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 *

110 related articles for article (PubMed ID: 3139339)

  • 1. Carrier detection in Sanfilippo A syndrome.
    Toone JR; Applegarth DA
    Clin Genet; 1988 Jun; 33(6):401-3. PubMed ID: 3139339
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Carrier detection for Sanfilippo A syndrome.
    Matalon R; Deanching M; Marback R; Michals K
    J Inherit Metab Dis; 1988; 11(2):158-60. PubMed ID: 3139927
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carrier detection in Sanfilippo syndrome type B: report of six families.
    Vance JM; Conneally PM; Wappner RS; Yu PL; Brandt IK; Pericak-Vance MA
    Clin Genet; 1981 Aug; 20(2):135-40. PubMed ID: 6796309
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Carrier detection for Sanfilippo A syndrome.
    Stone J; Brimble A; Pennock CA
    J Inherit Metab Dis; 1990; 13(2):184-6. PubMed ID: 2116549
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sanfilippo B disease in two related sibships. Biochemical studies in patients, parents and sibs.
    Liem KO; Giesberts MA; van de Kamp JJ; van Pelt JF; Hooghwinkel GJ
    Clin Genet; 1976 Nov; 10(5):273-8. PubMed ID: 825332
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sanfilippo B disease in two related sibships. Biochemical studies in patients and sibs.
    Liem KO; Hooghwinkel GJ
    Monogr Hum Genet; 1978; 10():11-5. PubMed ID: 102922
    [No Abstract]   [Full Text] [Related]  

  • 7. Sulphamidase activity in leucocytes, cultured skin fibroblasts and amniotic cells: diagnosis of the Sanfilippo A syndrome with the use of radiolabelled disaccharide substrate.
    Hopwood JJ; Elliott H
    Clin Sci (Lond); 1981 Dec; 61(6):729-35. PubMed ID: 6794973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sanfilippo disease, type C: three cases in the same family.
    Turki I; Kresse H; Scotto J; Tardieu M
    Neuropediatrics; 1989 May; 20(2):90-2. PubMed ID: 2500617
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sanfilippo B syndrome (MPS III B): altered residual alpha-N-acetylglucosaminidase activity in an unusual sibship.
    Di Natale P; Murino P; Pontarelli G; Salvatore D; Andria G
    Clin Chim Acta; 1982 Jul; 122(2):135-43. PubMed ID: 6809360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sanfilippo A syndrome in the fetus.
    Greenwood RS; Hillman RE; Alcala H; Sly WS
    Clin Genet; 1978 Mar; 13(3):241-50. PubMed ID: 147760
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sanfilippo D syndrome: estimation of N-acetylglucosamine-6-sulfatase activity with a radiolabeled monosulfated disaccharide substrate.
    Freeman C; Hopwood JJ
    Anal Biochem; 1989 Feb; 176(2):244-8. PubMed ID: 2500866
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [You make the diagnosis. Mucopolysaccharidosis III A (Sanfillipo A disease)].
    Howanietz H; Widhalm K
    Padiatr Padol; 1987; 22(4):361-4. PubMed ID: 3125511
    [No Abstract]   [Full Text] [Related]  

  • 13. Mucopolysaccharidosis type IIIC (Sanfilippo): early clinical presentation in a large Turkish pedigree.
    Sewell AC; Pontz BF; Benischek G
    Clin Genet; 1988 Aug; 34(2):116-21. PubMed ID: 3142713
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sanfilippo syndrome type C: assay for acetyl-CoA: alpha-glucosaminide N-acetyltransferase in leukocytes for detection of homozygous and heterozygous individuals.
    Klein U; van de Kamp JJ; von Figura K; Pohlmann R
    Clin Genet; 1981 Jul; 20(1):55-9. PubMed ID: 6794963
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A clinical study of the siblings of Sanfilippo B syndrome (MPS III B)].
    Tamagawa K; Nakajima S; Terauchi A; Koide H; Morimatsu Y; Nishiya O; Mimura A
    No To Hattatsu; 1983; 15(1):57-66. PubMed ID: 6401424
    [No Abstract]   [Full Text] [Related]  

  • 16. Sanfilippo type C syndrome in two sisters.
    Uvebrant P
    Acta Paediatr Scand; 1985 Jan; 74(1):137-9. PubMed ID: 3920864
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The laboratory diagnosis of Sanfilippo disease.
    Whiteman P; Young E
    Clin Chim Acta; 1977 Apr; 76(1):139-47. PubMed ID: 404099
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sanfilippo B syndrome (MPS III B): mild and severe forms within the same sibship.
    Andria G; Di Natale P; Del Giudice E; Strisciuglio P; Murino P
    Clin Genet; 1979 Jun; 15(6):500-4. PubMed ID: 157237
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patient.
    Gordon BA; Feleki V; Budreau CH; Tyler L
    Clin Biochem; 1975 Jun; 8(3):184-93. PubMed ID: 238759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C).
    van de Kamp JJ; Niermeijer MF; von Figura K; Giesberts MA
    Clin Genet; 1981 Aug; 20(2):152-60. PubMed ID: 6796310
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.