Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1 von Hackman, Peter, Sarparanta, Jaakko, Lehtinen, Sara, Vihola, Anna, Evilä, Anni, Jonson, Per Harald, Luque, Helena, Kere, Juha, Screen, Mark, Chinnery, Patrick F., Åhlberg, Gabrielle, Edström, Lars, Udd, Bjarne

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Safety and tolerability of NXY-059 for acute intracerebral hemorrhage : The CHANT trial von LYDEN, Patrick D, SHUAIB, Ashfaq, RODICHOK, Larry, WASIEWSKI, Warren W, AHLBERG, Gabrielle, LEES, Kennedy R, DAVALOS, Antoni, DAVIS, Stephen M, DIENER, Hans-Christoph, GROTTA, James C, ASHWOOD, Tim J, HARDEMARK, Hans-Goren, SVENSSON, Hannah H

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Kinetic analysis and test-retest variability of the radioligand [11C](R)-PK11195 binding to TSPO in the human brain - a PET study in control subjects von Jučaite, Aurelija, Cselényi, Zsolt, Arvidsson, Annie, Åhlberg, Gabrielle, Julin, Per, Varnäs, Katarina, Stenkrona, Per, Andersson, Jan, Halldin, Christer, Farde, Lars

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Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H von Borg, Kristian, Stucka, Rolf, Locke, Matthew, Melin, Eva, Åhlberg, Gabrielle, Klutzny, Ursula, Hagen, Maja von der, Huebner, Angela, Lochmüller, Hanns, Wrogemann, Klaus, Thornell, Lars-Eric, Blake, Derek J, Schoser, Benedikt

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Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI) von Prakash, Neha, Coffey, Christopher, Tanner, Caroline M., Kieburtz, Karl, Merchant, Kalpana, Foroud, Tatiana, Chahine, Lana M., Casaceli, Cindy, Dorsey, Ray, Wilson, Renee, Herzog, Margaret, Daegele, Nichole, Arnedo, Vanessa, Marek, Ken, Frank, Samuel, Jennings, Danna, Marek, Kenneth, Siderowf, Andrew, Coffey, Christopher, Tanner, Caroline, Simuni, Tanya, Shaw, Leslie, Trojanowski, John, Singleton, Andrew, Kieburtz, Karl, Toga, Arthur, Galasko, Douglas, Poewe, Werner, Foroud, Tatiana, Poston, Kathleen, Chowdhury, Sohini, Frasier, Mark, Kopil, Catherine, Wilson, Renee, Salerno, Christina, Caspell-Garcia, Chelsea, Crawford, Karen, Casalin, Paola, Weisz, Mali Gani, Orr-Urtreger, Avi, Montine, Thomas, Russell, David, Giladi, Nir, Standaert, David, Jankovic, Joseph, Saint-Hilaire, Marie, Rosenthal, Liana, Barone, Paolo, Marder, Karen, Santiago, Anthony, Bressman, Susan, Isaacson, Stuart, Martinez, Javiar Ruiz, Tai, Yen, Politis, Marios, Smejdir, Debra, Williams, Karen, Willeke, Diana, Peacock, Shawnees, Sommerfeld, Barbara, Wakeman, Katrina, Blair, Courtney, Guthrie, Stephanie, Harrell, Leigh, Thomas, Cathi-Ann, James, Raymond, Zimmerman, Grace, Brown, Victoria, Mule, Jennifer, Hilt, Ella, Ainscough, Susan, Ranola, Madelaine, Santana, Helen Mejia, Moreno, Juliana, Raymond, Deborah, Speketer, Krista, Croitoru, Ioana, Garrido, Alicia, Payne, Laura Marie, Viswanth, Veena, Severt, Lawrence, Facheris, Maurizio, Soares, Holly, Mintun, Mark A., Cedarbaum, Jesse, Biglan, Kevin, Sheikh, Zulfiqar Haider, Bingol, Baris, Fischer, Tanya, Sardi, Pablo, Egebjerg, Jan, Hillert, Gabrielle Ahlberg, Saba, Barbara, Umek, Robert, Post, Anke, Boess, Frank, Taylor, Kirsten, Grachev, Igor, Muglia, Pierandrea, Tauscher, Johannes

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Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectiona... von Simuni, Tanya, Uribe, Liz, Caspell-Garcia, Chelsea, Coffey, Christopher S, Siderowf, Andrew, Trojanowski, John Q, Shaw, Leslie M, Seibyl, John, Toga, Arthur W, Galasko, Doug, Tosun, Duygu, Poston, Kathleen, Weintraub, Daniel, Mollenhauer, Brit, Tanner, Caroline M, Kieburtz, Karl, Hutten, Samantha J, Bressman, Susan, Marek, Kenneth, Chowdhury, Sohini, Sherer, Todd, Casaceli, Cynthia, Dorsey, Ray, Wilson, Renee, Mahes, Sugi, Salerno, Christina, Crawford, Karen, Casalin, Paola, Malferrari, Giulia, Weisz, Mali Gani, Orr-Urtreger, Avi, Montine, Thomas, Baglieri, Chris, Russell, David, Giladi, Nir, Factor, Stewart, Hauser, Robert, Jankovic, Joseph, Saint-Hilaire, Marie, Richard, Irene, Shprecher, David, Brockmann, Katrina, Barone, Paolo, Espay, Alberto, Santiago, Anthony, Hu, Shu-Ching, Isaacson, Stuart, Corvol, Jean-Christophe, Ruiz Martinez, Javiar, Tolosa, Eduardo, Tai, Yen, Smejdir, Debra, Rees, Linda, Williams, Karen, Kausar, Farah, Richardson, Whitney, Willeke, Diana, Peacock, Shawnees, Sommerfeld, Barbara, Freed, Alison, Guthrie, Stephanie, Harrell, Leigh, Thomas, Cathi-Ann, James, Raymond, Zimmerman, Grace, Mule, Jennifer, Hilt, Ella, Ribb, Kori, Ainscough, Susan, Ranola, Madelaine, Mejia Santana, Helen, Moreno, Juliana, Raymond, Deborah, Carvajal, Lisbeth, Carvalo, Stephanie, Croitoru, Ioana, Garrido, Alicia, Payne, Laura Marie, Viswanth, Veena, Severt, Lawrence, Facheris, Maurizio, Cedarbaum, Jesse, Taylor, Peggy, Haider Sheikh, Zulfiqar, Fischer, Tanya, Sardi, Pablo, Forrat, Remi, Reith, Alastair, Ahlberg Hillert, Gabrielle, Saba, Barbara, Min, Chris, Umek, Robert, Mather, Joe, De Santi, Susan, Post, Anke, Boess, Frank, Taylor, Kirsten, Grachev, Igor, Muglia, Pierandrea, Merchant, Kaplana

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Longitudinal Measurements of Glucocerebrosidase activity in Parkinson’s patients von Wolf, Pavlina, Chiang, Ming Sum Ruby, Helesicova, Karolina, Zhang, Xiaokui Kate, Merchant, Kalpana, Scherzer, Clemens, Caspell‐Garcia, Chelsea, Blauwendraat, Cornelis, Foroud, Tatiana, Chahine, Lana M., Li, Gen, Sardi, Sergio Pablo, Marek, Kenneth, Siderowf, Andrew, Seibyl, John, Tanner, Caroline, Shaw, Leslie M, Trojanowski, John Q, Singleton, Andrew, Kieburtz, Karl, Toga, Arthur, Mollenhauer, Brit, Galasko, Douglas, Chahine, Lana M, Poewe, Werner, Poston, Kathleen, Reimer, Alyssa, Clark, Adrienne, Frasier, Mark, Kopil, Catherine, Chowdhury, Sohini, Sherer, Todd, Casaceli, Cynthia, Wilson, Renee, Salerno, Christina, Crawford, Karen, Malferrari, Giulia, Orr‐Urtreger, Avi, Montine, Thomas, Christini, Amanda, Russell, David, Factor, Stewart, Hogarth, Penelope, Standaert, David, Hauser, Robert, Jankovic, Joseph, Richard, Irene, Shprecher, David, Rosenthal, Liana, Rowe, Dominic, Santiago, Anthony, Hu, Shu‐Ching, Tolosa, Eduardo, Tai, Yen, Politis, Marios, Smejdir, Debra, Rees, Linda, Kausar, Farah, Richardson, Whitney, Willeke, Diana, Freed, Alison, Wakeman, Katrina, Blair, Courtney, Guthrie, Stephanie, Harrell, Leigh, Thomas, Cathi‐Ann, James, Raymond, Mule, Jennifer, Hilt, Ella, Ribb, Kori, Ainscough, Susan, Wethington, Misty, Ranola, Madelaine, Mejia Santana, Helen, Raymond, Deborah, Speketer, Krista, Carvajal, Lisbeth, Carvalo, Stephanie, Croitoru, Ioana, Payne, Laura Marie, Viswanth, Veena, Facheris, Maurizio, Soares, Holly, Mintun, Mark A, Cedarbaum, Jesse, Haider Sheikh, Zulfiqar, Bingol, Baris, Fischer, Tanya, Sardi, Pablo, Forrat, Remi, Reith, Alastair, Hillert, Gabrielle Ahlberg, Saba, Barbara, Umek, Robert, De Santi, Susan, Post, Anke, Boess, Frank, Taylor, Kirsten, Grachev, Igor, Avbersek, Andreja

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Longitudinal clinical and biomarker characteristics of non-manifesting LRRK2 G2019S carriers in the PPMI cohort von Simuni, Tanya, Merchant, Kalpana, Brumm, Michael C., Cho, Hyunkeun, Caspell-Garcia, Chelsea, Coffey, Christopher S., Chahine, Lana M., Alcalay, Roy N., Nudelman, Kelly, Foroud, Tatiana, Mollenhauer, Brit, Siderowf, Andrew, Tanner, Caroline, Iwaki, Hirotaka, Sherer, Todd, Marek, Kenneth

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Welander distal myopathy outside the Swedish population: phenotype and genotype von von Tell, Désirée, Somer, Hannu, Udd, Bjarne, Edström, Lars, Borg, Kristian, Åhlberg, Gabrielle

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Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus von VON TELL, Désirée, BRUDER, Carl E. G, ANDERSON, Louise V. B, ANVRET, Maria, AHLBERG, Gabrielle

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Welander distal myopathy : clinical and genetic studies von Åhlberg, Gabrielle

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New Combination 937 von ERIKSSON HAKAN, AHLBERG GABRIELLE

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Genetic linkage of Welander distal myopathy to chromosome 2p13 von Åhlberg, Gabrielle, Von Tell, Désirée, Borg, Kristian, Edström, Lars, Anvret, Maria

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Welander distal myopathy – an overview von Borg, Kristian, Åhlberg, Gabrielle, Anvret, Maria, Edström, Lars

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Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies von Åhlberg, Gabrielle, Borg, Kristian, Edström, Lars, Anvret, Maria

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Welander distal myopathy is not linked to other defined distal myopathy gene loci von Åhlberg, Gabrielle, Borg, Kristian, Edström, Lars, Anvret, Maria

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C4342T-mutation in the SCN4A gene on chromosome 17q in a Swedish family with paramyotonia congenita (Eulenburg) – correlations with clinical, neurophysiological and muscle biopsy d... von Borg, Kristian, Åhlberg, Gabrielle, Anvret, Maria

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Welander hereditary distal myopathy, a comparison to hereditary IBM (inclusion body myositis) and autosomal recessive distal myopathy with regard to molecular genetics von Åhlberg, Gabrielle, Borg, Kristian, Edström, Lars, Anvret, Maria

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Distribution of muscle degeneration in Welander distal myopathy—A magnetic resonance imaging and muscle biopsy study von Åhlberg, Gabrielle, Jakobsson, Finnbogi, Fransson, Annette, Moritz, Åke, Borg, Kristian, Edström, Lars

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Muscle fibre degeneration in distal myopathy (Welander)—Ultrastructure related to immunohistochemical observations on cytoskeletal proteins and Leu-19 antigen von Borg, Kristian, Åhlberg, Gabrielle, Hedberg, Birgitta, Edström, Lars

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