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 *

108 related articles for article (PubMed ID: 812167)

  • 21. Progressive genetic-metabolic diseases of the central nervous system in children.
    Rapin I
    Pediatr Ann; 1976 May; 5(5):313-49. PubMed ID: 818604
    [No Abstract]   [Full Text] [Related]  

  • 22. [Disorders of mucopolysaccharide and glycoprotein metabolism].
    Suzuki Y
    Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1304-10. PubMed ID: 2113302
    [No Abstract]   [Full Text] [Related]  

  • 23. [Macula findings in thesaurismoses].
    François J
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975; (73):223-65. PubMed ID: 54161
    [No Abstract]   [Full Text] [Related]  

  • 24. Isolation and characterization of oligosaccharides from urine of patients with abnormal glycoconjugate metabolism.
    Chester MA; Lennartson G; Lundblad A; Lundsten J; Nordén NE; Sjöblad S; Svensson S; Ockerman PA
    Monogr Hum Genet; 1978; 10():2-6. PubMed ID: 102924
    [No Abstract]   [Full Text] [Related]  

  • 25. Inborn errors of lysosomal catabolism--principles of heterozygote detection.
    Jolly RD; Desnick RJ
    Am J Med Genet; 1979; 4(3):293-307. PubMed ID: 117711
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Isoelectric focusing pattern of acid hydrolases in cultured fibroblasts, leucocytes and cell-free amniotic fluid.
    Christomanou H; Cáp C; Sandhoff K
    Neuropadiatrie; 1977 Aug; 8(3):238-52. PubMed ID: 578295
    [TBL] [Abstract][Full Text] [Related]  

  • 27. High-performance liquid chromatographic analysis of oligosaccharides and glycopeptides accumulating in lysosomal storage disorders.
    Kin NM; Wolfe LS
    Anal Biochem; 1980 Feb; 102(1):213-9. PubMed ID: 6766687
    [No Abstract]   [Full Text] [Related]  

  • 28. Abnormal lysosomal hydrolases excreted by cultured fibroblasts in I-cell disease (mucolipidosis II).
    Vladutiu GD; Rattazzi MC
    Biochem Biophys Res Commun; 1975 Dec; 67(3):956-64. PubMed ID: 1201084
    [No Abstract]   [Full Text] [Related]  

  • 29. [Use of the electron microscope in the diagnosis of various metabolic storage diseases].
    Porfiri B; Ricci R; Riccardi A; Segni G
    Minerva Pediatr; 1982 Feb; 34(4):139-50. PubMed ID: 6806599
    [No Abstract]   [Full Text] [Related]  

  • 30. [Hereditary diseases caused by disorders in glycoconjugate metabolism].
    Rozenfel'd EL
    Vopr Med Khim; 1977; (1):3-12. PubMed ID: 404759
    [No Abstract]   [Full Text] [Related]  

  • 31. Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.
    Hall CW; Liebaers I; Di Natale P; Neufeld EF
    Methods Enzymol; 1978; 50():439-56. PubMed ID: 26836
    [No Abstract]   [Full Text] [Related]  

  • 32. Biochemical screening for mucopolysaccharidosis, mucolipidosis and oligosaccharidosis.
    Humbel R
    Helv Paediatr Acta; 1975 Jul; 30(2):191-200. PubMed ID: 807540
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pseudo-clinical Fabry's disease without alpha galactosidase deficiency.
    Peltier A; Herbeuval E; Brondeau MT; Belleville F; Nabet P
    Biomedicine; 1977 May; 26(3):194-201. PubMed ID: 407951
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The mucopolysaccaridoses: clinical and biochemical correlations.
    Horwitz AL
    Am J Ment Defic; 1979 Sep; 84(2):113-23. PubMed ID: 115315
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Comparative ultrastructural investigations of livers in mucopolysaccharidoses and mucolipidoses (author's transl)].
    Blümcke S; Freitag F; Spranger J
    Verh Dtsch Ges Pathol; 1971; 55():394-9. PubMed ID: 4130735
    [No Abstract]   [Full Text] [Related]  

  • 36. [Phenotypes in heteroglycanoses and sphingolipidoses (author's transl)].
    Gehler J
    Monatsschr Kinderheilkd; 1981 Nov; 129(11):610-20. PubMed ID: 6798422
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Lysosomal storage diseases and the retina].
    Libert J
    J Fr Ophtalmol; 1978 Nov; 1(11):699-710. PubMed ID: 155092
    [No Abstract]   [Full Text] [Related]  

  • 38. Conjunctival biopsy for diagnosis of lysosomal disorders.
    Kenyon KR
    Prog Clin Biol Res; 1982; 82():103-22. PubMed ID: 6810369
    [No Abstract]   [Full Text] [Related]  

  • 39. [Microorganisms that produce alpha-galactosidase, alpha-mannosidase, alpha-fucosidase and beta-acetylglucosaminidase].
    Ulezlo IV; Zaprometova OM; Ozerskaia SM; Bezborodov AM
    Mikrobiologiia; 1980; 49(2):265-8. PubMed ID: 6248742
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization.
    Rattazzi MC; Brown JA; Davidson RG; Shows TB
    Birth Defects Orig Artic Ser; 1975; 11(3):232-5. PubMed ID: 812568
    [No Abstract]   [Full Text] [Related]  

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