Neurocognitive Characteristics of Individuals with Schizophrenia and Cocaine Dependence: Comparison of Currently Dependent and Remitted Groups

Por Peer, Jason, Bennett, Melanie E., Bellack, Alan S.
Publicado em 2009

Factors Associated with Weight Intervention Participation among People with Serious Mental Illness

Por Bennett, Lauren L., Cohen, Amy N., Young, Alexander S.
Publicado no J Nerv Ment Dis (2018)

Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitro

Por Wilson, Emma R., Kugathasan, Umaiyal, Abramov, Andrey Y., Clark, Alex J., Bennett, David L.H., Reilly, Mary M., Greensmith, Linda, Kalmar, Bernadett
Publicado no Neurobiol Dis (2018)

The RAISE Connection Program for Early Psychosis: Secondary Outcomes and Mediators and Moderators of Improvement

Por Marino, Leslie, Nossel, Ilana, Choi, Jean C., Nuechterlein, Keith, Wang, Yuanjia, Essock, Susan, Bennett, Melanie, McNamara, Karen, Mendon, Sapna, Dixon, Lisa
Publicado no J Nerv Ment Dis (2015)

Use of evoked potentials in preterm neonates.

Por Taylor, M. J., Saliba, E., Laugier, J.
Publicado em 1996

Case Series of Severe Neurologic Sequelae of Ebola Virus Disease during Epidemic, Sierra Leone

Por Howlett, Patrick J., Walder, Anna R., Lisk, Durodami R., Fitzgerald, Felicity, Sevalie, Stephen, Lado, Marta, N’jai, Abdul, Brown, Colin S., Sahr, Foday, Sesay, Foday, Read, Jonathon M., Steptoe, Paul J., Beare, Nicholas A.V., Dwivedi, Reena, Solbrig, Marylou, Deen, Gibrilla F., Solomon, Tom, Semple, Malcolm G., Scott, Janet T.
Publicado no Emerg Infect Dis (2018)

NMO-IgG: A Specific Biomarker for Neuromyelitis Optica

Por Weinshenker, Brian G., Wingerchuk, Dean M., Pittock, Sean J., Lucchinetti, Claudia F., Lennon, Vanda A.
Publicado em 2006

Management of Viral Central Nervous System Infections: A Primer for Clinicians

Por Bookstaver, P Brandon, Mohorn, Phillip L, Shah, Ansal, Tesh, Lauren D, Quidley, April M, Kothari, Ravish, Bland, Christopher M, Weissman, Sharon
Publicado no J Cent Nerv Syst Dis (2017)

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)

Twenty-nine Cases of Enterovirus-D68–associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview

Por Knoester, Marjolein, Helfferich, Jelte, Poelman, Randy, Van Leer-Buter, Coretta, Brouwer, Oebele F., Niesters, Hubert G. M.
Publicado no Pediatr Infect Dis J (2019)

Lepromatous leprosy and perianal tuberculosis: a case report and literature review

Por Parise-Fortes, Maria Rita, Lastória, Joel Carlos, Marques, Silvio Alencar, Putinatti, Maria Stella Ayres, Stolf, Hamilton Ometto, Marques, Mariângela Ester Alencar, Haddad, Vidal
Publicado em 2014

At-Risk Phenotype of Neurofibromatose-1 Patients: A Multicentre Case-Control Study

Por Sbidian, Emilie, Bastuji-Garin, Sylvie, Valeyrie-Allanore, Laurence, Ferkal, Salah, Lefaucheur, Jean P, Drouet, Alain, Brugière, Pierre, Vialette, Cédric, Combemale, Patrick, Barbarot, Sébastien, Wolkenstein, Pierre
Publicado em 2011

Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome

Por Kaissi, Ali Al, Grill, Franz, Safi, Hatem, Ghachem, Maher Ben, Chehida, Farid Ben, Klaushofer, Klaus
Publicado em 2007

AB 36. Primary lung carcinoid, a rare cause of paraparesis: report of a case and review of the literature

Por Visouli, Aikaterini N., Darwiche, Kaid, Kourtoglou, Georgios I., Zarogoulidis, Paul, Mpakas, Andreas, Machairiotis, Nikolaos, Stylianaki, Aikaterini, Christofis, Chistos, Katsikogiannis, Nikolaos, Tsakiridis, Kosmas, Courcoutsakis, Nicolaos, Zarogoulidis, Konstantinos
Publicado em 2012

Neurological impairment among heterozygote women for X-linked Adrenoleukodystrophy: a case control...

Por Habekost, Clarissa Troller, Schestatsky, Pedro, Torres, Vitor Felix, de Coelho, Daniella Moura, Vargas, Carmen Regla, Torrez, Vitor, Oses, Jean Pierre, Portela, Luis Valmor, Pereira, Fernanda dos Santos, Matte, Ursula, Jardim, Laura Bannach
Publicado em 2014

Distinct clinical, neuroimaging and genetic profiles of late-onset cobalamin C defects (cb1C): a report of 16 Chinese cases

Por Wang, Xianling, Yang, Yanhui, Li, Xuying, Li, Cunjiang, Wang, Chaodong
Publicado no Orphanet J Rare Dis (2019)

Muscle-Eye-Brain Disease

Por Shenoy, Anant M., Markowitz, Jennifer A., Bonnemann, Carsten G., Krishnamoorthy, Kalpathy, Bossler, Aaron D., Tseng, Brian S.
Publicado em 2010

Cluster headache

Por Leroux, Elizabeth, Ducros, Anne
Publicado em 2008

Late infantile metachromatic leukodystrophy: Clinical manifestations of five Taiwanese patients and Genetic features in Asia

Por Liaw, Hsiang-Ru, Lee, Hsiu-Fen, Chi, Ching-Shiang, Tsai, Chi-Ren
Publicado no Orphanet J Rare Dis (2015)

Texas Occurrence of Lyme Disease and Its Neurological Manifestations

Por Dandashi, Jad A, Nizamutdinov, Damir, Dayawansa, Samantha, Fonkem, Ekokobe, Huang, Jason H
Publicado no J Neuroinfect Dis (2016)