Hunter Syndrome.
Kumar P, Das PC, Das A.
JAMA Dermatol. 2022 Dec 1;158(12):1438. doi: 10.1001/jamadermatol.2022.4049.
Bow hunter syndrome.
Kühn AL, McGillicuddy GT, Singh J.
CMAJ. 2022 Nov 7;194(43):E1486. doi: 10.1503/cmaj.220607.
Hunter Syndrome: Is It Time to Make It Part of Newborn Screening?
Joseph R, DiCesare EB, Miller A.
Adv Neonatal Care. 2018 Dec;18(6):480-487. doi: 10.1097/ANC.0000000000000569.
Mucopolysaccharidosis type II (Hunter syndrome): Clinical and biochemical aspects of the disease and approaches to its diagnosis and treatment.
Mohamed S, He QQ, Singh AA, Ferro V.
Adv Carbohydr Chem Biochem. 2020;77:71-117. doi: 10.1016/bs.accb.2019.09.001. Epub 2019 Oct 26.
Mucopolysaccharidosis type II, Hunter's syndrome.
Tylki-Szymańska A.
Pediatr Endocrinol Rev. 2014 Sep;12 Suppl 1:107-13.
Bow Hunter's syndrome combined with ipsilateral vertebral artery dissection/pseudoaneurysm: case study and literature review.
Xue S, Shi H, Du X, Ma X.
Br J Neurosurg. 2023 Aug;37(4):911-915. doi: 10.1080/02688697.2020.1718604. Epub 2020 Feb 3.
Management of the behavioural manifestations of Hunter syndrome.
Roberts J, Stewart C, Kearney S.
Br J Nurs. 2016 Jan 14-27;25(1):22, 24, 26-30. doi: 10.12968/bjon.2016.25.1.22.
Hurler holes in Hunter syndrome.
Sharma R, Sharma V, Tiwari T, Goyal S.
BMJ Case Rep. 2021 Nov 11;14(11):e246765. doi: 10.1136/bcr-2021-246765.
Hunter syndrome with persistent thrombocytopenia.
Panigrahi I, Dhanorkar M, Didel S, Koganti RA.
BMJ Case Rep. 2019 Apr 20;12(4):e226518. doi: 10.1136/bcr-2018-226518.
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.
