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Advance Care Planning With Black Women with Breast Cancer: A Community Health Worker Model

Cancer control, 2023-03, Vol.30, p.10732748231162479

2023

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Aberrant expression of interleukin-10 in rheumatoid arthritis: Relationship with IL10 haplotypes and autoantibodies

Cytokine (Philadelphia, Pa.), 2017-07, Vol.95, p.88-96

2017

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TLR4 polymorphism and haplotype are associated with obesity and lipid profile in young population: a pilot study

Journal of endocrinological investigation, 2023-05, Vol.46 (5), p.903-913

2023

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Genetics and epidemiology of aniridia: Updated guidelines for genetic study

Archivos de la Sociedad Española de Oftalmología (English ed.), 2021-11

2021

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Analysis of IL10 haplotypes in primary Sjögren’s syndrome patients from Western Mexico: Relationship with mRNA expression, IL-10 soluble levels, and autoantibodies

Human immunology, 2015-07, Vol.76 (7), p.473-479

2015

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Tablet‐based electroencephalography diagnostics for patients with epilepsy in the West African Republic of Guinea

European journal of neurology, 2020-08, Vol.27 (8), p.1570-1577

2020

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A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

Journal of medical genetics, 2005-07, Vol.42 (7), p.588-594

2005

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Genetics and epidemiology of aniridia: Updated guidelines for genetic study

Archivos de la Sociedad Española de Oftalmología (English ed.), 2021-11, Vol.96, p.4-14

2021

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Macrophage migration inhibitory factor: Association of −794 CATT5–8 and −173 G>C polymorphisms with TNF-α in systemic lupus erythematosus

Human immunology, 2014-05, Vol.75 (5), p.433-439

2014

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Serial ctDNA analysis predicts clinical progression in patients with advanced urothelial carcinoma

British journal of cancer, 2022-02, Vol.126 (3), p.430-439

2022

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An evaluation of the efficacy and safety of erdafitinib for the treatment of bladder cancer

Expert opinion on pharmacotherapy, 2020-05, Vol.21 (8), p.863-870

2020

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Frequency distribution of interleukin-10 haplotypes (-1082 A>G, -819 C>T, and -592 C>A) in a Mexican population

Genetics and molecular research, 2016-11, Vol.15 (4)

2016

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Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C→T mutation in the mitochondrial 12S rRNA gene

Journal of medical genetics, 2006-11, Vol.43 (11), p.e54-e54

2006

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Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss

Journal of medical genetics, 2003-08, Vol.40 (8), p.632-636

2003

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Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss

Journal of medical genetics, 2002-07, Vol.39 (7), p.502-506

2002

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Attitudes toward Learning English and Procrastination in Students from a Private Institution Specialized in Foreign Languages in the City of Lima-Peru

Revista colombiana de psicología, 2021-12, Vol.30 (2), p.27-39

2021

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The reporting of blinding in physical medicine and rehabilitation randomized controlled trials: a systematic review

Journal of rehabilitation medicine, 2013-01, Vol.45 (1), p.6-13

2013

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A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

The New England journal of medicine, 2002-01, Vol.346 (4), p.243-249

2002

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A cysteine substitution in the zona pellucida domain of α-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family

Journal of medical genetics, 2001-05, Vol.38 (5), p.e13-13

2001

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Genética y epidemiología de la aniridia congénita: actualización de buenas prácticas para el diagnóstico genético

Archivos de la Sociedad Española de Oftalmología, 2021-11, Vol.96, p.4-14

2021

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Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene

Journal of medical genetics, 2002-12, Vol.39 (12), p.e82-e82

2002

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Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients

Journal of medical genetics, 2003-08, Vol.40 (8), p.636-639

2003

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Monoclonal Antibody-based TAS-ELISA for Quantitative Detection of Mycosphaerella fijiensis Antigens

Journal of phytopathology, 2007-12, Vol.155 (11-12), p.713-719

2007

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Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings

Clinical genetics, 2005-05, Vol.67 (5), p.438-440

2005

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Advance Care Planning With Black Women with Breast Cancer: A Community Health Worker Model

Aberrant expression of interleukin-10 in rheumatoid arthritis: Relationship with IL10 haplotypes and autoantibodies

TLR4 polymorphism and haplotype are associated with obesity and lipid profile in young population: a pilot study

Genetics and epidemiology of aniridia: Updated guidelines for genetic study

Analysis of IL10 haplotypes in primary Sjögren’s syndrome patients from Western Mexico: Relationship with mRNA expression, IL-10 soluble levels, and autoantibodies

Tablet‐based electroencephalography diagnostics for patients with epilepsy in the West African Republic of Guinea

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

Genetics and epidemiology of aniridia: Updated guidelines for genetic study

Macrophage migration inhibitory factor: Association of −794 CATT5–8 and −173 G>C polymorphisms with TNF-α in systemic lupus erythematosus

Serial ctDNA analysis predicts clinical progression in patients with advanced urothelial carcinoma

An evaluation of the efficacy and safety of erdafitinib for the treatment of bladder cancer

Frequency distribution of interleukin-10 haplotypes (-1082 A>G, -819 C>T, and -592 C>A) in a Mexican population

Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C→T mutation in the mitochondrial 12S rRNA gene

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss

Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss

Attitudes toward Learning English and Procrastination in Students from a Private Institution Specialized in Foreign Languages in the City of Lima-Peru

The reporting of blinding in physical medicine and rehabilitation randomized controlled trials: a systematic review

A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

A cysteine substitution in the zona pellucida domain of α-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family

Genética y epidemiología de la aniridia congénita: actualización de buenas prácticas para el diagnóstico genético

Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene

Prevalence and Evolutionary Origins of the del( GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients

Monoclonal Antibody-based TAS-ELISA for Quantitative Detection of Mycosphaerella fijiensis Antigens

Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings

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