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 *

116 related articles for article (PubMed ID: 698556)

  • 1. Indian childhood cirrhosis: an inherited disorder of tryptophan metabolism?
    Sur AM; Bhatti A
    Br Med J; 1978 Aug; 2(6136):529-31. PubMed ID: 698556
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Study of the role of tryptophan metabolism in Indian Childhood Cirrhosis.
    Srivastava JR; Rao ST; Sur BK
    Indian Pediatr; 1980 Jul; 17(7):587-91. PubMed ID: 7216409
    [No Abstract]   [Full Text] [Related]  

  • 3. [Role of tryptophan metabolism disorders in the etiology of mental retardation in children].
    Knapp A; Vel'tishchev IuE; Barashnev IuI; Grimm U; Kazantseva LZ
    Vopr Okhr Materin Det; 1978 Oct; 23(10):51-6. PubMed ID: 706273
    [No Abstract]   [Full Text] [Related]  

  • 4. [Proceedings: Pellagroid eruption and deep recurrent ataxia due to a tryptophan metabolism disorder].
    Nuyts JP; Gaudier B; Caridroit M; Leclerc F
    Pediatrie; 1975; 30(5):539. PubMed ID: 1178284
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial hypertryptophanemia, tryptophanuria and indoleketonuria.
    Snedden W; Mellor CS; Martin JR
    Clin Chim Acta; 1983 Jul; 131(3):247-56. PubMed ID: 6883719
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [New observations on fetal liver cirrhosis associated with hereditary tyrosinemia].
    Gourdeau H; Larochelle J; Bélanger M; Bélanger L
    Union Med Can; 1985 Sep; 114(9):762-4. PubMed ID: 3840613
    [No Abstract]   [Full Text] [Related]  

  • 7. Family exhibiting cerebellar-like ataxia, photosensitivity and shortness of stature - a new inborn error of tryptophan metabolism.
    Fenton DA; Wilkinson JD; Toseland PA
    J R Soc Med; 1983 Sep; 76(9):736-9. PubMed ID: 6620277
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Disorders of tryptophan metabolism in dermatology].
    Jouve I; Berbis P; Garnier JP; Privat Y
    Ann Dermatol Venereol; 1987; 114(12):1571-82. PubMed ID: 3328548
    [No Abstract]   [Full Text] [Related]  

  • 9. [Changes in metabolism of tryptophan of a familial type with mental deficiency].
    Giovannini M; Careddu P
    Pediatria (Napoli); 1967; 75(1):48-59. PubMed ID: 5601245
    [No Abstract]   [Full Text] [Related]  

  • 10. [On the pathology of tryptophan metabolism, with a report of another family with a deficiency simulating vitamin B6 deficiency].
    Knapp A; Wolfram G; Heilmann HH
    Dtsch Gesundheitsw; 1967 Dec; 22(52):2449-55. PubMed ID: 5597004
    [No Abstract]   [Full Text] [Related]  

  • 11. alpha-I antitrypsin enzyme deficiency in Indian childhood cirrhosis.
    Kishore N; Prasad R; Kumar A; Kishore B; Dayal RS; Sharma BB
    Trop Geogr Med; 1979 Sep; 31(3):339-45. PubMed ID: 316592
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Liver fibrosis in arginase deficiency.
    Jordá A; Portolés M; Rubio V; Capdevila A; Vilas J; García-Piño J
    Arch Pathol Lab Med; 1987 Aug; 111(8):691-2. PubMed ID: 3632278
    [No Abstract]   [Full Text] [Related]  

  • 13. Tryptophan metabolism in liver cirrhosis: influence of oral antibiotics on neuropsychiatric symptoms.
    Yoshida K; Hirayama C
    Tohoku J Exp Med; 1984 Jan; 142(1):35-41. PubMed ID: 6202023
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Study of the intermediate metabolism of tryptophan; tryptophan load test in cirrhosis].
    BENHAMOU E; LACROIX R
    C R Seances Soc Biol Fil; 1957; 151(3):545-8. PubMed ID: 13480029
    [No Abstract]   [Full Text] [Related]  

  • 15. [Skin manifestations in genetic disturbances of the amino acid metabolism].
    Knapp A
    Dermatol Monatsschr; 1970; 156(5):548-54. PubMed ID: 5509159
    [No Abstract]   [Full Text] [Related]  

  • 16. [Studies on tryptophan-nicotinic acid metabolism in hepatic cirrhosis in man. Preliminary note].
    RAGNO I; PINTO R
    Boll Soc Ital Biol Sper; 1961 Dec; 37():1296-7. PubMed ID: 14489890
    [No Abstract]   [Full Text] [Related]  

  • 17. [Infantile cirrhosis associated with neoproduction of alpha-fetoprotein. Further perspectives in hereditary tyrosinemia].
    Bélanger L; Bélanger M; Larochelle J
    Nouv Presse Med; 1972 May; 1(22):1503-4. PubMed ID: 5036712
    [No Abstract]   [Full Text] [Related]  

  • 18. The liver in siblings of patients with Indian childhood cirrhosis: a light and electron microscopic study.
    Nayak NC; Marwaha N; Kalra V; Roy S; Ghai OP
    Gut; 1981 Apr; 22(4):295-300. PubMed ID: 7239321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of copper in Indian childhood cirrhosis.
    Tanner MS
    Am J Clin Nutr; 1998 May; 67(5 Suppl):1074S-1081S. PubMed ID: 9587155
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Disorders of tryptophan-serotonin metabolism in liver cirrhosis].
    Shipov AA
    Klin Med (Mosk); 1973 Oct; 51(10):97-100. PubMed ID: 4787289
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.