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 *

90 related articles for article (PubMed ID: 4420281)

  • 1. [Hyperprolinemia type II].
    Thomsen B; Vetner M; Rosleff F; Reske-Nielsen E
    Ugeskr Laeger; 1974 Nov; 136(45):2530. PubMed ID: 4420281
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hyperprolinemia type I].
    Thomsen B; Vetner M; Rosleff F; Reske-Nielsen E
    Ugeskr Laeger; 1974 Oct; 136(44):2460-1. PubMed ID: 4420280
    [No Abstract]   [Full Text] [Related]  

  • 3. [Familial hyperprolinemia with nephropathy].
    Ortuño Mirete J; Guardiola Vicente JM; Botella García J
    Rev Clin Esp; 1970 Jul; 118(2):141-50. PubMed ID: 5486371
    [No Abstract]   [Full Text] [Related]  

  • 4. [Type I hyperprolinemia. Study of a familial case].
    Fontaine G; Farriaux JP; Dautrevaux M
    Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Type I hyperprolinemia: genotype/phenotype correlations.
    Guilmatre A; Legallic S; Steel G; Willis A; Di Rosa G; Goldenberg A; Drouin-Garraud V; Guet A; Mignot C; Des Portes V; Valayannopoulos V; Van Maldergem L; Hoffman JD; Izzi C; Espil-Taris C; Orcesi S; Bonafé L; Le Galloudec E; Maurey H; Ioos C; Afenjar A; Blanchet P; Echenne B; Roubertie A; Frebourg T; Valle D; Campion D
    Hum Mutat; 2010 Aug; 31(8):961-5. PubMed ID: 20524212
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Familial essential hyperprolinemia].
    Hainaut H; Hariga J; Willems C; Heusden A; Chapelle P
    Presse Med (1893); 1971 Apr; 79(21):945-8. PubMed ID: 5580522
    [No Abstract]   [Full Text] [Related]  

  • 8. [Hyperprolinemia type I].
    Endo F
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):152-4. PubMed ID: 9590013
    [No Abstract]   [Full Text] [Related]  

  • 9. [Familial hyperprolinemia].
    Dogan K; Dogan S; Lipovac K
    Neuropsihijatrija; 1968; 16(1):15-23. PubMed ID: 5191809
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy].
    Jeune M; Collombel C; Michel M; David M; Guibaud P; Guerrier G; Albert J
    Ann Pediatr (Paris); 1970 Feb; 17(2):349-63. PubMed ID: 5513158
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Hyperprolinaemia type II.
    Similä S
    Fla Dent J; 1970 Aug; 2(2):143-50. PubMed ID: 5271041
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

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

  • 15. Familial hyperprolinemia and mental retardation. A second metabolic type.
    Selkoe DJ
    Neurology; 1969 May; 19(5):494-502. PubMed ID: 5815222
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
    Minder FC; Dubach UC; Antener I
    Z Klin Med; 1965 Dec; 158(7):601-32. PubMed ID: 5869106
    [No Abstract]   [Full Text] [Related]  

  • 17. [Diseases caused by altered intermediate metabolism of amino acids].
    Bulgarelli R; Berio A
    Minerva Nipiol; 1969; 19(6):328-61 contd. PubMed ID: 4923874
    [No Abstract]   [Full Text] [Related]  

  • 18. [Familial hyperprolinemia--a case in a family].
    Oknińska A; Grygalewicz J; Kowalewska-Kantecka B; Iwańska J
    Pol Arch Med Wewn; 1974 Feb; 51(2):189-97. PubMed ID: 4816363
    [No Abstract]   [Full Text] [Related]  

  • 19. Type 2 hyperprolinemia: absence of delta1-pyrroline-5-carboxylic acid dehydrogenase activity.
    Valle DL; Phang JM; Goodman SI
    Science; 1974 Sep; 185(4156):1053-4. PubMed ID: 4369405
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.