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Gut microbiota: a key player in health and disease. A review focused on obesity

Journal of physiology and biochemistry, 2015-09, Vol.71 (3), p.509-525

2015

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Redox Status in Retinitis Pigmentosa

Advances in experimental medicine and biology, 2023, Vol.1415, p.443-448

2023

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Limited beneficial effects of piceatannol supplementation on obesity complications in the obese Zucker rat: gut microbiota, metabolic, endocrine, and cardiac aspects

Journal of physiology and biochemistry, 2016-09, Vol.72 (3), p.567-582

2016

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Synergistic activation of AMPK prevents from polyglutamine-induced toxicity in Caenorhabditis elegans

Pharmacological research, 2020-11, Vol.161, p.105105-105105, Article 105105

2020

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Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2

Human genetics, 2022-04, Vol.141 (3-4), p.737-758

2022

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Yugular venous catheter lodged in intercostal vein

Revista española de anestesiología y reanimación (English ed.), 2020-12, Vol.67 (10), p.568-569

2020

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Agomelatine: mechanism of action and pharmacological profile in relation to antidepressant properties

British journal of pharmacology, 2014-08, Vol.171 (15), p.3604-3619

2014

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The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

Journal of medical genetics, 2010-09, Vol.47 (9), p.640-642

2010

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Induction chemotherapy with paclitaxel, cisplatin and 5-fluorouracil for squamous cell carcinoma of the head and neck: long-term results of a phase II trial

Annals of oncology, 2002-10, Vol.13 (10), p.1665-1673

2002

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Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth

Clinical genetics, 2013-06, Vol.83 (6), p.565-570

2013

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The Added Value of Apparent Diffusion Coefficient to Cerebral Blood Volume in the Preoperative Grading of Diffuse Gliomas

American journal of neuroradiology : AJNR, 2012-04, Vol.33 (4), p.701-707

2012

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Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene

Clinical genetics, 2014-05, Vol.85 (5), p.470-475

2014

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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells

Scientific reports, 2019-08, Vol.9 (1), p.11829-15, Article 11829

2019

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Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect

Journal of medical genetics, 2005-04, Vol.42 (4), p.358-365

2005

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Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability

Clinical genetics, 2004-12, Vol.66 (6), p.525-529

2004

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Physical interaction between the serotonin transporter and neuronal nitric oxide synthase underlies reciprocal modulation of their activity

Proceedings of the National Academy of Sciences - PNAS, 2007-05, Vol.104 (19), p.8119-8124

2007

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Uso y tendencias de las técnicas bibliométricas en Ciencias Sociales y Humanas a nivel internacional

Revista española de documentación científica, 2020-05, Vol.16 (1), p.30-41

2020

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Severe Traumatic Head Injury: Prognostic Value of Brain Stem Injuries Detected at MRI

American journal of neuroradiology : AJNR, 2012-11, Vol.33 (10), p.1925-1931

2012

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Acute perfusion changes after spontaneous SAH: a perfusion CT study

Acta neurochirurgica, 2012-03, Vol.154 (3), p.405-412

2012

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Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patients

Clinical genetics, 2012-05, Vol.81 (5), p.491-494

2012

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Deconstructing vulnerability for psychosis: Meta-analysis of environmental risk factors for psychosis in subjects at ultra high-risk

European psychiatry, 2017-02, Vol.40, p.65-75

2017

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The induction of pain: an integrative review

Progress in neurobiology, 1999-01, Vol.57 (1), p.1-164

Millan, M J

1999

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Acute perfusion changes after spontaneous SAH: a perfusion CT study

Acta neurochirurgica, 2012-03, Vol.154 (3), p.405-412

2012

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The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4

Clinical genetics, 2007-04, Vol.71 (4), p.343-349

2007

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Functional analysis of splicing mutations in MYO7A and USH2A genes

Clinical genetics, 2011-03, Vol.79 (3), p.282-288

2011

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Gut microbiota: a key player in health and disease. A review focused on obesity

Redox Status in Retinitis Pigmentosa

Limited beneficial effects of piceatannol supplementation on obesity complications in the obese Zucker rat: gut microbiota, metabolic, endocrine, and cardiac aspects

Synergistic activation of AMPK prevents from polyglutamine-induced toxicity in Caenorhabditis elegans

Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2

Yugular venous catheter lodged in intercostal vein

Agomelatine: mechanism of action and pharmacological profile in relation to antidepressant properties

The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

Induction chemotherapy with paclitaxel, cisplatin and 5-fluorouracil for squamous cell carcinoma of the head and neck: long-term results of a phase II trial

Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth

The Added Value of Apparent Diffusion Coefficient to Cerebral Blood Volume in the Preoperative Grading of Diffuse Gliomas

Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene

The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells

Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect

Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability

Physical interaction between the serotonin transporter and neuronal nitric oxide synthase underlies reciprocal modulation of their activity

Uso y tendencias de las técnicas bibliométricas en Ciencias Sociales y Humanas a nivel internacional

Severe Traumatic Head Injury: Prognostic Value of Brain Stem Injuries Detected at MRI

Acute perfusion changes after spontaneous SAH: a perfusion CT study

Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patients

Deconstructing vulnerability for psychosis: Meta-analysis of environmental risk factors for psychosis in subjects at ultra high-risk

The induction of pain: an integrative review

Acute perfusion changes after spontaneous SAH: a perfusion CT study

The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4

Functional analysis of splicing mutations in MYO7A and USH2A genes

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