Navegar por autor "Rodríguez Pazos, Laura"

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations

2019- Montalván-Suárez, M.; Esperón Moldes, Uxía Saraiva; Rodríguez Pazos, Laura; Ordoñez Ugalde, Andrés; Moscoso, F.; [et al.]

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations

2019- Montalván‐Suárez, Martha; Saraiva Esperón, Uxía; Rodríguez Pazos, Laura; Ordóñez‐Ugalde, Andrés; Moscoso, Fernanda; [et al.]

Alopecia triangular temporal

2015- Monteagudo Sánchez, Benigno; León Muiños, Elvira; González Vilas, Daniel; Rodríguez Pazos, Laura

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

2011- Fachal Vilar, Laura; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Carracedo Álvarez, Ángel; [et al.]

ANCA-positive vasculitis induced by levamisole-adulterated cocaine and nephrotic syndrome: The kidney as an unusual target

2013- Álvarez Díaz, Hortensia; Mariño Callejo, Ana Isabel; Rodríguez Pazos, Laura; García Rodríguez, José Francisco; Gómez Buela, Inmaculada [et al.]

Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

2019- Esperón Moldes, Uxía Saraiva; Pardo Seco, Jacobo José; Montalván-Suárez, M.; Fachal Vilar, Laura; Ginarte Val, Manuel Javier; [et al.]

Birt-Hogg-Dube syndrome in a patient with localized fibrofolliculomas and a novel mutation in the FLCN gene

2011- Alonso González, Julio; Fernández Redondo, Virginia; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Rodríguez Pazos, Laura [et al.]

Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis

2012- Fachal Vilar, Laura; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Carracedo Álvarez, Ángel; [et al.]

Clinical and molecular classification of ichthyosis

2012- Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Rodríguez Pazos, Laura

Disseminated eruptive clear cell acanthoma with spontaneous regression: further evidence of an inflammatory origin?

2011- González Vilas, Daniel; Toribio Pérez, Jaime; Montero Pérez, Iria Carmen; García Gavín, Juan Ramón; Rodríguez Pazos, Laura; [et al.]

Endometriosis primaria: un diagnostico diferencial dentro de las lesiones nodulares umbilicales

2014- Monteagudo Sánchez, Benigno; Suarez Amor, Oscar Manuel; González Vilas, Daniel; De las Heras Soto, Cristina; Rodríguez Pazos, Laura; [et al.]

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis

2014- Fachal Vilar, Laura; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Carracedo Álvarez, Ángel; [et al.]

Kaposi sarcoma following postmastectomy lymphedema

2015- Toribio Pérez, Jaime; Montero Pérez, Iria Carmen; Suárez Peñaranda, Jose Manuel; Rodríguez Pazos, Laura; Alvarez Perez, Adriana Del Rosario; [et al.]

Lentiginous mosaicism and mosaic generalized neurofibromatosis type 1

2014- Toribio Pérez, Jaime; Rodríguez Pazos, Laura; Rodríguez Granados, María Teresa

Repositorio digital RUNA

Navegar por autor "Rodríguez Pazos, Laura"

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations ﻿

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations ﻿

Alopecia triangular temporal ﻿

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects. ﻿

ANCA-positive vasculitis induced by levamisole-adulterated cocaine and nephrotic syndrome: The kidney as an unusual target ﻿

Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population ﻿

Birt-Hogg-Dube syndrome in a patient with localized fibrofolliculomas and a novel mutation in the FLCN gene ﻿

Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis ﻿

Clinical and molecular classification of ichthyosis ﻿

Disseminated eruptive clear cell acanthoma with spontaneous regression: further evidence of an inflammatory origin? ﻿

Endometriosis primaria: un diagnostico diferencial dentro de las lesiones nodulares umbilicales ﻿

Enfermedad de Grover en fracaso renal crónico. ﻿

Epidermodisplasia verruciforme adquirida en una paciente transplantada renal ﻿

Eritema multiforme fotodistribuido ﻿

Erythema multiforme photoinduced by paroxetine and herpes simplex virus ﻿

Fotosensibilidad por tiazidas ﻿

Ictiosis congénitas autosómicas recesivas ﻿

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis ﻿

Kaposi sarcoma following postmastectomy lymphedema ﻿

Lentiginous mosaicism and mosaic generalized neurofibromatosis type 1 ﻿

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations

Alopecia triangular temporal

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

ANCA-positive vasculitis induced by levamisole-adulterated cocaine and nephrotic syndrome: The kidney as an unusual target

Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

Birt-Hogg-Dube syndrome in a patient with localized fibrofolliculomas and a novel mutation in the FLCN gene

Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis

Clinical and molecular classification of ichthyosis

Disseminated eruptive clear cell acanthoma with spontaneous regression: further evidence of an inflammatory origin?

Endometriosis primaria: un diagnostico diferencial dentro de las lesiones nodulares umbilicales

Enfermedad de Grover en fracaso renal crónico.

Epidermodisplasia verruciforme adquirida en una paciente transplantada renal

Eritema multiforme fotodistribuido

Erythema multiforme photoinduced by paroxetine and herpes simplex virus

Fotosensibilidad por tiazidas

Ictiosis congénitas autosómicas recesivas

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis

Kaposi sarcoma following postmastectomy lymphedema

Lentiginous mosaicism and mosaic generalized neurofibromatosis type 1