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5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction

artículo científico publicado en 2003

A 3'-UTR Polymorphism in Soluble Epoxide Hydrolase Gene Is Associated with Acute Rejection in Renal Transplant Recipients

artículo científico publicado en 2015

A CLCNKA polymorphism (rs10927887; p.Arg83Gly) previously linked to heart failure is associated with the estimated glomerular filtration rate in the RENASTUR cohort

artículo científico publicado en 2013

A Common APOE Polymorphism Is an Independent Risk Factor for Reduced Glomerular Filtration Rate in the Spanish RENASTUR Cohort

scientific article published on 16 May 2013

A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients.

artículo científico publicado en 2015

A Semiconductor Chip-Based Next Generation Sequencing Procedure for the Main Pulmonary Hypertension Genes

artículo científico publicado en 2015

A Single Nucleotide Polymorphism in the Il17ra Promoter Is Associated with Functional Severity of Ankylosing Spondylitis.

artículo científico publicado en 2016

A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees

artículo científico publicado en 2003

A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients.

artículo científico publicado en 2015

A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome patients.

artículo científico publicado en 2014

A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry

artículo científico publicado en 2017

A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies

artículo científico publicado en 2004

A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.

artículo científico publicado en 2011

A search for cyclophilin-A gene variants in cyclosporine A-treated renal transplanted patients

article

A search for new CYP3A4 variants as determinants of tacrolimus dose requirements in renal-transplanted patients.

artículo científico publicado en 2013

A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction

artículo científico publicado en 2004

ABCA1 polymorphisms and prognosis after myocardial infarction in young patients

artículo científico publicado en 2005

ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: a Next Generation Sequencing approach

artículo científico publicado en 2015

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms.

artículo científico publicado en 2014

Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.

artículo científico publicado en 2011

An elderly Jervell and Lange-Nielsen patient heterozygous compound for two new KCNQ1 mutations

scientific article published on 21 November 2016

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

artículo científico publicado en 2015

Analysis of theMicro-RNA-133andPITX3genes in Parkinson's disease

article

Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome

scientific article published on 31 August 2020

Apolipoprotein epsilon4 allele is associated with psoriasis severity

artículo científico publicado en 2010

Apolipoprotein epsilon4 allele is associated with psoriasis severity: reply

scientific article published on 07 February 2010

Assessing the role of TUBA4A gene in frontotemporal degeneration.

artículo científico publicado en 2015

Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia

artículo científico publicado en 2013

Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort

scientific article published on 05 March 2013

Association between a common KCNJ11 polymorphism (rs5219) and new-onset posttransplant diabetes in patients treated with Tacrolimus

scientific article published on 04 January 2012

Association between single nucleotide polymorphisms IL17RA rs4819554 and IL17E rs79877597 and Psoriasis in a Spanish cohort

artículo científico publicado en 2015

Association between the IL17RA rs4819554 polymorphism and reduced renal filtration rate in the Spanish RENASTUR cohort.

artículo científico publicado en 2015

Association between the Stin2 VNTR polymorphism of the serotonin transporter gene and treatment outcome in alcohol-dependent patients

artículo científico publicado en 2008

Association between the TNFalpha-308 A/G polymorphism and the onset-age of Alzheimer disease.

artículo científico publicado en 2002

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Bilineal inheritance of type 1 autosomal dominant polycystic kidney disease (ADPKD) and recurrent fetal loss

artículo científico publicado en 2008

CDKAL1 gene variants affect the anti-TNF response among Psoriasis patients

artículo científico publicado en 2015

Capillary Electrophoresis of PCR fragments with 5’-labelled primers for testing the SARS-Cov-2

scientific article published on 21 May 2020

Capillary electrophoresis of PCR fragments with 5´-labelled primers for testing the SARS-Cov-2

scientific article published on 10 July 2020

Cardiovascular risk factors influence response to biological therapies in psoriasis

artículo científico publicado en 2015

Characterization of Left Ventricular Non-Compaction Cardiomyopathy

artículo científico publicado en 2020

Chemokines (RANTES and MCP-1) and chemokine-receptors (CCR2 and CCR5) gene polymorphisms in Alzheimer's and Parkinson's disease.

artículo científico publicado en 2004

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

scientific article published on 26 November 2020

Clinical and analytical findings in Gitelman's syndrome associated with homozygosity for the c.1925 G>A SLC12A3 mutation

artículo científico publicado en 2009

Common European mitochondrial haplogroups in the risk for psoriasis and psoriatic arthritis

artículo científico publicado en 2011

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders

artículo científico publicado en 2020

Diagnostic impact of genetic testing in hypertrophic cardiomyopathy: The story of two families

artículo científico publicado en 2015

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT.

artículo científico publicado en 2017

Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease.

artículo científico publicado en 2012

Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children

artículo científico publicado en 2007

Effect of mitochondrial, APOE, ACE and NOS3 gene polymorphisms on cardiovascular risk factors among the Vaqueiros de Alzada, a Northern Spain human isolate.

artículo científico publicado en 2013

Effect of the FTO rs9930506 Polymorphism on the Main Comorbidities of the Cardiorenal Metabolic Syndrome in an Elderly Spanish Cohort

artículo científico publicado en 2014

Endoplasmic reticulum stress signals in defined human embryonic stem cell lines and culture conditions.

artículo científico publicado en 2010

Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families.

artículo científico publicado en 2013

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

artículo científico publicado en 2011

FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.

artículo científico publicado en 2010

FK506 affects mitochondrial protein synthesis and oxygen consumption in human cells

artículo científico publicado en 2013

Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry

artículo científico publicado en 2020

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier.

artículo científico publicado en 2010

Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy.

artículo científico publicado en 2010

Gene Variant in the NF-κB Pathway Inhibitor NFKBIA Distinguishes Patients with Psoriatic Arthritis within the Spectrum of Psoriatic Disease

scientific article published on 11 November 2019

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

scientific article published on 19 March 2019

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

artículo científico publicado en 2018

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

artículo científico publicado en 2018

Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report

artículo científico publicado en 2010

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic variation at IL12B, IL23R and IL23A is associated with psoriasis severity, psoriatic arthritis and type 2 diabetes mellitus

scientific article published on 11 June 2014

Genetic variation at the CCR5/CCR2 gene cluster and risk of psoriasis and psoriatic arthritis

artículo científico publicado en 2010

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

scientific article published on 02 July 2018

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

scientific article published on 02 September 2020

Genetic variation in the renin-angiotensin system and athletic performance

article by R Alvarez et al published 15 May 2000 in European Journal of Applied Physiology

Genetic variation of DKK3 may modify renal disease severity in ADPKD.

artículo científico publicado en 2010

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease

artículo científico publicado en 2003

Gut microbiota dysbiosis in a cohort of patients with psoriasis

artículo científico publicado en 2019

Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease

scientific article published on 01 January 2005

Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism

artículo científico publicado en 2005

Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?

scientific article published on 17 April 2015

Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect.

artículo científico publicado en 2004

Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients

scientific article published on 01 August 2003

IL-15 preferentially enhances functional properties and antigen-specific responses of CD4+CD28(null) compared to CD4+CD28+ T cells

artículo científico publicado en 2011

IL-1α (− 889) promoter polymorphism is a risk factor for osteomyelitis

artículo científico publicado en 2003

IL17RA in early-onset coronary artery disease: Total leukocyte transcript analysis and promoter polymorphism (rs4819554) association

scientific article published on 16 September 2020

Identification of epitopes and immunodominant regions on the MICA protein defined by alloantibodies from kidney transplant patients

artículo científico publicado en 2009

In vivo interleukin-6 protects neutrophils from apoptosis in osteomyelitis

artículo científico publicado en 2004

Influence of Fcγ Receptor Polymorphisms on Response to Anti-Tumor Necrosis Factor Treatment in Psoriasis

scientific article published on 01 December 2015

Influence of endothelial nitric oxide synthase polymorphisms in psoriasis risk

artículo científico publicado en 2011

Insights Into Hypertrophic Cardiomyopathy Evaluation Through Follow-up of a Founder Pathogenic Variant

artículo científico publicado en 2018

Interaction of insulin and PPAR-α genes in Alzheimer's disease: the Epistasis Project.

artículo científico publicado en 2011

Interactions between PPAR-α and inflammation-related cytokine genes on the development of Alzheimer's disease, observed by the Epistasis Project

artículo científico publicado en 2012

KCNQ1 gene variants and risk of new-onset diabetes in tacrolimus-treated renal-transplanted patients.

artículo científico publicado en 2011

KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort

artículo científico publicado en 2016

Lack of association between SNPsrs8176719(O blood group) and COVID-19: data from Spanish age matched patients and controls

artículo científico publicado en 2020

Lack of association between angiotensin I-converting enzyme insertion/deletion polymorphism and psoriasis or psoriatic arthritis in Spain.

artículo científico publicado en 2009

Lack of association between endothelin-1 gene variants and myocardial infarction

artículo científico publicado en 2009

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease.

artículo científico publicado en 2011

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy.

artículo científico publicado en 2011

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium

artículo científico publicado en 2015

Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: a case-control study in a Spanish population

artículo científico publicado en 2009

Metalloproteinase Polymorphisms and Bicuspid Aortic Valves ⬇️

artículo científico publicado el 1 de noviembre de 2010

MiRNA profile in the substantia nigra of Parkinson's disease and healthy subjects.

artículo científico publicado en 2014

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H

artículo científico publicado en 2010

Mitochondrial DNA haplogroups and risk of new-onset diabetes among tacrolimus-treated renal transplanted patients.

artículo científico publicado en 2014

Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy

artículo científico publicado en 2006

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.

artículo científico publicado en 2005

Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia

artículo científico publicado en 2011

Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete

artículo científico publicado en 2007

Mitochondrial transcription factor A (TFAM) gene variation and risk of late-onset Alzheimer's disease.

artículo científico publicado en 2008

Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease

artículo científico publicado en 2007

Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophy

artículo científico publicado en 2008

Mutation analysis of the LCE3B/LCE3C genes in Psoriasis

artículo científico publicado en 2010

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing

artículo científico publicado en 2014

Mutation analysis of the myocyte enhancer factor 2A gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy

artículo científico publicado en 2009

Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease.

artículo científico publicado en 2012

Mutational screening of the mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease

artículo científico publicado en 2008

Mutational screening of the mortalin gene (HSPA9) in Parkinson's disease

scientific article published on 06 August 2009

Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.

artículo científico publicado en 2010

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

scientific journal article

Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2009

Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms.

artículo científico publicado en 2006

N-acetyltransferase-2 polymorphisms and schizophrenia

artículo científico publicado en 2006

NFKBIZ and CW6 in Adalimumab Response Among Psoriasis Patients: Genetic Association and Alternative Transcript Analysis

artículo científico publicado en 2019

NFKBIZ in Psoriasis: Assessing the association with gene polymorphisms and report of a new transcript variant

artículo científico publicado en 2017

NKG2D and its ligands: active factors in the outcome of solid organ transplantation?

artículo científico

New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy

artículo científico publicado en 2012

New psoriasis susceptibility genes: momentum for skin-barrier disruption.

artículo científico publicado en 2011

Next generation sequencing of the NOTCH3 gene in a cohort of pulmonary hypertension patients

artículo científico publicado en 2016

Next generation sequencing search for uromodulin gene variants related with impaired renal function

artículo científico publicado en 2015

No association between Parkinson's disease and three polymorphisms in the eNOS, nNOS, and iNOS genes

artículo científico publicado en 2006

No differential DNA methylation of PARK2 in brain of Parkinson's disease patients and healthy controls.

artículo científico publicado en 2013

Non optical semi-conductor next generation sequencing of the main cardiac QT-interval duration genes in pooled DNA samples

artículo científico publicado en 2013

Pharmacogenetics of calcineurin inhibitors in renal transplantation

artículo científico publicado en 2009

Pharmacogenetics of tacrolimus after renal transplantation: analysis of polymorphisms in genes encoding 16 drug metabolizing enzymes

artículo científico publicado en 2011

Pharmacogenetics of tacrolimus: ready for clinical translation?

artículo científico publicado en 2011

Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients

artículo científico publicado en 2006

Profile of microRNAs differentially produced in hearts from patients with hypertrophic cardiomyopathy and sarcomeric mutations

scientific article published on 02 September 2011

Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls

artículo científico publicado en 2013

Profile of microRNAs in the plasma of hypertrophic cardiomyopathy patients compared to healthy controls.

artículo científico publicado en 2012

Psoriasis and type 2 diabetes risk among psoriatic patients in a Spanish population

artículo científico publicado en 2011

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy.

artículo científico publicado en 2017

Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene

artículo científico publicado en 2005

Renin-angiotensin system polymorphisms and renal scarring

artículo científico publicado en 2002

Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease

artículo científico publicado en 2009

Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.

artículo científico publicado en 2011

Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypes

artículo científico publicado en 2012

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy

artículo científico publicado en 2012

Role of serotonergic polymorphisms in the clinical severity of the panic disorder

artículo científico publicado en 2009

Role of syncope in predicting adverse outcomes in patients with suspected Brugada syndrome undergoing standardized flecainide testing.

artículo científico publicado en 2017

Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 genes in the risk of atherosclerosis and myocardial infarction

scientific article published on 31 March 2007

SNP rs11652075 in the CARD14 gene as a risk factor for psoriasis (PSORS2) in a Spanish cohort.

artículo científico publicado en 2013

Salt-losing tubulopathy and chronic dermatitis

artículo científico publicado en 2018

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients

artículo científico publicado en 2017

Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy

artículo científico publicado en 2008

Soluble co-signaling molecules predict long-term graft outcome in kidney-transplanted patients

artículo científico publicado en 2014

Spectral Analysis of the QT Interval Increases the Prediction Accuracy of Clinical Variables in Brugada Syndrome

artículo científico publicado en 2019

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients

artículo científico publicado en 2016

Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope.

artículo científico publicado en 2016

TGFBR2 gene mutational spectrum in aortic pathology

scientific article published on 01 January 2011

The Cw6 and late-cornified envelope genotype plays a significant role in anti-tumor necrosis factor response among psoriatic patients.

artículo científico publicado en 2015

The Epistasis Project: A Multi-Cohort Study of the Effects of BDNF, DBH, and SORT1 Epistasis on Alzheimer's Disease Risk

scientific article published on 01 January 2019

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain).

artículo científico publicado en 2013

The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19

artículo científico publicado en 2020

The NOS3 (27-bp repeat, intron 4) polymorphism is associated with susceptibility to osteomyelitis

artículo científico publicado en 2006

The Sp1/Egr1-tandem repeat polymorphism in the 5-lipoxygenase gene promoter is not associated with late onset Alzheimer disease

artículo científico publicado en 2008

The T-786C endothelial nitric oxide synthase genotype and coronary artery disease

artículo científico publicado en 2003

The TNFRSF1B rs1061622 polymorphism (p.M196R) is associated with biological drug outcome in Psoriasis patients

artículo científico publicado en 2014

The Ups and Downs of Genetic Diagnosis of Hypertrophic Cardiomyopathy

artículo científico publicado en 2015

The donor ABCB1 (MDR-1) C3435T polymorphism is a determinant of the graft glomerular filtration rate among tacrolimus treated kidney transplanted patients

artículo científico publicado en 2015

The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project

artículo científico publicado en 2010

The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease

artículo científico publicado en 2014

The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis Project

artículo científico publicado en 2013

The spectrum of SCN5A gene mutations in Spanish Brugada syndrome patients.

artículo científico publicado en 2010

Time-dependent responses to provocative testing with flecainide in the diagnosis of Brugada syndrome

artículo científico publicado en 2014

Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease

artículo científico publicado en 2019

Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project

artículo científico publicado en 2010

Unified criteria for ultrasonographic diagnosis of ADPKD.

artículo científico publicado en 2008

Variant-genetic and transcript-expression analysis showed a role for the chemokine-receptor CCR5 in COVID-19 severity

scholarly article by Helena Gil-Peña published in 2021

Variants in cardiac GATA genes associated with bicuspid aortic valve

scientific article published on 08 October 2018

Variation in the lipoprotein receptor-related protein, alpha2-macroglobulin and lipoprotein receptor-associated protein genes in relation to plasma lipid levels and risk of early myocardial infarction

artículo científico publicado en 2002

Vesicoureteric reflux and tumor necrosis factor-alpha gene polymorphism

artículo científico publicado en 2006

[Pharmacogenetics of tacrolimus: from bench to bedside?]

scientific article published on 01 January 2014

Detección directa de mutaciones malignas en pacientes con miocardiopatía hipertrófica ⬇️

artículo científico publicado el 1 de octubre de 2003

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