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 *

488 related articles for article (PubMed ID: 1168276)

  • 1. [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]  

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

  • 3. [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]  

  • 4. Inborn errors of organic acid metabolism.
    Green A
    Br J Hosp Med; 1989 May; 41(5):426-30, 432, 434. PubMed ID: 2663104
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnosis and therapy of organic acidurias.
    Sperl W
    Padiatr Padol; 1993; 28(1):3-8. PubMed ID: 8446425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [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]  

  • 8. [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]  

  • 9. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C
    Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974
    [No Abstract]   [Full Text] [Related]  

  • 10. [Prevention of congenital metabolic diseases. Early diagnosis by neonatal screening].
    Giovannini M; Riva E
    Minerva Med; 1979 Mar; 70(16):1137-46. PubMed ID: 440584
    [No Abstract]   [Full Text] [Related]  

  • 11. Prenatal diagnosis of inborn errors of metabolism.
    Mahoney MJ
    Clin Perinatol; 1979 Sep; 6(2):255-73. PubMed ID: 391465
    [No Abstract]   [Full Text] [Related]  

  • 12. [Metabolic disorders and corneal changes (author's transl)].
    François J
    Klin Monbl Augenheilkd; 1981 Jun; 178(6):419-23. PubMed ID: 6973662
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease.
    Vaca G; Hernández A; Ibarra B; Velázquez A; Olivares N; Sanchez-Corona J; Medina C; Cantú JM
    Arch Invest Med (Mex); 1981; 12(3):341-8. PubMed ID: 7294941
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal detection of heritable metabolic disorders.
    Thompson JN
    Pediatr Ann; 1978 Jun; 7(6):25-7, 30-1, 33-6 passim. PubMed ID: 97614
    [No Abstract]   [Full Text] [Related]  

  • 15. [Early detection of hereditary metabolic disturbances (author's transl)].
    Pfändler U
    Schweiz Rundsch Med Prax; 1975 Feb; 64(7):192-6. PubMed ID: 1167694
    [No Abstract]   [Full Text] [Related]  

  • 16. [Early diagnosis of enzymatic disorders in protein and carbohydrate metabolism].
    Otter G
    Offentl Gesundheitswes; 1970 Jan; 32(1):11-7. PubMed ID: 4245079
    [No Abstract]   [Full Text] [Related]  

  • 17. [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]  

  • 18. [Progress in the diagnosis of congenital metabolic central nervous system diseases. Review].
    Nevsímalová S
    Cesk Neurol; 1973 Mar; 36(2):120-7. PubMed ID: 4266580
    [No Abstract]   [Full Text] [Related]  

  • 19. [Suspected clinical diagnosis of genetic metabolic disorders in prevention and daily practice].
    Grosser V; Knapp A
    Z Arztl Fortbild (Jena); 1973 Dec; 67(24):1233-8. PubMed ID: 4791811
    [No Abstract]   [Full Text] [Related]  

  • 20. [Biochemical diagnosis of rare hereditary metabolic disorders. Experiences from a patient sample of the Innsbruck University Pediatric Clinic 1984-1987].
    Sperl W
    Padiatr Padol; 1990; 25(3):157-67. PubMed ID: 2381732
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.