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

178 related items for PubMed ID: 948541

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Renal failure in adult onset hypophosphatemic osteomalacia with Fanconi syndrome: a family study and review of the literature.
    Harrison NA, Bateman JM, Ledingham JG, Smith R.
    Clin Nephrol; 1991 Apr; 35(4):148-50. PubMed ID: 1649711
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [Adult-onset sex-linked familial hypophosphatemic osteomalacia].
    Radó J, Haris A, Szebenyi B.
    Orv Hetil; 1997 Jun 29; 138(26):1683-8. PubMed ID: 9289682
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Familial adult onset X-linked hypophosphataemic osteomalacia (report of a family; clinical and experimental studies).
    Radó JP, Haris A, Szebenyi B.
    Acta Physiol Hung; 1997 Jun 29; 85(3):199-214. PubMed ID: 10101535
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Fanconi's syndrome in adults (phospho-gluco-amino diabetes) and cancer].
    Lièvre JA, Camus JP, Benichou C, Guillien P, Louvet L.
    Ann Med Interne (Paris); 1969 Jun 29; 120(6):459-68. PubMed ID: 5807725
    [No Abstract] [Full Text] [Related]

  • 11. Inherited tubule disorders.
    DeFronzo RA, Thier SO.
    Hosp Pract (Off Ed); 1982 Feb 29; 17(2):111-7, 121-8. PubMed ID: 6281157
    [No Abstract] [Full Text] [Related]

  • 12. [Hypophosphatemia of a genetic origin].
    Escoubet B, Silve C.
    Nephrologie; 1992 Feb 29; 13(3):115-21. PubMed ID: 1641053
    [Abstract] [Full Text] [Related]

  • 13. Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance.
    Wrong OM, Norden AG, Feest TG.
    QJM; 1994 Aug 29; 87(8):473-93. PubMed ID: 7922301
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder.
    Econs MJ, McEnery PT.
    J Clin Endocrinol Metab; 1997 Feb 29; 82(2):674-81. PubMed ID: 9024275
    [Abstract] [Full Text] [Related]

  • 16. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].
    De Marchi S, Proto G, Jengo A, Collinassi P, Basile A.
    Minerva Med; 1983 Feb 25; 74(7):301-6. PubMed ID: 6828258
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Renal diabetes. Apropos of 103 cases in children].
    Lestradet H, Labrune B, Duval C, Deschamps I.
    Arch Fr Pediatr; 1979 Feb 25; 36(8):760-6. PubMed ID: 395917
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.