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 *

135 related articles for article (PubMed ID: 1166174)

  • 21. [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]  

  • 22. [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)].
    Koepp P; Grüttner R
    Klin Padiatr; 1975 Jan; 187(1):14-9. PubMed ID: 1168276
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Detection of amino acid metabolism inborn errors in neonatal age].
    Stoppoloni G
    Pediatria (Napoli); 1974 Mar; 82(1):79-95. PubMed ID: 4848445
    [No Abstract]   [Full Text] [Related]  

  • 24. [Amino acid metabolism and childhood pathology].
    Netakhata ZhN; Liapun SN
    Pediatriia; 1970; 49(12):63-73. PubMed ID: 4950145
    [No Abstract]   [Full Text] [Related]  

  • 25. Multiple neonatal screening for aminoacidopathies by ion exchange chromatography.
    Antonozzi I; Santagata G; Tofani R
    Ric Clin Lab; 1982; 12(3):507-15. PubMed ID: 7134749
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Metabolic homoiostasis and its disorders in the new-born infant. Recent acquisitions.
    Jaeken J; Eggermont E
    Acta Paediatr Belg; 1977; 30(4):205-12. PubMed ID: 347871
    [No Abstract]   [Full Text] [Related]  

  • 27. [Neonatal transitory tyrosinemia and other types of tyrosinemia].
    Lanza I
    Minerva Pediatr; 1976 Mar; 28(11):637-43. PubMed ID: 995075
    [No Abstract]   [Full Text] [Related]  

  • 28. Severe neonatal citrullinaemia.
    Danks DM; Tippett P; Zentner G
    Arch Dis Child; 1974 Jul; 49(7):579-81. PubMed ID: 4854268
    [No Abstract]   [Full Text] [Related]  

  • 29. [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]  

  • 30. [Biochemical and clinical correlations in children suspected of having lysosomal diseases].
    Tănase-Mogos I; Turcanu L; Petrescu L; Popescu M
    Physiologie; 1981; 18(1):37-45. PubMed ID: 6794050
    [No Abstract]   [Full Text] [Related]  

  • 31. [Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages].
    Simková M; Hyánek J; Karger P; Hoza J; Holub J; Viletová H
    Cesk Pediatr; 1976 Nov; 31(11):619-21. PubMed ID: 1035139
    [No Abstract]   [Full Text] [Related]  

  • 32. [Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1].
    Menne F; Enzenauer J; Matz D
    Med Klin; 1976 Apr; 71(17):724-8. PubMed ID: 775276
    [No Abstract]   [Full Text] [Related]  

  • 33. [Diagnostic and therapeutic management of inherited metabolic diseases in emergency and intensive care unit].
    de Lonlay P; Valayannopoulos V; Arnoux JB; Servais A; Charron B; Jacqmarcq O; Ottolenghi C; Hubert P
    Arch Pediatr; 2010 Jun; 17(6):947-8. PubMed ID: 20654974
    [No Abstract]   [Full Text] [Related]  

  • 34. Diagnosis of metabolic disease.
    Snyderman SE
    Pediatr Clin North Am; 1971 Feb; 18(1):199-208, ix. PubMed ID: 25868185
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset].
    Saudubray JM; Lyonnet S; Lombes A; Hervé F; Bonnefont JP; Munnich A; Ogier H
    J Genet Hum; 1989 Dec; 37(4-5):299-310. PubMed ID: 2635710
    [No Abstract]   [Full Text] [Related]  

  • 36. [Areas of applicability of thin-layer chromatography. Practical mass screening; data on intestinal mucosa lesions].
    Szabó B
    Padiatr Padol; 1983; 18(2):105-11. PubMed ID: 6856315
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Amino acid composition in blood and urine from healthy newborn infants: screening test for the detection of enxymopathies].
    Adrienne S
    Orv Hetil; 1969 Jun; 110(23):1315-20. PubMed ID: 5794637
    [No Abstract]   [Full Text] [Related]  

  • 38. Neonatal hepatitis in premature infants simulating hereditary tyrosinosis.
    Yu JS; Walker-Smith JA; Burnard ED
    Arch Dis Child; 1971 Jun; 46(247):306-9. PubMed ID: 5090663
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Screening for aminoacidopathies in newborns by means of an aminoacid analyzer. Reference values and statistical determinations (author's transl)].
    Antonozzi I; Del Castello PG; Morisi G; Ceccarelli P
    Ann Ist Super Sanita; 1978; 14(4):781-91. PubMed ID: 756692
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Free amino acids in plasma. Normal values in pediatrics].
    Cohen AL; Monesiglio JC
    Arch Argent Pediatr; 1971 Sep; 69(7):281-7. PubMed ID: 5113471
    [No Abstract]   [Full Text] [Related]  

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