Central syntropic effects elicited by trigeminal proprioceptive equilibrium in Alzheimer’s disease: a case report

Por De Cicco, Vincenzo
Publicado em 2012

Cerebro-afferent vessel and pupillary basal diameter variation induced by stomatognathic trigeminal proprioception: a case report

Por De Cicco, Vincenzo
Publicado em 2012

Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number...

Por Hwang, Eileen S., Morgan, Denise J., Pennington, Katie L., Owen, Leah A., Fingert, John H., Bernstein, Paul S., DeAngelis, Margaret M.
Publicado no BMC Med Genet (2019)

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)

Facial Reanimation After Facial Nerve Injury Using Hypoglossal to Facial Nerve Anastomosis: The Gruppo Otologico Experience

Por Tanbouzi Husseini, Sami, Kumar, David Victor, De Donato, Giuseppe, Almutair, Tamama, Sanna, Mario
Publicado em 2012

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

Por Jongmans, M C J, Admiraal, R J, van der Donk, K P, Vissers, L E L M, Baas, A F, Kapusta, L, van Hagen, J M, Donnai, D, de Ravel, T J, Veltman, J A, van Kessel, A Geurts, De Vries, B B A, Brunner, H G, Hoefsloot, L H, van Ravenswaaij, C M A
Publicado em 2006

Hypoganglionosis in pregnancy: a case report

Por Figueiredo, Ana, Martins, Isabel, Palma, Fátima, Alves, Maria José, de Barros, Carlos
Publicado em 2012

Sympathetic nerve traffic and circulating norepinephrine levels in RGS2-deficient mice

Por Tank, Jens, Obst, Michael, Diedrich, Andrè, Brychta, Robert J., Blumer, Kendall J., Heusser, Karsten, Jordan, Jens, Luft, Friedrich C., Gross, Volkmar
Publicado no Auton Neurosci (2007)

Facial Nerve Outcome after Vestibular Schwannoma Surgery: Our Experience

Por Rinaldi, Vittorio, Casale, Manuele, Bressi, Federica, Potena, Massimiliano, Vesperini, Emanuela, De Franco, Antonio, Silvestri, Sergio, Zini, Carlo, Salvinelli, Fabrizio
Publicado em 2012

Tone-in-Noise Detection Deficits in Elderly Patients with Clinically Normal Hearing

Por Ralli, Massimo, Greco, Antonio, De Vincentiis, Marco, Sheppard, Adam, Cappelli, Giampietro, Neri, Ilaria, Salvi, Richard
Publicado no Am J Otolaryngol (2018)

Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion

Por R.M. Pabón Meneses, G. Azcona Ganuza, J. Urriza Mena, A. Ibiricu Yanguas, L. Gila Useros, I. García de Gurtubay
Publicado em 2022-05-01

Hallazgos clínico-neurofisiológicos en neuropatías hereditarias sensibles a la presión con deleción del cromosoma 17p11.2

Por R.M. Pabón Meneses, G. Azcona Ganuza, J. Urriza Mena, A. Ibiricu Yanguas, L. Gila Useros, I. García de Gurtubay
Publicado em 2022-05-01

Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature

Por de Silva, Nipun Lakshitha, Weeratunga, Praveen, Umapathi, Thirugnanam, Malavige, Neelika, Chang, Thashi
Publicado no J Med Case Rep (2019)

Development and subsequent neural tube effects on the excitability of cultured Xenopus myocytes

Por DeCino, P, Kidokoro, Y
Publicado no J Neurosci (1985)

Expression of RAD21 Immunoreactivity in Myenteric Neurons of the Human and Mouse Small Intestine

Por Bianco, Francesca, Eisenman, Seth T., Colmenares Aguilar, Maria Gabriela, Bonora, Elena, Clavenzani, Paolo, Linden, David R., De Giorgio, Roberto, Farrugia, Gianrico, Gibbons, Simon J.
Publicado no Neurogastroenterol Motil (2018)

Drug-resistant epilepsy: Definition and treatment alternatives

Por F.J. López González, X. Rodríguez Osorio, A. Gil-Nagel Rein, M. Carreño Martínez, J. Serratosa Fernández, V. Villanueva Haba, A.J. Donaire Pedraza, J.M. Mercadé Cerdá
Publicado em 2015-09-01

Preliminary study of visual pathway in ocular hypertension patients using magnetic resonance diffusion tensor and 3D-OCT

Por Zhi Tan, Rong Huang, Qing Guo, De-Mao Liang, Yan-Hua Pang
Publicado em 2020-08-01

Recurrent Optic Neuritis as the Initial Symptom in Demyelinating Diseases

Por Falcão-Gonçalves, Alessandra Billi, Bichuetti, Denis Bernardi, de Oliveira, Enedina Maria Lobato
Publicado no J Clin Neurol (2018)

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing

Por Quintáns, B., Pardo, J., Campos, B., Barros, F., Volpini, V., Carracedo, Á., Sobrido, M.J.
Publicado em 2011

Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies

Por Semmler, Anna-Lena, Sacconi, Sabrina, Bach, J Elisa, Liebe, Claus, Bürmann, Jan, Kley, Rudolf A, Ferbert, Andreas, Anderheiden, Roland, Van den Bergh, Peter, Martin, Jean-Jacques, De Jonghe, Peter, Neuen-Jacob, Eva, Müller, Oliver, Deschauer, Marcus, Bergmann, Markus, Schröder, J Michael, Vorgerd, Matthias, Schulz, Jörg B, Weis, Joachim, Kress, Wolfram, Claeys, Kristl G
Publicado no Orphanet J Rare Dis (2014)