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 *

123 related articles for article (PubMed ID: 1048197)

  • 21. The occurrence of gamma-aminobutyric acid in human tissues other than brain.
    Zachmann M; Tocci P; Nyhan WL
    J Biol Chem; 1966 Mar; 241(6):1355-8. PubMed ID: 4222879
    [No Abstract]   [Full Text] [Related]  

  • 22. Hydroxylysinuria.
    Hoefnagel D; Pomeroy J
    Lancet; 1970 Jun; 760(1):1342-3. PubMed ID: 4194840
    [No Abstract]   [Full Text] [Related]  

  • 23. Screening for metabolic disorders associated with mental retardation.
    Hill A; Zaleski WA
    Clin Biochem; 1972 Mar; 5(1):33-45. PubMed ID: 5022447
    [No Abstract]   [Full Text] [Related]  

  • 24. Amino acid abnormalities in a mentally retarded population.
    Kelly S; Swift H
    Am J Epidemiol; 1967 Mar; 85(2):250-8. PubMed ID: 6021375
    [No Abstract]   [Full Text] [Related]  

  • 25. A study of aminoacidemia and aminoaciduria in epileptic children.
    Tudor I; Tănase-Mogoş I; Tănăsie E; Bădescu E; Răşcanu M
    Neurol Psychiatr (Bucur); 1976; 14(4):277-82. PubMed ID: 1024264
    [No Abstract]   [Full Text] [Related]  

  • 26. Amino acid transport and mental retardation.
    Gruemer HD; Grannis GF; Hetland LB; Costantini ML
    Clin Chem; 1971 Nov; 17(11):1129-31. PubMed ID: 5166687
    [No Abstract]   [Full Text] [Related]  

  • 27. [Inborn errors of amino acid metabolism].
    Endo F
    Nihon Rinsho; 2004 Nov; 62 Suppl 11():562-6. PubMed ID: 15628476
    [No Abstract]   [Full Text] [Related]  

  • 28. A prospective community survey for aminoacidaemias.
    Komrower GM; Griffiths MJ; Fowler B; Lambert AM
    Proc R Soc Med; 1968 Mar; 61(3):294-6. PubMed ID: 5689917
    [No Abstract]   [Full Text] [Related]  

  • 29. [Long-term personal experience in the diagnosis of amino acidopathies by chromatography of serum according to the method of Scriver et al].
    Berio A
    Minerva Pediatr; 1985 Dec; 37(23-24):947-54. PubMed ID: 3834309
    [No Abstract]   [Full Text] [Related]  

  • 30. Metabolism of sulfur-containing amino acids in a patient excreting -mercaptolactate-cysteine disulfide.
    Crawhall JC; Purkiss P; Stanbury JB
    Biochem Med; 1973 Feb; 7(1):103-11. PubMed ID: 4684079
    [No Abstract]   [Full Text] [Related]  

  • 31. Tyrosinaemia and tyrosyluria in infancy.
    Wong PW; Lambert AM; Komrower GM
    Dev Med Child Neurol; 1967 Oct; 9(5):551-62. PubMed ID: 6066020
    [No Abstract]   [Full Text] [Related]  

  • 32. Screening for aminoaciduria: a critical evaluation of four techniques and a survey of a mentally retarded population.
    Tippett PA; Danks DM
    Aust Paediatr J; 1972 Oct; 8(5):255-63. PubMed ID: 4658964
    [No Abstract]   [Full Text] [Related]  

  • 33. Metabolic traits in mentally retarded children as compared with normal populations: monoaminodicarboxylic acids and their half amides and total amino acids.
    Hirsch W; Mex A; Vogel F
    J Ment Defic Res; 1969 Jun; 13(2):130-42. PubMed ID: 5794287
    [No Abstract]   [Full Text] [Related]  

  • 34. Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase.
    Schulman JD; Goodman SI; Mace JW; Patrick AD; Tietze F; Butler EJ
    Biochem Biophys Res Commun; 1975 Jul; 65(1):68-74. PubMed ID: 238530
    [No Abstract]   [Full Text] [Related]  

  • 35. A new method for screening of hyperammonemia.
    Tada K; Tateda H; Metoki K
    Adv Exp Med Biol; 1982; 153():19-27. PubMed ID: 7164897
    [No Abstract]   [Full Text] [Related]  

  • 36. Studies on amino acid metabolism in citrullinuria.
    Mohyuddin F; Rathbun JC; McMurray WC
    Am J Dis Child; 1967 Jan; 113(1):152-6. PubMed ID: 6015893
    [No Abstract]   [Full Text] [Related]  

  • 37. Implications for clinical implementation of results of metabolic screening for amino acidopathies in the newborn.
    Griffiths MI
    Arch Dis Child; 1971 Dec; 46(250):881. PubMed ID: 5129202
    [No Abstract]   [Full Text] [Related]  

  • 38. Intellectual development in patients with untreated histidinemia. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan.
    Tada K; Tateda H; Arashima S; Sakai K; Kitagawa T; Aoki K; Suwa S; Kawamura M; Oura T; Takesada M; Kuroda Y; Yamashita F; Matsuda I; Naruse H
    J Pediatr; 1982 Oct; 101(4):562-3. PubMed ID: 7119955
    [No Abstract]   [Full Text] [Related]  

  • 39. Free amino acid pattern in the liver from the patients with amino acid disorders: postmortem diagnosis of inborn errors of amino acid metabolism.
    Tada K; Yoshida T; Arakawa T
    Tohoku J Exp Med; 1970 Jul; 101(3):223-6. PubMed ID: 5455854
    [No Abstract]   [Full Text] [Related]  

  • 40. [Physiological and pathological aminoacidurias].
    Brodehl J
    Monatsschr Kinderheilkd (1902); 1973 May; 121(5):190-200. PubMed ID: 4713389
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.