Molar tooth sign in Joubert syndrome: clinical, radiologic, and pathologic significance (Q33866376)

29 July 2017

title

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

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29 July 2017

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B L Maria

1

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29 July 2017

R G Quisling

2

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29 July 2017

L C Rosainz

3

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29 July 2017

A T Yachnis

4

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29 July 2017

J Gitten

5

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29 July 2017

D Dede

6

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29 July 2017

E Fennell

7

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29 July 2017

publication date

1 June 1999

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Journal of Child Neurology

29 July 2017

published in

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29 July 2017

volume

14

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29 July 2017

issue

6

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29 July 2017

page(s)

368-376

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

29 July 2017

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

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Vermian agenesis and unsegmented midbrain tectum. Case report

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Joubert-Boltshauser syndrome with polydactyly in siblings

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

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The Joubert syndrome associated with bilateral chorioretinal coloboma.

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Chorioretinal coloboma and Joubert syndrome: a nonrandom association

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Joubert syndrome associated with unilateral ptosis and Leber congenital amaurosis

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Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibship

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MRI of Joubert's syndrome

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

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Neurobehavioral development in Joubert syndrome

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Joubert syndrome associated with Leber amaurosis and multicystic kidneys

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Joubert syndrome associated with multicystic kidney disease and hepatic fibrosis

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Tracing neuroepithelial cells of the mesencephalic and metencephalic alar plates during cerebellar ontogeny in quail-chick chimaeras

21 January 2018

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Chick/quail chimeras with partial cerebellar grafts: an analysis of the origin and migration of cerebellar cells.

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Zebrafish pax[b] is involved in the formation of the midbrain-hindbrain boundary

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

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Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development

21 January 2018

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Clinical and molecular analysis in Joubert syndrome

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Involvement of Wnt-1 in the formation of the mes/metencephalic boundary

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Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP

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10.1177/088307389901400605

21 January 2018

Identifiers

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