(Q33425273)

26 July 2017

1 reference

title

Malformations of the midbrain and hindbrain: a retrospective study and review of the literature (English)

1 reference

26 July 2017

Ozlem Alkan

1

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26 July 2017

Osman Kizilkilic

series ordinal

2

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26 July 2017

Tulin Yildirim

series ordinal

3

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26 July 2017

publication date

1 April 2009

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26 July 2017

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26 July 2017

volume

8

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26 July 2017

issue

3

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26 July 2017

page(s)

355-365

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MRI in children with mental retardation

26 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS12311-009-0104-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-009-0104-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-009-0104-X

Revised classification of posterior fossa cysts and cystlike malformations based on the results of multiplanar MR imaging.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-009-0104-X

Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-009-0104-X

[Development and the developmental disorders of human brain. I. Early development of the cerebrum]

21 January 2018

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12 December 2020

Genetic disorders and cerebellar structural abnormalities in childhood

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12 December 2020

A new approach to the development of the cerebellum provided by the quail-chick marker system.

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12 December 2020

Distinguishing the four genetic causes of Jouberts syndrome-related disorders.

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12 December 2020

The cells and molecules that make a cerebellum.

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12 December 2020

Analysis and classification of cerebellar malformations.

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12 December 2020

Abnormalities of cerebellar foliation and fissuration: classification, neurogenetics and clinicoradiological correlations

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12 December 2020

Rhombencephalosynapsis: cerebellar embryogenesis

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12 December 2020

Neurogenetics of the cerebellar system.

1 reference

12 December 2020

A developmental classification of malformations of the brainstem

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12 December 2020

Etiological classification of CNS malformations: integration of molecular genetic and morphological criteria

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12 December 2020

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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12 December 2020

Ultrastructure and pathogenesis of intracranial arachnoid cysts

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12 December 2020

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation

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12 December 2020

Genotypes and phenotypes of Joubert syndrome and related disorders

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12 December 2020

Neuropathologic and MR imaging correlation in a neonatal case of cerebellar cortical dysplasia

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12 December 2020

Defective glycosylation in muscular dystrophy

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12 December 2020

New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey

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12 December 2020

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

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12 December 2020

Spectrum of malformations of the hindbrain (cerebellum, pons, and medulla) in a cohort of children with high rate of parental consanguinity

1 reference

12 December 2020

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

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12 December 2020

Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation.

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12 December 2020

Meckel syndrome: genetics, perinatal findings, and differential diagnosis

1 reference

12 December 2020

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

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12 December 2020

The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation

1 reference

12 December 2020

New concepts on posterior fossa malformations

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12 December 2020

Development and malformations of the cerebellum in mice

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12 December 2020

Partial rhombencephalosynapsis.

1 reference

12 December 2020

Human malformations of the midbrain and hindbrain: review and proposed classification scheme

1 reference

12 December 2020

Genetic regulation of cerebellar development

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12 December 2020

The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome

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12 December 2020

Molecular genetic classification of central nervous system malformations

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12 December 2020

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

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12 December 2020

Cerebellar cortical dysplasia: MR findings in a complex entity.

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12 December 2020

Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.

1 reference

12 December 2020

Engrailed, Wnt and Pax genes regulate midbrain--hindbrain development

1 reference

12 December 2020

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

1 reference

12 December 2020

A different approach to cysts of the posterior fossa

1 reference

12 December 2020

Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

1 reference

12 December 2020

Cystic malformations of the posterior cranial fossa originating from a defect of the posterior membranous area. Mega cisterna magna and persisting Blake's pouch: two separate entities

1 reference

12 December 2020

Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification

1 reference

12 December 2020

10.1007/S12311-009-0104-X

Identifiers

DOI

1 reference

Dimensions Publication ID

26 July 2017

1049128573

0 references

1 reference