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1.
Adv Exp Med Biol ; 987: 177-184, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28971457

RESUMO

Scientific advances in biomedical disciplines have allowed us to identify the underlying causes of many diseases with increased comprehension-leading the way towards precision medicine. In this context, unique disease and medical traits pave the way for the development of adapted disease management, drugs and therapies tailored to each patient. Bearing in mind that reductionism, an approach that has dominated biomedical research for many years and has resulted in the identification of definite cellular phenotypes and human diseases which are linked with specific integral molecules, we strongly believe that Alzheimer's Disease, one of the most common neurodegenerative diseases, could not be applied to the model of one disease-one assay-one drug. Regarding the discrete complexities in the molecular pathogenesis combined with the limited knowledge of inherited and sporadic forms of Alzheimer's disease, the great heterogeneity in the clinical development, as well as the plethora of validated biomarkers that have been proposed for early diagnosis or prognosis of the disease, we presume that a radically different way of thinking is in demand for comprehensive explanations of the molecular pathogenesis of the disease. In this article we highlight the most recent advances made in the omics field of systems biology towards a more complete understanding of Alzheimer's disease mechanisms, emphasizing to the paramount emergence of the development of various high-throughput strategies applied to the omics sciences.


Assuntos
Doença de Alzheimer/genética , Doença de Alzheimer/metabolismo , Pesquisa Biomédica/métodos , Biologia de Sistemas/métodos , Genômica/métodos , Humanos , Metabolômica/métodos , Medicina de Precisão/métodos , Proteômica/métodos
2.
Adv Exp Med Biol ; 987: 199-212, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28971459

RESUMO

New research data on Alzheimer's Disease define it as a clinicobiological entity, which has a long preclinical and presymptomatic phase. Emphasis has been given in early detection and diagnosis, which will allow professionals, caregivers and patients themselves to plan and adjust better to the response of the disease. Primary care physicians, who most often are the first to witness and perceive cognitive impairment, may play a central role in the diagnostic procedure, but frequently they are reluctant to be engaged to the screening procedure. The aim of this study is to model a practical guideline for mental assessment and screening, which will be part of a whole step-to-step medical instruction policy for primary care physicians. After a careful review of the literature, we propose a two-visits approach. This approach combines the measures to be administered in each visit, with a detailed list of close-ended questions on the factors concerning Alzheimer's screening. The tests are automatically available to the physician through hyperlink connection and the scores are immediately calculated. Clinical trials will follow to test the validity of the proposed guidance.


Assuntos
Doença de Alzheimer/diagnóstico , Cognição , Programas de Rastreamento/métodos , Médicos de Atenção Primária , Doença de Alzheimer/psicologia , Humanos , Testes Neuropsicológicos/normas , Guias de Prática Clínica como Assunto/normas , Reprodutibilidade dos Testes , Literatura de Revisão como Assunto , Sensibilidade e Especificidade
3.
Bioinformation ; 7(2): 91-5, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21938211

RESUMO

A permutation-based algorithm is introduced for the representation of closed RNA secondary structures. It is an efficient 'loopless' algorithm, which generates the permutations on base-pairs of 'k-noncrossing' setting partitions. The proposed algorithm reduces the computational complexity of known similar techniques in O(n), using minimal change ordering and transposing of not adjacent elements.

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