Demyelinating Peripheral Neuropathy Caused by the p.R160H Mutation in the LITAF Gene

por Peddareddygari, Leema Reddy, Grewal, Raji P.
Publicado 2023

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 2015

Clinical and Genetic Analysis of a Patient with CMT4J

por Peddareddygari, Leema Reddy, Grewal, Raji P.
Publicado 2022

Intrafamilial Phenotypic Variability Associated with the I1739V Mutation in the SCN9A Gene

por Peddareddygari, Leema Reddy, Grewal, Raji P.
Publicado 2021

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

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

Clinical and Genetic Analysis of an Asian Indian Family with Charcot-Marie-Tooth Disease Type 4C

por Grewal, Raji P., Oberoi, Kinsi, Peddareddygari, Leema Reddy
Publicado 2018

Limb Girdle Muscular Dystrophy due to Digenic Inheritance of DES and CAPN3 Mutations

por Peddareddygari, Leema Reddy, Oberoi, Kinsi, Grewal, Raji P.
Publicado 2018

Novel Titin Gene Mutation Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy

por Peddareddygari, Leema Reddy, Oberoi, Kinsi, Grewal, Raji P
Publicado 2022

Genotype phenotype analysis in a family carrying truncating mutations in the titin gene

por Peddareddygari, Leema Reddy, Baisre-de León, Ada, Grewal, Raji P
Publicado 2021

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 2016

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

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

Positive Germline Selection in Pedigrees With Multiple Endocrine Neoplasia Type 2 Carrying V804M Mutation in the RET Gene

por Peddareddygari, Leema Reddy, Fay, Angela Musial, Shifrin, Alexander L., Grewal, Raji P.
Publicado 2016

Inclusion-Body Myositis Associated with Alzheimer's Disease

por Levacic, Danijela, Peddareddygari, Leema Reddy, Nochlin, David, Sharer, Leroy R., Grewal, Raji P.
Publicado 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 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 2010

Lance–Adams syndrome associated with cerebellar pathology

por Waddell, Adam, Dirweesh, Ahmed, Ordonez, Fausto, Kososky, Charles, Reddy Peddareddygari, Leema, Grewal, Raji P.
Publicado 2017

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 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 2016

Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies

por Traylor, Matthew, Persyn, Elodie, Tomppo, Liisa, Klasson, Sofia, Abedi, Vida, Bakker, Mark K, Torres, Nuria, Li, Linxin, Bell, Steven, Rutten-Jacobs, Loes, Tozer, Daniel J, Griessenauer, Christoph J, Zhang, Yanfei, Pedersen, Annie, Sharma, Pankaj, Jimenez-Conde, Jordi, Rundek, Tatjana, Grewal, Raji P, Lindgren, Arne, Meschia, James F, Salomaa, Veikko, Havulinna, Aki, Kourkoulis, Christina, Crawford, Katherine, Marini, Sandro, Mitchell, Braxton D, Kittner, Steven J, Rosand, Jonathan, Dichgans, Martin, Jern, Christina, Strbian, Daniel, Fernandez-Cadenas, Israel, Zand, Ramin, Ruigrok, Ynte, Rost, Natalia, Lemmens, Robin, Rothwell, Peter M, Anderson, Christopher D, Wardlaw, Joanna, Lewis, Cathryn M, Markus, Hugh S
Publicado 2021

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 2017