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 *

67 related articles for article (PubMed ID: 5557313)

  • 21. [On the increased excretion of taurine and beta aminoisobutyric acid in urine following irradiation and the sensitivity of these biochemical reactions].
    Bigwood EJ
    Strahlenschutz Forsch Prax; 1964; 4():183-97. PubMed ID: 5878289
    [No Abstract]   [Full Text] [Related]  

  • 22. Homocystinuria. Trial treatment of a 5-year old severely retarded child with a natural diet low in methionine.
    Carson NA
    Am J Dis Child; 1967 Jan; 113(1):95-7. PubMed ID: 6015915
    [No Abstract]   [Full Text] [Related]  

  • 23. [Hereditary digestive enzyme defects].
    Rey J
    Med Chir Dig; 1972; 1(1):41-4 contd. PubMed ID: 5054004
    [No Abstract]   [Full Text] [Related]  

  • 24. [Primary, transitory and secondary cystathionineuria].
    Endres W
    Fortschr Med; 1978 May; 96(18):982. PubMed ID: 649003
    [No Abstract]   [Full Text] [Related]  

  • 25. [Laboratorium technics for the diagnosis of inborn errors of amino acid metabolism].
    Trijbels JM; van Munster PJ
    Maandschr Kindergeneeskd; 1969 Jun; 37(1):9-16. PubMed ID: 5789978
    [No Abstract]   [Full Text] [Related]  

  • 26. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA; Ismail Z; Embong KH; Mohamad SA
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():130-3. PubMed ID: 8629091
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Prolinuria].
    Tada K
    Saishin Igaku; 1969 Jun; 24(6):1226-34. PubMed ID: 5805578
    [No Abstract]   [Full Text] [Related]  

  • 28. [Congenital cystathioninuria. B6-dependent].
    Bravo Mata M; Escribano Rey MD; Alonso Martín A; Alonso Fernández JR
    An Esp Pediatr; 1993 Sep; 39(3):260-4. PubMed ID: 8250445
    [No Abstract]   [Full Text] [Related]  

  • 29. The Vodskov Project VII: the amino acids in plasma and urine determined by ion exchange chromatography in a selected patient material and in a normal material.
    Espersen O; Paaby P
    Dan Med Bull; 1971 Aug; 18(4):88-99. PubMed ID: 5570689
    [No Abstract]   [Full Text] [Related]  

  • 30. Methionine malabsorption syndrome.
    Hooft C; Timmermans J; Snoeck J; Antener I; Oyaert W; Van den Hende C
    Ann Paediatr; 1965; 205(1):73-104. PubMed ID: 5897673
    [No Abstract]   [Full Text] [Related]  

  • 31. The relationship between the urinary level of some amino acids and the occurrence of metabolic diseases associated with psychic disorders.
    Mogoş T; Tănase I; Pănuş C; Mincu I
    Rom J Intern Med; 1994; 32(3):221-5. PubMed ID: 7866339
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Amino acids of plasma and urine in muscular dystrophies.
    Bank WJ; Rowland LP; Ipsen J
    Trans Am Neurol Assoc; 1968; 93():185-7. PubMed ID: 5711014
    [No Abstract]   [Full Text] [Related]  

  • 33. [B6-dependent xanthurenic aciduria].
    Tada K; Yokoyama Y
    Tanpakushitsu Kakusan Koso; 1968 Apr; 13(4):311-8. PubMed ID: 5749458
    [No Abstract]   [Full Text] [Related]  

  • 34. [Chromatographic studies of aminoaciduria in rickets].
    Wolyńska-Bochner S
    Ann Acad Med Stetin; 1966; 12():489-507. PubMed ID: 5921239
    [No Abstract]   [Full Text] [Related]  

  • 35. [Homocystinuria (apropos of a case)].
    Gaudier B; François P; Biserte G; Nuyts JP; Bombart E
    Pediatrie; 1966 Dec; 21(8):889-98. PubMed ID: 5985819
    [No Abstract]   [Full Text] [Related]  

  • 36. No evidence of isovalthinuria in isovaleric acidemia-- brief note.
    Kodama H; Fujii Y; Mizuhara S; Tanaka K
    Acta Med Okayama (1952); 1970 Feb; 24(1):107-9. PubMed ID: 4246447
    [No Abstract]   [Full Text] [Related]  

  • 37. Studies on the metabolism of the phenolic acids in hereditary tyrosinemia by a gas-liquid chromatographic method.
    Gentz J; Lindblad B; Lindstedt S; Zetterström R
    J Lab Clin Med; 1969 Aug; 74(2):185-202. PubMed ID: 5799507
    [No Abstract]   [Full Text] [Related]  

  • 38. Roentgen findings in homocystinuria.
    Smith SW
    Am J Roentgenol Radium Ther Nucl Med; 1967 May; 100(1):147-54. PubMed ID: 6023889
    [No Abstract]   [Full Text] [Related]  

  • 39. General anesthesia for patient with type III homocystinuria (tetrahydrofolate reductase deficiency).
    Yamada T; Hamada H; Mochizuki S; Sutoh M; Tsuji M; Kawamoto M; Yuge O
    J Clin Anesth; 2005 Nov; 17(7):565-7. PubMed ID: 16297760
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Facial dysmorphism associated with ketoglutaric acid].
    Delgado Luengo W; Fleitas Cabello H; Solís Áñez E; Miranda Contreras L; Morales-Machín A
    An Pediatr (Barc); 2011 Mar; 74(3):204-6. PubMed ID: 21345758
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.