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 *

212 related articles for article (PubMed ID: 10095889)

  • 1. [Extensive Mongolian spot related to Hurler disease].
    Rybojad M; Moraillon I; Ogier de Baulny H; Prigent F; Morel P
    Ann Dermatol Venereol; 1999 Jan; 126(1):35-7. PubMed ID: 10095889
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Extensive Mongolian spots: a clinical sign merits special attention.
    Ashrafi MR; Shabanian R; Mohammadi M; Kavusi S
    Pediatr Neurol; 2006 Feb; 34(2):143-5. PubMed ID: 16458829
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Hurler syndrome. Early diagnosis and successful enzyme replacement therapy: a new therapeutic approach. Case report].
    Dupont C; El Hachem C; Harchaoui S; Ribault V; Amiour M; Guillot M; Maire I; Froissart R; Guffon-Fouilhoux N
    Arch Pediatr; 2008 Jan; 15(1):45-9. PubMed ID: 18162380
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence of Mongolian spots in Nigerian children in Ile-Ife, Nigeria.
    Onayemi O; Adejuyigbe EA; Torimiro SE; Oyelami O; Jegede OA
    Niger J Med; 2001; 10(3):121-3. PubMed ID: 11806010
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources.
    Souillet G; Guffon N; Maire I; Pujol M; Taylor P; Sevin F; Bleyzac N; Mulier C; Durin A; Kebaili K; Galambrun C; Bertrand Y; Froissart R; Dorche C; Gebuhrer L; Garin C; Berard J; Guibaud P
    Bone Marrow Transplant; 2003 Jun; 31(12):1105-17. PubMed ID: 12796790
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hurler's disease.
    Bhaduri G; Chatterjee S; Sarkar AD; Mukherjee SP; Todani A
    J Indian Med Assoc; 2005 Jul; 103(7):385-6, 398. PubMed ID: 16366193
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mucopolysaccharidosis type I: clinical and biochemical study.
    Bassyouni HT; Afifi HH; el-Awadi MK; Meguid NA
    East Mediterr Health J; 2000; 6(2-3):359-66. PubMed ID: 11556024
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Atypical Mongolian Spots With Hurler's Disease: A Case Report.
    Athanti S; Mouzam S; Sohail Ahmed M
    Cureus; 2024 Apr; 16(4):e58501. PubMed ID: 38765368
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Compound Hurler-Scheie disease in 3 siblings].
    Goldberg G; Grützner P
    Klin Monbl Augenheilkd; 1985 Aug; 187(2):120-3. PubMed ID: 3932747
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hurler's syndrome--early clinical suspicion].
    Søreide K; Søreide JA; Laerdal A; Søreide E; Johannessen F
    Tidsskr Nor Laegeforen; 2002 Jun; 122(16):1552-5. PubMed ID: 12119781
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Frequency and characteristics of mongolian spots among Turkish children in Aegean region.
    Egemen A; Ikizoğlu T; Ergör S; Mete Asar G; Yilmaz O
    Turk J Pediatr; 2006; 48(3):232-6. PubMed ID: 17172067
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early diagnosis of Hurler's syndrome with the aid of the identification of the characteristic gibbus deformity.
    Belmont PJ; Polly DW
    Mil Med; 1998 Oct; 163(10):711-4. PubMed ID: 9795551
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mucopolysaccharidoses. New therapeutic possibilities increase the need of early diagnosis].
    Malm G; Bondeson ML; von Döbeln U; Månsson JE
    Lakartidningen; 2002 Apr; 99(16):1804-9. PubMed ID: 12043480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mucopolysaccharidoses type I and IVA: clinical features and consanguinity in Tunisia.
    Khedhiri S; Chkioua L; Bouzidi H; Dandana A; Ben Turkia H; Miled A; Laradi S
    Pathol Biol (Paris); 2009 Jul; 57(5):392-7. PubMed ID: 18584975
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extensive mongolian spots in an infant with Hurler syndrome.
    Grant BP; Beard JS; de Castro F; Guiglia MC; Hall BD
    Arch Dermatol; 1998 Jan; 134(1):108-9. PubMed ID: 9449925
    [No Abstract]   [Full Text] [Related]  

  • 18. Natural history of extensive Mongolian spots in mucopolysaccharidosis type II (Hunter syndrome): a survey among 52 Japanese patients.
    Ochiai T; Suzuki Y; Kato T; Shichino H; Chin M; Mugishima H; Orii T
    J Eur Acad Dermatol Venereol; 2007 Sep; 21(8):1082-5. PubMed ID: 17714129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mongolian spots: How important are they?
    Gupta D; Thappa DM
    World J Clin Cases; 2013 Nov; 1(8):230-2. PubMed ID: 24340274
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.