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 *

180 related articles for article (PubMed ID: 100026)

  • 21. [Detection of metabolic diseases].
    Adriaenssens K; Van Sande M
    Acta Neurol Psychiatr Belg; 1968 Oct; 68(10):719-28. PubMed ID: 4976725
    [No Abstract]   [Full Text] [Related]  

  • 22. Biochemistry of mental disorders. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1969; 427():1-40. PubMed ID: 4980629
    [No Abstract]   [Full Text] [Related]  

  • 23. Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe.
    Wachtel U
    Hum Nutr Appl Nutr; 1986; 40 Suppl 1():61-9. PubMed ID: 3528074
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Metabolic myopathies: a guide and update for clinicians.
    Burr ML; Roos JC; Ostör AJ
    Curr Opin Rheumatol; 2008 Nov; 20(6):639-47. PubMed ID: 18946322
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Biochemistry of mental retardation].
    Yoshida M; Seyama Y; Yamakwa T
    Nihon Rinsho; 1976 Sep; 34(9):2726-34. PubMed ID: 825670
    [No Abstract]   [Full Text] [Related]  

  • 26. [G M1 gangliosidosis, type II].
    Carton D
    Acta Paediatr Belg; 1970; 24(2):75-82. PubMed ID: 5490875
    [No Abstract]   [Full Text] [Related]  

  • 27. [Nutrition in congenital metabolic diseases].
    Plöchl E
    Padiatr Padol; 1984; 19(4):343-8. PubMed ID: 6504543
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Congenital metabolic disorders with eye manifestations].
    Oura T; Kozaki M
    Ganka; 1969 Nov; 11(11):872-83. PubMed ID: 5391925
    [No Abstract]   [Full Text] [Related]  

  • 29. Neurological aspects of folate and vitamin B12 metabolism.
    Reynolds EH
    Clin Haematol; 1976 Oct; 5(3):661-96. PubMed ID: 788983
    [No Abstract]   [Full Text] [Related]  

  • 30. Pathogenesis of mental retardation in amino acid disorders.
    Tada K
    Int J Neurol; 1976; 11(1):73-84. PubMed ID: 1017916
    [No Abstract]   [Full Text] [Related]  

  • 31. Investigations in enzyme replacement therapy in lipid storage diseases.
    Brady RO; Pentchev PG; Gal AG
    Fed Proc; 1975 Apr; 34(5):1310-5. PubMed ID: 804420
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Breast milk feeding in infants with inherited metabolic disorders other than phenylketonuria - a 10-year single-center experience.
    Pichler K; Michel M; Zlamy M; Scholl-Buergi S; Ralser E; Jörg-Streller M; Karall D
    J Perinat Med; 2017 Apr; 45(3):375-382. PubMed ID: 27564695
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Inborn errors of metabolism with preferred localization in the central nervous system].
    Peiffer J
    Verh Dtsch Ges Pathol; 1982; 66():213-33. PubMed ID: 7184239
    [No Abstract]   [Full Text] [Related]  

  • 34. Mental retardation in methemoglobinemia due to diaphorase deficiency.
    Fialkow PJ; Browder JA; Sparkes RS; Motulsky AG
    N Engl J Med; 1965 Oct; 273(16):840-5. PubMed ID: 4378489
    [No Abstract]   [Full Text] [Related]  

  • 35. [Lysosomes and lysosomal storage diseases].
    Lie KK; Lie SO
    Tidsskr Nor Laegeforen; 1975 Jan; 95(2):88-94, 83. PubMed ID: 803727
    [No Abstract]   [Full Text] [Related]  

  • 36. [Autosomal recessive diseases with mental retardation].
    Fernández-Carvajal I; Telleria JJ; Alonso M; Palencia R; Durán M; López B; Navarro N; de Diego-Otero Y; Blanco A
    Rev Neurol; 2006 Jan; 42 Suppl 1():S39-43. PubMed ID: 16506131
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Inborn errors of metabolism.
    Kolodny EH; Cable WJ
    Ann Neurol; 1982 Mar; 11(3):221-32. PubMed ID: 6807191
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Impact of selected inborn errors of metabolism on prenatal and neonatal development.
    Illsinger S; Das AM
    IUBMB Life; 2010 Jun; 62(6):403-13. PubMed ID: 20503433
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Clinical and neuropathological observations on a familial disease with mental retardation, myoclonus and neuronal accumulation of gangliosides].
    Bertinelli RP; Bollea G; Borri P; Maccagnani F; Palladini G; Sagui G
    Minerva Pediatr; 1975 May; 27(19):1095-104. PubMed ID: 1134467
    [No Abstract]   [Full Text] [Related]  

  • 40. [Screening of newborns for inborn errors of metabolism by tandem mass spectrometry].
    Simonsen H
    Ugeskr Laeger; 2002 Nov; 164(48):5607-12. PubMed ID: 12523003
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.