Search Results - "Salazar, Mario R"
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Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry
Published in NPJ Parkinson's Disease (02-06-2017)“…Mutations in Leucine Repeat Rich Kinase 2 (LRRK2) , primarily located in codons G2019 and R1441, represent the most common genetic cause of Parkinson’s disease…”
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Predictors of electrocardiographic change, cardiac troponin elevation, and survival after major vascular surgery: a community hospital experience
Published in The American surgeon (01-07-2007)“…Cardiovascular disease is the leading cause of perioperative morbidity and mortality after vascular surgery. The purpose of this study was to identify risk…”
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Small Bowel Ischemia in a Sickle Cell Patient
Published in Case reports in gastroenterology (31-03-2009)“…We report a case of small bowel ischemia secondary to sickle cell disease. Acute bowel ischemia is an uncommon presentation of patients with sickle cell…”
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Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort
Published in Journal of Huntington's disease (2015)“…Late onset cases of Huntington disease (HD), with onset ≥60 years, account for up to 20% of HD cases worldwide. Clinical features include mild motor…”
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Neurogenetics in Peru: clinical, scientific and ethical perspectives
Published in Journal of community genetics (01-07-2015)“…Neurogenetics, the science that studies the genetic basis of the development and function of the nervous system, is a discipline of recent development in Peru,…”
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Erratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry
Published in NPJ Parkinson's Disease (19-01-2018)“…A correction to this article has been published and is linked from the HTML version of this article…”
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Homocistinuria, una enfermedad metabólica de diagnóstico tardío en el Perú
Published in Revista de neuro-psiquiatría (30-12-2015)“…La Homocistinuria, es un desorden metabólico autosómico recesivo, cuya forma clásica es causada por deficiencia de cistationina β-sintasa, debido a mutaciones…”
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Percutaneous biopsy in evaluation of lung nodules
Published in Journal of the Society of Laparoendoscopic Surgeons (01-07-2004)“…Management of an indeterminate pulmonary nodule is a diagnostic challenge that commonly confronts primary care physicians and specialists. Patients often…”
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