Publications by authors named "Celsa Quinteiro"

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Analysis of IGF(CA)19 and IGFBP3-202A/C gene polymorphisms in patients with acromegaly: association with clinical presentation and response to treatments.
Ana M Ramos-Leví, Mónica Marazuela, Amalia Paniagua, Celsa Quinteiro, Javier Riveiro

Eur J Endocrinol· February 2015

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Pituitary stalk dysgenesis-induced hypopituitarism in adult patients: prevalence, evolution of hormone dysfunction and genetic analysis.
Eva Fernandez-Rodriguez, Celsa Quinteiro, Jesus Barreiro, Mónica Marazuela, Inmaculada Pereiro

Neuroendocrinology· July 2011

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LIF, a Novel STAT5-Regulated Gene, Is Aberrantly Expressed in Myeloproliferative Neoplasms.
Elisa M Salas, María J García-Barchino, Sara Labiano, Mikhail Shugay, Manuel Pérez-Encinas, Celsa Quinteiro

Genes Cancer· May 2011

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Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant.
Silvia Parajes, Arturo González-Quintela, Joaquín Campos, Celsa Quinteiro, Fernando Domínguez

BMC Genet· December 2010

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Pegvisomant-induced liver injury is related to the UGT1A1*28 polymorphism of Gilbert's syndrome.
Ignacio Bernabeu, Mónica Marazuela, Tomás Lucas, Lourdes Loidi, Cristina Alvarez-Escolá, Celsa Quinteiro

J Clin Endocrinol Metab· May 2010

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The exon 3-deleted growth hormone receptor is associated with better response to pegvisomant therapy in acromegaly.
Ignacio Bernabeu, Cristina Alvarez-Escolá, Celsa Quinteiro, Tomás Lucas, Manel Puig-Domingo

J Clin Endocrinol Metab· January 2010

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The role of inbreeding in the extinction of a European royal dynasty.
Gonzalo Alvarez, Francisco C Ceballos, Celsa Quinteiro

PLoS One· July 2009

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Functional characterization of three CYP21A2 sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system.
Caroline Bleicken, Lourdes Loidi, Vivek Dhir, Silvia Parajes, Celsa Quinteiro

Hum Mutat· February 2009

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Serum TNF-alpha levels in relation to alcohol consumption and common TNF gene polymorphisms.
Arturo Gonzalez-Quintela, Joaquin Campos, Lourdes Loidi, Celsa Quinteiro, Luis-Fernando Perez

Alcohol· September 2008

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High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.
Silvia Parajes, Celsa Quinteiro, Fernando Domínguez, Lourdes Loidi

PLoS One· May 2008

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Liver enzyme levels in relation to a common polymorphism in the CD14 promoter gene.
Arturo Gonzalez-Quintela, Joaquin Campos, Celsa Quinteiro, Francisco Gude

Eur J Gastroenterol Hepatol· February 2007

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High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect.
Lourdes Loidi, Celsa Quinteiro, Silvia Parajes, Jesús Barreiro, Domingo G Lestón

Clin Endocrinol (Oxf)· March 2006

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Gene by environment interaction: the -159C/T polymorphism in the promoter region of the CD14 gene modifies the effect of alcohol consumption on serum IgE levels.
Joaquin Campos, Francisco Gude, Celsa Quinteiro, Carmen Vidal, Arturo Gonzalez-Quintela

Alcohol Clin Exp Res· January 2006

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Relation of tumor necrosis factor (TNF) gene polymorphisms with serum concentrations and in vitro production of TNF-alpha and interleukin-8 in heavy drinkers.
Arturo González-Quintela, Maria-Jesus Dominguez-Santalla, Lourdes Loidi, Celsa Quinteiro, Luis F Perez

Alcohol· July 2005

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The -159C/T polymorphism in the promoter region of the CD14 gene is associated with advanced liver disease and higher serum levels of acute-phase proteins in heavy drinkers.
Joaquin Campos, Arturo Gonzalez-Quintela, Celsa Quinteiro, Francisco Gude, Luis-Fernando Perez

Alcohol Clin Exp Res· July 2005

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Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein.
Lourdes Loidi, Lidia Castro-Feijóo, Jesús Barreiro, Celsa Quinteiro, Paloma Cabanas

J Pediatr Endocrinol Metab· June 2005

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Novel mutation involving the translation initiation codon of the growth hormone receptor gene (GHR) in a patient with Laron syndrome.
Celsa Quinteiro, Lidia Castro-Feijoo, Lourdes Loidi, Jesus Barreiro, Maria de la Fuente

J Pediatr Endocrinol Metab· March 2003

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