Treatment of excessive daytime sleepiness in patients with Parkinson's Disease with modafinil von NIEVES, Anette V, LANG, Anthony E

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Acute onset dystonic camptocormia caused by lenticular lesions von Nieves, Anette V., Miyasaki, Janis M., Lang, Anthony E.

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Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study von Westenberger, Ana, Skrahina, Volha, Usnich, Tatiana, Beetz, Christian, Vollstedt, Eva-Juliane, Laabs, Björn-Hergen, Paul, Jefri J, Curado, Filipa, Skobalj, Snezana, Gaber, Hanaa, Olmedillas, Maria, Bogdanovic, Xenia, Ameziane, Najim, Schell, Nathalie, Aasly, Jan Olav, Afshari, Mitra, Agarwal, Pinky, Aldred, Jason, Alonso-Frech, Fernando, Anderson, Roderick, Araújo, Rui, Arkadir, David, Avenali, Micol, Balal, Mehmet, Benizri, Sandra, Bette, Sagari, Bhatia, Perminder, Bonello, Michael, Braga-Neto, Pedro, Brauneis, Sarah, Cardoso, Francisco Eduardo Costa, Cavallieri, Francesco, Classen, Joseph, Cohen, Lisa, Coletta, Della, Crosiers, David, Cullufi, Paskal, Dashtipour, Khashayar, Demirkiran, Meltem, de Carvalho Aguiar, Patricia, De Rosa, Anna, Djaldetti, Ruth, Dogu, Okan, Dos Santos Ghilardi, Maria Gabriela, Eggers, Carsten, Elibol, Bulent, Ellenbogen, Aaron, Ertan, Sibel, Fabiani, Giorgio, Falkenburger, Björn H, Farrow, Simon, Fay-Karmon, Tsviya, Ferencz, Gerald J, Fonoff, Erich Talamoni, Fragoso, Yara Dadalti, Genç, Gençer, Gorospe, Arantza, Grandas, Francisco, Gruber, Doreen, Gudesblatt, Mark, Gurevich, Tanya, Hagenah, Johann, Hanagasi, Hasmet A, Hassin-Baer, Sharon, Hauser, Robert A, Hernández-Vara, Jorge, Herting, Birgit, Hinson, Vanessa K, Hogg, Elliot, Hu, Michele T, Hummelgen, Eduardo, Hussey, Kelly, Infante, Jon, Isaacson, Stuart H, Jauma, Serge, Koleva-Alazeh, Natalia, Kuhlenbäumer, Gregor, Kühn, Andrea, Litvan, Irene, López-Manzanares, Lydia, Luxmore, McKenzie, Manandhar, Sujeena, Marcaud, Veronique, Markopoulou, Katerina, Marras, Connie, McKenzie, Mark, Matarazzo, Michele, Merello, Marcelo, Mollenhauer, Brit, Morgan, John C, Mullin, Stephen, Musacchio, Thomas, Myers, Bennett, Negrotti, Anna, Nieves, Anette, Nitsan, Zeev, Oskooilar, Nader, Öztop-Çakmak, Özgür, Pal, Gian, Pavese, Nicola

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Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study von Westenberger, Ana, Skrahina, Volha, Usnich, Tatiana, Beetz, Christian, Vollstedt, Eva-Juliane, Laabs, Bjoern-Hergen, Paul, Jefri J, Curado, Filipa, Skobalj, Snezana, Gaber, Hanaa, Olmedillas, Maria, Bogdanovic, Xenia, Ameziane, Najim, Schell, Nathalie, Aasly, Jan Olav, Afshari, Mitra, Agarwal, Pinky, Aldred, Jason, Alonso-Frech, Fernando, Anderson, Roderick, Araujo, Rui, Arkadir, David, Avenali, Micol, Balal, Mehmet, Benizri, Sandra, Bette, Sagari, Bhatia, Perminder, Bonello, Michael, Braga-Neto, Pedro, Brauneis, Sarah, Cardoso, Francisco Eduardo Costa, Cavallieri, Francesco, Classen, Joseph, Cohen, Lisa, Coletta, Della, Crosiers, David, Cullufi, Paskal, Dashtipour, Khashayar, Demirkiran, Meltem, Aguiar, Patricia de Carvalho, De Rosa, Anna, Djaldetti, Ruth, Dogu, Okan, Ghilardi, Maria Gabriela dos Santos, Eggers, Carsten, Elibol, Bulent, Ellenbogen, Aaron, Ertan, Sibel, Fabiani, Giorgio, Falkenburger, Bjoern H, Farrow, Simon, Fay-Karmon, Tsviya, Ferencz, Gerald J, Fonoff, Erich Talamoni, Fragoso, Yara Dadalti, Genc, Gencer, Gorospe, Arantza, Grandas, Francisco, Gruber, Doreen, Gudesblatt, Mark, Gurevich, Tanya, Hagenah, Johann, Hanagasi, Hasmet A, Hassin-Baer, Sharon, Hauser, Robert A, Hernandez-Vara, Jorge, Herting, Birgit, Hinson, Vanessa K, Hogg, Elliot, Hu, Michele T, Hummelgen, Eduardo, Hussey, Kelly, Infante, Jon, Isaacson, Stuart H, Jauma, Serge, Koleva-Alazeh, Natalia, Kuhlenbaeumer, Gregor, Kuehn, Andrea, Litvan, Irene, Lopez-Manzanares, Lydia, Luxmore, McKenzie, Manandhar, Sujeena, Marcaud, Veronique, Markopoulou, Katerina, Marras, Connie, McKenzie, Mark, Matarazzo, Michele, Merello, Marcelo, Mollenhauer, Brit, Morgan, John C, Mullin, Stephen, Musacchio, Thomas, Myers, Bennett, Negrotti, Anna, Nieves, Anette, Nitsan, Zeev, Oskooilar, Nader, Oztop-Cakmak, Ozgur, Pal, Gian, Pavese, Nicola

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Randomized trial of IPX066, carbidopa/levodopa extended release, in early Parkinson's disease von Pahwa, Rajesh, Lyons, Kelly E, Hauser, Robert A, Fahn, Stanley, Jankovic, Joseph, Pourcher, Emmanuelle, Hsu, Ann, O'Connell, Martin, Kell, Sherron, Gupta, Suneel

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Conversion to carbidopa and levodopa extended-release (IPX066) followed by its extended use in patients previously taking controlled-release carbidopa-levodopa for advanced Parkins... von Tetrud, James, Nausieda, Paul, Kreitzman, David, Liang, Grace S, Nieves, Anette, Duker, Andrew P, Hauser, Robert A, Farbman, Eric S, Ellenbogen, Aaron, Hsu, Ann, Kell, Sherron, Khanna, Sarita, Rubens, Robert, Gupta, Suneel

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Heterozygosity for a mutation in the Parkin gene leads to later onset Parkinson disease von FOROUD, T, UNIACKE, S. K, LIU, L, PANKRATZ, N, RUDOLPH, A, HALTER, C, SHULTS, C, MARDER, K, CONNEALLY, P. M, NICHOLS, W. C

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Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia von Pankratz, Nathan, Byder, Lisa, Halter, Cheryl, Rudolph, Alice, Shults, Clifford W., Conneally, P. Michael, Foroud, Tatiana, Nichols, William C.

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Significant Linkage of Parkinson Disease to Chromosome 2q36-37 von Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana

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Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations von Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana

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Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families von Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Murrell, Jill, Rudolph, Alice, Shults, Clifford W., Conneally, P. Michael, Foroud, Tatiana

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Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease von Nichols, William C., Uniacke, Sean K., Pankratz, Nathan, Reed, Terry, Simon, David K., Halter, Cheryl, Rudolph, Alice, Shults, Clifford W., Conneally, P. Michael, Foroud, Tatiana

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Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea von Fox, Susan H., Nieves, Anette, Bergeron, Catherine, Lang, Anthony E.

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Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study von Westenberger, Ana, Skrahina, Volha, Usnich, Tatiana, Laabs, Björn-hergen, Paul, Jefri J, Curado, Filipa, Skobalj, Snezana, Olmedillas, Maria, Bogdanovic, Xenia, Schell, Nathalie, Agarwal, Pinky, Anderson, Roderick, Araújo, Rui, Arkadir, David, Avenali, Micol, Benizri, Sandra, Bette, Sagari, Braga-neto, Pedro, Cardoso, Francisco Eduardo Costa, Crosiers, David, Demirkiran, Meltem, De Carvalho Aguiar, Patricia, Djaldetti, Ruth, Dogu, Okan, Dos Santos Ghilardi, Maria Gabriela, Eggers, Carsten, Elibol, Bulent, Ertan, Sibel, Fabiani, Giorgio, Falkenburger, Björn H, Farrow, Simon, Fay-karmon, Tsviya, Ferencz, Gerald J, Fonoff, Erich Talamoni, Fragoso, Yara Dadalti, Gruber, Doreen, Gudesblatt, Mark, Gurevich, Tanya, Hagenah, Johann, Hanagasi, Hasmet A, Hassin-baer, Sharon, Hu, Michele T, Hummelgen, Eduardo, Hussey, Kelly, Infante, Jon, Kuhlenbäumer, Gregor, Kühn, Andrea, Manandhar, Sujeena, Markopoulou, Katerina, Marras, Connie, Mckenzie, Mark, Merello, Marcelo, Mollenhauer, Brit, Myers, Bennett, Negrotti, Anna, Nitsan, Zeev, Pavese, Nicola, Percesepe, Antonio, Piccoli, Tommaso, Prell, Tino, Pulera, Mark, Raw, Jason, Reetz, Kathrin, Reiner, Johnathan, Rosenberg, David, Ruiz-lopez, Marta, Santos-lobato, Bruno Lopes, Saunders-pullman, Rachel, Schlesinger, Ilana, Schofield, Christine M, Schumacher-schuh, Artur F, Scott, Burton, Sesar, Ángel, Silverdale, Monty, Sophia, Rani, Spitz, Mariana, Stocchi, Fabrizio, Tai, Yen F, Terwecoren, Annelies, Thonke, Sven, Tönges, Lars, Tumas, Vitor, Urban, Peter Paul, Vacca, Laura, Valente, Enza Maria, Valzania, Franco, Vela-desojo, Lydia, Weill, Caroline, Weise, David, Wojcieszek, Joanne, Yalcin-cakmakli, Gul, Zittel, Simone, Zlotnik, Yair, Balck, Alexander, Hanssen, Henrike, Borsche, Max, Lohmann, Katja, Kasten, Meike, Brüggemann, Norbert, Bauer, Peter

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The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update von Maurer, Marcus, Magerl, Markus, Betschel, Stephen, Aberer, Werner, Ansotegui, Ignacio J., Aygören‐Pürsün, Emel, Banerji, Aleena, Bara, Noémi‐Anna, Boccon‐Gibod, Isabelle, Bork, Konrad, Bouillet, Laurence, Boysen, Henrik Balle, Brodszki, Nicholas, Busse, Paula J., Bygum, Anette, Caballero, Teresa, Cancian, Mauro, Castaldo, Anthony, Cohn, Danny M., Csuka, Dorottya, Farkas, Henriette, Gompels, Mark, Gower, Richard, Grumach, Anete S., Guidos‐Fogelbach, Guillermo, Hide, Michihiro, Kang, Hye‐Ryun, Kaplan, Allen Phillip, Katelaris, Constance, Kiani‐Alikhan, Sorena, Lei, Wei‐Te, Lockey, Richard, Longhurst, Hilary, Lumry, William R., MacGinnitie, Andrew, Malbran, Alejandro, Martinez Saguer, Inmaculada, Matta, Juan José, Nast, Alexander, Nguyen, Dinh, Nieto‐Martinez, Sandra A., Pawankar, Ruby, Peter, Jonathan, Porebski, Grzegorz, Prior, Nieves, Reshef, Avner, Riedl, Marc, Ritchie, Bruce, Rafique Sheikh, Farrukh, Smith, William B., Spaeth, Peter J., Stobiecki, Marcin, Toubi, Elias, Varga, Lilian Agnes, Weller, Karsten, Zanichelli, Andrea, Zhi, Yuxiang, Zuraw, Bruce, Craig, Timothy

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International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency von Caballero, Teresa, MD, PhD, Farkas, Henriette, MD, PhD, DSc, Bouillet, Laurence, MD, PhD, Bowen, Tom, MD, Gompel, Anne, MD, PhD, Fagerberg, Christina, MD, Bjökander, Janne, MD, Bork, Konrad, MD, Bygum, Anette, MD, Cicardi, Marco, MD, de Carolis, Caterina, MD, Frank, Michael, MD, Gooi, Jimmy H.C., MD, Longhurst, Hilary, MD, Martínez-Saguer, Inmaculada, MD, Nielsen, Erik Waage, MD, Obtulowitz, Krystina, MD, Perricone, Roberto, MD, Prior, Nieves, MD

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Cutaneous Expression of Familial Cancer Syndromes von Andersen, Anne-Johanne, Schierbeck, Juliane, Bygum, Anette, Puente-Pablo, Nieves

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Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group von Cicardi, M., Aberer, W., Banerji, A., Bas, M., Bernstein, J. A., Bork, K., Caballero, T., Farkas, H., Grumach, A., Kaplan, A. P., Riedl, M. A., Triggiani, M., Zanichelli, A., Zuraw, B.

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International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency von Farkas, H., Martinez‐Saguer, I., Bork, K., Bowen, T., Craig, T., Frank, M., Germenis, A. E., Grumach, A. S., Luczay, A., Varga, L., Zanichelli, A., Aberer, Werner, Andrejevic, Sladjana, Aygoeren‐Pürsün, Emel, Banerji, Alena, Bara, Noemi‐Anna, Bas, Murat, Bernstein, Jonathan, Betschel, Stephen, Björkander, Janne, Boccon‐Gibod, Isabelle, Bouillet, Laurence, Bova, Maria, Boysen, Henrik Halle, Branco‐Ferreira, Manuel, Bygum, Anette, Caballero, Teresa, Cancian, Mauro, Castaldo, Anthony, Christiansen, Sandra, Cicardi, Marco, Drouet, Christian, Fabiani, Jose, Gompels, Mark, Gonzalez‐Quevedo, Maria Teresa, Gooi, Jimmy, Gower, Richard, Gökmen, Nihal Mete, Grivcheva‐Panovska, Vesna, Guilarte, Mar, Gülbahar, Okan, Hack, Erik, Hakl, Roman, Harmat, György, Jeseňák, Miloš, Jolles, Stephen, Kaplan, Allen, Katelaris, Connie, Kosnik, Mitja, Kőhalmi, Kinga Viktória, Leibovich, Iris, Levi, Marcel, Li, Henry, Longhurst, Hilary J., Lumry, William, Magerl, Markus, Malbran, Alejandro, Martin, Ludovic, Maurer, Marcus, Mihály, Enikő, Moldovan, Dumitru, Murdjeva, Mariana, Nagy, Imola Beatrix, Nielsen, Erik W., Nieto, Sandra, Nordenfelt, Patrik, Obtulowitzc, Kristine, Pedrosa, Maria, Porębski, Grzegorz, Prior, Nieves, Reshef, Avner, Riedl, Marc A., Rosenkranz, Bernd, Schmid‐Grendelmeier, Peter, Péter, Spath, Speletas, Matthaios, Staevska, Maria, Stobiecki, Marcin, Triggiani, Massimo, Veszeli, Nóra, Wuillemin, Walter, Xiang, Zhi Yu, Yamamoto, Beverley, Zuraw, Bruce

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The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update von Maurer, Marcus, Magerl, Markus, Betschel, Stephen, Aberer, Werner, Ansotegui, Ignacio J., Aygören-Pürsün, Emel, Banerji, Aleena, Bara, Noémi-Anna, Boccon-Gibod, Isabelle, Bork, Konrad, Bouillet, Laurence, Boysen, Henrik Balle, Brodszki, Nicholas, Busse, Paula J., Bygum, Anette, Caballero, Teresa, Cancian, Mauro, Castaldo, Anthony J., Cohn, Danny M., Csuka, Dorottya, Farkas, Henriette, Gompels, Mark, Gower, Richard, Grumach, Anete S., Guidos-Fogelbach, Guillermo, Hide, Michihiro, Kang, Hye-Ryun, Kaplan, Allen P., Katelaris, Constance H., Kiani-Alikhan, Sorena, Lei, Wei-Te, Lockey, Richard F., Longhurst, Hilary, Lumry, William, MacGinnitie, Andrew, Malbran, Alejandro, Martinez Saguer, Inmaculada, Matta Campos, Juan José, Nast, Alexander, Nguyen, Dinh, Nieto-Martinez, Sandra A., Pawankar, Ruby, Peter, Jonathan, Porebski, Grzegorz, Prior, Nieves, Reshef, Avner, Riedl, Marc, Ritchie, Bruce, Sheikh, Farrukh Rafique, Smith, William B., Spaeth, Peter J., Stobiecki, Marcin, Toubi, Elias, Varga, Lilian Agnes, Weller, Karsten, Zanichelli, Andrea, Zhi, Yuxiang, Zuraw, Bruce, Craig, Timothy

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