Neurological manifestations of xeroderma pigmentosum due to XPA gene mutation

Rubens Paulo A Salomão; José Luiz Pedroso; Orlando G P Barsottini

doi:10.1136/practneurol-2018-001888

Article menu

Article
Text
Article
info
Citation
Tools
Share
Rapid Responses
Article
metrics
Alerts

PDF

Image of the moment

Neurological manifestations of xeroderma pigmentosum due to XPA gene mutation

Share this article

Click the icon of the social media platform on which you would like to share this article.

Share This Article:

Email this article to a friend

We will not keep your email address; we ask for it so your friend knows the email isn't spam.

Your email: *

Your name: *

Send to: *

Enter multiple addresses on separate lines or separate them with commas.

You are going to email the following Neurological manifestations of xeroderma pigmentosum due to XPA gene mutation

Message subject: (Your Name) has forwarded a page to you from Practical Neurology

Message body: (Your Name) thought you would like to see this page from the Practical Neurology web site.

Your personal message:

CAPTCHA

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Read the full text or download the PDF:

Log in using your username and password

For personal accounts OR managers of institutional accounts

Username *

Password *

Forgot your log in details?Register a new account?

Forgot your user name or password?

Other content recommended for you

Fragile X associated tremor/ataxia syndrome (FXTAS) with dementia in a female harbouring FMR1 premutation
Y Karmon et al., Journal of Neurology, Neurosurgery & Psychiatry, 2008
Corneal endothelium in xeroderma pigmentosum: clinical specular microscopy study
Ashik Mohamed et al., British Journal of Ophthalmology, 2015
Vitamin B12 deficiency: an unusual cause for recurrent generalised seizures with pancytopaenia
Kushal Naha et al., BMJ Case Reports, 2012
Relapsing CD8+ encephalitis—looking for a solution
Sharfaraz Salam et al., BMJ Case Reports, 2016
Clinical trial on the efficacy and safety of NPC-15 for patients with xeroderma pigmentosum exaggerated sunburn reaction type: XP-1 study protocol for a multicentre, double-blinded, placebo-controlled, two-group crossover study followed by a long-term open study in Japan
Mariko Tsujimoto et al., BMJ Open, 2023
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair
Porcia T Bradford et al., Journal of Medical Genetics, 2010
Neurology and the skin
Orest Hurko et al., Journal of Neurology, Neurosurgery & Psychiatry, 1999
Xeroderma pigmentosum
Sandra Webb, BMJ, 2008
Ocular surface biopsies of patients with xeroderma pigmentosum in the United Kingdom: a retrospective observational case series
John Vekinis et al., British Journal of Ophthalmology, 2020
Community perspectives on the magnitude of Xeroderma pigmentosum and care-seeking practices in Micheweni district, Pemba: a mixed-methods cross-sectional study
Lucas E Matemba et al., BMJ Open, 2024

Log in using your username and password

Main menu

Log in using your username and password

You are here

Share this article

Email this article to a friend

Request permissions

Read the full text or download the PDF:

Log in using your username and password

Other content recommended for you