Identification of Novel Mutations in Spatacsin and Apolipoprotein B Genes in a Patient with Spastic Paraplegia and Hypobetalipoproteinemia

Por Peddareddygari, Leema Reddy, Grewal, Raji P.
Publicado no Case Rep Genet (2015)

Congenital Insensitivity to Pain: A Case Report and Review of the Literature

Por Peddareddygari, Leema Reddy, Oberoi, Kinsi, Grewal, Raji P.
Publicado em 2014

Factors Affecting Phenotype Variability in a Family with CMT2B: Gender and LRSAM1 Genotype

Por Peddareddygari, Leema Reddy, Oberoi, Kinsi, Vellore, Jaasrini Reddy, Grewal, Raji P.
Publicado no Case Rep Neurol (2016)

An analysis of <it>Methylenetetrahydrofolate reductase </it>and <it>Glutathione S-transferase omega-1 genes </it>as modifiers of the cerebral response to ischemia

Por Sen Souvik, Levenstien Mark A, Dutra Ana, Peddareddygari Leema, Grewal Raji P
Publicado em 2009-07-01

Kikuchi-Fujimoto Disease Associated with Myasthenia Gravis: A Case Report

Por Onasanya, Olukayode, Nochlin, David, Casas, Victor, Peddareddygari, Leema Reddy, Grewal, Raji P.
Publicado em 2010

Inclusion-Body Myositis Associated with Alzheimer's Disease

Por Levacic, Danijela, Peddareddygari, Leema Reddy, Nochlin, David, Sharer, Leroy R., Grewal, Raji P.
Publicado em 2013

An analysis of Methylenetetrahydrofolate reductase and Glutathione S-transferase omega-1 genes as modifiers of the cerebral response to ischemia

Por Peddareddygari, Leema Reddy, Dutra, Ana Virginia, Levenstien, Mark A, Sen, Souvik, Grewal, Raji P
Publicado em 2009

Hyperhomocysteinemia is Associated with Aortic Atheroma Progression in Stroke/TIA Patients

Por Sen, Souvik, Reddy, P. Leema, Grewal, Raji P., Busby, Marjorie, Chang, Patricia, Hinderliter, Alan
Publicado em 2010

Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic stroke

Por Dutra, Ana VC, Lin, Hsiu-Fen, Juo, Suh-Hang H, Mohrenweiser, Harvey, Sen, Souvik, Grewal, Raji P
Publicado em 2006

Role of Therapeutic Plasma Exchange in Treatment of Tumefactive Multiple Sclerosis-Associated Low CD4 and CD8 Levels

Por Lew, Kristen, Mewada, Nishith, Ramanujam, Sahana, Hassanzadeh, Bahareh, Donahue, John E., Peddareddygari, Leema Reddy, Moser, Robert, Kososky, Charles, Grewal, Raji P.
Publicado no Case Rep Neurol (2016)

Somatic and Germline Instability of the ATTCT Repeat in Spinocerebellar Ataxia Type 10

Por Matsuura, Tohru, Fang, Ping, Lin, Xi, Khajavi, Mehrdad, Tsuji, Kuniko, Rasmussen, Astrid, Grewal, Raji P., Achari, Madhureeta, Alonso, Maria E., Pulst, Stefan M., Zoghbi, Huda Y., Nelson, David L., Roa, Benjamin B., Ashizawa, Tetsuo
Publicado em 2004

X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1

Por Quinzii, Catarina M., Vu, Tuan H., Min, K. Christopher, Tanji, Kurenai, Barral, Sandra, Grewal, Raji P., Kattah, Andrea, Camaño, Pilir, Otaegui, David, Kunimatsu, Teruhito, Blake, David M., Wilhelmsen, Kirk C., Rowland, Lewis P., Hays, Arthur P., Bonilla, Eduardo, Hirano, Michio
Publicado em 2008

Agreement between TOAST and CCS ischemic stroke classification: The NINDS SiGN Study

Por McArdle, Patrick F., Kittner, Steven J., Ay, Hakan, Brown, Robert D., Meschia, James F., Rundek, Tatjana, Wassertheil-Smoller, Sylvia, Woo, Daniel, Andsberg, Gunnar, Biffi, Alessandro, Brenner, David A., Cole, John W., Corriveau, Roderick, de Bakker, Paul I.W., Delavaran, Hossein, Dichgans, Martin, Grewal, Raji P., Gwinn, Katrina, Huq, Mohammed, Jern, Christina, Jimenez-Conde, Jordi, Jood, Katarina, Kaplan, Robert C., Katschnig, Petra, Katsnelson, Michael, Labovitz, Daniel L., Lemmens, Robin, Li, Linxin, Lindgren, Arne, Markus, Hugh S., Peddareddygari, Leema R., Pedersén, Annie, Pera, Joanna, Redfors, Petra, Roquer, Jaume, Rosand, Jonathan, Rost, Natalia S., Rothwell, Peter M., Sacco, Ralph L., Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie, Thijs, Vincent, Tiedt, Steffen, Valenti, Raffaella, Worrall, Bradford B.
Publicado no Neurology (2014)

Etiologic Ischemic Stroke Phenotypes in the NINDS Stroke Genetics Network

Por Ay, Hakan, Arsava, Ethem Murat, Andsberg, Gunnar, Benner, Thomas, Brown, Robert D., Chapman, Sherita N., Cole, John W., Delavaran, Hossein, Dichgans, Martin, Engström, Gunnar, Giralt-Steinhauer, Eva, Grewal, Raji P., Gwinn, Katrina, Jern, Christina, Jimenez-Conde, Jordi, Jood, Katarina, Katsnelson, Michael, Kissela, Brett, Kittner, Steven J., Kleindorfer, Dawn O., Labovitz, Daniel L., Lanfranconi, Silvia, Lee, Jin-Moo, Lehm, Manuel, Lemmens, Robin, Levi, Chris, Li, Linxin, Lindgren, Arne, Markus, Hugh S., McArdle, Patrick F., Melander, Olle, Norrving, Bo, Peddareddygari, Leema Reddy, Pedersén, Annie, Pera, Joanna, Rannikmäe, Kristiina, Rexrode, Kathryn M., Rhodes, David, Rich, Stephen S., Roquer, Jaume, Rosand, Jonathan, Rothwell, Peter M., Rundek, Tatjana, Sacco, Ralph L., Schmidt, Reinhold, Schürks, Markus, Seiler, Stephan, Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie, Thijs, Vincent, Woodfield, Rebecca, Worrall, Bradford B., Meschia, James F.
Publicado no Stroke (2014)

Genetic variation at 16q24.2 is associated with small vessel stroke

Por Traylor, Matthew, Malik, Rainer, Nalls, Mike A., Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S., Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Eilis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W.T., Ikram, M. Arfan, Launer, Lenore J., Seshadri, Sudha, Hamilton‐Bruce, Monica Anne, Jimenez‐Conde, Jordi, Cole, John W., Schmidt, Reinhold, Słowik, Agnieszka, Lemmens, Robin, Lindgren, Arne, Melander, Olle, Grewal, Raji P., Sacco, Ralph L., Rundek, Tatjana, Rexrode, Kathryn, Arnett, Donna K., Johnson, Julie A., Benavente, Oscar R., Wasssertheil‐Smoller, Sylvia, Lee, Jin‐Moo, Pulit, Sara L., Wong, Quenna, Rich, Stephen S., de Bakker, Paul I.W., McArdle, Patrick F., Woo, Daniel, Anderson, Christopher D., Xu, Huichun, Heitsch, Laura, Fornage, Myriam, Jern, Christina, Stefansson, Kari, Thorsteinsdottir, Unnur, Gretarsdottir, Solveig, Lewis, Cathryn M., Sharma, Pankaj, Sudlow, Cathie L.M., Rothwell, Peter M., Boncoraglio, Giorgio B., Thijs, Vincent, Levi, Chris, Meschia, James F., Rosand, Jonathan, Kittner, Steven J., Mitchell, Braxton D., Dichgans, Martin, Worrall, Bradford B., Markus, Hugh S.
Publicado no Ann Neurol (2017)

The NINDS Stroke Genetics Network: a genome-wide association study of ischemic stroke and its subtypes

Por Pulit, Sara L., McArdle, Patrick F., Wong, Quenna, Malik, Rainer, Gwinn, Katrina, Achterberg, Sefanja, Algra, Ale, Amouyel, Philippe, Anderson, Christopher D., Arnett, Donna K., Arsava, Ethem Murat, Attia, John, Ay, Hakan, Bartz, Traci M., Battey, Thomas, Benavente, Oscar R., Bevan, Steve, Biffi, Alessandro, Bis, Joshua C., Blanton, Susan H., Boncoraglio, Giorgio B., Brown, Robert D., Burgess, Annette I., Carrera, Caty, Chapman Smith, Sherita N., Chasman, Daniel I., Chauhan, Ganesh, Chen, Wei-Min, Cheng, Yu-Ching, Chong, Michael, Cloonan, Lisa K., Cole, John W., Cotlarciuc, Ioana, Cruchaga, Carlos, Cuadrado-Godia, Elisa, Dave, Tushar, Dawson, Jesse, Debette, Stéphanie, Delavaran, Hossein, Dell, Cameron A., Dichgans, Martin, Doheny, Kimberly F., Dong, Chuanhui, Duggan, David J., Engström, Gunnar, Evans, Michele K., Pallejà, Xavier Estivill, Faul, Jessica D., Fernández-Cadenas, Israel, Fornage, Myriam, Frossard, Philippe M., Furie, Karen, Gamble, Dale M., Gieger, Christian, Giese, Anne-Katrin, Giralt-Steinhauer, Eva, González, Hector M., Goris, An, Gretarsdottir, Solveig, Grewal, Raji P., Grittner, Ulrike, Gustafsson, Stefan, Han, Buhm, Hankey, Graeme J., Heitsch, Laura, Higgins, Peter, Hochberg, Marc C., Holliday, Elizabeth, Hopewell, Jemma C., Horenstein, Richard B., Howard, George, Ikram, M. Arfan, Ilinca, Andreea, Ingelsson, Erik, Irvin, Marguerite R., Jackson, Rebecca D., Jern, Christina, Conde, Jordi Jiménez, Johnson, Julie A., Jood, Katarina, Kahn, Muhammad S., Kaplan, Robert, Kappelle, L. Jaap, Kardia, Sharon L.R., Keene, Keith L., Kissela, Brett M., Kleindorfer, Dawn O., Koblar, Simon, Labovitz, Daniel, Launer, Lenore J., Laurie, Cathy C., Laurie, Cecelia A., Lee, Cue Hyunkyu, Lee, Jin-Moo, Lehm, Manuel, Lemmens, Robin, Levi, Christopher, Leys, Didier, Lindgren, Arne, Longstreth, W. T., Maguire, Jane, Manichaikul, Ani, Markus, Hugh S., McClure, Leslie A., McDonough, Caitrin W., Meisinger, Christa, Melander, Olle, Meschia, James F., Mola-Caminal, Marina, Montaner, Joan, Mosley, Thomas H., Müller-Nurasyid, Martina, Nalls, Mike A., O’Connell, Jeffrey R., O’Donnell, Martin, Ois, Ángel, Papanicolaou, George J., Paré, Guillaume, Peddareddygari, Leema Reddy, Pedersén, Annie, Pera, Joanna, Peters, Annette, Poole, Deborah, Psaty, Bruce M., Rabionet, Raquel, Raffeld, Miriam R., Rannikmäe, Kristiina, Rasheed, Asif, Redfors, Petra, Reiner, Alex P., Rexrode, Kathryn, Ribasés, Marta, Rich, Stephen S., Robberecht, Wim, Rodriguez-Campello, Ana, Rolfs, Arndt, Roquer, Jaume, Rose, Lynda M., Rosenbaum, Daniel, Rost, Natalia S., Rothwell, Peter M., Rundek, Tatjana, Ryan, Kathleen A., Sacco, Ralph L., Sale, Michèle M., Saleheen, Danish, Salomaa, Veikko, Sánchez-Mora, Cristina, Schmidt, Carsten Oliver, Schmidt, Helena, Schmidt, Reinhold, Schürks, Markus, Scott, Rodney, Segal, Helen C., Seiler, Stephan, Seshadri, Sudha, Sharma, Pankaj, Shuldiner, Alan R., Silver, Brian, Slowik, Agnieszka, Smith, Jennifer A., Söderholm, Martin, Soriano, Carolina, Sparks, Mary J., Stanne, Tara, Stefansson, Kari, Stine, O. Colin, Strauch, Konstantin, Sturm, Jonathan, Sudlow, Cathie LM, Tajuddin, Salman M., Talbert, Robert L., Tatlisumak, Turgut, Thijs, Vincent, Thorleifsson, Gudmar, Thorsteindottir, Unnur, Tiedt, Steffen, Traylor, Matthew, Trompet, Stella, Valant, Valerie, Waldenberger, Melanie, Walters, Matthew, Wang, Liyong, Wassertheil-Smoller, Sylvia, Weir, David R., Wiggins, Kerri L., Williams, Stephen R., Wloch-Kopec, Dorota, Woo, Daniel, Woodfield, Rebecca, Wu, Ona, Xu, Huichun, Zonderman, Alan B., Worrall, Bradford B., de Bakker, Paul I.W., Kittner, Steven J., Mitchell, Braxton D., Rosand, Jonathan
Publicado no Lancet Neurol (2015)