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 *

88 related articles for article (PubMed ID: 420125)

  • 21. [Hyperlysinemia and hyperammonemia].
    Rabier D; Parvy P; Bardet J; Kamoun P
    Ann Biol Clin (Paris); 1991; 49(1):45-8. PubMed ID: 1904697
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Blood ammonia in portal hypertension and liver diseases in children.
    Michalowicz-Wojczyńska E
    Pol Med J; 1969; 8(5):1101-10. PubMed ID: 5310033
    [No Abstract]   [Full Text] [Related]  

  • 23. Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolism.
    Baumgartner ER; Bachmann C; Brechbühler T; Wick H
    Pediatr Res; 1975 Jul; 9(7):559-64. PubMed ID: 240144
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Acute hepatic failure in children.
    Riely CA
    Yale J Biol Med; 1984; 57(2):161-84. PubMed ID: 6433587
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Effect of pyrrolizidine alkaloid-induced hepatic disease on plasma amino acid patterns in the horse.
    Gulick BA; Liu IK; Qualls CW; Gribble DH; Rogers QR
    Am J Vet Res; 1980 Nov; 41(11):1894-8. PubMed ID: 7212423
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Combined use of tandem mass spectrometry with urine gas chromatography/mass spectrometry is useful for diagnosis of inborn errors of metabolism in children].
    Xie LJ; Zhu JX; Zhu XD; Li HJ; Han LS; Gu XF
    Zhongguo Dang Dai Er Ke Za Zhi; 2008 Feb; 10(1):31-4. PubMed ID: 18289467
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Reye's syndrome in the United States from 1981 through 1997.
    Belay ED; Bresee JS; Holman RC; Khan AS; Shahriari A; Schonberger LB
    N Engl J Med; 1999 May; 340(18):1377-82. PubMed ID: 10228187
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Atypical clinical course of ornithine transcarbamylase deficiency due to a new mutant (comparison with Reye's disease).
    Krieger I; Snodgrass PJ; Roskamp J
    J Clin Endocrinol Metab; 1979 Mar; 48(3):388-92. PubMed ID: 429491
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: an eight-year experience.
    Vatanavicharn N; Ratanarak P; Liammongkolkul S; Sathienkijkanchai A; Wasant P
    Clin Chim Acta; 2012 Jul; 413(13-14):1141-4. PubMed ID: 22465081
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Plasma alpha-amino-n-butyric acid to leucine ratio in perspective.
    Dienstag JL; Isselbacher KJ
    Gastroenterology; 1978 Nov; 75(5):928. PubMed ID: 29818
    [No Abstract]   [Full Text] [Related]  

  • 31. Abnormalities of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of patients with Reye's syndrome.
    Sinatra F; Yoshida T; Applebaum M; Masion Hoogenraad NJ; Sunshine P
    Pediatr Res; 1975 Nov; 9(11):829-33. PubMed ID: 171618
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Atypical nonketotic hyperglycinemia with a defective glycine transport system in nervous tissue.
    Mayor F; Martin A; Rodriguez-Pombo P; Garcia MJ; Benavides J; Ugarte M
    Neurochem Pathol; 1984-1985 Winter; 2(4):233-49. PubMed ID: 6537469
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prevalence of selected disorders of inborn errors of metabolism in suspected cases at a tertiary care hospital in Karachi.
    Satwani H; Raza J; Hanai J; Nomachi S
    J Pak Med Assoc; 2009 Dec; 59(12):815-9. PubMed ID: 20201170
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [Reye's syndrome: pathogenetic problems (author's transl)].
    Sabetta G; Castro M; Donfrancesco A; Castelli P; Lucidi V; Lubrano R; Ruberto U; Qaddourah M
    Pediatr Med Chir; 1981; 3(6):555-7. PubMed ID: 7343954
    [TBL] [Abstract][Full Text] [Related]  

  • 36. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects.
    Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K
    Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Viral infections and prolonged fever after liver transplantation in young children with inborn errors of metabolism.
    Huang HP; Chien YH; Huang LM; Ni YH; Chang MH; Ho MC; Lee PH; Hwu WL
    J Formos Med Assoc; 2005 Sep; 104(9):623-9. PubMed ID: 16276436
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Nonketotic hyperglycinemia. Glycine accumulation due to absence of glycerine cleavage in brain.
    Perry TL; Urquhart N; MacLean J; Evans ME; Hansen S; Davidson GF; Applegarth DA; MacLeod PJ; Lock JE
    N Engl J Med; 1975 Jun; 292(24):1269-73. PubMed ID: 1128590
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Inherited metabolic disorders in Thailand.
    Wasant P; Svasti J; Srisomsap C; Liammongkolkul S
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S700-9. PubMed ID: 12403250
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Reye's syndrome].
    Berghuis M; van Vught AJ; de Klerk JB; Huber J
    Tijdschr Kindergeneeskd; 1987 Dec; 55(6):216-25. PubMed ID: 3327194
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.