21. [Fanconi-Bickel syndrome].
    Koch HC; Mallmann R
    Klin Padiatr; 1990; 202(6):422-6. PubMed ID: 2266709
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Debré-De Toni-Fanconi syndrome with glycogenosis of the liver].
    Bauer B
    Klin Wochenschr; 1968 Mar; 46(6):317-28. PubMed ID: 5245557
    [No Abstract]   [Full Text] [Related]  

  • 23. Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease.
    Weinstein DA; Wolfsdorf JI
    Eur J Pediatr; 2002 Oct; 161 Suppl 1():S35-9. PubMed ID: 12373568
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cornstarch therapy in type I glycogen-storage disease.
    Wergowske GL; Carmody TJ
    N Engl J Med; 1984 Jul; 311(2):128-9. PubMed ID: 6588292
    [No Abstract]   [Full Text] [Related]  

  • 25. Nocturnal enteral nutrition is therapeutic for growth failure in Fanconi-Bickel syndrome.
    Pennisi A; Maranda B; Benoist JF; Baudouin V; Rigal O; Pichard S; Santer R; Romana Lepri F; Novelli A; Ogier de Baulny H; Dionisi-Vici C; Schiff M
    J Inherit Metab Dis; 2020 May; 43(3):540-548. PubMed ID: 31816104
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An infant with severe combined immunodeficiency syndrome, an alpha-thalassemia trait and renal Fanconi syndrome.
    van de Moesdijk D; van Weel-Sipman MH
    Bone Marrow Transplant; 2000 Jul; 26(1):97-9. PubMed ID: 10918411
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Clinical aspects and enzymologic diagnosis of glycogenosis type 1].
    Bührdel P; Zimmermann G; Theile H; Braun W; Beyreiss K
    Kinderarztl Prax; 1977 May; 45(5):211-8. PubMed ID: 267792
    [No Abstract]   [Full Text] [Related]  

  • 28. [Glycogenosis type I. Therapy (author's transl)].
    López MJ; Escribano A; Brines J; Colomer J
    An Esp Pediatr; 1980 Aug; 13(8):689-99. PubMed ID: 6933881
    [TBL] [Abstract][Full Text] [Related]  

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

  • 30. Fanconi syndrome associated with use of tenofovir in HIV-infected patients: a case report and review of the literature.
    Quimby D; Brito MO
    AIDS Read; 2005 Jul; 15(7):357-64. PubMed ID: 16044577
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Looking a gift horse in the mouth: effects of cornstarch therapy and other implications of glycogen storage disease on oral hygiene and dentition.
    Farrington FH; Duncan LL; Roth KS
    Pediatr Dent; 1995; 17(4):311-4. PubMed ID: 7567637
    [No Abstract]   [Full Text] [Related]  

  • 32. [Corn starch in the treatment of patients with glycogenosis type I and III].
    Galiano Segovia MJ; Moreno Villares JM; Medina Benítez E; Manzanares López-Manzanares J; Urruzuno Tellería P; León Sanz M
    Nutr Hosp; 1998; 13(5):228-32. PubMed ID: 9830843
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome.
    Simşek E; Savaş-Erdeve S; Sakamoto O; Doğanci T; Dallar Y
    Turk J Pediatr; 2009; 51(2):166-8. PubMed ID: 19480329
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Liver glycogenosis: first 2 Brazilian cases with double enzyme defect].
    Seibt FL; Mello de Oliveira JA; Santoro JR; Alcantara A; Dora GL; Pena GA
    Ann Histochim; 1973; 18(3):253-65. PubMed ID: 4526225
    [No Abstract]   [Full Text] [Related]  

  • 35. Cornstarch therapy in type I glycogen-storage disease.
    Chen YT; Cornblath M; Sidbury JB
    N Engl J Med; 1984 Jan; 310(3):171-5. PubMed ID: 6581385
    [No Abstract]   [Full Text] [Related]  

  • 36. [Multiple calcium oxalate stone formation in a patient with glycogen storage disease type I (von Gierke's disease) and renal tubular acidosis type I: a case report].
    Kanematsu A; Segawa T; Kakehi Y; Takeuchi H
    Hinyokika Kiyo; 1993 Jul; 39(7):645-8. PubMed ID: 8362684
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Orthotopic liver transplantation for type I glycogenosis unresponsive to medical therapy.
    Sokal EM; Lopez-Silvarrey A; Buts JP; Otte JB
    J Pediatr Gastroenterol Nutr; 1993 May; 16(4):465-7. PubMed ID: 8315558
    [No Abstract]   [Full Text] [Related]  

  • 38. A family with a dominant form of idiopathic Fanconi syndrome leading to renal failure in adult life.
    Patrick A; Cameron JS; Ogg CS
    Clin Nephrol; 1981 Dec; 16(6):289-92. PubMed ID: 7032774
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The Fanconi syndrome associated with hepatic glycogenosis and abnormal metabolism of galactose.
    Garty R; Cooper M; Tabachnik E
    J Pediatr; 1974 Dec; 85(6):821-3. PubMed ID: 4529611
    [No Abstract]   [Full Text] [Related]  

  • 40. [Rare case of viral hepatitis coexisting with Gierke disease (glycogenosis)].
    Bychkova VI
    Sov Med; 1977 Jan; (1):146-7. PubMed ID: 265631
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.