Citation Impact
Citing Papers
Leishmaniasis
2018 Standout
Visceral leishmaniasis: what are the needs for diagnosis, treatment and control?
2007 Standout
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
On the Anglocentricities of current reading research and practice: The perils of overreliance on an "outlier" orthography.
2008 Standout
Newborn Hearing Screening — A Silent Revolution
2006 Standout
Natural products: An evolving role in future drug discovery
2011 Standout
Musical Training Influences Linguistic Abilities in 8-Year-Old Children: More Evidence for Brain Plasticity
2008 Standout
Cognitive functions correlate with white matter architecture in a normal pediatric population: A diffusion tensor MRI study
2005 Standout
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
The spectrum of hearing loss due to mitochondrial DNA defects
2000
Structural and Functional Diversity of Connexin Genes in the Mouse and Human Genome
2002 Standout
Evaluating Penicillin Allergies Without Skin Testing
2019
Detection of Leishmania infantum cryptic infection in asymptomatic blood donors living in an endemic area (Eivissa, Balearic Islands, Spain) by different diagnostic methods
2003
Hereditary deafness and phenotyping in humans
2002
Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes
2008
Mitochondrial DNA and disease
2005
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins
2000
Specific reading disability (dyslexia): what have we learned in the past four decades?
2004 Standout
Broca’s area: Nomenclature, anatomy, typology and asymmetry
2009 Standout
Sensorineural hearing loss in children
2005 Standout
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss
2005
Natural products to drugs: natural product-derived compounds in clinical trials
2008 Standout
Leishmaniases in Northern Greece: seroprevalence of the infection and incidence of the disease during the period 2001–2006
2008
The neurological basis of developmental dyslexia: An overview and working hypothesis
2000
The genetics of deafness
2003
LeishVet guidelines for the practical management of canine leishmaniosis
2011 Standout
Genetic Factors in Aminoglycoside Toxicity
1999
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Anatomical correlates of dyslexia: frontal and cerebellar findings
2003
Asymptomatic Leishmania Infection: A New Challenge for Leishmania Control
2014
Asymptomatic leishmaniasis in kala-azar endemic areas of Malda district, West Bengal, India
2017
IgG1 as a Potential Biomarker of Post-chemotherapeutic Relapse in Visceral Leishmaniasis, and Adaptation to a Rapid Diagnostic Test
2014
Safety and Outcomes of Oral Graded Challenges to Amoxicillin without Prior Skin Testing
2018
Mitochondrial deafness
2007
A new gene (DYX3) for dyslexia is located on chromosome 2.
1999
Sexually Transmitted Infections Treatment Guidelines, 2021
2021 Standout
The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
2005 Standout
Pore-forming activity and structural autoinhibition of the gasdermin family
2016 StandoutNature
The deafness gene DFNA5 induces programmed cell death through mitochondria and MAPK-related pathways
2015
Therapeutic Glucocorticoid-Induced TNF Receptor-Mediated Amplification of CD4+ T Cell Responses Enhances Antiparasitic Immunity
2010 StandoutNobel
Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss
2002
Advances in leishmaniasis
2005 Standout
Developments in Diagnosis of Visceral Leishmaniasis in the Elimination Era
2015
Point-of-Care Diagnostics for Global Health
2008 Standout
Molecular Genetics of Hearing Loss
2001
Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3
2003
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
2003
Clinical Practice Guideline: Sudden Hearing Loss (Update)
2019 Standout
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections
2003
Brain morphometry in reading-disabled twins
1999
Genetics of Sensory Mechanotransduction
2002 StandoutNobel
Works of Luis Moral being referenced
Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
1998
A leishmanin skin test survey in the human population of l'Alacantí Region (Spain): implications for the epidemiology of Leishmania infantum infection in southern Europe
2002
Oral challenge without skin tests in children with non‐severe beta‐lactam hypersensitivity: Time to change the paradigm?
2017