Interactive and sex‐specific life‐history responses of Culex pipiens mosquito larvae to multiple environmental factors von Alcalay, Y., Puzhevsky, D., Tsurim, I., Scharf, I., Ovadia, O.

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Isolated recurrent myelitis in a persistent MOG positive patient von Anis, S., Regev, K., Pittock, S.J., Flanagan, E.P., Alcalay, Y., Gadoth, A.

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A30 BIOMARKERS IN THORACIC ONCOLOGY: PREDICTING OUTCOMES: A Combined Score Of Biomarkers In Sputum May Be An Indicator For Lung Cancer von Bar-Shai, A, Shenhar-Tsarfaty, S, Ahimor, A, Ophir, N, Siterman, M, Rotem, M, Alcalay, Y, Schwarz, Y, Fireman, E M

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C32 ASTHMA: PRE-CLINICAL STUDIES: Fingerprint Of Lung Fluid Ultra-Fine-Particles, A Novel Marker Of Acute Lung Inflammation von Bar-Shai, A, Fireman, E, Alcalay, Y, Sagiv, A, Alon, R

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A46 OCCUPATION, OBESITY, AND LUNG HEALTH: Functional And Inflammatory Abnormalities In Artificial Stone Exposed Workers von Ophir, N, Alcalay, Y, Bar-Shai, A, Israeli-shany, L, Korenstein, R, Kramer, M, Fireman, E M

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Popeye domain containing 1 (Popdc1/Bves) is a caveolae-associated protein involved in ischemia tolerance von Alcalay, Y, Hochhauser, E, Kliminski, V, Dick, J, Zahalka, MA, Parnes, D, Schlesinger, H, Abassi, Z, Shainberg, A, Schindler, RFR, Brand, T, Kessler-Icekson, G

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The existence of gender difference in IL-1Ra gene polymorphism von Bessler, Hanna, Osovsky, Micky, Beilin, Benzion, Alcalay, Yifat, Sirota, Lea

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The association between Mediterranean diet adherence and Parkinson's disease von Alcalay, Roy N., Gu, Yian, Mejia-Santana, Helen, Cote, Lucien, Marder, Karen S., Scarmeas, Nikolaos

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Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies von Krohn, Lynne, Öztürk, Tuğba Nur, Vanderperre, Benoît, Ouled Amar Bencheikh, Bouchra, Ruskey, Jennifer A., Laurent, Sandra B., Spiegelman, Dan, Postuma, Ronald B., Arnulf, Isabelle, Hu, Michele T. M., Dauvilliers, Yves, Högl, Birgit, Stefani, Ambra, Monaca, Christelle Charley, Plazzi, Giuseppe, Antelmi, Elena, Ferini‐Strambi, Luigi, Heidbreder, Anna, Rudakou, Uladzislau, Cochen De Cock, Valérie, Young, Peter, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Greenbaum, Lior, Liong, Christopher, Gagnon, Jean‐François, Desautels, Alex, Hassin‐Baer, Sharon, Montplaisir, Jacques Y., Dupré, Nicolas, Rouleau, Guy A., Fon, Edward A., Trempe, Jean‐François, Lamoureux, Guillaume, Alcalay, Roy N., Gan‐Or, Ziv

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SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease von Alcalay, Roy N., Mallett, Victoria, Vanderperre, Benoît, Tavassoly, Omid, Dauvilliers, Yves, Wu, Richard Y.J., Ruskey, Jennifer A., Leblond, Claire S., Ambalavanan, Amirthagowri, Laurent, Sandra B., Spiegelman, Dan, Dionne‐Laporte, Alexandre, Liong, Christopher, Levy, Oren A., Fahn, Stanley, Waters, Cheryl, Kuo, Sheng‐Han, Chung, Wendy K., Ford, Blair, Marder, Karen S., Kang, Un Jung, Hassin‐Baer, Sharon, Greenbaum, Lior, Trempe, Jean‐Francois, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Clark, Lorraine N., Langlois, Melanie, Dion, Patrick A., Fon, Edward A., Dupre, Nicolas, Rouleau, Guy A., Gan‐Or, Ziv

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α-Synuclein in blood exosomes immunoprecipitated using neuronal and oligodendroglial markers distinguishes Parkinson’s disease from multiple system atrophy von Dutta, Suman, Hornung, Simon, Kruayatidee, Adira, Maina, Katherine N., del Rosario, Irish, Paul, Kimberly C., Wong, Darice Y., Duarte Folle, Aline, Markovic, Daniela, Palma, Jose-Alberto, Serrano, Geidy E., Adler, Charles H., Perlman, Susan L., Poon, Wayne W., Kang, Un Jung, Alcalay, Roy N., Sklerov, Miriam, Gylys, Karen H., Kaufmann, Horacio, Fogel, Brent L., Bronstein, Jeff M., Ritz, Beate, Bitan, Gal

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Toward a biomarker panel measured in CNS-originating extracellular vesicles for improved differential diagnosis of Parkinson's disease and multiple system atrophy von Taha, Hash Brown, Hornung, Simon, Dutta, Suman, Fenwick, Leony, Lahgui, Otmane, Howe, Kathryn, Elabed, Nour, Del Rosario, Irish, Wong, Darice Y, Duarte Folle, Aline, Markovic, Daniela, Palma, Jose-Alberto, Kang, Un Jung, Alcalay, Roy N, Sklerov, Miriam, Kaufmann, Horacio, Fogel, Brent L, Bronstein, Jeff M, Ritz, Beate, Bitan, Gal

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Early‐Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation von Kim, Christine Y., Wirth, Thomas, Hubsch, Cécile, Németh, Andrea H., Okur, Volkan, Anheim, Mathieu, Drouot, Nathalie, Tranchant, Christine, Rudolf, Gabrielle, Chelly, Jamel, Tatton‐Brown, Katrina, Blauwendraat, Cornelis, Vonsattel, Jean Paul G., Cortes, Etty, Alcalay, Roy N., Chung, Wendy K.

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Reply to “PPP2R5D Genetic Mutations and Early Onset Parkinsonism” von Kim, Christine Y., Wirth, Thomas, Hubsch, Cécile, Németh, Andrea H., Okur, Volkan, Anheim, Mathieu, Drouot, Nathalie, Tranchant, Christine, Rudolf, Gabrielle, Chelly, Jamel, Tatton‐Brown, Katrina, Blauwendraat, Cornelis, Vonsattel, Jean Paul G., Cortes, Etty, Alcalay, Roy N., Chung, Wendy K.

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GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder von Gan‐Or, Ziv, Mirelman, Anat, Postuma, Ronald B., Arnulf, Isabelle, Bar‐Shira, Anat, Dauvilliers, Yves, Desautels, Alex, Gagnon, Jean‐François, Leblond, Claire S., Frauscher, Birgit, Alcalay, Roy N., Saunders‐Pullman, Rachel, Bressman, Susan B., Marder, Karen, Monaca, Christelle, Högl, Birgit, Orr‐Urtreger, Avi, Dion, Patrick A., Montplaisir, Jacques Y., Giladi, Nir, Rouleau, Guy A.

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Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets von Kia, Demis A, Zhang, David, Guelfi, Sebastian, Manzoni, Claudia, Hubbard, Leon, Reynolds, Regina H, Botía, Juan, Ryten, Mina, Ferrari, Raffaele, Lewis, Patrick A, Williams, Nigel, Trabzuni, Daniah, Hardy, John, Wood, Nicholas W

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The impact of a nationwide hands‐on workshop on the diagnostic rates and management of obstetrical anal sphincter Injuries in Israel von Ginath, S., Alcalay, M., Ben Ami, M., Bssam Abbas, Y., Cohen, G., Condrea, A., Feit, H., Gershi, H., Gold, R., Goldschmidt, E., Gordon, D., Groutz, A., Lavy, Y., Levy, G., Lowenstein, L., Marcus, N., Padoa, A., Samuelof, A., Tevet, A., Weintraub, A. Y.

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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome von Storm, Catherine S., Kia, Demis A., Almramhi, Mona M., Bandres-Ciga, Sara, Finan, Chris, Hingorani, Aroon D., Wood, Nicholas W.

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The role of the melanoma gene MC1R in Parkinson disease and REM sleep Behavior Disorder von Gan-Or, Ziv, Mohsin, Noreen, Girard, Simon L, Montplaisir, Jacques Y, Ambalavanan, Amirthagowri, Strong, Stephanie, Mallett, Victoria, Laurent, Sandra B, Bourassa, Cynthia V, Boivin, Michel, Langlois, Melanie, Arnulf, Isabelle, Högl, Birgit, Frauscher, Birgit, Monaca, Christelle, Desautels, Alex, Gagnon, Jean-François, Postuma, Ronald B, Dion, Patrick A, Dauvilliers, Yves, Dupre, Nicolas, Alcalay, Roy N, Rouleau, Guy A

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Correction to: α-Synuclein in blood exosomes immunoprecipitated using neuronal and oligodendroglial markers distinguishes Parkinson’s disease from multiple system atrophy von Dutta, Suman, Hornung, Simon, Kruayatidee, Adira, Maina, Katherine N., del Rosario, Irish, Paul, Kimberly C., Wong, Darice Y., Duarte Folle, Aline, Markovic, Daniela, Palma, Jose-Alberto, Serrano, Geidy E., Adler, Charles H., Perlman, Susan L., Poon, Wayne W., Kang, Un Jung, Alcalay, Roy N., Sklerov, Miriam, Gylys, Karen H., Kaufmann, Horacio, Fogel, Brent L., Bronstein, Jeff M., Ritz, Beate, Bitan, Gal

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