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au.\*:("COTO, Eliecer")

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P53 allelic loss and outcome in patients with squamous cell carcinoma of the head and neckRODRIGO, Juan P; COTO, Eliecer; GONZALEZ, Maria V et al.European archives of oto-rhino-laryngology. 2001, Vol 258, Num 5, pp 255-258, issn 0937-4477Article

Early-onset Parkinson's disease associated with a new parkin mutation in a Spanish familyALVAREZ, Victoria; GUISASOLA, Luis M; MOREIRA, Vanessa G et al.Neuroscience letters. 2001, Vol 313, Num 1-2, pp 108-110, issn 0304-3940Article

Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 geneCOTO, Eliecer; ARMENTA, Daniel; ESPINOSA, Raul et al.Movement disorders. 2005, Vol 20, Num 12, pp 1626-1629, issn 0885-3185, 4 p.Article

Profile of microRNAs in the plasma of hypertrophic cardiomyopathy patients compared to healthy controlsPALACIN, Maria; COTO, Eliecer; REGUERO, Julián R et al.International journal of cardiology. 2013, Vol 167, Num 6, pp 3075-3076, issn 0167-5273, 2 p.Article

A DNA polymorphism at the α2-macroglobulin gene is associated with the severity of rheumatoid arthritisZAPICO, Isabel; COTO, Eliecer; RODRIGUEZ, Amado et al.Journal of rheumatology. 2000, Vol 27, Num 10, pp 2308-2311, issn 0315-162XArticle

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)REGUERO, Julián R; GOMEZ, Juan; MARTIN, María et al.International journal of cardiology. 2013, Vol 168, Num 4, pp 4555-4556, issn 0167-5273, 2 p.Article

Prevalence and spectmm of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patientsGARCIA-CASTRO, Monica; REGUERO, Julian R; MORIS, César et al.International journal of cardiology. 2007, Vol 121, Num 1, pp 115-116, issn 0167-5273, 2 p.Article

ABCA1 polymorphisms and prognosis after myocardial infarction in young patientsMARTIN, Maria; GONZALEZ, Pelayo; REGUERO, J. J. R et al.International journal of cardiology. 2006, Vol 110, Num 2, pp 267-268, issn 0167-5273, 2 p.Article

Variation in the LRP-associated protein gene (LRPAP1) is associated with late-onset Alzheimer diseaseSANCHEZ, Lourdes; ALVAREZ, Victoria; GONZALEZ, Pelayo et al.American journal of medical genetics. 2001, Vol 105, Num 1, pp 76-78, issn 0148-7299Conference Paper

Apolipoprotein ε4 allele is associated with psoriasis severityCOTO-SEGURA, Pablo; COTO, Eliecer; ALVAREZ, Victoria et al.Archives of dermatological research (Print). 2010, Vol 302, Num 2, pp 145-149, issn 0340-3696, 5 p.Article

Pharmacogenetics of Calcineurin Inhibitors in Renal TransplantationCOTO, Eliecer; TAVIRA, Beatriz.Transplantation. 2009, Vol 88, Num 3, issn 0041-1337, S62-S67, SUPConference Paper

The Sp1/Egr1-tandem Repeat Polymorphism in the 5-Lipoxygenase Gene Promoter is not Associated With Late Onset Alzheimer DiseaseALVAREZ, Victoria; GONZALEZ, Pelayo; CORAO, Ana I et al.Alzheimer disease and associated disorders. 2008, Vol 22, Num 2, pp 177-180, issn 0893-0341, 4 p.Article

Lack of association between polymorphisms of the coagulation factor VII and myocardial infarction in middle-aged Spanish menBATALLA, Alberto; ALVAREZ, Ruth; REGUERO, Julian R et al.International journal of cardiology. 2001, Vol 80, Num 2-3, pp 209-212, issn 0167-5273Article

Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effectGARCIA-CASTRO, Monica; REGUERO, Julian R; ALVAREZ, Victoria et al.International journal of cardiology. 2005, Vol 102, Num 3, pp 501-507, issn 0167-5273, 7 p.Article

Renin-angiotensin system polymorphisms and renal scarringPARDO, Rafael; MALAGA, Serafin; COTO, Eliecer et al.Pediatric nephrology (Berlin, West). 2003, Vol 18, Num 2, pp 110-114, issn 0931-041X, 5 p.Article

Genetic alterations in squamous cell carcinomas of the hypopharynx with correlations to clinicopathological featuresRODRIGO, Juan P; GONZALEZ, Maria V; LAZO, Pedro S et al.Oral oncology (1997). 2002, Vol 38, Num 4, pp 357-363, issn 1368-8375Article

Variation at the angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of Esophageal varices among patients with alcoholic cirrhosisCOTO, Eliecer; RODRIGO, Luis; ALVAREZ, Ruth et al.Journal of cardiovascular pharmacology. 2001, Vol 38, Num 6, pp 833-839, issn 0160-2446Article

Psoriasis and type 2 diabetes risk among psoriatic patients in a Spanish populationARMESTO, Susana; SANTOS-JUANES, Jorge; GALACHE-OSUNA, Cristina et al.Australasian journal of dermatology. 2012, Vol 53, Num 2, pp 128-130, issn 0004-8380, 3 p.Article

Profile of MicroRNAs Differentially Produced in Hearts from Patients with Hypertrophic Cardiomyopathy and Sarcomeric MutationsPALACIN, Maria; REGUERO, Julian R; MARTIN, Maria et al.Clinical chemistry (Baltimore, Md.). 2011, Vol 57, Num 11, pp 1614-1616, issn 0009-9147, 3 p.Article

Association Between the STin2 VNTR Polymorphism of the Serotonin Transporter Gene and Treatment Outcome in Alcohol-Dependent PatientsFLOREZ, Gerardo; SAIZ, Pilar; GARCIA-PORTILLA, Paz et al.Alcohol and alcoholism (Oxford). 2008, Vol 43, Num 5, pp 516-522, issn 0735-0414, 7 p.Article

No association between Parkinson's disease and three polymorphisms in the eNOS, nNOS, and iNoS genesHUERTA, Cecilia; SANCHEZ-FERRERO, Elena; COTO, Eliecer et al.Neuroscience letters. 2007, Vol 413, Num 3, pp 202-205, issn 0304-3940, 4 p.Article

Influence of endothelial nitric oxide synthase polymorphisms in psoriasis riskCOTO-SEGURA, Pablo; COTO, Eliecer; MAS-VIDAL, Albert et al.Archives of dermatological research (Print). 2011, Vol 303, Num 6, pp 445-449, issn 0340-3696, 5 p.Article

Lack of association between angiotensin I-converting enzyme insertion/deletion polymorphism and psoriasis or psoriatic arthritis in SpainCOTO-SEGURA, Pablo; ALVAREZ, Victoria; SOTO-SANCHEZ, Javier et al.International journal of dermatology. 2009, Vol 48, Num 12, pp 1320-1323, issn 0011-9059, 4 p.Article

Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer diseaseALVAREZ, Victoria; MATA, Ignacio F; GONZALEZ, Pelayo et al.American journal of medical genetics. 2002, Vol 114, Num 5, pp 574-577, issn 0148-7299Article

Analysis of the Micro-RNA-133 and PITX3 Genes in Parkinson's DiseaseDE MENA, Lorena; COTO, Eliecer; MENENDEZ, Manuel et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 6, pp 1234-1239, issn 1552-4841, 6 p.Article

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