BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 4663897)

  • 1. Congenital hypophosphatasia. Report on two cases with special reference to phosphoethanolamine excretion.
    Terheggen HG; Schildberg C; Schürer W; Van Sande M; Bützler O
    Monogr Hum Genet; 1972; 6():188. PubMed ID: 4663897
    [No Abstract]   [Full Text] [Related]  

  • 2. [Congenital hypophosphatasia].
    Terheggen HG; Wischermann A
    Monatsschr Kinderheilkd; 1984 Jul; 132(7):512-22. PubMed ID: 6147751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterogeneity of adult hypophosphatasia. Report of severe and mild cases.
    Weinstein RS; Whyte MP
    Arch Intern Med; 1981 May; 141(6):727-31. PubMed ID: 7235780
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical, laboratory, and genetic investigations of hypophosphatasia: support for autosomal dominant inheritance with homozygous lethality.
    Eastman JR; Bixler D
    J Craniofac Genet Dev Biol; 1983; 3(3):213-34. PubMed ID: 6643650
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neutrophil alkaline phosphatase (NAP) score in the diagnosis of hypophosphatasia.
    Iqbal SJ; Davies T; Cole R; Whitaker P; Chapman C
    Clin Chim Acta; 2000 Dec; 302(1-2):49-57. PubMed ID: 11074063
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Hypophosphatasia in the adult. Considerations apropos of a case].
    Rico Lenza H; Paniagua Garrido MC; Rosa García M; Huertas García-Alejo R
    Rev Clin Esp; 1982 Sep; 166(5):255-6. PubMed ID: 6216561
    [No Abstract]   [Full Text] [Related]  

  • 7. Lethal and mild hypophosphatasia in half-sibs.
    Eastman J; Bixler D
    J Craniofac Genet Dev Biol; 1982; 2(1):35-44. PubMed ID: 7130355
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypophosphatasia: biochemical screening of a Dutch kindred and evidence that urinary excretion of inorganic pyrophosphate is a marker for the disease.
    Macfarlane JD; Poorthuis BJ; van de Kamp JJ; Russell RG; Caswell AM
    Clin Chem; 1988 Sep; 34(9):1937-41. PubMed ID: 2843309
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hypophosphatasia with normal urinary phosphoethanolamine in a 22-month-old girl].
    Tecza S; Prandota J; Morawska Z; Rudzka M; Panków-Prandota L
    Pediatr Pol; 1980 Jun; 55(6):791-6. PubMed ID: 7413330
    [No Abstract]   [Full Text] [Related]  

  • 10. Serum alkaline phosphatase, serum pyrophosphatase, phosphorylethanolamine and inorganic pyrophosphate in plasma and urine. A genetic and clinical study of hypophosphatasia.
    Sørensen SA; Flodgaard H; Sørensen E
    Monogr Hum Genet; 1978; 10():66-9. PubMed ID: 214699
    [No Abstract]   [Full Text] [Related]  

  • 11. Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening.
    Chodirker BN; Evans JA; Seargeant LE; Cheang MS; Greenberg CR
    Am J Hum Genet; 1990 Feb; 46(2):280-5. PubMed ID: 2301398
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Hypophosphatasia].
    Meberg A; Torstenson T
    Tidsskr Nor Laegeforen; 1974 Apr; 94(10):641-3. PubMed ID: 4826792
    [No Abstract]   [Full Text] [Related]  

  • 13. Infantile hypophosphatasia--linkage with the RH locus.
    Chodirker BN; Evans JA; Lewis M; Coghlan G; Belcher E; Philipps S; Seargeant LE; Sus C; Greenberg CR
    Genomics; 1987 Nov; 1(3):280-2. PubMed ID: 3128473
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pseudohypophosphatasia.
    Sarkar AK; Ghosh SK; Mitra P; Mandal S; Mukhopadhyay S; Mathew J
    Indian J Pediatr; 1997; 64(2):256-61. PubMed ID: 10771846
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hypophosphatasia in an adult, with late clinical manifestations (author's transl)].
    Paolaggi JB; Job C; Durigon M; Alterescu R; Auquier L
    Nouv Presse Med; 1978 Dec; 7(47):4285-9. PubMed ID: 745977
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal recessive adult-onset hypophosphatasia.
    Harraway JR; Sheard JM; Soule SJ; Florkowski CM; George PM
    Pathology; 2005 Dec; 37(6):563-5. PubMed ID: 16373239
    [No Abstract]   [Full Text] [Related]  

  • 17. Clinical, biochemical and genetic spectrum of low alkaline phosphatase levels in adults.
    Riancho-Zarrabeitia L; García-Unzueta M; Tenorio JA; Gómez-Gerique JA; Ruiz Pérez VL; Heath KE; Lapunzina P; Riancho JA
    Eur J Intern Med; 2016 Apr; 29():40-5. PubMed ID: 26783040
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Serum alkaline phosphatase in hypophosphatasia.
    Warshaw JB; Littlefield JW; Fishman WH; Inglis NR; Stolbach LL
    J Clin Invest; 1971 Oct; 50(10):2137-42. PubMed ID: 5116205
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypophosphatasia (adult form): quantitation of serum alkaline phosphatase isoenzyme activity in a large kindred.
    Millán JL; Whyte MP; Avioli LV; Fishman WH
    Clin Chem; 1980 Jun; 26(7):840-5. PubMed ID: 7379306
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The diagnosis of the early infantile form of hypophosphatasia tarda.
    Svejcar J; Walther A
    Humangenetik; 1975 May; 28(1):49-56. PubMed ID: 1150259
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.