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 *

120 related articles for article (PubMed ID: 6406726)

  • 1. Ocular manifestations of Hurler/Scheie phenotype in two sibs.
    Chijiiwa T; Inomata H; Yamana Y; Kaibara N
    Jpn J Ophthalmol; 1983; 27(1):54-62. PubMed ID: 6406726
    [No Abstract]   [Full Text] [Related]  

  • 2. Letter: In-vitro confirmation of genetic compound of the Hurler and Scheie syndromes.
    Danes BS
    Lancet; 1974 Apr; 1(7859):680. PubMed ID: 4132345
    [No Abstract]   [Full Text] [Related]  

  • 3. Decreased corneal opacity and improved vision in a patient with mucopolysaccharidosis I (Hurler-Scheie) treated with enzyme replacement therapy (laronidase, Aldurazyme).
    Cáceres-Marzal C; García-Reymundo M; Solana J; de Arévalo B; Vaquerizo J; Galán E
    Am J Med Genet A; 2008 Jul; 146A(13):1768-70. PubMed ID: 18546328
    [No Abstract]   [Full Text] [Related]  

  • 4. [Cytogenetic studies in children with visual disorders].
    Muşeţeanu P; Garoiu M; Duca-Marinescu D; Carangiu M; Friciu E; Ionescu B; Maximilian C
    Stud Cercet Endocrinol; 1972; 23(5):333-5. PubMed ID: 4219458
    [No Abstract]   [Full Text] [Related]  

  • 5. [Mucopolysaccharidosis type I, Hurler-Scheie phenotype with ocular involvement. Clinical and ultrastructural study].
    Girard B; Hoang-Xuan T; D'Hermies F; Savoldelli M; Bennouna M; Poenaru L; Maroteaux P; Pouliquen Y
    J Fr Ophtalmol; 1994; 17(4):286-95. PubMed ID: 8089412
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited eye diseases.
    Whitwell J
    Practitioner; 1975 May; 214(1283):621-630. PubMed ID: 1079941
    [No Abstract]   [Full Text] [Related]  

  • 7. Hurler-Scheie phenotype with parental consanguinity. Report of an additional case supporting the concept of genetic heterogeneity.
    Kaibara N; Katsuki I; Hotokebuchi T; Takagishi K; Kure T
    Clin Orthop Relat Res; 1983 May; (175):233-6. PubMed ID: 6404579
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Further electroretinographic studies of patients with mucopolysaccharidoses.
    Leung LS; Weinstein GW; Hobson RR
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):32-40. PubMed ID: 5006141
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Mucopolysaccharidosis of the Pfaundler-Hurler type with spastic tetraparesis and retinitis pigmentosa of two adult sisters].
    Schäfer U; Rödl W
    Fortschr Neurol Psychiatr Grenzgeb; 1972 Aug; 40(8):409-39. PubMed ID: 4263397
    [No Abstract]   [Full Text] [Related]  

  • 11. [Hurler syndrome(MPS IH), Scheie syndrome(MPS IS)].
    Matsushita Y; Kuroiwa Y
    Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):460-1. PubMed ID: 11031992
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetics and counselling in ophthalmology.
    Keith CG
    Aust J Ophthalmol; 1981 Feb; 9(1):74-6. PubMed ID: 6793033
    [No Abstract]   [Full Text] [Related]  

  • 13. The relative frequency of the Hurler and Hunter syndromes.
    McKusick VA
    N Engl J Med; 1970 Oct; 283(16):853-4. PubMed ID: 4989786
    [No Abstract]   [Full Text] [Related]  

  • 14. Ocular and genetic features of Cockayne's syndrome.
    Pearce WG
    Can J Ophthalmol; 1972 Oct; 7(4):435-44. PubMed ID: 4652816
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. Four novel mutations underlying mild or intermediate forms of alpha-L-iduronidase deficiency (MPS IS and MPS IH/S).
    Tieu PT; Bach G; Matynia A; Hwang M; Neufeld EF
    Hum Mutat; 1995; 6(1):55-9. PubMed ID: 7550232
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Hurler/Scheie phenotype in children from a consanguineous marriage: case report with electronmicroscopy of the conjunctiva and ERG.
    Jensen OA; Pedersen C; Vestermark S; Warburg M
    Metab Pediatr Ophthalmol; 1980; 4(3):133-4. PubMed ID: 6779061
    [No Abstract]   [Full Text] [Related]  

  • 19. Ocular manifestations in female carriers of X-linked disorders.
    Nowakowski R
    J Am Optom Assoc; 1995 Jun; 66(6):352-6. PubMed ID: 7673594
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular biology in ocular disorders.
    Keith CG
    Med J Aust; 1993 May; 158(9):615-8. PubMed ID: 8479380
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.