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TLR2–TLR4/CD14 polymorphisms and predisposition to severe invasive infections by Neisseria meningitidis and Streptococcus pneumoniae

Medicina intensiva, 2014-08, Vol.38 (6), p.356-362

2014

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Neuropatía auditiva autosómica dominante y variante DIAPH3 (c.-173C>T)

Acta otorrinolaringológica española, 2017-05, Vol.68 (3), p.183-185

2017

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A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A → G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene

Genomics (San Diego, Calif.), 1992-02, Vol.12 (2), p.417-418

1992

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Relevancia de las nuevas pruebas genéticas en el diagnóstico de la talla baja con dismorfias

Medicina clínica, 2016-12, Vol.147 (12), p.e67-e68

2016

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Autosomal dominant auditory neuropathy and variant DIAPH3 (c.-173C>T)

Acta otorrinolaringológica española (English), 2017-05, Vol.68 (3), p.183-185

2017

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Autosomal Dominant Auditory Neuropathy and Variant DIAPH3 (c.-173C>T)

Acta otorrinolaringológica española (English), 2017-05, Vol.68 (3), p.183-185

2017

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Autosomal dominant auditory neuropathy and variant DIAPH3 (c.-173C>T)

Acta otorrinolaringologica espanola, 2017-05, Vol.68 (3), p.183

2017

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Farmacogenética en el tratamiento del asma

Anales de pediatría (Barcelona, Spain : 2003), 2006, Vol.64 (3), p.221-223

2006

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Pharmacogenetics in the treatment of asthma

Anales de pediatría (Barcelona, Spain : 2003), 2006-03, Vol.64 (3), p.221-223

2006

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Screening for non-deltaF508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy

American journal of human genetics, 1991, Vol.48 (6), p.1127-1132

1991

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Agenesis of vas deferens and cystic fibrosis

Actas urologicas españolas, 1997-09, Vol.21 (8), p.773-776

1997

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Building a federated research infrastructure for a policy-rapid response

European journal of public health, 2021-10, Vol.31 (Supplement_3)

2021

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Changes in severity, mortality, and virus genome among a Spanish cohort of patients hospitalized with SARS-CoV-2

Scientific reports, 2021-09, Vol.11 (1), p.18844-18844, Article 18844

2021

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Evaluating process-mining interoperability: stroke case analysis on Italian health real-world data

European journal of public health, 2020-09, Vol.30 (Supplement_5)

2020

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Neonatal screening for cystic fibrosis

Anales españoles de pediatría, 2002-07, Vol.57 (1), p.60

2002

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Effectiveness of a clinical test in the preselection of children with suspected fragile X syndrome

Anales españoles de pediatría, 2001-04, Vol.54 (4), p.326

2001

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Serum antibodies against Haemophilus influenzae in children from the province of Valladolid (Spain)

Anales españoles de pediatría, 1996-11, Vol.45 (5), p.487

1996

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Value of salivary antibodies for determining seropositivity to measles, rubella, and mumps in children and adults

Anales españoles de pediatría, 1997-11, Vol.47 (5), p.499

1997

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Serum eosinophil cationic protein in children with allergic and nonallergic inflammation

Anales españoles de pediatría, 1996-03, Vol.44 (3), p.245

1996

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Measurement and comparison of the rheumatoid factors class IgG, IgM and IgA in chronic juvenile rheumatoid arthritis

Anales españoles de pediatría, 1989-12, Vol.31 (6), p.554

1989

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TLR2–TLR4/CD14 polymorphisms and predisposition to severe invasive infections by Neisseria meningitidis and Streptococcus pneumoniae

Medicina intensiva (English ed.), 2014-08, Vol.38 (6), p.356-362

2014

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Eficacia de un test clínico como preselección de niños con sospecha de síndrome X frágil

Anales de pediatría (Barcelona, Spain : 2003), 2001, Vol.54 (4), p.326-330

2001

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TLR2–TLR4/CD14 polymorphisms and predisposition to severe invasive infections by Neisseria meningitidis and Streptococcus pneumoniae

Neuropatía auditiva autosómica dominante y variante DIAPH3 (c.-173C>T)

A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A → G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene

Relevancia de las nuevas pruebas genéticas en el diagnóstico de la talla baja con dismorfias

Autosomal dominant auditory neuropathy and variant DIAPH3 (c.-173C>T)

Autosomal Dominant Auditory Neuropathy and Variant DIAPH3 (c.-173C>T)

Autosomal dominant auditory neuropathy and variant DIAPH3 (c.-173C>T)

Farmacogenética en el tratamiento del asma

Pharmacogenetics in the treatment of asthma

Screening for non-deltaF508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy

Agenesis of vas deferens and cystic fibrosis

Building a federated research infrastructure for a policy-rapid response

Changes in severity, mortality, and virus genome among a Spanish cohort of patients hospitalized with SARS-CoV-2

Evaluating process-mining interoperability: stroke case analysis on Italian health real-world data

Neonatal screening for cystic fibrosis

Effectiveness of a clinical test in the preselection of children with suspected fragile X syndrome

Serum antibodies against Haemophilus influenzae in children from the province of Valladolid (Spain)

Value of salivary antibodies for determining seropositivity to measles, rubella, and mumps in children and adults

Serum eosinophil cationic protein in children with allergic and nonallergic inflammation

Measurement and comparison of the rheumatoid factors class IgG, IgM and IgA in chronic juvenile rheumatoid arthritis

TLR2–TLR4/CD14 polymorphisms and predisposition to severe invasive infections by Neisseria meningitidis and Streptococcus pneumoniae

Eficacia de un test clínico como preselección de niños con sospecha de síndrome X frágil

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