Artigos e Materiais de Revistas Científicas - FCM

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Artigos e Materiais de Revistas Científicas - FCM

 

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  • do Nascimento, Andre Luiz; dos Santos, Neide Ferreira; Pelagio, Fernanda Campos; Teixeira, Simone Aparecida; De Moraes Ferrari, Elenice A.; Langone, Francesco (AmsterdamElsevier, 2012)
    Temporal lobe epilepsy (TLE) is the most common type of human epilepsy and has been related with extensive loss of hippocampal pyramidal and dentate hilar neurons and gliosis. Many characteristics of TLE are reproduced in ...
  • Costa Araujo, Priscila Pereira; Marcello, Marjory Alana; Tincani, Alfio Jose; Trindade Guilhen, Ana Carolina; Morari, Elaine Cristina; Ward, Laura Sterian (JenaElsevier, 2012)
    Literature has consistently shown associations of BRAFV600E mutation with papillary thyroid cancer clinical features. However, the clinical utility of BRAF expression has not been clinically explored so far. We studied 67 ...
  • Solomon, Benjamin D.; Bear, Kelly A.; Wyllie, Adrian; Keaton, Amelia A.; Dubourg, Christele; David, Veronique; Mercier, Sandra; Odent, Sylvie; Hehr, Ute; Paulussen, Aimee; Clegg, Nancy J.; Delgado, Mauricio R.; Bale, Sherri J.; Lacbawan, Felicitas; Ardinger, Holly H.; Aylsworth, Arthur S.; Bhengu, Ntombenhle Louisa; Braddock, Stephen; Brookhyser, Karen; Burton, Barbara; Gaspar, Harald; Grix, Art; Horovitz, Dafne; Kanetzke, Erin; Kayserili, Hulya; Lev, Dorit; Nikkel, Sarah M.; Norton, Mary; Roberts, Richard; Saal, Howard; Schaefer, G. B.; Schneider, Adele; Smith, Erika K.; Sowry, Ellen; Spence, M. Anne; Shalev, Stavit A.; Steiner, Carlos E.; Thompson, Elizabeth M.; Winder, Thomas L.; Balog, Joan Z.; Hadley, Donald W.; Zhou, Nan; Pineda-Alvarez, Daniel E.; Roessler, Erich; Muenke, Maximilian (LondonB M J Publishing Group, 2012)
    Background Holoprosencephaly (HPE), the most common malformation of the human forebrain, may result from mutations in over 12 genes. Sonic Hedgehog (SHH) was the first such gene discovered; mutations in SHH remain the most ...
  • do Nascimento, Andre Luiz; dos Santos, Neide Ferreira; Pelagio, Fernanda Campos; Teixeira, Simone Aparecida; de Moraes Ferrari, Elenice A.; Langone, Francesco (AmsterdamElsevier, 2012)
  • Freitas, Erika L.; Gribble, Susan M.; Simioni, Milena; Vieira, Tarsis P.; Prigmore, Elena; Krepischi, Ana C.; Rosenberg, Carla; Pearson, Peter L.; Melo, Debora G.; Gil-da-Silva-Lopes, Vera Lucia (AmsterdamElsevier, 2012)
    Submicroscopic chromosomal anomalies play an important role in the etiology of craniofacial malformations, including midline facial defects with hypertelorism (MFDH). MFDH is a common feature combination in several conditions, ...