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 *

174 related articles for article (PubMed ID: 3074716)

  • 41. [Ocular diagnosis in hereditary lysosomal diseases].
    Cantani A; Ciarnella Cantani A; Giardini O; Lendvai D; Santillo C
    Minerva Pediatr; 1980 Nov; 32(22):1283-92. PubMed ID: 7219368
    [No Abstract]   [Full Text] [Related]  

  • 42. [Metabolic problems related to various encephalopathies in children].
    Cotte J; Kohler C
    Rev Neuropsychiatr Infant; 1967; 15(4):287-318. PubMed ID: 5602322
    [No Abstract]   [Full Text] [Related]  

  • 43. Operational experience of a large urban neonatal referral unit.
    Murdock A; Sutton M; Linsao L; Tilak K; Reid M; Llewellyn MA; Swyer PR
    Can Med Assoc J; 1969 Sep; 101(6):351-3. PubMed ID: 5387725
    [No Abstract]   [Full Text] [Related]  

  • 44. [Various unusual congenital and metabolic myopathies].
    Walton J
    Rev Neurol (Paris); 1970 Jul; 123(1):23-8. PubMed ID: 5516327
    [No Abstract]   [Full Text] [Related]  

  • 45. [Contribution of electron microscopy of cultures of fibroblasts in the diagnosis of hereditary metabolic diseases].
    Jaffray JY; Charbonne F; Rousseau P; Malpuech G; Meyer M; Labbe A; Malet P
    Pathol Biol (Paris); 1986 Feb; 34(2):91-8. PubMed ID: 3517782
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [lysosomes and storage disease].
    Raivio K
    Duodecim; 1981; 97(2):51-5. PubMed ID: 7249962
    [No Abstract]   [Full Text] [Related]  

  • 47. [Inborn errors of metabolism with neurological manifestations in the neonatal period].
    Campistol J
    Medicina (B Aires); 2007; 67(6 Pt 1):561-8. PubMed ID: 18422082
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A survey of inborn errors of metabolism in Ireland 1965-1976.
    Coffey VP; Moore PT; Martin M
    Ir Med J; 1977 Mar; 70(4):132-9. PubMed ID: 852971
    [No Abstract]   [Full Text] [Related]  

  • 49. [Screening for inborn errors of metabolism in infancy].
    Mrskos A; Brunecký Z
    Kinderarztl Prax; 1966 Dec; 34(12):529-32. PubMed ID: 5980997
    [No Abstract]   [Full Text] [Related]  

  • 50. Diagnosis of lysosomal storage diseases by the ultrastructural study of conjunctival biopsies.
    Libert J
    Pathol Annu; 1980; 15(Pt 1):37-66. PubMed ID: 7443310
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Inborn errors of metabolism in infancy and early childhood: an update.
    Raghuveer TS; Garg U; Graf WD
    Am Fam Physician; 2006 Jun; 73(11):1981-90. PubMed ID: 16770930
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Screening of 1,000 patients for inborn errors of metabolism.
    Tobon H; Amenta JS
    Pa Med; 1970 Oct; 73(10):49-55. PubMed ID: 5479564
    [No Abstract]   [Full Text] [Related]  

  • 53. [The prevention and treatment of metabolic encephalopathies].
    Frézal J; Rey J
    Rev Neuropsychiatr Infant; 1967; 15(4):319-24. PubMed ID: 5602323
    [No Abstract]   [Full Text] [Related]  

  • 54. [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]  

  • 55. [Problems in practical medical genetics].
    Fradin ; Girard ; Jeune ; Paufique ; Robert
    Lyon Med; 1969 Jul; 222(27):11-41. PubMed ID: 4249539
    [No Abstract]   [Full Text] [Related]  

  • 56. [Screening for congenital metabolic disorders. Indication and results].
    Bickel H
    Monatsschr Kinderheilkd; 1983 Jun; 131(6):323-7. PubMed ID: 6888386
    [No Abstract]   [Full Text] [Related]  

  • 57. [Hereditary enzyme defects of the urea cycle].
    Colombo JP
    Ergeb Inn Med Kinderheilkd; 1971; 31():97-130. PubMed ID: 4933544
    [No Abstract]   [Full Text] [Related]  

  • 58. Peroxidase in ceroid-lipofuscinosis.
    Den Tandt WR; Martin JJ
    J Neurol Sci; 1978 Sep; 38(2):191-3. PubMed ID: 712383
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Hereditary diseases in Finland; rare flora in rare soul.
    Norio R; Nevanlinna HR; Perheentupa J
    Ann Clin Res; 1973 Jun; 5(3):109-41. PubMed ID: 4584134
    [No Abstract]   [Full Text] [Related]  

  • 60. [Malabsorption syndromes in childhood].
    Mei V
    Clin Pediatr (Bologna); 1967 Dec; 49(12):733-76. PubMed ID: 4878228
    [No Abstract]   [Full Text] [Related]  

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