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 *

109 related articles for article (PubMed ID: 3834309)

  • 41. [Enzymatic disturbances in the urea cycle].
    Colombo JP
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):29-31. PubMed ID: 4098700
    [No Abstract]   [Full Text] [Related]  

  • 42. [Early diagnosis of congenital metabolic diseases].
    Steuer W
    Rev Clin Esp; 1971 Jun; 121(6):521-6. PubMed ID: 5131308
    [No Abstract]   [Full Text] [Related]  

  • 43. [Amino-aciduria and amino-acidemia as a clinical and diagnostic problem in child neuropsychiatry].
    Milovanović D; Radojcić B
    Srp Arh Celok Lek; 1976 Jun; 104(6):457-62. PubMed ID: 1025761
    [No Abstract]   [Full Text] [Related]  

  • 44. [Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies].
    Thiriar MJ; Szliwowski HB; Vis HL
    Acta Neurol Psychiatr Belg; 1968 Mar; 68(3):216-27. PubMed ID: 4972603
    [No Abstract]   [Full Text] [Related]  

  • 45. [Study of aminoaciduria and aminoacidemia by chromato-ion-ophoresis. Technic and application to the dynamic study of various amino acid metabolic disorders].
    Vovan L; Perrimond H; Pierron H; Orsini A
    Pediatrie; 1967 Sep; 22(6):732-3. PubMed ID: 5621096
    [No Abstract]   [Full Text] [Related]  

  • 46. [Screening on aminoacid opathies in newborn infants].
    Stoppoloni G; Santinelli R
    Pediatria (Napoli); 1976 Dec; 84(4):604-16. PubMed ID: 1035798
    [No Abstract]   [Full Text] [Related]  

  • 47. [Homocystinuria].
    Hooft C; Carton D
    Verh K Vlaam Acad Geneeskd Belg; 1967; 29(2):119-51. PubMed ID: 6078458
    [No Abstract]   [Full Text] [Related]  

  • 48. [The spectrum of amino acids in mental retardation and epilepsy in childhood].
    Wiechert P; Cammann R; Gierow W
    Padiatr Grenzgeb; 1977; 16(6):355-61. PubMed ID: 611435
    [No Abstract]   [Full Text] [Related]  

  • 49. [Indications of renal and intestinal amino acid malabsorption in Lowe's syndrome].
    Colombo JP
    Schweiz Med Wochenschr; 1971 Jul; 101(26):968-72. PubMed ID: 5143472
    [No Abstract]   [Full Text] [Related]  

  • 50. [Comparison of free amino acids in capillary and venous blood serum of children and adolescents with phenylketonuria and leucinosis].
    Liappis N; Schlebusch H; Mallmann R
    Klin Padiatr; 1992; 204(2):107-10. PubMed ID: 1583848
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Results of screening for inborn errors of aminoacid metabolism in adult and infant patients from psychiatric institutions (author's transl)].
    Hyánek J; Turek S; Kríz J; Trísková J; Homolka J; Kopejtková H
    Cas Lek Cesk; 1975 Mar; 114(10-11):307-8. PubMed ID: 1139573
    [No Abstract]   [Full Text] [Related]  

  • 52. Routine investigation of amino acid patterns in blood serum and urine by thin-layer electrophoresis.
    Fahie-Wilson MN
    J Med Lab Technol; 1969 Oct; 26(4):363-70. PubMed ID: 5355354
    [No Abstract]   [Full Text] [Related]  

  • 53. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Kroll S; Zebisch P; Toussaint W
    Fortschr Med; 1972 Apr; 90(11):423-8. PubMed ID: 4680607
    [No Abstract]   [Full Text] [Related]  

  • 54. [Familial essential hyperprolinemia].
    Hainaut H; Hariga J; Willems C; Heusden A; Chapelle P
    Presse Med (1893); 1971 Apr; 79(21):945-8. PubMed ID: 5580522
    [No Abstract]   [Full Text] [Related]  

  • 55. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
    Shih VE; Efron ML; Moser HW
    Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534
    [No Abstract]   [Full Text] [Related]  

  • 56. The pathogenesis of mental retardation in phenylketonuria and other inborn errors of amino acid metabolism.
    Menkes JH
    Pediatrics; 1967 Feb; 39(2):297-308. PubMed ID: 5335144
    [No Abstract]   [Full Text] [Related]  

  • 57. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D; Tebib N; Kaabachi N; Ben Dridi MF; Mebazaa A
    Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277
    [No Abstract]   [Full Text] [Related]  

  • 58. [Type I hyperprolinemia. Study of a familial case].
    Fontaine G; Farriaux JP; Dautrevaux M
    Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477
    [No Abstract]   [Full Text] [Related]  

  • 59. A simple screening test for histidinuria.
    Gerber MG; Gerber DA
    Pediatrics; 1969 Jan; 43(1):40-3. PubMed ID: 5764066
    [No Abstract]   [Full Text] [Related]  

  • 60. [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]  

    [Previous]   [Next]    [New Search]
    of 6.