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 *

80 related articles for article (PubMed ID: 4247489)

  • 21. [Hereditary mucopolysaccharidoses (literature survey)].
    Pashin IuV
    Vopr Okhr Materin Det; 1972 Jun; 17(6):49-52. PubMed ID: 4262644
    [No Abstract]   [Full Text] [Related]  

  • 22. The role of lysosomes in the pathogeny of storage diseases.
    Hers HG
    Arch Belg Dermatol Syphiligr; 1972; 28(1):51-7. PubMed ID: 4266285
    [No Abstract]   [Full Text] [Related]  

  • 23. Interactions between acid hydrolases of human liver and mucopolysaccharides.
    Kint JA; Huys A
    Arch Int Physiol Biochim; 1973 May; 81(2):375-6. PubMed ID: 4126229
    [No Abstract]   [Full Text] [Related]  

  • 24. Angiokeratoma corporis diffusum with alpha-L-fucosidase deficiency.
    Epinette WW; Norins AL; Drew AL; Zeman W; Patel V
    Arch Dermatol; 1973 May; 107(5):754-7. PubMed ID: 4634000
    [No Abstract]   [Full Text] [Related]  

  • 25. G-M1-gangliosidosis. Correlation of clinical and biochemical data.
    Suzuki Y; Crocker AC; Suzuki K
    Arch Neurol; 1971 Jan; 24(1):58-64. PubMed ID: 4249736
    [No Abstract]   [Full Text] [Related]  

  • 26. Generalized gangliosidosis: impaired cleavage of galactose from a mucopolysaccharide and a glycoprotien.
    MacBrinn MC; Okada S; Ho MW; Hu CC; O'Brien JS
    Science; 1969 Feb; 163(3870):946-7. PubMed ID: 4236799
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [The mucopolysaccharidoses: modern diagnostic, etiopathogenetic and therapeutic trends. Enzymatic and ultrastructural study of a case of Sanfilippo's disease].
    Collina A; Pirazzoli P; Cicognani A; Tassoni P; Salardi S; Cacciari E
    Minerva Pediatr; 1972 Nov; 24(41):2072-83. PubMed ID: 4264713
    [No Abstract]   [Full Text] [Related]  

  • 28. Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis.
    Sly WS; Quinton BA; McAlister WH; Rimoin DL
    J Pediatr; 1973 Feb; 82(2):249-57. PubMed ID: 4265197
    [No Abstract]   [Full Text] [Related]  

  • 29. I-cell disease, mucolipidosis II. Pathological, histochemical, ultrastructural and biochemical observations in four cases.
    Gilbert EF; Dawson G; zu Rhein GM; Opitz JM; Spranger
    Z Kinderheilkd; 1973; 114(4):259-92. PubMed ID: 4353613
    [No Abstract]   [Full Text] [Related]  

  • 30. [A new type of mucopolysaccharidosis].
    von Figura K; Kresse H
    Dtsch Med Wochenschr; 1972 Jan; 97(4):134. PubMed ID: 4257567
    [No Abstract]   [Full Text] [Related]  

  • 31. Inborn errors of complex carbohydrate metabolism.
    Spranger J
    Am J Med Genet; 1987 Oct; 28(2):489-99. PubMed ID: 2962491
    [No Abstract]   [Full Text] [Related]  

  • 32. Selective noncompetitive assimilation of bovine testicular beta-galactosidase and bovine liver beta-glucuronidase by generalized gangliosidosis fibroblasts.
    Hieber V; Distler J; Myerowitz R; Schmickel RD; Jourdian GW
    J Clin Invest; 1980 Apr; 65(4):879-84. PubMed ID: 6766954
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Quantitative aspects of mucopolysaccharide degradation correction in Sanfilippo-B-fibroblasts due to N-acetyl-alpha-D-glucosaminidase].
    Kresse H; von Figura K
    Hoppe Seylers Z Physiol Chem; 1972 Oct; 353(10):1541-2. PubMed ID: 4265375
    [No Abstract]   [Full Text] [Related]  

  • 34. Histochemical studies on enzymes acting on glycosyl compounds, phosphoryl-containing anhydrides and phosphoamides in human carious dentine.
    Larmas M
    Acta Odontol Scand; 1972 May; 30(2):201-18. PubMed ID: 4262582
    [No Abstract]   [Full Text] [Related]  

  • 35. Mannosidosis: clinical, fine-structural and biochemical findings in three cases.
    Autio S; Nordén NE; Ockerman PA; Riekkinen P; Rapola J; Louhimo T
    Acta Paediatr Scand; 1973 Nov; 62(6):555-65. PubMed ID: 4358183
    [No Abstract]   [Full Text] [Related]  

  • 36. Ganglioside storage diseases.
    O'Brien JS; Okada S; Ho MW; Fillerup DL; Veath ML; Adams K
    Fed Proc; 1971; 30(3):956-69. PubMed ID: 4252532
    [No Abstract]   [Full Text] [Related]  

  • 37. Human intestinal disaccharidase activity. II. Diseases of the small intestine and deficiency states.
    Welsh JD; Rohrer GV; Drewry R; May JC; Walker A
    Arch Intern Med; 1966 Apr; 117(4):495-503. PubMed ID: 5906641
    [No Abstract]   [Full Text] [Related]  

  • 38. [Recent contributions of electron microscopy and of tissue culture in the study of some storage diseases: mucopolysaccharidoses and lipidoses].
    Tondeur M; Vamos-Hurwitz E; Loeb H
    Acta Paediatr Belg; 1970; 24(3):355-84. PubMed ID: 4250299
    [No Abstract]   [Full Text] [Related]  

  • 39. Neuro-visceral storage disease in infancy and childhood.
    Med J Aust; 1971 Nov; 2(20):990-2. PubMed ID: 4257077
    [No Abstract]   [Full Text] [Related]  

  • 40. Tissue culture and study of cystic fibrosis and other inherited diseases.
    N Engl J Med; 1968 Sep; 279(10):547-8. PubMed ID: 4233593
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.