Artigos e Materiais de Revistas Científicas - LIM/42

Artigos e Materiais de Revistas Científicas - LIM/42

 

A coleção de Artigos e Materiais de Revistas Científicas engloba artigos originais, artigos de revisão, artigos de atualização, artigos técnicos, relatos de experiências, resenhas, ensaios, editoriais, cartas ao editor, debates, notas científicas e técnicas, depoimentos, entrevistas e pontos de vista. Consideram-se como artigos científicos originais os trabalhos redigidos para divulgação de informações e resultados sobre determinada pesquisa científica, publicados em periódico científico após avaliação por outros pesquisadores.

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  • BATISTA, Rafael Loch; RODRIGUES, Andresa di Santi; NISHI, Mirian Yumie; GOMES, Nathalia Lisboa; FARIA JUNIOR, Jose Antonio Diniz; MORAES, Daniela Rodrigues de; CARVALHO, Luciani Renata; COSTA, Elaine Maria Frade; DOMENICE, Sorahia; MENDONCA, Berenice Bilharinho (PERGAMON-ELSEVIER SCIENCE LTD, OXFORD, ENGLAND, 2017)
    Androgen insensitivity syndrome (AIS) is the most common cause of 46,XY disorders of sex development (46,XY DSD). This syndrome is an X-linked inheritance disease and it is caused by mutations in the human androgen receptor ...
  • FRANCA, Monica M.; FUNARI, Mariana F. A.; LERARIO, Antonio M.; NISHI, Mirian Y.; PITA, Carmem C.; FONTENELE, Eveline G. P.; MENDONCA, Berenice B. (SPRINGER, NEW YORK, USA, 2017)
    Purpose Primary ovarian failure (POF) is characterized by amenorrhea, hypoestrogenism, and elevated gonadotropin levels in women leading to infertility under the age of 40 years. POF is a heterogeneous disease with different ...
  • GRINSPON, R. P.; BEDECARRAS, P.; BALLERINI, M. G.; INIGUEZ, G.; ROCHA, A.; RESENDE, E. A. Mantovani Rodrigues; BRITO, V. N.; MILANI, C.; GACITUA, V. Figueroa; CHIESA, A.; KESELMAN, A.; GOTTLIEB, S.; BORGES, M. F.; ROPELATO, M. G.; PICARD, J. -Y.; CODNER, E.; REY, R. A. (WILEY-BLACKWELL, HOBOKEN, USA, 2011)
    Male patients with an extra sex chromosome or autosome are expected to present primary hypogonadism at puberty owing to meiotic germ-cell failure. Scarce information is available on trisomy 21, a frequent autosomal aneuploidy. ...
  • HALPERN, B.; FARIA, A. M.; HALPERN, A. (PROUS SCIENCE, SA-THOMSON REUTERS, BARCELONA, SPAIN, 2011)
    The combination of bupropion and naltrexone is one of the most promising new possibilities for the treatment of obesity in an era of increasing prevalence of this disease and decreasing options for its pharmacological ...
  • ARAUJO, Ricardo Vieira; MACIEL, Ceres; HARTFELDER, Klaus; CAPURRO, Margareth Lara (PERGAMON-ELSEVIER SCIENCE LTD, OXFORD, ENGLAND, 2011)
    Insect disease vectors show diminished fecundity when infected with Plasmodium. This phenomenon has already been demonstrated in laboratory models such as Aedes aegypti, Anopheles gambiae and Anopheles stephensi. This study ...
  • RODRIGUES, Luiza Souza; CAU, Ana Carolina Arias; BUSSMANN, Luciane Zgoda; BASTIDA, Gabriela; BRUNETTO, Oscar H.; CORREA, Pedro Henrique Silveira; MARTIN, Regina Matsunaga (SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIA, RIO DE JANEIRO, RJ, BRAZIL, 2011)
    A loss of calcium-sensing receptor (CASR) function due to inactivating mutations can cause familial hypocalciuric hypercalcemia (FHH) or neonatal severe hyperparathyroidism (NSHPT). NSHPT represents the most severe expression ...
  • ALATZOGLOU, Kyriaki S.; KELBERMAN, Daniel; COWELL, Christopher T.; PALMER, Rodger; ARNHOLD, Ivo J. P.; MELO, Maria E.; SCHNABEL, Dirk; GRUETERS, Annette; DATTANI, Mehul T. (ENDOCRINE SOC, CHEVY CHASE, USA, 2011)
    Backgound and Aims: Correct gene dosage of SOX3 is critical for the development of the hypothalamo-pituitary axis. Both overdosage of SOX3, as a result of gene duplication, and loss of function resulting from expansion of ...
  • FARIA, Andre M.; PEREZ, Ricardo V.; MARCONDES, Jose A. M.; FREIRE, Daniel S.; BLASBALG, Roberto; SOARES JR., Jose; SIMOES, Kleber; HAYASHIDA, Sylvia A. Y.; PEREIRA, Maria A. A. (NATURE PUBLISHING GROUP, NEW YORK, USA, 2011)
    Background. A 33-year-old woman presented to an endocrinology clinic with a 5-year history of secondary amenorrhea. 2 years before presentation, she had noticed progressively worsening signs of virilization. Investigations. ...
  • DANILOVIC, Debora Lucia Seguro; MARTIN, Regina Matsunaga; CARUSO, Pedro; MARUI, Suemi (HOSPITAL CLINICAS, UNIV SAO PAULO, SAO PAULO, BRAZIL, 2011)
  • SILVA, Thatiana Evilen da; NISHI, Mirian Yumie; COSTA, Elaine Maria Frade; MARTIN, Regina Matsunaga; CARVALHO, Filomena Marino; MENDONCA, Berenice Bilharinho; DOMENICE, Sorahia (SPRINGER, NEW YORK, USA, 2011)
    WT1 mutations have been described in a variety of syndromes, including Denys-Drash syndrome (DDS), which is characterized by predisposition to Wilms' tumor, genital abnormalities and development of early nephropathy. The ...

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