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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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Unilateral ptosis as the initial sign of multiple myeloma

Neurologia (Barcelona, Spain), 2016-05, Vol.31 (4), p.282

2016

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Ptosis palpebral unilateral como debut de mieloma múltiple

Neurología (Barcelona, Spain), 2016-05, Vol.31 (4), p.282-283

2016

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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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Supported discharge shortens hospital stay in patients hospitalized because of an exacerbation of COPD

The European respiratory journal, 2001-06, Vol.17 (6), p.1138-1142

2001

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Unilateral ptosis as the initial sign of multiple myeloma

Neurología (Barcelona, English ed. ), 2016-05, Vol.31 (4), p.282-283

2016

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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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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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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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A prospective observational study of the effectiveness, safety, and effect on fatigue of darbepoetin alfa for the treatment of chemotherapy-induced anaemia

Current medical research and opinion, 2008-10, Vol.24 (10), p.2931-2942

2008

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Resolution of Nephrotic Syndrome Secondary Heroin-Associated Renal Amyloidosis

Nephrology, dialysis, transplantation, 1990, Vol.5 (2), p.158-158

1990

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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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Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy

American journal of human genetics, 1991-06, Vol.48 (6), p.1127-1132

1991

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Frequency of cystic fibrosis mutations and associated haplotype distribution in Slovak CF patients

Advances in experimental medicine and biology, 1991, Vol.290, p.383

1991

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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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Organizational models for the hematology areas of the district hospitals of Catalonia

Sangre (Zaragoza), 1996-06, Vol.41 (3), p.211

1996

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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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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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Anaemia and macroglossia as the first clinical features of multiple myeloma and amyloidosis

Sangre (Zaragoza), 1995-10, Vol.40 (5), p.435

1995

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

Unilateral ptosis as the initial sign of multiple myeloma

Ptosis palpebral unilateral como debut de mieloma múltiple

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

Supported discharge shortens hospital stay in patients hospitalized because of an exacerbation of COPD

Unilateral ptosis as the initial sign of multiple myeloma

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

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

Pharmacogenetics in the treatment of asthma

A prospective observational study of the effectiveness, safety, and effect on fatigue of darbepoetin alfa for the treatment of chemotherapy-induced anaemia

Resolution of Nephrotic Syndrome Secondary Heroin-Associated Renal Amyloidosis

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

Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy

Frequency of cystic fibrosis mutations and associated haplotype distribution in Slovak CF patients

Neonatal screening for cystic fibrosis

Organizational models for the hematology areas of the district hospitals of Catalonia

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

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)

Anaemia and macroglossia as the first clinical features of multiple myeloma and amyloidosis

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