Browse by Author "Barros Angueira, Francisco"

Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2

2014- Leis Trabazo, María Rosaura; Barros Angueira, Francisco; Loidi Fernández, Lourdes; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; [et al.]

Hypoxia-inducible factors in OSCC

2011- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

Immunohistochemical localization of C1 subunit of V-ATPase (ATPase C1) in oral squamous cell cancer and normal oral mucosa

2012- Barros Angueira, Francisco; García García, Abel; Antúnez López, José Ramón

Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Fernández Prieto, Montserrat; Castro Gago, Manuel; Gómez Lado, María del Carmen; [et al.]

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Perez Gay, Laura; Eiris Puñal, Jesús; [et al.]

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing.

2011- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Barros Angueira, Francisco; Campos Balea, Begoña; Quintans Castro, Beatriz; [et al.]

New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients

2013- Echarri Piudo, Ana; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Cruz Guerrero, Raquel; [et al.]

p16(INK4a)/CDKN2 expression and its relationship with oral squamous cell carcinoma is our current knowledge enough?

2011- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

P21Waf1/CIP1 is a poor diagnostic and prognostic marker for OSCC although its expression increases in patients with N1 regional metastasis

2015- Barros Angueira, Francisco

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response

2011- Echarri Piudo, Ana; Castro Alvariño, Javier; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; [et al.]

Progressive heterotopic ossification: the arduousness of an accurate diagnosis

2014- Barros Angueira, Francisco; Couce Pico, María Luz; Dosil Gallardo, Silvia; García Magán, Carlos; Fernández Seara, María José [et al.]

Quantitative determination of c-myc facilitates the assessment of prognosis of OSCC patients

2014- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

Rasopathies: Assessment of growth, genetic study, genotype-phenotype correlation and therapeutic response to GH in noonan syndrome

2014- Barros Angueira, Francisco; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; Castro Feijoo, Lidia; Barreiro Conde, Jesús [et al.]

Successful treatment of hypokalemic periodic paralysis with topiramate

2012- Sobrido Gómez, María Jesús; Barros Angueira, Francisco; Quintans Castro, Beatriz; Pardo Fernández, Julio; López Ferreiro, Ana; [et al.]

The loss of p16 expression worsens the prognosis of OSCC

2015- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome

2013- Casanueva Freijo, Felipe; Barros Angueira, Francisco

The role of carbonic anhydrase IX in hypoxia control in OSCC

2013- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

RUNA digital repository

Browse by Author "Barros Angueira, Francisco"

Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2 ﻿

Hypoxia-inducible factors in OSCC ﻿

Immunohistochemical localization of C1 subunit of V-ATPase (ATPase C1) in oral squamous cell cancer and normal oral mucosa ﻿

Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder ﻿

LEOPARD syndrome: Clinical characteristics and molecular study ﻿

Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia ﻿

Microdeleción 2q23.1 y hallazgos sindrómicos ﻿

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes ﻿

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing. ﻿

New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients ﻿

p16(INK4a)/CDKN2 expression and its relationship with oral squamous cell carcinoma is our current knowledge enough? ﻿

P21Waf1/CIP1 is a poor diagnostic and prognostic marker for OSCC although its expression increases in patients with N1 regional metastasis ﻿

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response ﻿

Progressive heterotopic ossification: the arduousness of an accurate diagnosis ﻿

Quantitative determination of c-myc facilitates the assessment of prognosis of OSCC patients ﻿

Rasopathies: Assessment of growth, genetic study, genotype-phenotype correlation and therapeutic response to GH in noonan syndrome ﻿

Successful treatment of hypokalemic periodic paralysis with topiramate ﻿

The loss of p16 expression worsens the prognosis of OSCC ﻿

The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome ﻿

The role of carbonic anhydrase IX in hypoxia control in OSCC ﻿

Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2

Hypoxia-inducible factors in OSCC

Immunohistochemical localization of C1 subunit of V-ATPase (ATPase C1) in oral squamous cell cancer and normal oral mucosa

Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder

LEOPARD syndrome: Clinical characteristics and molecular study

Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia

Microdeleción 2q23.1 y hallazgos sindrómicos

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing.

New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients

p16(INK4a)/CDKN2 expression and its relationship with oral squamous cell carcinoma is our current knowledge enough?

P21Waf1/CIP1 is a poor diagnostic and prognostic marker for OSCC although its expression increases in patients with N1 regional metastasis

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response

Progressive heterotopic ossification: the arduousness of an accurate diagnosis

Quantitative determination of c-myc facilitates the assessment of prognosis of OSCC patients

Rasopathies: Assessment of growth, genetic study, genotype-phenotype correlation and therapeutic response to GH in noonan syndrome

Successful treatment of hypokalemic periodic paralysis with topiramate

The loss of p16 expression worsens the prognosis of OSCC

The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome

The role of carbonic anhydrase IX in hypoxia control in OSCC