List of works - Natividad Cuadrado Corrales

A Recurrent Nonsense Mutation Occurring as a de novo Event in a Patient with Recessive Dystrophic Epidermolysis Bullosa

scientific article published on 18 August 2011

A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes

scientific article published on 05 July 2012

A prevalent mutation with founder effect in Spanish Recessive Dystrophic Epidermolysis Bullosa families.

scientific article

Altered glycosylation of acetylcholinesterase in Creutzfeldt-Jakob disease.

scientific article published on 8 November 2005

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

scientific article published on 01 September 2000

Apolipoprotein E allelic variants predict dementia in elderly patients with memory impairment.

scientific article published in July 1995

CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathies.

scientific article published in February 2007

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

scientific article

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

scientific article

Fatal familial insomnia: clinical, neuropathological, and genetic description of a Spanish family.

scientific article

In vivo assessment of acute UVB responses in normal and Xeroderma Pigmentosum (XP-C) skin-humanized mouse models.

scientific article

Recessive dystrophic epidermolysis bullosa: the origin of the c.6527insC mutation in the Spanish population

article

Revertant mosaicism due to a second-site mutation in COL7A1 in a patient with recessive dystrophic epidermolysis bullosa

scientific article published on 24 June 2010

The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation.

scientific article published on 22 February 2010

Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex.

scientific article published in September 2011

X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient.

scientific article published on 04 June 2010

List of works by Natividad Cuadrado Corrales

A Recurrent Nonsense Mutation Occurring as a de novo Event in a Patient with Recessive Dystrophic Epidermolysis Bullosa

A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes

A prevalent mutation with founder effect in Spanish Recessive Dystrophic Epidermolysis Bullosa families.

Altered glycosylation of acetylcholinesterase in Creutzfeldt-Jakob disease.

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

Apolipoprotein E allelic variants predict dementia in elderly patients with memory impairment.

CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathies.

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

Fatal familial insomnia: clinical, neuropathological, and genetic description of a Spanish family.

In vivo assessment of acute UVB responses in normal and Xeroderma Pigmentosum (XP-C) skin-humanized mouse models.

Recessive dystrophic epidermolysis bullosa: the origin of the c.6527insC mutation in the Spanish population

Revertant mosaicism due to a second-site mutation in COL7A1 in a patient with recessive dystrophic epidermolysis bullosa

The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation.

Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex.

X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient.