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 *

127 related articles for article (PubMed ID: 144057)

  • 41. Neurochemistry of the mucopolysaccharidoses: brain glycosaminoglycans in normals and four types of mucopolysaccharidoses.
    Constantopoulos G; McComb RD; Dekaban AS
    J Neurochem; 1976 May; 26(5):901-8. PubMed ID: 131847
    [No Abstract]   [Full Text] [Related]  

  • 42. Differentiation of mucopolysaccharidoses by analyses of the excreted sulfated mucopolysaccharides.
    Cohen DM; Mourão PA; Dietrich CP
    Clin Chim Acta; 1977 Nov; 80(3):555-62. PubMed ID: 144036
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Human beta-glucuronidase deficiency mucopolysaccharidosis: identification of cross-reactive antigen in cultured fibroblasts of deficient patients by enzyme immunoassay.
    Bell CE; Sly WS; Brot FE
    J Clin Invest; 1977 Jan; 59(1):97-105. PubMed ID: 401508
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mucopolysaccharidosis in a domestic short-haired cat--a disease distinct from that seen in the Siamese cat.
    Haskins ME; Jezyk PF; Desnick RJ; McDonough SK; Patterson DF
    J Am Vet Med Assoc; 1979 Aug; 175(4):384-7. PubMed ID: 115818
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Morphological and biochemical findings in a case of mucopolysaccharidosis type III A (Sanfilippo's disease type A).
    Witting C; Müller KM; Kresse H; Figura KV; Marx H
    Beitr Pathol; 1975; 154(3):324-38. PubMed ID: 805586
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Atypical radiological features of beta-glucuronidase deficiency (mucopolysaccharidosis VII) occurring in an elderly patient from an inbred kindred.
    Chapman S; Gray RG; Constable TJ; Bundey S
    Br J Radiol; 1989 May; 62(737):491-4. PubMed ID: 2496886
    [No Abstract]   [Full Text] [Related]  

  • 47. Early manifestations of multiple sulfatase deficiency.
    Burk RD; Valle D; Thomas GH; Miller C; Moser A; Moser H; Rosenbaum KN
    J Pediatr; 1984 Apr; 104(4):574-8. PubMed ID: 6142938
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Clinical heterogeneity in Sanfilippo disease (mucopolysaccharidosis III) type D: presentation of two new cases.
    Coppa GV; Giorgi PL; Felici L; Gabrielli O; Donti E; Bernasconi S; Kresse H; Paschke E; Mastropaolo C
    Eur J Pediatr; 1983 Apr; 140(2):130-3. PubMed ID: 6411475
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Test for mucopolysaccharidoses: simple method for quantitative estimation of urinary glycosaminoglycans.
    Calatroni A
    Clin Chem; 1972 Mar; 18(3):266-9. PubMed ID: 4259853
    [No Abstract]   [Full Text] [Related]  

  • 50. Morquio-B disease, spondyloepiphyseal dysplasia associated with acid beta-galactosidase deficiency. Report of three cases in one family.
    van Gemund JJ; Giesberts MA; Eerdmans RF; Blom W; Kleijer WJ
    Hum Genet; 1983; 64(1):50-4. PubMed ID: 6409799
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mucopolysaccharidosis type VII: characterization of mutations and molecular heterogeneity.
    Tomatsu S; Fukuda S; Sukegawa K; Ikedo Y; Yamada S; Yamada Y; Sasaki T; Okamoto H; Kuwahara T; Yamaguchi S
    Am J Hum Genet; 1991 Jan; 48(1):89-96. PubMed ID: 1702266
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Keratan and herparan sulfaturia: glucosamine-6-sulfate deficiency.
    Matalon R; Wappner R; Deanching M; Brandt IK; Horwitz A
    Ann Clin Lab Sci; 1982; 12(3):234-8. PubMed ID: 6212020
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Hereditary lysosomal diseases in Mexico. II. Laboratory diagnosis of mucopolysaccharidosis and mucolipidosis].
    Zetina ME; Gonzalez-Noriega A
    Rev Invest Clin; 1990; 42(3):165-73. PubMed ID: 2125355
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduria.
    Haust MD; Gordon BA; Hong R; Choi JH; Langer LO; Spranger J; Opitz JM
    Am J Med Genet; 1985 Sep; 22(1):1-27. PubMed ID: 2931979
    [No Abstract]   [Full Text] [Related]  

  • 55. Mucopolysaccharidosis VII: postmortem biochemical and pathological findings in a young adult with beta-glucuronidase deficiency.
    Vogler C; Levy B; Kyle JW; Sly WS; Williamson J; Whyte MP
    Mod Pathol; 1994 Jan; 7(1):132-7. PubMed ID: 8159643
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Locus differentiation of hereditary mucopolysaccharidoses].
    Odinokova ON; Lebedeva TV; Krasnopol'skaia KD; Freĭdin MI
    Vopr Med Khim; 1986; 32(2):45-9. PubMed ID: 3085344
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Postmortem observations on beta-glucuronidase deficiency presenting as hydrops fetalis.
    Irani D; Kim HS; El-Hibri H; Dutton RV; Beaudet A; Armstrong D
    Ann Neurol; 1983 Oct; 14(4):486-90. PubMed ID: 6685450
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Clinical, radiological, biochemical, and genetic aspects of the Sanfilippo disease, apropos of 3 cases].
    Dhondt JL; Farriaux JP; Fournier A; Fontaine G
    J Genet Hum; 1974 Jun; 22(2):109-32. PubMed ID: 4278846
    [No Abstract]   [Full Text] [Related]  

  • 59. The use of alpha-L-iduronidase activity determinations in leucocytes for the detection of Hurler and Scheie syndromes.
    Liem KO; Hooghwinkel GJ
    Clin Chim Acta; 1975 Apr; 60(2):259-62. PubMed ID: 805007
    [No Abstract]   [Full Text] [Related]  

  • 60. Reclassification of previously reported cases of mucopolysaccharidosis type IS to mucopolysaccharidosis type VI.
    Constantopoulos G; Stowens DW; Barranger JA
    Clin Chim Acta; 1982 Sep; 124(1):137-9. PubMed ID: 6812996
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.