Joubert syndrome: a clinico-radiological study (Q30606593)

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Language	Label	Description	Also known as
English	Joubert syndrome: a clinico-radiological study	scientific article

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scholarly article

1 reference

Europe PubMed Central

25 June 2017

Joubert syndrome: a clinico-radiological study (English)

1 reference

Europe PubMed Central

25 June 2017

Joubert syndrome

1 reference

based on heuristic

inferred from title

author name string

Kendall B

1

1 reference

Europe PubMed Central

25 June 2017

Kingsley D

2

1 reference

Europe PubMed Central

25 June 2017

Lambert SR

3

1 reference

Europe PubMed Central

25 June 2017

Taylor D

4

1 reference

Europe PubMed Central

25 June 2017

Finn P

5

1 reference

Europe PubMed Central

25 June 2017

publication date

1 January 1990

1 reference

Europe PubMed Central

25 June 2017

1 reference

Europe PubMed Central

25 June 2017

31

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Europe PubMed Central

25 June 2017

6

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Europe PubMed Central

25 June 2017

502-506

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Europe PubMed Central

25 June 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dandy-Walker syndrome: analysis of 21 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Dandy-Walker syndrome. A clinicopathological study based on 28 cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Joubert-Boltshauser syndrome with polydactyly in siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Joubert's syndrome. Apropos of 5 cases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow Saccades in Spinocerebellar Degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uncommon syndromes of cerebellar vermis aplasia. I: Joubert syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Joubert syndrome: a case confirmed by computerized tomography

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Joubert syndrome: clinical and polygraphic observations in a further case

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar-dependent adaptive control of primate saccadic system

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's congenital amaurosis. Relationship of structural CNS anomalies to psychomotor retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary syndrome of congenital retinal blindness (Leber), polycystic kidneys and maldevelopment of the brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/2352633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00340131

1 reference

Europe PubMed Central

25 June 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

25 June 2017

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