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 *

105 related articles for article (PubMed ID: 4843066)

  • 21. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
    Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G
    Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466
    [No Abstract]   [Full Text] [Related]  

  • 22. Urinary excretion of argininosuccinic acid.
    Palmer T; Oberholzer VG; Levin B; Burgess EA
    Clin Chim Acta; 1973 Sep; 47(3):443-8. PubMed ID: 4744836
    [No Abstract]   [Full Text] [Related]  

  • 23. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies].
    Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
    Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971
    [No Abstract]   [Full Text] [Related]  

  • 24. Comparison of exchange transfusion, peritoneal dialysis, and hemodialysis for the treatment of hyperammonemia in an anuric newborn infant.
    Donn SM; Swartz RD; Thoene JG
    J Pediatr; 1979 Jul; 95(1):67-70. PubMed ID: 480015
    [No Abstract]   [Full Text] [Related]  

  • 25. [Screening of 80,000 newborn infants at delivery, for amino acid metabolism].
    Greven-Brauns G; Mulkens E
    Arch Belg Med Soc; 1975 Apr; 33(4):253-7. PubMed ID: 1231644
    [No Abstract]   [Full Text] [Related]  

  • 26. The lure of treatment: expanded newborn screening and the curious case of histidinemia.
    Brosco JP; Sanders LM; Dharia R; Guez G; Feudtner C
    Pediatrics; 2010 Mar; 125(3):417-9. PubMed ID: 20156889
    [No Abstract]   [Full Text] [Related]  

  • 27. [Screening of newborn infants for inborn errors of metabolism].
    Halvorsen S; Skjelkvåle L
    Tidsskr Nor Laegeforen; 1970 Jan; 90(2):233-5. PubMed ID: 5430194
    [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. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles].
    Plöchl E
    Wien Med Wochenschr; 1970 Oct; 120(41):707-11. PubMed ID: 4918107
    [No Abstract]   [Full Text] [Related]  

  • 30. [Diagnosis and acute treatment of inborn metabolic diseases in infants].
    Lund AM; Christensen E; Skovby F
    Ugeskr Laeger; 2002 Nov; 164(48):5613-9. PubMed ID: 12523004
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New approaches to the diagnosis and treatment of inborn errors or urea synthesis.
    Batshaw ML; Thomas GH; Brusilow SW
    Pediatrics; 1981 Aug; 68(2):290-7. PubMed ID: 7267240
    [No Abstract]   [Full Text] [Related]  

  • 32. [Arginino-succinate aciduria].
    Dogan K; Schmutzer L; Dogan S; Lipovac K; Rudar D
    Neuropsihijatrija; 1973; 21(3-4):237-46. PubMed ID: 4805065
    [No Abstract]   [Full Text] [Related]  

  • 33. Clinical aspects of disorders of the urea cycle.
    Snyderman SE
    Pediatrics; 1981 Aug; 68(2):284-9, 295-7. PubMed ID: 7267239
    [No Abstract]   [Full Text] [Related]  

  • 34. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease].
    Raven EJ
    Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645
    [No Abstract]   [Full Text] [Related]  

  • 35. 3-Methylcrotonyl-CoA carboxylase deficiency: metabolic decompensation in a noncompliant child detected through newborn screening.
    Ficicioglu C; Payan I
    Pediatrics; 2006 Dec; 118(6):2555-6. PubMed ID: 17142544
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The critically ill child: acute metabolic disease in infancy and early childhood.
    O'Brien D; Goodman SI
    Pediatrics; 1970 Oct; 46(4):620-6. PubMed ID: 5503697
    [No Abstract]   [Full Text] [Related]  

  • 37. [Early diagnosis of congenital metabolic diseases].
    Steuer W
    Cah Med; 1971 Oct; 12(12):1009-13. PubMed ID: 5130231
    [No Abstract]   [Full Text] [Related]  

  • 38. [Study of a case of methylmalonic acidemia of neonatal onset. Therapeutic value of peritoneal dialysis. Discussion of vitamin B 12 sensitivity].
    Saudubray JM; Boisse J; Charpentier C; Lemonnier A; Mozziconacci P
    Arch Fr Pediatr; 1972; 29(6):676-7. PubMed ID: 5078375
    [No Abstract]   [Full Text] [Related]  

  • 39. [Value of peritoneal dialysis in the emergency treatment of metabolic diseases of constitutional origin revealed in the neonatal period].
    Saudubray JM; Fournet JP; Cloup M
    Ann Med Interne (Paris); 1971 Dec; 122(12):1279-83. PubMed ID: 5151629
    [No Abstract]   [Full Text] [Related]  

  • 40. [Findings in certain neonatal amino acid diseases. Current means of diagnosis and treatment].
    Giardini O; Corrado G; Martinelli M; D'Eufemia P
    Minerva Pediatr; 1978 Dec; 30(24):1943-7. PubMed ID: 753961
    [No Abstract]   [Full Text] [Related]  

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