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A real world multi center study on efficacy and safety of natalizumab in Indian patients with multiple sclerosis

Autor: Mathew, Thomas, Kamath, Vikram, John, Saji K, Netravathi, M, Iyer, Rajesh B, Raghavendra, S, Kumar, Suresh, Neeharika, M.L., Gupta, Salil, Murgod, Uday, Shivakumar, R., Annadure, Ravi K, Ichaporia, Nasli, Rohatgi, Anshu, Nair, Sruthi S, Yareeda, Sireesha, Anand, Bawani, Singh, Prabhjeet, Renukaradhya, Umashankar, Arulselvan, V., Reddy, Y Muralidhar, Surya, Nirmal, Sarma, G.R.K., Nadig, Raghunandan, Deepalam, Saikanth, Sharath Kumar, G.G., Satishchandra, P., Singhal, Bhim Sen, Parry, Gareth

Publikováno v: In Multiple Sclerosis and Related Disorders October 2022 66

Congenital myasthenic syndrome: Ten years clinical experience from a quaternary care south-Indian hospital

Autor: Wadwekar, Vaibhav, Nair, Sruthi S., Tandon, Vaibhav, Kuruvilla, Abraham, Nair, Muralidharan

Publikováno v: In Journal of Clinical Neuroscience February 2020 72:238-243

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Genotype-phenotype correlations in valosin-containing protein disease

Autor: Schiava, Marianela, Ikenaga, Chiseko, Villar-Quiles, Rocío Nur, Caballero-Ávila, Marta, Topf, Ana, Nishino, Ichizo, Kimonis, Virginia, Udd, Bjarne, Schoser, Benedikt, Zanoteli, Edmar, Souza, Paulo Victor Sgobbi, Tasca, Giorgio, Lloyd, Thomas, Lopez-de Munain, Adolfo, Paradas, Carmen, Pegoraro, Elena, Nadaj-Pakleza, Aleksandra, De Bleecker, Jan, Badrising, Umesh, Alonso-Jiménez, Alicia, Kostera-Pruszczyk, Anna, Miralles, Francesc, Shin, Jin-Hong, Bevilacqua, Jorge Alfredo, Olivé, Montse, Vorgerd, Matthias, Kley, Rudi, Brady, Stefen, Williams, Timothy, Domínguez-González, Cristina, Papadimas, George K, Warman-Chardon, Jodi, Claeys, Kristl G, de Visser, Marianne, Muelas, Nuria, LaForet, Pascal, Malfatti, Edoardo, Alfano, Lindsay N, Nair, Sruthi S, Manousakis, Georgios, Kushlaf, Hani A, Harms, Matthew B, Nance, Christopher, Ramos-Fransi, Alba, Rodolico, Carmelo, Hewamadduma, Channa, Cetin, Hakan, García-García, Jorge, Pál, Endre, Farrugia, Maria Elena, Lamont, Phillipa J, Quinn, Colin, Nedkova-Hristova, Velina, Peric, Stojan, Luo, Sushan, Oldfors, Anders, Taylor, Kate, Ralston, Stuart, Stojkovic, Tanya, Weihl, Conrad, Diaz-Manera, Jordi, VCP International Study Group

Publikováno v: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Journal of neurology, neurosurgery and psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 93(10), 1099-1111. BMJ PUBLISHING GROUP
Journal of Neurology, Neurosurgery and Psychiatry, 93(10):328921, 1099-1111. BMJ Publishing Group

[ntroduction] Valosin-containing protein (VCP) disease, caused by mutations in the VCP gene, results in myopathy, Paget's disease of bone (PBD) and frontotemporal dementia (FTD). Natural history and genotype-phenotype correlation data are limited. Th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f2d1f3b8c1678f2ecadb77fcd371913
https://hdl.handle.net/1887/3505241