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Clinical, Laboratory, And Molecular Evaluation Of 105 Patients With A Phenotype Of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome

Journal of allergy and clinical immunology, 2009-02, Vol.123 (2), p.S148-S148

2009

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Monkeypox outbreak in Madrid (Spain): Clinical and virological aspects

The Journal of infection, 2022-10, Vol.85 (4), p.412-417

2022

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Severe Food Allergy as a Variant of IPEX Syndrome Caused by a Deletion in a Noncoding Region of the FOXP3 Gene

Gastroenterology (New York, N.Y. 1943), 2007-05, Vol.132 (5), p.1705-1717

2007

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Comèl-Netherton Syndrome - New Insight Into The Molecular Basis of this Rare Syndrome Characterized by Atopic Diathesis and Immune Deficiency

Journal of allergy and clinical immunology, 2007, Vol.119 (1), p.S11-S11

2007

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Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis

The Journal of clinical investigation, 2007-02, Vol.117 (2), p.407-418

2007

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Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect

Clinical immunology (Orlando, Fla.), 2006, Vol.119, p.S131-S132

2006

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Evaluation of Signaling Events in 2 Related X-SCID Patients with the Same Hypomorphic IL2RG Mutation but Different Clinical Phenotypes

Clinical immunology (Orlando, Fla.), 2008-01, Vol.127, p.S72-S73

2008

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Rapid Suppression of Activation Markers and Cytokine Secretion in Human CD4+CD25- T Cells by Cord Blood Derived CD4+CD25+FOXP3+ T Regulatory Cells

Clinical immunology (Orlando, Fla.), 2008-01, Vol.127, p.S72-S72

2008

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The Naturally Occurring Splice Variant of FOXP3 Lacking Exon 2 is not Sufficient to Maintain Immune Homeostasis and Prevent IPEX in vivo in Humans

Clinical immunology (Orlando, Fla.), 2009-01, Vol.131, p.S7-S7

2009

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Atypical presentation of IL-12 receptor β1 deficiency with pneumococcal sepsis and disseminated nontuberculous mycobacterial infection in a 19-month-old girl born to nonconsanguineous US residents

Journal of allergy and clinical immunology, 2010, Vol.125 (1), p.264-265

2010

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Novel Missense Mutation P.M37K in IKBA Results in Impaired NF-κB Activation Causing Ectodermal Dysplasia with Immunodeficiency and Autoimmune Polyendocrinopathy

JOURNAL OF CLINICAL IMMUNOLOGY, 2012, Vol.32 (2), p.377

2012

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Relevance of biallelic vs monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2008, Vol.154, p.207

2008

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Era feliz y no lo sabía

Káñina, 2019-06, Vol.43 (1), p.135-136

Añover, Verónica

2019

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Maternal age modulates the effects of early-pregnancy L-proline supplementation on the birth-weight of piglets

Animal reproduction science, 2017-06, Vol.181, p.63-68

2017

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Polyphenols and IUGR pregnancies: Maternal hydroxytyrosol supplementation improves prenatal and early-postnatal growth and metabolism of the offspring

PloS one, 2017-05, Vol.12 (5), p.e0177593-e0177593

2017

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Effects of the inclusion of two extracts derived from the olive industry on growth performance, antiparasitic protection, and antioxidant activity in broiler chicken diets from 0 to 45 d

Livestock science, 2024-09, Vol.287, p.105534, Article 105534

2024

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Polyphenols and IUGR Pregnancies: Effects of Maternal Hydroxytyrosol Supplementation on Placental Gene Expression and Fetal Antioxidant Status, DNA-Methylation and Phenotype

International journal of molecular sciences, 2019-03, Vol.20 (5), p.1187

2019

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La pena de muerte en la Restauración: una historia del cambio social

Historia y Política: Ideas, Procesos y Movimientos Sociales, 2016-05 (35), p.203-230

Bascuñán Añover, Óscar

2016

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Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH 17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome

Journal of allergy and clinical immunology, 2008, Vol.122 (1), p.181-187

2008

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Le cabaret des mémoires par Joachim Schnerf (review)

The French review, 2023-10, Vol.97 (1), p.252-252

Anover, Véronique

2023

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Nu-propriétaire par Patrick Varetz (review)

The French review, 2023-03, Vol.96 (3), p.244-244

Anover, Véronique

2023

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Des ambitieux by Isabelle Siac (review)

The French review, 2011, Vol.85 (2), p.408-409

Añover, Véronique

2011

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Ovulation rate, embryo mortality and intrauterine growth retardation in obese swine with gene polymorphisms for leptin and melanocortin receptors

Theriogenology, 2011, Vol.75 (1), p.34-41

2011

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L'absente de tous bouquets by Catherine Mavrikakis (review)

The French review, 2022-05, Vol.95 (4), p.255-255

Anover, Véronique

2022

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FOXP3 Inhibits Activation-Induced NFAT2 Expression in T Cells Thereby Limiting Effector Cytokine Expression

The Journal of immunology (1950), 2009-07, Vol.183 (2), p.907-915

2009

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Clinical, Laboratory, And Molecular Evaluation Of 105 Patients With A Phenotype Of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome

Monkeypox outbreak in Madrid (Spain): Clinical and virological aspects

Severe Food Allergy as a Variant of IPEX Syndrome Caused by a Deletion in a Noncoding Region of the FOXP3 Gene

Comèl-Netherton Syndrome - New Insight Into The Molecular Basis of this Rare Syndrome Characterized by Atopic Diathesis and Immune Deficiency

Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis

Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect

Evaluation of Signaling Events in 2 Related X-SCID Patients with the Same Hypomorphic IL2RG Mutation but Different Clinical Phenotypes

Rapid Suppression of Activation Markers and Cytokine Secretion in Human CD4+CD25- T Cells by Cord Blood Derived CD4+CD25+FOXP3+ T Regulatory Cells

The Naturally Occurring Splice Variant of FOXP3 Lacking Exon 2 is not Sufficient to Maintain Immune Homeostasis and Prevent IPEX in vivo in Humans

Atypical presentation of IL-12 receptor β1 deficiency with pneumococcal sepsis and disseminated nontuberculous mycobacterial infection in a 19-month-old girl born to nonconsanguineous US residents

Novel Missense Mutation P.M37K in IKBA Results in Impaired NF-κB Activation Causing Ectodermal Dysplasia with Immunodeficiency and Autoimmune Polyendocrinopathy

Relevance of biallelic vs monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Era feliz y no lo sabía

Maternal age modulates the effects of early-pregnancy L-proline supplementation on the birth-weight of piglets

Polyphenols and IUGR pregnancies: Maternal hydroxytyrosol supplementation improves prenatal and early-postnatal growth and metabolism of the offspring

Effects of the inclusion of two extracts derived from the olive industry on growth performance, antiparasitic protection, and antioxidant activity in broiler chicken diets from 0 to 45 d

Polyphenols and IUGR Pregnancies: Effects of Maternal Hydroxytyrosol Supplementation on Placental Gene Expression and Fetal Antioxidant Status, DNA-Methylation and Phenotype

La pena de muerte en la Restauración: una historia del cambio social

Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH 17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome

Le cabaret des mémoires par Joachim Schnerf (review)

Nu-propriétaire par Patrick Varetz (review)

Des ambitieux by Isabelle Siac (review)

Ovulation rate, embryo mortality and intrauterine growth retardation in obese swine with gene polymorphisms for leptin and melanocortin receptors

L'absente de tous bouquets by Catherine Mavrikakis (review)

FOXP3 Inhibits Activation-Induced NFAT2 Expression in T Cells Thereby Limiting Effector Cytokine Expression

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