(Q43612745)

25 November 2017

title

Defect of cerebellar Purkinje cell histogenesis associated with type I and type II renal cystic disease (English)

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25 November 2017

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5

J Opitz

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25 November 2017

S Kornguth

1

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25 November 2017

L Knobeloch

series ordinal

2

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25 November 2017

C Viseskul

series ordinal

3

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25 November 2017

E Gilbert

series ordinal

4

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25 November 2017

publication date

1 September 1977

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25 November 2017

published in

Acta Neuropathologica

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25 November 2017

volume

40

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25 November 2017

issue

1

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25 November 2017

page(s)

1-9

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Fine structure of the cerebellar cortex in Menkes Kinky-hair disease. X-chromosome-linked copper malabsorption

25 November 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00688568

Congenital hydrocephalus with defective development of the cerebellar vermis (Dandy-Walker syndrome) clinical and anatomical findings in two cases with particular reference to the so-called atresia of the foramina of Magendie and Luschka

21 January 2018

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12 December 2020

Specialized membrane junctions between neurons in the vertebrate cerebellar cortex

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12 December 2020

Differentiation of Purkinje cells and their relationship to other components of developing cerebellar cortex in man

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12 December 2020

Congenital Hydrocephalus due to Atresia of the Foramen of Magendie

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12 December 2020

Histogenesis of cortical layers in human cerebellum, particularly the lamina dissecans.

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12 December 2020

Cerebro-hepato-renal syndrome. Report of a case with histochemical and ultrastructural observations

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12 December 2020

The synaptic glomerulus and the intrinsic neuron in the dorsal lateral geniculate nucleus of the cat.

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12 December 2020

Brain hypoxia studied in mouse central nervous system cultures. I. Sequential cellular changes

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12 December 2020

Permanence and fate of paramembranous synaptic specializations in "mutants" experimental animals

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12 December 2020

The developmental effects of congenital hydrocephalus (ch) in the mouse

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12 December 2020

The role of climbing fibers in the formation of Purkinje cell dendrites

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12 December 2020

Familial renal dysplasia. Microdissection studies in siblings with associated central nervous system and hepatic malformations

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12 December 2020

THE TANGENTIAL ORGANIZATION OF THE VISUAL CORTEX

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12 December 2020

NEONATAL POLYCYSTIC KIDNEY WITH BRAIN DEFECT.

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12 December 2020

Organization of the primate retina: electron microscopy

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12 December 2020

The Dandy-Walker syndrome or the so-called atresia of the foramen Magendie.

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12 December 2020

THE DANDY-WALKER SYNDROME

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12 December 2020

Congenital Malformations in Autosomal Trisomy Syndromes

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12 December 2020

An electron microscopic study of cycasin-induced cerebellar alterations.

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12 December 2020

Thiophen induced granule cell necrosis in the rat cerebellum an electron microscopic study

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12 December 2020

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

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12 December 2020

The Fine Structure of Astrocytes in the Adult Staggerer

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12 December 2020

[Histological findings in case of congenital pigmentary retinal degeneration]

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12 December 2020

The effects of reduced climbing and parallel fibre input on Purkinje cell dendritic growth

1 reference

12 December 2020

The renal lesion in syndromes of multiple congenital malformations. Cerebrohepatorenal syndrome; Jeune asphyxiating thoracic dystrophy; tuberous sclerosis; Meckel syndrome

1 reference

12 December 2020

Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00688568

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25 November 2017

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