PubMed (Bookshelf cited) for id: 7734

Year	Number of Results
1971	1
1973	1
1977	1
1981	1
1986	1
1990	1
2000	1
2003	1
2005	2
2006	2
2007	2
2008	3
2009	2
2010	2
2011	5
2012	4
2013	7
2014	7
2015	1
2016	2
2017	7
2022	1
2024	0

1

Variation among DNA banking consent forms: points for clinicians to bank on.

Huang SJ, Amendola LM, Sternen DL. Huang SJ, et al. J Community Genet. 2022 Aug;13(4):389-397. doi: 10.1007/s12687-022-00601-3. Epub 2022 Jul 14. J Community Genet. 2022. PMID: 35834113 Free PMC article.

2

Presentation and Treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome).

Stapleton M, Kubaski F, Mason RW, Yabe H, Suzuki Y, Orii KE, Orii T, Tomatsu S. Stapleton M, et al. Expert Opin Orphan Drugs. 2017;5(4):295-307. doi: 10.1080/21678707.2017.1296761. Epub 2017 Mar 8. Expert Opin Orphan Drugs. 2017. PMID: 29158997 Free PMC article.

3

Clinical outcomes in idursulfase-treated patients with mucopolysaccharidosis type II: 3-year data from the hunter outcome survey (HOS).

Muenzer J, Giugliani R, Scarpa M, Tylki-Szymańska A, Jego V, Beck M. Muenzer J, et al. Orphanet J Rare Dis. 2017 Oct 3;12(1):161. doi: 10.1186/s13023-017-0712-3. Orphanet J Rare Dis. 2017. PMID: 28974237 Free PMC article.

4

Pathophysiology, evaluation, and management of sleep disorders in the mucopolysaccharidoses.

Rapoport DM, Mitchell JJ. Rapoport DM, et al. Mol Genet Metab. 2017 Dec;122S:49-54. doi: 10.1016/j.ymgme.2017.08.008. Epub 2017 Aug 25. Mol Genet Metab. 2017. PMID: 28964643 Free article. Review.

5

Mucopolysaccharidosis type I, II and VI and response to enzyme replacement therapy: Results from a single-center case series study.

Franco JFDS, El Dib R, Agarwal A, Soares D, Milhan NVM, Albano LMJ, Kim CA. Franco JFDS, et al. Intractable Rare Dis Res. 2017 Aug;6(3):183-190. doi: 10.5582/irdr.2017.01036. Intractable Rare Dis Res. 2017. PMID: 28944140 Free PMC article.

6

Survival in idursulfase-treated and untreated patients with mucopolysaccharidosis type II: data from the Hunter Outcome Survey (HOS).

Burton BK, Jego V, Mikl J, Jones SA. Burton BK, et al. J Inherit Metab Dis. 2017 Nov;40(6):867-874. doi: 10.1007/s10545-017-0075-x. Epub 2017 Sep 8. J Inherit Metab Dis. 2017. PMID: 28887757

7

Early hematopoietic stem cell transplantation in a patient with severe mucopolysaccharidosis II: A 7 years follow-up.

Barth AL, de Magalhães TSPC, Reis ABR, de Oliveira ML, Scalco FB, Cavalcanti NC, Silva DSE, Torres DA, Costa AAP, Bonfim C, Giugliani R, Llerena JC Jr, Horovitz DDG. Barth AL, et al. Mol Genet Metab Rep. 2017 Jun 8;12:62-68. doi: 10.1016/j.ymgmr.2017.05.010. eCollection 2017 Sep. Mol Genet Metab Rep. 2017. PMID: 28649514 Free PMC article.

8

Genotype-phenotype relationship in mucopolysaccharidosis II: predictive power of IDS variants for the neuronopathic phenotype.

Vollebregt AAM, Hoogeveen-Westerveld M, Kroos MA, Oussoren E, Plug I, Ruijter GJ, van der Ploeg AT, Pijnappel WWMP. Vollebregt AAM, et al. Dev Med Child Neurol. 2017 Oct;59(10):1063-1070. doi: 10.1111/dmcn.13467. Epub 2017 May 25. Dev Med Child Neurol. 2017. PMID: 28543354 Free article.

9

CNS-directed gene therapy for the treatment of neurologic and somatic mucopolysaccharidosis type II (Hunter syndrome).

Motas S, Haurigot V, Garcia M, Marcó S, Ribera A, Roca C, Sánchez X, Sánchez V, Molas M, Bertolin J, Maggioni L, León X, Ruberte J, Bosch F. Motas S, et al. JCI Insight. 2016 Jun 16;1(9):e86696. doi: 10.1172/jci.insight.86696. JCI Insight. 2016. PMID: 27699273 Free PMC article.

10

Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).

da Silva EM, Strufaldi MW, Andriolo RB, Silva LA. da Silva EM, et al. Cochrane Database Syst Rev. 2016 Feb 5;2(2):CD008185. doi: 10.1002/14651858.CD008185.pub4. Cochrane Database Syst Rev. 2016. PMID: 26845288 Free PMC article. Review.

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