Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 13

1.

Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome).

Popowska E, Rathmann M, Tylki-Szymanska A, Bunge S, Steglich C, Schwinger E, Gal A.

Hum Mutat. 1995;5(1):97-100. No abstract available.

PMID:
7728156
[PubMed - indexed for MEDLINE]
2.

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene.

Hopwood JJ, Bunge S, Morris CP, Wilson PJ, Steglich C, Beck M, Schwinger E, Gal A.

Hum Mutat. 1993;2(6):435-42. Review.

PMID:
8111411
[PubMed - indexed for MEDLINE]
3.

Hunter disease in the Spanish population: molecular analysis in 31 families.

Gort L, Chabás A, Coll MJ.

J Inherit Metab Dis. 1998 Aug;21(6):655-61. Review.

PMID:
9762601
[PubMed - indexed for MEDLINE]
4.

[Mutation analysis in Hunter patients].

Villani GR, Balzano N, Grosso M, Di Natale P.

Pediatr Med Chir. 1996 Jan-Feb;18(1):71-83. Review. Italian.

PMID:
8685029
[PubMed - indexed for MEDLINE]
5.

[Mucopolysaccharidosis type II (Hunter syndrome)].

Sukegawa K, Tomatsu S, Kondo N, Orii T.

Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):435-8. Review. Japanese. No abstract available.

PMID:
9645102
[PubMed - indexed for MEDLINE]
6.

Multidisciplinary management of Hunter syndrome.

Muenzer J, Beck M, Eng CM, Escolar ML, Giugliani R, Guffon NH, Harmatz P, Kamin W, Kampmann C, Koseoglu ST, Link B, Martin RA, Molter DW, Muñoz Rojas MV, Ogilvie JW, Parini R, Ramaswami U, Scarpa M, Schwartz IV, Wood RE, Wraith E.

Pediatrics. 2009 Dec;124(6):e1228-39. doi: 10.1542/peds.2008-0999. Epub 2009 Nov 9. Review.

PMID:
19901005
[PubMed - indexed for MEDLINE]
Free Article
7.

[Hunter syndrome].

Matsushita Y, Kuroiwa Y.

Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):462-3. Review. Japanese. No abstract available.

PMID:
11031993
[PubMed - indexed for MEDLINE]
8.

Mucopolysaccharidosis type II in females: case report and review of literature.

Tuschl K, Gal A, Paschke E, Kircher S, Bodamer OA.

Pediatr Neurol. 2005 Apr;32(4):270-2. Review.

PMID:
15797184
[PubMed - indexed for MEDLINE]
9.

Idursulfase in Hunter syndrome treatment.

Zareba G.

Drugs Today (Barc). 2007 Nov;43(11):759-67. doi: 10.1358/dot.2007.43.11.1157619. Review.

PMID:
18174963
[PubMed - indexed for MEDLINE]
10.

Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy.

Wraith JE, Scarpa M, Beck M, Bodamer OA, De Meirleir L, Guffon N, Meldgaard Lund A, Malm G, Van der Ploeg AT, Zeman J.

Eur J Pediatr. 2008 Mar;167(3):267-77. Epub 2007 Nov 23. Review.

PMID:
18038146
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning.

Winchester B, Young E, Geddes S, Genet S, Hurst J, Middleton-Price H, Williams N, Webb M, Habel A, Malcolm S.

Am J Med Genet. 1992 Dec 1;44(6):834-8. Review.

PMID:
1481858
[PubMed - indexed for MEDLINE]
12.

Mucopolysaccharidosis type II: an update on mutation spectrum.

Froissart R, Da Silva IM, Maire I.

Acta Paediatr Suppl. 2007 Apr;96(455):71-7. Review.

PMID:
17391447
[PubMed - indexed for MEDLINE]
13.

The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensus.

Muenzer J, Bodamer O, Burton B, Clarke L, Frenking GS, Giugliani R, Jones S, Rojas MV, Scarpa M, Beck M, Harmatz P.

Eur J Pediatr. 2012 Jan;171(1):181-8. doi: 10.1007/s00431-011-1606-3. Epub 2011 Oct 29.

PMID:
22037758
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk