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Climate versus carbon dioxide controls on biomass burning: a model analysis of the glacial–interglacial contrast

Biogeosciences, 2014-11, Vol.11 (21), p.6017-6027

2014

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Sex combs reduced (Scr) regulatory region of Drosophila revisited

Molecular genetics and genomics : MGG, 2017-08, Vol.292 (4), p.773-787

2017

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Evidence of neofunctionalization after the duplication of the highly conserved Polycomb group gene Caf1-55 in the obscura group of Drosophila

Scientific reports, 2017-01, Vol.7 (1), p.40536, Article 40536

2017

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Molecular population genetics of the Polycomb genes in Drosophila subobscura

PloS one, 2017-09, Vol.12 (9), p.e0185005-e0185005

2017

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Sexual group composition and shelter geometry affect collective decision-making: the case of Periplaneta americana

Insectes sociaux, 2020-11, Vol.67 (4), p.523-530

2020

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Results of a prospective phase II trial with ofatumumab as part of reduced intensity conditioning regimen in high‐risk non‐Hodgkin B lymphoma patients: A GELTAMO trial

Hematological oncology, 2017-06, Vol.35 (S2), p.346-347

2017

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Adaptive selection and coevolution at the proteins of the Polycomb repressive complexes in Drosophila

Heredity, 2016-02, Vol.116 (2), p.213-223

2016

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Results of a prospective phase II trial with ofatumumab as part of reduced intensity conditioning regimen in high‐risk non‐ H odgkin B lymphoma patients: A GELTAMO trial

Hematological oncology, 2017-06, Vol.35 (S2), p.346-347

2017

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Prader-Willi and Angelman syndromes: 21 years of experience

Anales de pediatría (Barcelona, Spain : 2003), 2012-09, Vol.77 (3), p.151-157

2012

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Myotonic dystrophy. 18 years experience in a neuropaediatric clinic

Anales de pediatría (Barcelona, Spain : 2003), 2010-02, Vol.72 (2), p.133-138

2010

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Implicación de los polimorfismos C677T y A1298C del gen MTHFR en el desarrollo de los defectos del tubo neural en la población española

Medicina clínica, 2003-04, Vol.120 (12), p.441-442

2003

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Distrofia miotónica. Nuestra experiencia de 18 años en consulta de Neuropediatría

Anales de pediatría (Barcelona, Spain : 2003), 2010-02, Vol.72 (2), p.133-138

2010

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Molecular population genetics of the Polycomb genes in Drosophila subobscura

PloS one, 2017-09

2017

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Síndrome de Gorlin neonatal asociado a hemimegalencefalia confirmado por estudio genético

Revista de neurologiá, 2006, Vol.43 (4), p.251

2006

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Síndromes de Prader-Willi y de Angelman. Expriencia de 21 años

Anales de pediatría (Barcelona, Spain : 2003), 2012-09, Vol.77 (3), p.151-157

2012

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Detección precoz de episodios de hipomanía en pacientes con trastorno afectivo

Revista de psiquiatría y salud mental, 2012-04, Vol.5 (2), p.89-97

2012

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Serum and gene expression levels of CT‐1, IL‐6, and TNF‐α after a lifestyle intervention in obese children

Pediatric diabetes, 2018-03, Vol.19 (2), p.217-222

2018

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Zeolite screening for the separation of gas mixtures containing SO2, CO2 and CO

Physical chemistry chemical physics : PCCP, 2014-10, Vol.16 (37), p.19884-19893

2014

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Coffee Consumption and the Risk of Depression in a Middle-Aged Cohort: The SUN Project

Nutrients, 2018-09, Vol.10 (9), p.1333

2018

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Adherence to the Mediterranean diet and risk of stroke and stroke subtypes

European journal of epidemiology, 2019-04, Vol.34 (4), p.337-349

2019

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Canine-coronavirus (CCV) characterization in Spain. Epidemiological aspects

Journal of veterinary medicine. Series B, 1994-01, Vol.41 (1-10), p.249-256

1994

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Epicardial and liver fat implications in albuminuria: a retrospective study

Cardiovascular diabetology, 2024-08, Vol.23 (1), p.308-14

2024

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Association between yogurt consumption and the risk of metabolic syndrome over 6 years in the SUN study

BMC public health, 2015-02, Vol.15 (1), p.170-170, Article 170

2015

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Síndrome de inversión duplicación del cromosoma 15 (INVDUP15) «de novo»: presentación de tres casos clínicos

Revista del laboratorio clínico, 2011, Vol.4 (4), p.186-195

2011

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Hereditary juvenile cobalamin deficiency due to mutations in GIF gene

Anales de pediatría (Barcelona, Spain : 2003), 2008-07, Vol.69 (1), p.56-58

2008

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Climate versus carbon dioxide controls on biomass burning: a model analysis of the glacial–interglacial contrast

Sex combs reduced (Scr) regulatory region of Drosophila revisited

Evidence of neofunctionalization after the duplication of the highly conserved Polycomb group gene Caf1-55 in the obscura group of Drosophila

Molecular population genetics of the Polycomb genes in Drosophila subobscura

Sexual group composition and shelter geometry affect collective decision-making: the case of Periplaneta americana

Results of a prospective phase II trial with ofatumumab as part of reduced intensity conditioning regimen in high‐risk non‐Hodgkin B lymphoma patients: A GELTAMO trial

Adaptive selection and coevolution at the proteins of the Polycomb repressive complexes in Drosophila

Results of a prospective phase II trial with ofatumumab as part of reduced intensity conditioning regimen in high‐risk non‐ H odgkin B lymphoma patients: A GELTAMO trial

Prader-Willi and Angelman syndromes: 21 years of experience

Myotonic dystrophy. 18 years experience in a neuropaediatric clinic

Implicación de los polimorfismos C677T y A1298C del gen MTHFR en el desarrollo de los defectos del tubo neural en la población española

Distrofia miotónica. Nuestra experiencia de 18 años en consulta de Neuropediatría

Molecular population genetics of the Polycomb genes in Drosophila subobscura

Síndrome de Gorlin neonatal asociado a hemimegalencefalia confirmado por estudio genético

Síndromes de Prader-Willi y de Angelman. Expriencia de 21 años

Detección precoz de episodios de hipomanía en pacientes con trastorno afectivo

Serum and gene expression levels of CT‐1, IL‐6, and TNF‐α after a lifestyle intervention in obese children

Zeolite screening for the separation of gas mixtures containing SO2, CO2 and CO

Coffee Consumption and the Risk of Depression in a Middle-Aged Cohort: The SUN Project

Adherence to the Mediterranean diet and risk of stroke and stroke subtypes

Canine-coronavirus (CCV) characterization in Spain. Epidemiological aspects

Epicardial and liver fat implications in albuminuria: a retrospective study

Association between yogurt consumption and the risk of metabolic syndrome over 6 years in the SUN study

Síndrome de inversión duplicación del cromosoma 15 (INVDUP15) «de novo»: presentación de tres casos clínicos

Hereditary juvenile cobalamin deficiency due to mutations in GIF gene

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