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52. Genetic background in pediatric pulmonary arterial hypertension. Should we change the current recommendations for genetic testing?

53. Eisenmenger syndrome: is it the same entity in adulthood and pediatric age?

54. Nutrition During Pregnancy, Lactation and Early Childhood and its Implications for Maternal and Long-Term Child Health

55. Fibre intake is associated with cardiovascular health in european children

56. Influence of total sugar intake on metabolic blood markers at 8 years of age in the Childhood Obesity Project

64. Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial

67. The LifeCycle Project-EU Child Cohort Network: a federated analysis infrastructure and harmonized data of more than 250,000 children and parents

68. Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.

69. A Heritage Science Workflow to Preserve and Narrate a Rural Archeological Landscape Using Virtual Reality: The Cerro del Castillo of Belmez and Its Surrounding Environment (Cordoba, Spain)

70. Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

71. Idiopathic pulmonary hypertension in Spanish pediatric registry: clinical characterization, management, and risk factors for survival

72. Pulmonary hypertension and congenital heart disease: medical treatment and risk factors for survival

73. Impact of smoking habit on platelet reactivity in a cohort of patients admitted due to an acute coronary syndrome

74. Is “one size fits all” anti-aggregation really effective? Variability in the response to P2Y12 receptor inhibitors in obese patients

75. Pretriscuspid shunt and Eisenmenger syndrome: a deadly combination

76. Pulmonary arterial hypertension in Spanish pediatric registry age: clinical characterization, management and survival

97. Current perspectives in Bietti crystalline dystrophy

98. Transforming growth factor beta-induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients

99. To the Editor

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