Epidemiology of Sanfilippo syndrome: results of a systematic literature review

[1] Valstar MJ(2008)Sanfilippo syndrome: a mini-review J Inherit Metab Dis 31 240-252

[2] Ruijter GJ(2015)Sanfilippo syndrome: causes, consequences, and treatments Appl Clin Genet 8 269-281

[3] van Diggelen OP(2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement PLoS Med 6 e1000097-808

[4] Poorthuis BJ(2007)Strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies BMJ 335 806-41

[5] Wijburg FA(2014)The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): a changing landscape Mol Genet Metab 113 34-370

[6] Fedele AO(2013)Lifetime risk estimators in epidemiological studies of Krabbe disease: review and Monte Carlo comparison Rare Dis 1 e25212-1581

[7] Moher D(1998)A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK J Med Genet 35 366-396

[8] Liberati A(2000)Incidence of inborn errors of metabolism in British Columbia, 1969–1996 Pediatrics 105 e10-785

[9] Tetzlaff J(2008)Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence Acta Paediatr 97 1577-299

[10] Altman DG(2010)The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations J Inherit Metab Dis 33 387-979

[1] Valstar MJ(2008)Sanfilippo syndrome: a mini-review J Inherit Metab Dis 31 240-252

[2] Ruijter GJ(2015)Sanfilippo syndrome: causes, consequences, and treatments Appl Clin Genet 8 269-281

[3] van Diggelen OP(2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement PLoS Med 6 e1000097-808

[4] Poorthuis BJ(2007)Strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies BMJ 335 806-41

[5] Wijburg FA(2014)The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): a changing landscape Mol Genet Metab 113 34-370

[6] Fedele AO(2013)Lifetime risk estimators in epidemiological studies of Krabbe disease: review and Monte Carlo comparison Rare Dis 1 e25212-1581

[7] Moher D(1998)A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK J Med Genet 35 366-396

[8] Liberati A(2000)Incidence of inborn errors of metabolism in British Columbia, 1969–1996 Pediatrics 105 e10-785

[9] Tetzlaff J(2008)Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence Acta Paediatr 97 1577-299

[10] Altman DG(2010)The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations J Inherit Metab Dis 33 387-979