Search Results - "MISBAHUDDIN, A"

A Performance Study of a Fast-Rate WLAN Fingerprint Measurement Collection Method by Schmidt, Erick, Mohammed, Misbahuddin A., Akopian, David

“…Indoor positioning systems exploiting wireless local area network (WLAN) signal measurements, such as received signal strength (RSS), are gaining popularity…”
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How satisfied are cervical dystonia patients after 3 years of botulinum toxin type A treatment? Results from a prospective, long-term observational study by Colosimo, Carlo, Charles, David, Misra, Vijay P., Maisonobe, Pascal, Om, Savary

“…Background Patients with cervical dystonia (CD) typically require regular injections of botulinum toxin to maintain symptomatic control. We aimed to document…”
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Secondary normal pressure hydrocephalus post gamma knife radiosurgery for treatment of vestibular schwannoma by Krommyda, M, Pollock, J, Misbahuddin, A

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INTEREST IN CD2, a global patient-centred study of long-term cervical dystonia treatment with botulinum toxin by Misra, Vijay P., Colosimo, Carlo, Charles, David, Chung, Tae Mo, Maisonobe, Pascal, Om, Savary

“…Background Longitudinal cohort studies provide important information about the clinical effectiveness of an intervention in the routine clinical setting, and…”
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Correction to: How satisfied are cervical dystonia patients after 3 years of botulinum toxin type A treatment? Results from a prospective, long-term observational study by Colosimo, Carlo, Charles, David, Misra, Vijay P., Maisonobe, Pascal, Om, Savary

“…The article How satisfied are cervical dystonia patients after 3 years of botulinum toxin type A treatment?…”
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POC20 Do patients like being present when their letters are dictated, and does it matter? by De Silva, R, Misbahuddin, A, Grayson, K, Mikhail, S

“…Patients in the UK have a right to receive copies of correspondence relating to their treatment, and some clinicians dictate letters in their presence too…”
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A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm by MISBAHUDDIN, A, PLACZEK, M. R, CHAUDHURI, K. R, WOOD, N. W, BHATIA, K. P, WARNER, T. T

“…Abnormalities in dopamine neurotransmission are thought to underlie the generation of dystonic movements. The authors performed a case-control allelic…”
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Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene by Placzek, M R, Misbahuddin, A, Chaudhuri, K Ray, Wood, N W, Bhatia, K P, Warner, T T

“…The objective was to assess whether polymorphisms in the dopamine receptor and transporter genes are associated with development of primary cervical dystonia…”
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Dystonia: an update on genetics and treatment by Misbahuddin, A, Warner, T T

“…Recent years have seen many advances in our understanding of the genetics of the dystonias, with 13 loci identified to date. The DYT1 gene, which causes most…”
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Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C by Pelletier, Félixe, Cayami, Ferdy K, Mirchi, Amytice, Saikali, Stephan, Tran, Luan T, Ulrick, Nicole, van Spaendonk, Rosalina M L, Naidu, Sakkubai, Pohl, Daniela, Gibson, William T, Demos, Michelle, Goizet, Cyril, Tejera-Martin, Ingrid, Potic, Ana, Fogel, Brent L, Brais, Bernard, Sylvain, Michel, Sébire, Guillaume, Lourenço, Charles Marques, Catsman-Berrevoets, Coriene, Pinto, Pedro S, Tirupathi, Sandya, Strømme, Petter, Gieruszczak-Bialek, Dorota, Krägeloh-Mann, Ingeborg, Mierzewska, Hanna, Philippi, Heike, Rankin, Julia, Atik, Tahir, Banwell, Brenda, Benko, William S, Blaschek, Astrid, Bley, Annette, Boltshauser, Eugen, Bratkovic, Drago, Brozova, Klara, Cimas, Icíar, Clough, Christopher, Dinopoulos, Argirios, Dolan, Gail, Faletra, Flavio, Fernandez, Raymond, Fletcher, Janice, Garcia Garcia, Maria Eugenia, Gasparini, Paolo, Gburek-Augustat, Janina, Gonzalez Moron, Dolores, Hamati, Aline, Harting, Inga, Hertzberg, Christoph, Hill, Alan, Kauffman, Marcelo, Kluger, Gerhard, Kotzaeridou, Urania, La Piana, Roberta, Liston, Eriskay, McClintock, William, McEntagart, Meriel, McKenzie, Fiona, Melançon, Serge, Misbahuddin, Anjum, Suri, Mohnish, Monton, Fernando I, Murphy, Raymond P J, Nickel, Miriam, Onay, Hüseyin, Orcesi, Simona, Özkınay, Ferda, Patzer, Steffi, Pedro, Helio, Pineda Marfa, Mercedes, Pizzino, Amy, Plecko, Barbara, Poll-The, Bwee Tien, Popovic, Vera, Rating, Dietz, Rioux, Marie-France, Ronan, Anne, Ostergaard, John R, Rossignol, Elsa, Sanchez-Carpintero, Rocio, Schossig, Anna, Sønderberg Roos, Laura K, Synofzik, Matthis, Sztriha, László, Tibussek, Daniel, Timmann, Dagmar, Tonduti, Davide, van de Warrenburg, Bart P, Vázquez-López, Maria, Venkateswaran, Sunita, Wasling, Pontus, Webster, Richard I, Wiegand, Gert, Yoon, Grace, Rotteveel, Joost, Schiffmann, Raphael, Vanderver, Adeline, Martos-Moreno, Gabriel Á, Bernard, Geneviève

“…Abstract Context 4H or POLR3-related leukodystrophy is an autosomal recessive disorder typically characterized by hypomyelination, hypodontia, and…”
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Natural History of Vanishing White Matter by Hamilton, Eline M. C., van der Lei, Hannemieke D. W., Lourenço, Charles M., Naidu, Sakkubai, Mierzewska, Hanna, de Vet, Henrica C. W., Uitdehaag, Bernard M. J., Lissenberg‐Witte, Birgit I., Aldhalaan, H., Alves, D., Appleton, R., Arslan, E.A., Baethmann, M., Banwell, B., Barbot, C., Bertini, E., Bley, A., Bollen, L., Boltshauser, E., Bower, S., Bravo Oro, A., Campos, M.M., Carr, L., Chan, A.K.J., Clarke, A., Crow, Y., Csányi, B., Del Rossario Aldao, M., D'Hooghe, M., El Helou, J, Fallon, P., Ferlini, A., Ferro, J.M., Fluss, J., Fontenelle, L., Garone, C., Geldhoff, M., Glamuzina, E., Góes, F., Gonzalez, V., Guarda, C., Gulati, S., Güler, S., Horvath, R., Jagadeesh, S., Kaczorowska, M., Kankirawatana, P., Karall, D., King, M.D., Krägeloh‐Mann, I., Lehman, A., Liptai, Z., Livingston, J.H., Maes, M., Majumdar, A., Mandel, H., McEntagart, M., Morton, R., Moura de Souza, C.F., Mundy, H., Naess, K., Naismith, K., Newton, R.W., Noetzel, M.J., O'Brien, B, Okálová, K., Østergaard, J.R., Pato Pato, A., Pera, J., Perlman, S., Philippart, M., Régal, L., Rice, C.M., Rossignol, E., Rubin, J.P., Salvi, F., Sampaio, H., Sánchez Herrero, J., Santos, E., Sessa, M., Sharma, S., Shearn, J., Shoffner, J., Skranes, J.S., Sparagana, S.P., Storey, E., Sztriha, L., Tatli, B., Tekturk, P., Tennison, M., Tirupathi, S., Toledo Bravo de Laguna, L., Tuna, M.A., Valverde, A., van Coster, R., Vasconcelos, M., Vogt, H., von Kleist‐Retzow, J.C., Wong, S.S.N., Yavuz, H.

“…Objective To comprehensively describe the natural history of vanishing white matter (VWM), aiming at improving counseling of patients/families and providing…”
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Posterior subthalamic area deep brain stimulation for treatment of tremor and dystonia in Wilson's disease by Low, Hu Liang, Alexander, Sian K., Misbahuddin, Anjum, Gillett, Godfrey T.

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011 Multifocal intracranial haemorrhage as a manifestation of reversible cerebral vasoconstriction syndrome by Tuohy, O, Osman, C O, Chawda, S C, Chaudhuri, A C, Misbahuddin, A M

“…A 56-year-old lady presented 3 days following the acute onset of a severe, occipital headache on examination a right homonymous hemianopia was detected. CT…”
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Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells by Misbahuddin, Anjum, Placzek, Mark R., Taanman, Jan-Willem, Gschmeissner, Steve, Schiavo, Giampietro, Cooper, J. Mark, Warner, Thomas T.

“…A single GAG deletion in the DYT1 gene causes primary early‐onset, generalized torsion dystonia. The DYT1 protein product, torsinA, belongs to the AAA+ family…”
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A Performance Study of a Fast-Rate WLAN Fingerprint Measurement Collection Method by Schmidt, Erick, Mohammed, Misbahuddin A, Akopian, David

“…IEEE Trans. Instrum. Meas., vol. 67, no. 10, pp. 2273-2281, Oct. 2018 Indoor positioning systems exploiting WLAN signal measurements such as Received Signal…”
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Analysis of the ϵ-sarcoglycan gene in familial and sporadic myoclonus-dystonia: Evidence for genetic heterogeneity by Valente, Enza-Maria, Misbahuddin, Anjum, Brancati, Francesco, Placzek, Mark R., Garavaglia, Barbara, Salvi, Sergio, Nemeth, Andrea, Shaw-Smith, Charles, Nardocci, Nardo, Bentivoglio, Anna-Rita, Berardelli, Alfredo, Eleopra, Roberto, Dallapiccola, Bruno, Warner, Thomas T.

“…The ϵ‐sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus for inherited myoclonus–dystonia. Linkage to the SGCE locus has…”
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