Myotilinopathy: refining the clinical and myopathological phenotype von Olivé, Montse, Goldfarb, Lev G., Shatunov, Alexey, Fischer, Dirk, Ferrer, Isidro

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Numerical modeling of induction heating systems with load of azimuthal periodicity von Mannanov, Emil, Galunin, Sergei, Shatunov, Alexey

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Does Thrombosis Play a Causal Role in Lacunar Stroke and Cerebral Small Vessel Disease? von Koohi, Fatemeh, Harshfield, Eric L, Shatunov, Alexey, Markus, Hugh S

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Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy von Kaminska, Anna, Strelkov, Sergei V, Goudeau, Bertrand, Olivé, Montse, Dagvadorj, Ayush, Fidzianska, Anna, Simon-Casteras, Monique, Shatunov, Alexey, Dalakas, Marinos C, Ferrer, Isidro, Kwiecinski, Hubert, Vicart, Patrick, Goldfarb, Lev G

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The Impact of Long-Term Hypoxia on the Antioxidant Defense System in the Siberian Frog Rana amurensis von Shekhovtsov, Sergei V., Vorontsova, Yana L., Slepneva, Irina A., Smirnov, Dmitry N., Khrameeva, Ekaterina E., Shatunov, Alexey, Poluboyarova, Tatiana V., Bulakhova, Nina A., Meshcheryakova, Ekaterina N., Berman, Daniil I., Glupov, Viktor V.

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Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy von Dagvadorj, Ayush, Petersen, Robert B., Lee, Hee Suk, Cervenakova, Larisa, Shatunov, Alexey, Budka, Herbert, Brown, Paul, Gambetti, Pierluigi, Goldfarb, Lev G.

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Inclusion body myositis with human immunodeficiency virus infection: Four cases with clonal expansion of viral-specific T cells von Dalakas, Marinos C., Rakocevic, Goran, Shatunov, Alexey, Goldfarb, Lev, Raju, Raghavan, Salajegheh, Mohammad

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Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23 von Shatunov, Alexey, Sambuughin, Nyamkhishig, Jankovic, Joseph, Elble, Rodger, Lee, Hee Suk, Singleton, Andrew B., Dagvadorj, Ayush, Ji, Jay, Zhang, Yiping, Kimonis, Virginia E., Hardy, John, Hallett, Mark, Goldfarb, Lev G.

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Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy von Olivé, Montse, Odgerel, Zagaa, Martínez, Amaia, Poza, Juan José, Bragado, Federico García, Zabalza, Ramón J, Jericó, Ivonne, Gonzalez-Mera, Laura, Shatunov, Alexey, Lee, Hee Suk, Armstrong, Judith, Maraví, Elías, Arroyo, Maria Ramos, Pascual-Calvet, Jordi, Navarro, Carmen, Paradas, Carmen, Huerta, Mariano, Marquez, Fabian, Rivas, Eduardo Gutierrez, Pou, Adolf, Ferrer, Isidre, Goldfarb, Lev G

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Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin von Piñol-Ripoll, Gerard, Shatunov, Alexey, Cabello, Ana, Larrodé, Pilar, de la Puerta, Iris, Pelegrín, Juana, Ramos, Feliciano J, Olivé, Montse, Goldfarb, Lev G

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Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies von Bär, Harald, Goudeau, Bertrand, Wälde, Sarah, Casteras-Simon, Monique, Mücke, Norbert, Shatunov, Alexey, Goldberg, Y. Paul, Clarke, Charles, Holton, Janice L., Eymard, Bruno, Katus, Hugo A., Fardeau, Michel, Goldfarb, Lev, Vicart, Patrick, Herrmann, Harald

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In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy von SHATUNOV, Alexey, OLIVE, Montse, STRAUB, Volker, HILTON-JONES, David, DAMIAN, Maxwell S, KAMINSKA, Anna, VICART, Patrick, BUSHBY, Kate, DALAKAS, Marinos C, SAMBUUGHIN, Nyamkhishig, FERRER, Isidro, GOEBEL, Hans H, ODGEREL, Zagaa, GOLDFARB, Lev G, STADELMANN-NESSLER, Christine, IRLBACHER, Kerstin, VAN LANDEGHEM, Frank, BAYARSAIKHAN, Munkhuu, LEE, Hee-Suk, GOUDEAU, Bertrand, CHINNERY, Patrick F

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Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient von Olivé, Montse, Shatunov, Alexey, Gonzalez, Laura, Carmona, Olga, Moreno, Dolores, Quereda, Lidia Gonzalez, Martinez-Matos, J.A, Goldfarb, Lev G, Ferrer, Isidro

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Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutation von Pruszczyk, Piotr, Kostera-Pruszczyk, Anna, Shatunov, Alexey, Goudeau, Bertrand, Dramiñska, Agnieszka, Takeda, Kazuyo, Sambuughin, Nyamkhishig, Vicart, Patrick, Strelkov, Sergei V, Goldfarb, Lev G, Kamiñska, Anna

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Hypoglycosylation of α-dystroglycan in patients with hereditary IBM due to GNE mutations von Huizing, Marjan, Rakocevic, Goran, Sparks, Susan E, Mamali, Ioanna, Shatunov, Alexey, Goldfarb, Lev, Krasnewich, Donna, Gahl, William A, Dalakas, Marinos C

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Does Thrombosis Play a Causal Role in Lacunar Stroke and Cerebral Small Vessel Disease? von Koohi, Fatemeh, Harshfield, Eric L, Shatunov, Alexey, Markus, Hugh S

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Clinical and Myopathological Characteristics of Desminopathy Caused by a Mutation in Desmin Tail Domain von Maddison, Paul, Damian, Maxwell S., Sewry, Caroline, McGorrian, Catherine, Winer, John B., Odgerel, Zagaa, Shatunov, Alexey, Lee, Hee Suk, Goldfarb, Lev G.

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The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation von Vrabie, Alexandra, Goldfarb, Lev G, Shatunov, Alexey, Nägele, Andrea, Fritz, Peter, Kaczmarek, Ingo, Goebel, Hans H

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Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene von Olivé, Montse, Armstrong, Judith, Miralles, Francesc, Pou, Adolf, Fardeau, Michel, Gonzalez, Laura, Martínez, Francesca, Fischer, Dirk, Martínez Matos, Juan Antonio, Shatunov, Alexey, Goldfarb, Lev, Ferrer, Isidre

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Short communication: Generalized muscle pseudo-hypertrophy and stiffness associated with the myotilin Ser55Phe mutation: A novel myotilinopathy phenotype? von Gamez, Josep, Armstrong, Judith, Shatunov, Alexey, Selva-O'Callaghan, Albert, Dominguez-Oronoz, Rosa, Ortega, Arantxa, Goldfarb, Lev, Ferrer, Isidre, Olive, Montse

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