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 *

156 related articles for article (PubMed ID: 5805578)

  • 1. [Prolinuria].
    Tada K
    Saishin Igaku; 1969 Jun; 24(6):1226-34. PubMed ID: 5805578
    [No Abstract]   [Full Text] [Related]  

  • 2. [Results of a period of research (1967-1974) in the field of disorders of transport amino acid and metabolism using chromatographic, electrophoretic and dosimetric methods].
    Berio A; Allegranza A; Scapaticci E; Cadoni M; Camozzi C; Cavallo V; Di Stefano A; Santos JG
    Minerva Pediatr; 1975 Sep; 27(30):1609-23. PubMed ID: 1177852
    [No Abstract]   [Full Text] [Related]  

  • 3. Cystathioninuria and renal iminoglycinuria in a pedigree.
    Whelan DT; Scriver CR
    N Engl J Med; 1968 Apr; 278(17):924-7. PubMed ID: 5644557
    [No Abstract]   [Full Text] [Related]  

  • 4. [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]  

  • 5. [Familial iminoglycinuria].
    Ohura T
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):569-71. PubMed ID: 9645136
    [No Abstract]   [Full Text] [Related]  

  • 6. Prolinuria: defect in intestinal absorption of imino acids and glycine.
    Morikawa T; Tada K; Ando T; Yoshida T; Yokoyama Y; Arakawa T
    Tohoku J Exp Med; 1966 Oct; 90(2):105-16. PubMed ID: 5971079
    [No Abstract]   [Full Text] [Related]  

  • 7. [Hyperprolinemia and hydroxyprolinemia].
    Berger R; Broyer M
    Presse Med (1893); 1969 May; 77(26):957-8. PubMed ID: 5795142
    [No Abstract]   [Full Text] [Related]  

  • 8. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants.
    Turner B; Brown DA
    Med J Aust; 1972 Jan; 1(2):62-5. PubMed ID: 5025157
    [No Abstract]   [Full Text] [Related]  

  • 9. [Hyperglycinemia].
    Hyánek J; Posísil R; Hoza J; Mechlová J; Kapras J; Podhradská O; Kopejtková H; Hejduková H; Viletová H; Kunová V
    Cesk Pediatr; 1975 Nov; 30(11):543-5. PubMed ID: 1212727
    [No Abstract]   [Full Text] [Related]  

  • 10. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".
    Statter M; Ben-Zvi A; Shina A; Schein R; Russell A
    Helv Paediatr Acta; 1976 Aug; 31(2):173-82. PubMed ID: 955941
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hyperprolinemia. I. Study of a large family.
    Potter JL; Waickman FJ
    J Pediatr; 1973 Oct; 83(4):635-8. PubMed ID: 4729989
    [No Abstract]   [Full Text] [Related]  

  • 12. Hyperprolinemia: clinical and biochemical family study.
    Woody NC; Snyder CH; Harris JA
    Pediatrics; 1969 Oct; 44(4):554-63. PubMed ID: 5346634
    [No Abstract]   [Full Text] [Related]  

  • 13. Iminoglycinuria in a child in Czechoslovakia.
    Blehová B; Păzoutová N; Hyánek J; Jirásek J
    Humangenetik; 1973 Jul; 19(2):207-10. PubMed ID: 4744406
    [No Abstract]   [Full Text] [Related]  

  • 14. The relationship between proline and hydroxyproline urinary excretion in human as an index of collagen catabolism.
    Nusgens B; Lapiere CM
    Clin Chim Acta; 1973 Oct; 48(2):203-11. PubMed ID: 4758883
    [No Abstract]   [Full Text] [Related]  

  • 15. Defective hydroxyproline metabolism in type II hyperprolinemia.
    Goodman SI; Mace JW; Miles BS; Teng CC; Brown SB
    Biochem Med; 1974 Aug; 10(4):329-36. PubMed ID: 4851275
    [No Abstract]   [Full Text] [Related]  

  • 16. Congenital renal dysplasia, retinal dysplasia and mental retardation associated with hyperprolinuria and hyper-oh-prolinuria.
    Rokkones T; Loken AC
    Acta Paediatr Scand; 1968 May; 57(3):225-9. PubMed ID: 5706039
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.
    Jackson SH; Dennis AW; Greenberg M
    Can Med Assoc J; 1975 Oct; 113(8):759, 762-3. PubMed ID: 803128
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial iminoglycinuria. An inborn error of renal tubular transport.
    Rosenberg LE; Durant JL; Elsas LJ
    N Engl J Med; 1968 Jun; 278(26):1407-13. PubMed ID: 5652624
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hyperprolinuria].
    Blehová B; Pazoutová N; Hyánek J; Cerovská E; Rákosníková M
    Cesk Pediatr; 1974 Jul; 29(6):335-7. PubMed ID: 4847100
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.