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 *

202 related articles for article (PubMed ID: 4213627)

  • 1. 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]  

  • 2. [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]  

  • 3. [Two differentiated types of gargoylism--Hurler's and Hunter's].
    Likavcan M; Vajda P
    Cesk Pediatr; 1972 Aug; 27(8):391-3. PubMed ID: 4626309
    [No Abstract]   [Full Text] [Related]  

  • 4. Hurler's, Hunter's and Morquio's syndromes. A biochemical study in the light of current views of the underlying defects.
    Dean MF; Muir H; Ewins RJ
    Biochem J; 1971 Aug; 123(5):883-94. PubMed ID: 4256532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome).
    Berg K; Danes BS; Bearn AG
    Am J Hum Genet; 1968 Jul; 20(4):398-401. PubMed ID: 4969416
    [No Abstract]   [Full Text] [Related]  

  • 6. Intrauterine diagnosis of the hurler and hunter syndromes.
    Fratantoni JC; Neufeld EF; Uhlendorf BW; Jacobson CB
    N Engl J Med; 1969 Mar; 280(13):686-8. PubMed ID: 4179670
    [No Abstract]   [Full Text] [Related]  

  • 7. Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.
    Tønnesen T; Lykkelund C; Güttler F
    Hum Genet; 1982; 60(2):167-71. PubMed ID: 6210620
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Unusual findings in 2 patients with Hunter's disease].
    Fiehring C; Schramm G; Würbach G; Meerbach W; Koskowski H; Hoffmann W; Hellinger J; Buttenberg H
    Dtsch Gesundheitsw; 1970 Jan; 25(2):78-82. PubMed ID: 4245072
    [No Abstract]   [Full Text] [Related]  

  • 9. [Familial cases of Hunter's syndrome].
    Kawamura N; Narikawa J; Takahira T; Ito K; Kato M
    Nihon Rinsho; 1973 Aug; 31(8):2606-9. PubMed ID: 4203266
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hunter's disease: study of a family from the plain of Paestum].
    Carlomagno S; Federico A; Pinto L; Balbi R; Vitolo G; Guazzi GC
    Acta Neurol (Napoli); 1973; 28(3):323-49. PubMed ID: 4270001
    [No Abstract]   [Full Text] [Related]  

  • 11. Letter: Hurler's syndrome with clear corneas.
    Gardner RJ; Hay JR
    Lancet; 1974 Oct; 2(7884):845. PubMed ID: 4138321
    [No Abstract]   [Full Text] [Related]  

  • 12. The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.
    Fratantoni JC; Hall CW; Neufeld EF
    Proc Natl Acad Sci U S A; 1968 Jun; 60(2):699-706. PubMed ID: 4236091
    [No Abstract]   [Full Text] [Related]  

  • 13. Letter: Question raised regarding diagnosis of Hunter syndrome.
    Kelly TE
    Pediatrics; 1974 Oct; 54(4):522-3. PubMed ID: 4213222
    [No Abstract]   [Full Text] [Related]  

  • 14. Mucopolysaccharidosis II (Hunter's syndrome).
    Arch Dermatol; 1970 Nov; 102(5):578-80. PubMed ID: 4248769
    [No Abstract]   [Full Text] [Related]  

  • 15. The submicroscopic structure of connective tissue in a case of Hunter's syndrome. I. Polarisation microscopic examinations.
    Józsa L
    Acta Morphol Acad Sci Hung; 1971; 19(3):301-11. PubMed ID: 4260201
    [No Abstract]   [Full Text] [Related]  

  • 16. [Mucopolysaccharidosis type II (Hurler-Hunter) in siblings. Electron microscopic study].
    Tichý J; Cihula J; Vortel V
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1972; 15(2):173-9. PubMed ID: 4209410
    [No Abstract]   [Full Text] [Related]  

  • 17. Hunter's syndrome and Cooley's anaemia in the same patient. Effect of multiple transfusions.
    Bartsocas CS; Papasotiriou N; Karageorga M; Moser HW
    Acta Paediatr Scand; 1973 Jan; 62(1):66-8. PubMed ID: 4632385
    [No Abstract]   [Full Text] [Related]  

  • 18. [Delayed form of mucopolysaccharidosis II. (Hunter's syndrome): Occurrence in 4 brothers].
    Najjar Z; Ciorlia R; Mendes FT; Toledo SP; de Ulhoa-Cintra AB
    Rev Hosp Clin Fac Med Sao Paulo; 1976; 31(1):47-61. PubMed ID: 815978
    [No Abstract]   [Full Text] [Related]  

  • 19. Relative frequency of the Hurler and Hunter syndromes.
    N Engl J Med; 1970 Dec; 283(26):1466-8. PubMed ID: 4991513
    [No Abstract]   [Full Text] [Related]  

  • 20. [Type II mucolipidosis (I-cell disease)].
    Walbaum R; Dehaene P; Scharfman W; Farriaux JP; Tondeur M; Vamos-Hurwitz E; Kint JA; Van Hoof F
    Arch Fr Pediatr; 1973; 30(6):577-93. PubMed ID: 4375946
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.