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Artigos Publicados

Artigo de Pesquisa

Alpha amylase and alpha glucosidase inhibitory activities of isolated total saponins and tannins of Dialium guineense stem bark

Onoagbe

Background: Dialium guineense belongs to the Leguminosae family, and grows in dense forests in Africa along the southern edge of the Sahel. The bark, leav..Veja mais»

Artigo de Pesquisa

Designed Mentorship, Career Development, Learning and Psychological Growth across Generations: A Study of a Mentoring Program in an International Industrial Company

Max Rapp Ricciardi and Trevor Archer

The purpose of the present study was: 1) to evaluate workplace mentoring programs from the perspectives of the mentors and protégés. 2) To compare the evolution of thr..Veja mais»

Artigo de Pesquisa

Metals Contents in Black Tea and Evaluation of Potential Human Health Risks to Consumers

Naglaa F Soliman

Tea is one of the most common beverages in all over the world. Next to water, it is the most consumed beverage. During the last decades, there has been an extensive increase in ..Veja mais»

Editorial

A Decent Imperfection Control on Silicon Material

Jacob Dwinell

Silicon material is quite possibly the most well-known material utilizing in semiconductor industry because of its great exhibition as far as material construction, mechanical s..Veja mais»

Relato de caso

Neuromyelitis Optica Spectrum Disorders Associated To Posterior Reversible Encephalopathy Syndrome: Pathogenesis, Diagnosis, Treatment and Evolution: A Case Report and Literature Review

Benmoh Y, Hamid M, Arrami A, Alaoui MY, Satte A, Mounach J, Bichra MZ, Elfenni J and Bourazza A

Introduction: Neurmyelitis Optica Spectrum Disorders (NMOSD) is a rare central nervous demyelinating autoimmune disease. Posterior Reversible Encephalopathy Syn..Veja mais»

Artigo de revisão

Dental Phenotypes in Van der Woude Syndrome: An Integrative Review

Aline Cris tina da Silva Trevizan, Pollyana Pereira Teotonio dos Santos, Maria Carolina de Moraes Pereira, Lucimara Teixeira das Neves

Introduction: Van der Woude Syndrome (VWS) consists of a genetic abnormality attributed to mutations in the IRF6 gene, characterized by the presence of paramedi..Veja mais»