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 *

308 related articles for article (PubMed ID: 6888384)

  • 1. [Metabolic emergencies in the newborn infant].
    Bremer HJ
    Monatsschr Kinderheilkd; 1983 Jun; 131(6):317-20. PubMed ID: 6888384
    [No Abstract]   [Full Text] [Related]  

  • 2. Inborn errors of metabolism (IEM) -- an Indian perspective.
    Kumta NB
    Indian J Pediatr; 2005 Apr; 72(4):325-32. PubMed ID: 15876762
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I; Ciortoloman H; Grigorescu G; Popescu M; Ankăr V
    Physiologie; 1978; 15(4):239-43. PubMed ID: 106407
    [No Abstract]   [Full Text] [Related]  

  • 5. [Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
    Menne F; Enzenauer J; Matz D
    Med Klin; 1976 Apr; 71(18):779-85. PubMed ID: 178988
    [No Abstract]   [Full Text] [Related]  

  • 6. An approach to the diagnosis of overwhelming metabolic disease in early infancy.
    Nyhan WL
    Curr Probl Pediatr; 1977 Apr; ():1-20. PubMed ID: 856539
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Diagnosis of inborn errors of metabolism. (principles and results of investigation of 3,000 persons)].
    Farriaux JP; Adam E; Fontaine G; Delecour M
    Lille Med; 1968 Oct; 13(8):864-72. PubMed ID: 5743598
    [No Abstract]   [Full Text] [Related]  

  • 8. [Detection of congenital metabolic diseases with mental retardation].
    Colombo JP
    Rev Otoneuroophtalmol; 1971 Nov; 43(7):328-33. PubMed ID: 5159706
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. Perinatal diagnosis of the inborn errors of metabolism.
    Elsas LJ
    J Med Assoc Ga; 1971 Sep; 60(9):308-11. PubMed ID: 5093796
    [No Abstract]   [Full Text] [Related]  

  • 11. [The early recognition of congenital metabolic diseases].
    Steuber W
    Munch Med Wochenschr; 1971 Mar; 113(13):463-7. PubMed ID: 5108281
    [No Abstract]   [Full Text] [Related]  

  • 12. [Neonatal diagnosis of maple syrup urine disease and trial of exchange transfusion].
    Statter M; Ben-Zvi A; Russell A
    Harefuah; 1976 Oct; 91(7):167-9. PubMed ID: 1002028
    [No Abstract]   [Full Text] [Related]  

  • 13. [Metabolic emergencies in the newborn infant].
    Doménech E; Rodríguez-Luis JC; Méndez A; Cortabarría C; Ormazábal C
    An Esp Pediatr; 1984 Sep; 21(4):309-20. PubMed ID: 6535400
    [No Abstract]   [Full Text] [Related]  

  • 14. Screening for inborn errors of metabolism in infancy.
    Hudson FP
    Nurs Mirror Midwives J; 1975 Aug; 141(9):64-6. PubMed ID: 1041391
    [No Abstract]   [Full Text] [Related]  

  • 15. [Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests].
    Schmid-Rüter E
    Fortschr Med; 1978 Jun; 96(24):1289-93. PubMed ID: 96002
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968; 401():1-57. PubMed ID: 4973455
    [No Abstract]   [Full Text] [Related]  

  • 17. [Newborn infant screening program in Switzerland].
    Gitzelmann R
    Bull Schweiz Akad Med Wiss; 1972 Sep; 28(5):294-301. PubMed ID: 4645587
    [No Abstract]   [Full Text] [Related]  

  • 18. Postmortem diagnosis of metabolic disorders. The finding of maple syrup urine disease in a case of sudden and unexpected death in infancy.
    Hallock J; Morrow G; Karp LA; Barness LA
    Am J Dis Child; 1969 Oct; 118(4):649-51. PubMed ID: 5820611
    [No Abstract]   [Full Text] [Related]  

  • 19. [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]  

  • 20. Screening for genetic disorders.
    Berry HK
    Fed Proc; 1975 Nov; 34(12):2134-9. PubMed ID: 1102335
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.