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 *

145 related articles for article (PubMed ID: 1200680)

  • 1. Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs.
    Pavone L; Mollica F; Levy HL
    Arch Dis Child; 1975 Aug; 50(8):637-41. PubMed ID: 1200680
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Type II hyperprolinaemia in a pedigree of Irish travellers (nomads).
    Flynn MP; Martin MC; Moore PT; Stafford JA; Fleming GA; Phang JM
    Arch Dis Child; 1989 Dec; 64(12):1699-707. PubMed ID: 2624476
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dietary treatment in hyperprolinaemia type II.
    Similä S
    Acta Paediatr Scand; 1974 Mar; 63(2):249-56. PubMed ID: 4820590
    [No Abstract]   [Full Text] [Related]  

  • 4. Low proline diet in type I hyperprolinaemia.
    Harries JT; Piesowicz AT; Seakins JW; Francis DE; Wolff OH
    Arch Dis Child; 1971 Feb; 46(245):72-81. PubMed ID: 5555491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hydroxyproline metabolism in type II hyperprolinaemia.
    Similä S
    Ann Clin Biochem; 1979 Jul; 16(4):177-81. PubMed ID: 533224
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital.
    Yadav GC; Reavey PC
    J Inherit Metab Dis; 1988; 11(3):277-84. PubMed ID: 3148069
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hyperprolinaemia: a disease which does not need treatment?
    Mollica F; Pavone L
    Acta Paediatr Scand; 1976 Mar; 65(2):206-8. PubMed ID: 943900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hyperprolinaemia in two successive generations of a North American Indian family.
    Perry TL; Hardwick DF; Lowry RB; Hansen S
    Ann Hum Genet; 1968 May; 31(4):401-7. PubMed ID: 4299764
    [No Abstract]   [Full Text] [Related]  

  • 9. Type II hyperprolinaemia with renal involvement.
    Bellet H; Morin D; Daudet H; Dumas ML; Valette H; Magnan de Bornier B; Dumas R
    J Inherit Metab Dis; 1991; 14(5):846-7. PubMed ID: 1779641
    [No Abstract]   [Full Text] [Related]  

  • 10. Hyperprolinaemia.
    Piesowicz AT
    Arch Dis Child; 1968 Dec; 43(232):748. PubMed ID: 5702251
    [No Abstract]   [Full Text] [Related]  

  • 11. Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome.
    Goodman BK; Rutberg J; Lin WW; Pulver AE; Thomas GH
    J Inherit Metab Dis; 2000 Dec; 23(8):847-8. PubMed ID: 11196113
    [No Abstract]   [Full Text] [Related]  

  • 12. A patient with hypophosphatasia and hyperprolinaemia.
    De Vries HR; Duran M; De Bree PK; Wadman SK
    Neth J Med; 1978; 21(1):28-34. PubMed ID: 634414
    [No Abstract]   [Full Text] [Related]  

  • 13. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
    Mollica F; Pavone L; Antener I
    Pediatrics; 1971 Aug; 48(2):225-31. PubMed ID: 5560617
    [No Abstract]   [Full Text] [Related]  

  • 14. Intravenous proline tolerance in a patient with hyperprolinaemia type II and his relatives.
    Similä S
    Helv Paediatr Acta; 1970 Jul; 25(3):287-92. PubMed ID: 5518053
    [No Abstract]   [Full Text] [Related]  

  • 15. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P; Willems C; Heusden AM; Hainaut H; Gottschalk C
    J Genet Hum; 1969 Oct; 17(3):297-315. PubMed ID: 5387412
    [No Abstract]   [Full Text] [Related]  

  • 16. Non-ketotic hyperglycinaemia in a family with an unusual phenotype.
    Ando T; Nyhan WL; Bicknell J; Harris R; Stern J
    J Inherit Metab Dis; 1978; 1(3):79-83. PubMed ID: 116082
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Iminoglycinuria--a "harmless" inborn error of metabolism?
    Fraser GR; Friedmann AI; Patton VM; Wade DN; Woolf LI
    Humangenetik; 1968; 6(4):362-7. PubMed ID: 5713621
    [No Abstract]   [Full Text] [Related]  

  • 18. N-(pyrrole-2-carboxyl) glycine a diagnostic marker of hyperprolinaemia type II: mass spectra of trimethylsilyl derivatives.
    Walker V; Mills GA
    Clin Chim Acta; 2009 Jul; 405(1-2):153-4. PubMed ID: 19376100
    [No Abstract]   [Full Text] [Related]  

  • 19. Hyperprolinaemia type 2.
    Emery FA; Goldie L; Stern J
    J Ment Defic Res; 1968 Sep; 12(3):187-95. PubMed ID: 4972625
    [No Abstract]   [Full Text] [Related]  

  • 20. Hydroxyprolinemia: an apparently harmless familial metabolic disorder.
    Pelkonen R; Kivirikko KI
    N Engl J Med; 1970 Aug; 283(9):451-6. PubMed ID: 4393577
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.