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N Cuadrado-Corrales

Showing results (1-10 of 11) with videos related to

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Revista De Neurologia|August 22, 2000
[Immunohistochemistry techniques in prion diseases]I Gonzalo-Pascual, N Cuadrado-Corrales
Revista De Neurologia|August 22, 2000
[Neuropathology of the new variant of Creutzfeldt-Jakob disease]I Gonzalo-Pascual, N Cuadrado-Corrales
Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob diseaseB Van Everbroeck, A J E Green, E Vanmechelen, et al.
Neurologia (Barcelona, Spain)|March 7, 2008
[Usefulness of the 14-3-3 test for the diagnosis of sCJD evaluated by a Spanish reference center]N Cuadrado-Corrales, A Jiménez-Huete, C Albo, et al.
Dermatology (Basel, Switzerland)|June 5, 2010
X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patientA Hernández-Martín, N Cuadrado-Corrales, S Ciria-Abad, et al.
European Journal of Neurology|January 26, 2007
CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathiesA Green, P Sanchez-Juan, A Ladogana, et al.
Neurology|August 23, 2006
CSF tests in the differential diagnosis of Creutzfeldt-Jakob diseaseP Sanchez-Juan, A Green, A Ladogana, et al.
Neurology|September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Pocchiari, S Collins, et al.
The British Journal of Dermatology|February 27, 2010
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutationM J Escámez, M García, N Cuadrado-Corrales, et al.
The British Journal of Dermatology|June 1, 2011
Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplexM García, J L Santiago, A Terrón, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Revista De Neurologia|August 22, 2000
[Immunohistochemistry techniques in prion diseases]I Gonzalo-Pascual, N Cuadrado-Corrales
Revista De Neurologia|August 22, 2000
[Neuropathology of the new variant of Creutzfeldt-Jakob disease]I Gonzalo-Pascual, N Cuadrado-Corrales
Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob diseaseB Van Everbroeck, A J E Green, E Vanmechelen, et al.
Neurologia (Barcelona, Spain)|March 7, 2008
[Usefulness of the 14-3-3 test for the diagnosis of sCJD evaluated by a Spanish reference center]N Cuadrado-Corrales, A Jiménez-Huete, C Albo, et al.
Dermatology (Basel, Switzerland)|June 5, 2010
X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patientA Hernández-Martín, N Cuadrado-Corrales, S Ciria-Abad, et al.
European Journal of Neurology|January 26, 2007
CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathiesA Green, P Sanchez-Juan, A Ladogana, et al.
Neurology|August 23, 2006
CSF tests in the differential diagnosis of Creutzfeldt-Jakob diseaseP Sanchez-Juan, A Green, A Ladogana, et al.
Neurology|September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Pocchiari, S Collins, et al.
The British Journal of Dermatology|February 27, 2010
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutationM J Escámez, M García, N Cuadrado-Corrales, et al.
The British Journal of Dermatology|June 1, 2011
Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplexM García, J L Santiago, A Terrón, et al.
Pageof 2