Oral peripheral nerve sheath tumors: A clinicopathological and immunohistochemical study of 32 cases in a Brazilian population

Por Franco, Talita, de Freitas Filho, Silas-Antonio-Juvencio, Muniz, Laís-Borges, de Faria, Paulo-Rogério, Loyola, Adriano-Mota, Cardoso, Sérgio-Vitorino
Publicado no J Clin Exp Dent (2017)

An atypical case of neurosarcoidosis presenting with neovascular glaucoma

Por Vereecken, Melissa, Hollanders, Karolien, De Bruyn, Deborah, Ninclaus, Virginie, De Zaeytijd, Julie, De Schryver, Ilse
Publicado no J Ophthalmic Inflamm Infect (2018)

Unilateral Idiopathic Sensory Trigeminal Nerve Paralysis in a Dog

Por Maria Luíza de Melo Dias, Ana Carolina Mortari
Publicado no Acta Scientiae Veterinariae (2017)

A rare case of concomitant sicca keratopathy and ipsilateral central facial palsy in Wallenberg’s dorsolateral medullary syndrome

Por De Bruyn, Deborah, Van Aken, Elisabeth, Herman, Kristien
Publicado no GMS Ophthalmol Cases (2017)

Carpal tunnel syndrome: long-term nerve conduction studies in 261 hands Síndrome do tunel do carpo...

Por Dante Guilherme Velasco Hardoim, Guilherme Bueno de Oliveira, João Aris Kouyoumdjian
Publicado em 2009-03-01

Loss of H3K27 tri-methylation is a diagnostic marker for Malignant Peripheral Nerve Sheath Tumors and an indicator for an inferior survival

Por Cleven, Arjen H.G., Al Sannaa, Ghadah A., Bruijn, Inge Briaire-de, Ingram, Davis R., van de Rijn, Matt, Rubin, Brian P., de Vries, Maurits, Watson, Kelsey, Torres, Keila E., Wang, Wei-Lien, van Duinen, Sjoerd, Hogendoorn, Pancras C. W., Lazar, Alexander J., Bovée, Judith V.M.G.
Publicado no Mod Pathol (2016)

Jaw reflexes and masseter electromyograms in mesencephalic and pontine lesions: an electrodiagnostic study.

Por Ongerboer De Visser, B W, Goor, C
Publicado em 1976

Critical Illness Neuromyopathy Complicating Akinetic Crisis in Parkinsonism: Report of 3 Cases

Por Capasso, Margherita, De Angelis, Maria Vittoria, Di Muzio, Antonio, Anzellotti, Francesca, Bonanni, Laura, Thomas, Astrid, Onofrj, Marco
Publicado no Medicine (Baltimore) (2015)

X-linked spinal and bulbar muscular atrophy (Kennedy's disease) with long-term electrophysiological evaluation: case report Atrofia muscular bulbo-espinal ligada ao cromossomo X (doença de Kennedy) com...

Por João Aris Kouyoumdjian, Maria da Penha Ananias Morita, Rogério Gayer Machado de Araújo
Publicado em 2005-03-01

Papiloma de plexo coroide em um cão

Por Marta Cristina Thomas Heckler, Didier Quevedo Cagnini, Renata dos Santos Ramos, Luiz Henrique de Araújo Machado
Publicado no Acta Scientiae Veterinariae (2013)

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Por Greenberg, F, Guzzetta, V, Montes de Oca-Luna, R, Magenis, R E, Smith, A C, Richter, S F, Kondo, I, Dobyns, W B, Patel, P I, Lupski, J R
Publicado em 1991

Optic Nerve Hypoplasia Syndrome: A Review of the Epidemiology and Clinical Associations

Por Garcia-Filion, Pamela, Borchert, Mark
Publicado em 2013

First case of congenital idiopathic hypohidrosis in China

Por Shi, Ge, Zhu, Cheng-Yao, Zhou, Ying, Yang, Yan-Ping, Fan, Yi-Ming
Publicado no An Bras Dermatol (2015)

Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype

Por Lamers, Ideke J.C., Reijnders, Margot R.F., Venselaar, Hanka, Kraus, Alison, Jansen, Sandra, de Vries, Bert B.A., Houge, Gunnar, Gradek, Gyri Aasland, Seo, Jieun, Choi, Murim, Chae, Jong-Hee, van der Burgt, Ineke, Pfundt, Rolph, Letteboer, Stef J.F., van Beersum, Sylvia E.C., Dusseljee, Simone, Brunner, Han G., Doherty, Dan, Kleefstra, Tjitske, Roepman, Ronald
Publicado no Am J Hum Genet (2017)

Histomorphometric and sympathetic innervation of the human superficial temporal artery

Por Sreenivasulu Reddy, Pramod Kumar, Keerthana Prasad
Publicado em 2011-01-01

Bilateral stapes agenesis: What can we find?

Por Mathieu Bergeron, Mathieu Côté
Publicado em 2017-01-01

A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3

Por Chew, Sheena, Balasubramanian, Ravikumar, Chan, Wai-Man, Kang, Peter B., Andrews, Caroline, Webb, Bryn D., MacKinnon, Sarah E., Oystreck, Darren T., Rankin, Jessica, Crawford, Thomas O., Geraghty, Michael, Pomeroy, Scott L., Crowley, William F., Jabs, Ethylin Wang, Hunter, David G., Grant, Patricia E., Engle, Elizabeth C.
Publicado em 2013

A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity

Por Roberti, Domenico, Conforti, Renata, Giugliano, Teresa, Brogna, Barbara, Tartaglione, Immacolata, Casale, Maddalena, Piluso, Giulio, Perrotta, Silverio
Publicado no Front Genet (2018)

Evaluation of agreement between tests for the diagnosis of leprosy

Por Alison R. Silva, Marcos Fabiano A. Queiroz, Edna A. Y. Ishikaw, Maria do Perpétuo S. A. Silvestre, Marilia B. Xavier
Publicado no Jornal Brasileiro de Patologia e Medicina Laboratorial (2017)