(Q33874309)

29 July 2017

Clinical features and revised diagnostic criteria in Joubert syndrome (English)

1 reference

29 July 2017

0 references

1 reference

B L Maria

1

1 reference

29 July 2017

E Boltshauser

series ordinal

2

1 reference

29 July 2017

S C Palmer

series ordinal

3

1 reference

29 July 2017

T X Tran

series ordinal

4

1 reference

29 July 2017

1 September 1999

1 reference

Journal of Child Neurology

29 July 2017

1 reference

29 July 2017

14

1 reference

29 July 2017

583-90; discussion 590-1

1 reference

29 July 2017

9

1 reference

Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation

29 July 2017

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert Syndrome: Episodic Hyperpnea, Abnormal Eye Movements, Retardation and Ataxia, Associated with Dysplasia of the Cerebellar Vermis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert syndrome: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Follow-up in children with Joubert syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

"Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Clinical and molecular analysis in Joubert syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

CHARGE and Joubert syndromes are different.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

CHARGE and Joubert syndromes: are they a single disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert syndrome associated with unilateral ptosis and Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Molar tooth sign in Joubert syndrome: clinical, radiologic, and pathologic significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Neurobehavioral development in Joubert syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Autistic features in Joubert syndrome: a genetic disorder with agenesis of the cerebellar vermis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

MR imaging of Joubert's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert syndrome: a clinico-radiological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Magnetic resonance imaging features and classification of central nervous system malformations in Joubert syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Neuropathology of Joubert syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Autism and autistic behavior in Joubert syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert syndrome associated with multicystic kidney disease and hepatic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Clinical nosologic and genetic aspects of Joubert and related syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Joubert syndrome associated with Leber amaurosis and multicystic kidneys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

The Joubert syndrome associated with bilateral chorioretinal coloboma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400906

10.1177/088307389901400906

21 January 2018

Identifiers

DOI

0 references

1 reference