(Q48561063)

English

Cranial CT and MRI in diseases with DNA repair defects

scientific article published in January 1992

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

Cranial CT and MRI in diseases with DNA repair defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

author name string

P Demaerel

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

B E Kendall

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

D Kingsley

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

34

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

117-121

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

Cockayne syndrome: magnetic resonance images of the brain in a severe form with early onset

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MRI in Cockayne syndrome type I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dwarfism with retinal atrophy and deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cockayne syndrome: Unusual neuropathological findings and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs; probably a syndrome entity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High field MR imaging of the brain in pseudohypoparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CAMFAK syndrome: a demyelinating inherited disease similar to Cockayne syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

EEG and CT abnormalities in xeroderma pigmentosum

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cockayne syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diseases with DNA damage-processing defects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cockayne syndrome: MRI correlates of hypomyelination

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MRI of brain abnormalities in Cockayne syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Xeroderma pigmentosum presenting clinical features of spinocerebellar degeneration]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MRI in the diagnosis of Cockayne's syndrome. One case

1 reference

https://pubmed.ncbi.nlm.nih.gov/1603308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00588156

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/1603308

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