BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 6438322)

  • 41. Placenta analysis of prenatally diagnosed patients reveals early GAG storage in mucopolysaccharidoses II and VI.
    Baldo G; Matte U; Artigalas O; Schwartz IV; Burin MG; Ribeiro E; Horovitz D; Magalhaes TP; Elleder M; Giugliani R
    Mol Genet Metab; 2011 Jun; 103(2):197-8. PubMed ID: 21427013
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Elevated cerebral spinal fluid biomarkers in children with mucopolysaccharidosis I-H.
    Raymond GV; Pasquali M; Polgreen LE; Dickson PI; Miller WP; Orchard PJ; Lund TC
    Sci Rep; 2016 Dec; 6():38305. PubMed ID: 27910891
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prenatal diagnosis of vitamin D-dependent rickets, type II: response to 1,25-dihydroxyvitamin D in amniotic fluid cells and fetal tissues.
    Weisman Y; Jaccard N; Legum C; Spirer Z; Yedwab G; Even L; Edelstein S; Kaye AM; Hochberg Z
    J Clin Endocrinol Metab; 1990 Oct; 71(4):937-43. PubMed ID: 2169482
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Residual α-L-iduronidase activity in fibroblasts of mild to severe Mucopolysaccharidosis type I patients.
    Oussoren E; Keulemans J; van Diggelen OP; Oemardien LF; Timmermans RG; van der Ploeg AT; Ruijter GJ
    Mol Genet Metab; 2013 Aug; 109(4):377-81. PubMed ID: 23786846
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Delivery of an Adeno-Associated Virus Vector into Cerebrospinal Fluid Attenuates Central Nervous System Disease in Mucopolysaccharidosis Type II Mice.
    Hinderer C; Katz N; Louboutin JP; Bell P; Yu H; Nayal M; Kozarsky K; O'Brien WT; Goode T; Wilson JM
    Hum Gene Ther; 2016 Nov; 27(11):906-915. PubMed ID: 27510804
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Biochemical differentiation of Hurler's and Hunter's diseases by fracionation of heparitin sulfate].
    Maroteaux P
    Rev Eur Etud Clin Biol; 1970 Feb; 15(2):203-5. PubMed ID: 4245695
    [No Abstract]   [Full Text] [Related]  

  • 47. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes.
    Mueller OT; Shows TB; Opitz JM
    Am J Med Genet; 1984 Jul; 18(3):547-56. PubMed ID: 6433708
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans.
    Mossman J; Patrick AD
    Prenat Diagn; 1982 Jul; 2(3):169-76. PubMed ID: 6815629
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Antenatal diagnosis of Hurler disease.
    Henderson H; Whiteman P
    Lancet; 1976 Nov; 2(7993):1024-5. PubMed ID: 62242
    [No Abstract]   [Full Text] [Related]  

  • 50. Antenatal detection of Hurler's syndrome.
    Brock DJ; Gordon H; Seligman S; Lobo Ede H
    Lancet; 1971 Dec; 2(7737):1324-5. PubMed ID: 4143577
    [No Abstract]   [Full Text] [Related]  

  • 51. Mucopolysaccharidosis type V. (Scheie syndrome). A postmortem study by multidisciplinary techniques with emphasis on the brain.
    Dekaban AS; Constantopoulos G; Herman MM; Steusing JK
    Arch Pathol Lab Med; 1976 May; 100(5):237-45. PubMed ID: 817693
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).
    Chen CP; Lin SP; Tzen CY; Hwu WL; Chern SR; Chuang CK; Chiang SS; Wang W
    Genet Couns; 2007; 18(1):49-56. PubMed ID: 17515300
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The diagnosis of mucopolysaccharidoses by electron microscopy of skin biopsies.
    Bioulac P; Mercier M; Beylot C; Fontan D
    J Cutan Pathol; 1975; 2(4):179-90. PubMed ID: 172535
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Light and electron microscopy of the cornea in systemic mucopolysaccharidosis type I-S (Scheie's syndrome).
    Rummelt V; Meyer HJ; Naumann GO
    Cornea; 1992 Jan; 11(1):86-92. PubMed ID: 1559353
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Transplantation of fetal fibroblasts and correction of enzymatic deficiencies in patients with Hunter's or Hurler's disorders.
    Adinolfi M; McColl I; Chase D; Fensom AH; Welsh K; Brown S; Marsh J; Thick M; Dean M
    Transplantation; 1986 Sep; 42(3):271-4. PubMed ID: 3092412
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Histopathological diagnosis of a type vii mucopolysaccharidosis after pregnancy termination.
    Delbecque K; Gaillez S; Schaaps JP
    Fetal Pediatr Pathol; 2009; 28(1):1-8. PubMed ID: 19116811
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A familial occurrence of a mucopolysaccharidosis: Hurler's or Hunter's syndrome?
    Bhambhani R; Singh SM; Kuspira J; Muntjewerff N
    Hum Hered; 1974; 24(2):219-24. PubMed ID: 4213627
    [No Abstract]   [Full Text] [Related]  

  • 58. Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type II.
    Uttarilli A; Ranganath P; Matta D; Md Nurul Jain J; Prasad K; Babu AS; Girisha KM; Verma IC; Phadke SR; Mandal K; Puri RD; Aggarwal S; Danda S; Sankar VH; Kapoor S; Bhat M; Gowrishankar K; Hasan AQ; Nair M; Nampoothiri S; Dalal A
    Clin Genet; 2016 Dec; 90(6):496-508. PubMed ID: 27146977
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Detection of the carrier state of Hurler's syndrome by assay of alpha-L-iduronidase in leukocytes.
    Dulaney JT; Milunsky A; Moser HW
    Clin Chim Acta; 1976 Jun; 69(2):305-10. PubMed ID: 819189
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mucopolysaccharidosis type I.
    Wraith JE; Jones S
    Pediatr Endocrinol Rev; 2014 Sep; 12 Suppl 1():102-6. PubMed ID: 25345091
    [TBL] [Abstract][Full Text] [Related]  

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