(Q24655161)

2

0 references

K Hoffmann

3

0 references

A Diers

4

0 references

C Zimmer

5

0 references

K Sperling

6

0 references

S Mundlos

Journal of Medical Genetics

7

0 references

language of work or name

English

0 references

publication date

May 2006

0 references

published in

0 references

volume

43

0 references

issue

5

0 references

page(s)

461-4

0 references

cites work

Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564522

Accelerated evolution of nervous system genes in the origin of Homo sapiens

7 April 2017

1 reference

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Genetic links between brain development and brain evolution

7 April 2017

1 reference

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Movement disorders: classifications

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564522

Role of the cerebellum in the control and adaptation of gait in health and disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564522

Development and developmental disorders of the human cerebellum

28 September 2017

1 reference

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Origin of human bipedalism: The knuckle-walking hypothesis revisited

28 September 2017

1 reference

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Evidence that humans evolved from a knuckle-walking ancestor

28 September 2017

1 reference

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Creeping patterns of human adults and infants

28 September 2017

1 reference

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Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations

28 September 2017

1 reference

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Brain functional activity during gait in normal subjects: a SPECT study.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564522

Atavisms and atavistic mutations.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564522

Autosomal recessive cerebellar hypoplasia in the Hutterite population.

30 May 2018

1 reference

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Frontal ataxia in childhood

28 November 2018

1 reference

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A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze Family.

28 November 2018

1 reference

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The development of mature gait

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16371500

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16371500

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Origin of human bipedalism: The knuckle-walking hypothesis revisited

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16371500