BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 3201597)

  • 21. [Ornithine-transcarbamylase deficiency: prognostic difficulties].
    Sanjurjo Crespo P; Sasieta Altuna M; Rubio Zamora V; Prats Viñas JM; Vallo Boado A
    An Esp Pediatr; 1991 Dec; 35(6):407-8. PubMed ID: 1793191
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Use of immunocytochemical analysis of a duodenal biopsy specimen to identify a carrier of ornithine transcarbamylase deficiency.
    Hamano Y; Kodama H; Fujikawa Y; Tanaka Y; Nishimura K; Yanagisawa M
    N Engl J Med; 1988 Jun; 318(23):1521-3. PubMed ID: 3367962
    [No Abstract]   [Full Text] [Related]  

  • 23. [Hyperammonemia in children].
    Skovby F
    Ugeskr Laeger; 1988 Oct; 150(44):2638-41. PubMed ID: 3201596
    [No Abstract]   [Full Text] [Related]  

  • 24. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461
    [No Abstract]   [Full Text] [Related]  

  • 25. Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblasts.
    Rapp B; Häberle J; Linnebank M; Wermuth B; Marquardt T; Harms E; Koch HG
    Eur J Pediatr; 2001 May; 160(5):283-7. PubMed ID: 11388595
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fatal clinical course of ornithine transcarbamylase deficiency in an adult heterozygous female patient.
    Heringlake S; Böker K; Manns M
    Digestion; 1997; 58(1):83-6. PubMed ID: 9018015
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Family studies in ornithine transcarbamylase deficiency.
    Svirklys LG; Wilcken B; Hammond J; Mackinlay AG; O'Sullivan WJ
    Arch Dis Child; 1988 Mar; 63(3):297-302. PubMed ID: 3355210
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
    Tuchman M; Yudkoff M
    Mol Genet Metab; 1999 Jan; 66(1):10-5. PubMed ID: 9973542
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Prenatal diagnosis of inborn errors of metabolism].
    Matsuda I
    Nihon Rinsho; 1978 May; Suppl():1326-7. PubMed ID: 691339
    [No Abstract]   [Full Text] [Related]  

  • 30. Ornithine transcarbamylase deficiency: ten new mutations and high proportion of de novo mutations in heterozygous females.
    Oppliger Leibundgut E; Liechti-Gallati S; Colombo JP; Wermuth B
    Hum Mutat; 1997; 9(5):409-11. PubMed ID: 9143919
    [No Abstract]   [Full Text] [Related]  

  • 31. [Hyperammonemia in the newborn through ornithine transcarbamylase deficiency (author's transl)].
    Plöchl E; Hilbe W; Bachmann C
    Padiatr Padol; 1981; 16(2):179-88. PubMed ID: 7243329
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Hyperammonemia due to an inborn error of metabolism. Ornithine-transcarbamylase deficiency].
    Chevrel B
    Presse Med (1893); 1969 Sep; 77(40):1370. PubMed ID: 5821578
    [No Abstract]   [Full Text] [Related]  

  • 33. Molecular diagnosis of inborn errors of metabolism.
    McGill JJ
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():121-3. PubMed ID: 11400748
    [No Abstract]   [Full Text] [Related]  

  • 34. [Pre- and postnatal diagnosis of organoacidopathies].
    Hoffmann GF; Jakobs C; Rating D; Sweetman L; Trefz FK
    Monatsschr Kinderheilkd; 1990 Jul; 138(7):381-8. PubMed ID: 2204822
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diagnosis of inborn errors of metabolism.
    Wong HB
    J Singapore Paediatr Soc; 1986; 28(1-2):45-53. PubMed ID: 3762077
    [No Abstract]   [Full Text] [Related]  

  • 36. [Hyperammonemia in pediatric diseases].
    Cathelineau L
    Arch Fr Pediatr; 1979; 36(7):724-35. PubMed ID: 394697
    [No Abstract]   [Full Text] [Related]  

  • 37. [Neonatal hyperammonemia].
    Jaeken J; Devlieger H; Evens M; Casaer P; Eggermont E
    Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Prenatal diagnosis of metabolic hereditary diseases].
    Poenaru L
    Rev Prat; 1987 Oct; 37(43):2620-7. PubMed ID: 3423673
    [No Abstract]   [Full Text] [Related]  

  • 39. Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.
    Levin B; Dobbs RH; Burgess EA; Palmer T
    Arch Dis Child; 1969 Apr; 44(234):162-9. PubMed ID: 5779427
    [No Abstract]   [Full Text] [Related]  

  • 40. [Biological diagnosis of hereditary metabolic diseases. From selective screening to the mutant-cell bank].
    Divry P; Maire I; Mathieu M
    Ann Biol Clin (Paris); 1988; 46(6):381-6. PubMed ID: 3052190
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.