Management of mucopolysaccharidosis type III - PubMed (original) (raw)

Review

Management of mucopolysaccharidosis type III

M A Cleary et al. Arch Dis Child. 1993 Sep.

No abstract available

PubMed Disclaimer

Similar articles

• Developmental and degenerative patterns associated with cognitive, behavioural and motor difficulties in the Sanfilippo syndrome: an epidemiological study.
  Nidiffer FD, Kelly TE. Nidiffer FD, et al. J Ment Defic Res. 1983 Sep;27 (Pt 3):185-203. doi: 10.1111/j.1365-2788.1983.tb00291.x. J Ment Defic Res. 1983. PMID: 6415286
• Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing clinicians.
  Fraser J, Wraith JE, Delatycki MB. Fraser J, et al. Clin Genet. 2002 Nov;62(5):418-21. doi: 10.1034/j.1399-0004.2002.620512.x. Clin Genet. 2002. PMID: 12431260
• Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A: implications for evaluation of new therapies.
  McDowell GA, Cowan TM, Blitzer MG, Greene CL. McDowell GA, et al. Am J Med Genet. 1993 Nov 15;47(7):1092-5. doi: 10.1002/ajmg.1320470732. Am J Med Genet. 1993. PMID: 7507293
• Musculoskeletal manifestations of Sanfilippo Syndrome (mucopolysaccharidosis type III).
  White KK, Karol LA, White DR, Hale S. White KK, et al. J Pediatr Orthop. 2011 Jul-Aug;31(5):594-8. doi: 10.1097/BPO.0b013e31821f5ee9. J Pediatr Orthop. 2011. PMID: 21654471 Review.
• [Sanfilippo's disease--accompanying findings in maxillofacial surgery as an aid to differential diagnosis of type III mucopolysaccharidosis].
  Radtke J. Radtke J. Dtsch Z Mund Kiefer Gesichtschir. 1988 Jul-Aug;12(4):289-92. Dtsch Z Mund Kiefer Gesichtschir. 1988. PMID: 3149221 Review. German. No abstract available.

Cited by

• Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC.
  Marcó S, Pujol A, Roca C, Motas S, Ribera A, Garcia M, Molas M, Villacampa P, Melia CS, Sánchez V, Sánchez X, Bertolin J, Ruberte J, Haurigot V, Bosch F. Marcó S, et al. Dis Model Mech. 2016 Sep 1;9(9):999-1013. doi: 10.1242/dmm.025171. Epub 2016 Aug 4. Dis Model Mech. 2016. PMID: 27491071 Free PMC article.
• Sanfilippo syndrome: consensus guidelines for clinical care.
  Muschol N, Giugliani R, Jones SA, Muenzer J, Smith NJC, Whitley CB, Donnell M, Drake E, Elvidge K, Melton L, O'Neill C; MPS III Guideline Development Group. Muschol N, et al. Orphanet J Rare Dis. 2022 Oct 27;17(1):391. doi: 10.1186/s13023-022-02484-6. Orphanet J Rare Dis. 2022. PMID: 36303195 Free PMC article. Review.
• Natural history of Sanfilippo syndrome in Spain.
  Delgadillo V, O'Callaghan Mdel M, Gort L, Coll MJ, Pineda M. Delgadillo V, et al. Orphanet J Rare Dis. 2013 Dec 6;8:189. doi: 10.1186/1750-1172-8-189. Orphanet J Rare Dis. 2013. PMID: 24314109 Free PMC article.
• NAGLU mutations underlying Sanfilippo syndrome type B.
  Schmidtchen A, Greenberg D, Zhao HG, Li HH, Huang Y, Tieu P, Zhao HZ, Cheng S, Zhao Z, Whitley CB, Di Natale P, Neufeld EF. Schmidtchen A, et al. Am J Hum Genet. 1998 Jan;62(1):64-9. doi: 10.1086/301685. Am J Hum Genet. 1998. PMID: 9443878 Free PMC article.
• Electroclinical Features of Epilepsy in Mucopolysaccharidosis III: Outcome Description in a Cohort of 15 Italian Patients.
  Barone R, Fiumara A, Gulisano M, Cirnigliaro L, Cocuzza MD, Guida C, Pettinato F, Greco F, Elia M, Rizzo R. Barone R, et al. Front Neurol. 2021 Jul 19;12:705423. doi: 10.3389/fneur.2021.705423. eCollection 2021. Front Neurol. 2021. PMID: 34349725 Free PMC article.

References

1. 1. Clin Genet. 1981 Aug;20(2):152-60 - PubMed
2. 1. Am J Med Genet. 1987 Sep;28(1):125-9 - PubMed
3. 1. Bone Marrow Transplant. 1991;7 Suppl 2:71 - PubMed
4. 1. Can J Anaesth. 1988 Jan;35(1):67-73 - PubMed
5. 1. Aust Paediatr J. 1987 Dec;23(6):329-34 - PubMed

Publication types

MeSH terms

LinkOut - more resources

• Full Text Sources

  • Europe PubMed Central
  • PubMed Central

• Other Literature Sources

  • The Lens - Patent Citations Database