(Q38079401)

English

Behavioural phenotypes of the mucopolysaccharide disorders: a systematic literature review of cognitive, motor, social, linguistic and behavioural presentation in the MPS disorders

scientific article published on 06 February 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

Behavioural phenotypes of the mucopolysaccharide disorders: a systematic literature review of cognitive, motor, social, linguistic and behavioural presentation in the MPS disorders (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

mucopolysaccharide

1 reference

based on heuristic

inferred from title

systematic review

1 reference

based on heuristic

inferred from title

author name string

E M Cross

1

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

D J Hare

2

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

publication date

6 February 2013

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

36

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

189-200

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

The prevalence and phenomenology of self-injurious and aggressive behaviour in genetic syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Managing depression in primary care: A meta-synthesis of qualitative and quantitative research from the UK to identify barriers and facilitators

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Behaviour in mucopolysaccharide disorders

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Physical performance testing in mucopolysaccharidosis I: a pilot study

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Gross motor abilities in children with Hurler syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Annotation: behavioural phenotypes: a window onto the biology of behaviour

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Sleep disturbance in Sanfilippo syndrome: a parental questionnaire study

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Functional analysis of problem behavior: a review

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Strengthening behavioral research on genetic mental retardation syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Early clinical markers of central nervous system involvement in mucopolysaccharidosis type II.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Natural progression of neurological disease in mucopolysaccharidosis type II.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Development itself is the key to understanding developmental disorders

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Mucopolysaccharidosis type III (Sanfilippo disease) in Sweden: clinical presentation of 22 children diagnosed during a 30-year period

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Sleep disorders in Sanfilippo syndrome: a polygraphic study.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Is Sanfilippo type B in your mind when you see adults with mental retardation and behavioral problems?

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Self‐Injurious Behaviour in Children with Learning Disabilities: Recent Advances in Assessment and Intervention

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

A clinical study of 77 patients with mucopolysaccharidosis type II

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Cognitive development in patients with Mucopolysaccharidosis type III (Sanfilippo syndrome).

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10545-012-9572-0

21 January 2018

Clinical variability in Sanfilippo B disease: a report on six patients in two related sibships

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The natural history of the severe form of Hunter's syndrome: a study based on 52 cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early presentation in the mucopolysaccharide disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C)

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Otologic manifestations of Hunter syndrome and their relationship with speech development

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developmental and degenerative patterns associated with cognitive, behavioural and motor difficulties in the Sanfilippo syndrome: an epidemiological study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up on seven adult patients with mild Sanfilippo B-disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

When is a behavioural phenotype not a phenotype?

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A)

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sleep problems in children with Sanfilippo syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maroteaux-Lamy syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measuring behavioral phenotypes: provocations from the "new genetics".

1 reference

https://pubmed.ncbi.nlm.nih.gov/23385295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10545-012-9572-0

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38079401&oldid=2201244924"