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Journal Abstract Search

136 related items for PubMed ID: 4313225

  • 1. Genetic modes of transmission in metabolic bone disease.
    Jackson CE, Mock LF.
    Clin Orthop Relat Res; 1970; 68():238-50. PubMed ID: 4313225
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary metabolic bone diseases.
    Harrison HE, Harrison HC.
    Clin Orthop Relat Res; 1964; 33():147-63. PubMed ID: 5889018
    [No Abstract] [Full Text] [Related]

  • 3. Metabolic bone disease in children.
    Steendijk R.
    Clin Orthop Relat Res; 1971; 77():247-75. PubMed ID: 4335242
    [No Abstract] [Full Text] [Related]

  • 4. Fanconi or not Fanconi? Lowe syndrome revisited.
    Kleta R.
    Clin J Am Soc Nephrol; 2008 Sep; 3(5):1244-5. PubMed ID: 18667737
    [No Abstract] [Full Text] [Related]

  • 5. Hereditary tubular disorders of the Fanconi type and the idiopathic Fanconi syndrome.
    Bickel H, Manz F.
    Prog Clin Biol Res; 1989 Sep; 305():111-35. PubMed ID: 2668968
    [No Abstract] [Full Text] [Related]

  • 6. Eye signs of hypophosphatasia.
    Brenner RL, Smith JL, Cleveland WW, Bejar RL, Lockhart WS.
    Arch Ophthalmol; 1969 May; 81(5):614-7. PubMed ID: 4305610
    [No Abstract] [Full Text] [Related]

  • 7. [A case of inborn hypophosphatasia].
    Wolyńska-Bochner S, Woloszczuk K.
    Pediatr Pol; 1969 May; 44(5):611-4. PubMed ID: 4307196
    [No Abstract] [Full Text] [Related]

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  • 9. Manifestations of genetic diseases in the human pulp.
    Witkop CJ.
    Oral Surg Oral Med Oral Pathol; 1971 Aug; 32(2):278-316. PubMed ID: 4327157
    [No Abstract] [Full Text] [Related]

  • 10. Inorganic pyrophosphate in plasma in normal persons and in patients with hypophosphatasia, osteogenesis imperfecta, and other disorders of bone.
    Russell RG, Bisaz S, Donath A, Morgan DB, Fleisch H.
    J Clin Invest; 1971 May; 50(5):961-9. PubMed ID: 4324072
    [Abstract] [Full Text] [Related]

  • 11. [Clinical aspects and biochemical diagnosis of hypophosphatasia].
    Mühlbach R, Lindenhayn K, Krüger E.
    Beitr Orthop Traumatol; 1970 Jan; 17(1):74-6. PubMed ID: 4324396
    [No Abstract] [Full Text] [Related]

  • 12. Osteogenesis imperfecta and other heritable disorders of bone.
    Paterson CR.
    Baillieres Clin Endocrinol Metab; 1997 Apr; 11(1):195-213. PubMed ID: 9222492
    [Abstract] [Full Text] [Related]

  • 13. [Genetic bases of metabolic tubular nephropathies].
    Savi M.
    Minerva Med; 1979 Oct 13; 70(44):3001-13. PubMed ID: 386171
    [No Abstract] [Full Text] [Related]

  • 14.
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  • 15. Hereditary tubular disorders.
    Woolf LI.
    Monogr Pathol; 1979 Oct 13; 20():218-38. PubMed ID: 388203
    [No Abstract] [Full Text] [Related]

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  • 18. [Description of a case of hypophosphatasia].
    Varcasia E, Agostinelli O.
    Minerva Pediatr; 1969 Sep 29; 21(39):1840-5. PubMed ID: 4312049
    [No Abstract] [Full Text] [Related]

  • 19. [Hypophosphatasia in children].
    Verbitskaia LI, Dumnova AG.
    Pediatriia; 1966 Aug 29; 45(8):86-8. PubMed ID: 4305050
    [No Abstract] [Full Text] [Related]

  • 20. [Hereditary forms of rickets].
    Fanconi A, Prader A.
    Schweiz Med Wochenschr; 1972 Aug 05; 102(31):1073-8. PubMed ID: 4349077
    [No Abstract] [Full Text] [Related]

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