Cervical stability training with and without core stability training for patients with cervical disc herniation: A randomized, single‐blind study von Buyukturan, B., Guclu‐Gunduz, A., Buyukturan, O., Dadali, Y., Bilgin, S., Kurt, E.E.

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Role of ultrasonography in detection of the localization of the nasoenteric tube von Dagli, R, Bayir, H, Dadali, Y, Tokmak, T, Erbesler, Z

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Kinetics of Methyl Iodide Tribosorption on the Solid-Phase Salt KI von Shubin, A. A., Dadali, Yu. V., Mitchenko, S. A.

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Züchner, Stephan, Mersiyanova, Irina V, Muglia, Maria, Bissar-Tadmouri, Nisrine, Rochelle, Julie, Dadali, Elena L, Zappia, Mario, Nelis, Eva, Patitucci, Alessandra, Senderek, Jan, Parman, Yesim, Evgrafov, Oleg, Jonghe, Peter De, Takahashi, Yuji, Tsuji, Shoij, Pericak-Vance, Margaret A, Quattrone, Aldo, Battologlu, Esra, Polyakov, Alexander V, Timmerman, Vincent, Schröder, J Michael, Vance, Jeffery M

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Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes von Bychkov, I.O., Itkis, Y.S., Tsygankova, P.G., Krylova, T.D., Mikhaylova, S.V., Klyushnikov, S.A., Pechatnikova, N.L., Degtyareva, A.V., Nikolaeva, E.A., Seliverstov, Y.A., Kurbatov, S.A., Dadali, E.L., Rudenskaya, G.E., Illarioshkin, S.N., Zakharova, E.Y.

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Elevated levels of mitochondrial CoQ10 induce ROS-mediated apoptosis in pancreatic cancer von Dadali, Tulin, Diers, Anne R., Kazerounian, Shiva, Muthuswamy, Senthil K., Awate, Pallavi, Ng, Ryan, Mogre, Saie, Spencer, Carrie, Krumova, Katerina, Rockwell, Hannah E., McDaniel, Justice, Chen, Emily Y., Gao, Fei, Diedrich, Karl T., Vemulapalli, Vijetha, Rodrigues, Leonardo O., Akmaev, Viatcheslav R., Thapa, Khampaseuth, Hidalgo, Manuel, Bose, Arindam, Vishnudas, Vivek K., Moser, A. James, Granger, Elder, Kiebish, Michael A., Gesta, Stephane, Narain, Niven R., Sarangarajan, Rangaprasad

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Presentation of Rare Phenotypes Associated with the FKBP10 Gene von Merkuryeva, Elena S, Markova, Tatiana V, Kenis, Vladimir M, Agranovich, Olga E, Dan, Ivan M, Kotalevskaya, Yulia Y, Shchagina, Olga A, Ryzhkova, Oxana P, Fomenko, Sergei S, Dadali, Elena L, Kutsev, Sergey I

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Multigene panel testing results in patients with dyslipidemia von Vasiluev, P.A., Ivanova, O.N., Ezhov, M.V., Chubykina, U.V., Prus, Y., Semenova, N., Guseva, D., Malyshev, P., Zakharova, E., Dadali, E.

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Epidemiology of Hereditary Diseases in the Karachay-Cherkess Republic von Zinchenko, Rena A, Makaov, Amin Kh, Marakhonov, Andrey V, Galkina, Varvara A, Kadyshev, Vitaly V, El'chinova, Galina I, Dadali, Elena L, Mikhailova, Lyudmila K, Petrova, Nika V, Petrina, Nina E, Vasilyeva, Tatyana A, Gundorova, Polina, Polyakov, Alexander V, Alexandrova, Oksana Y, Kutsev, Sergey I, Ginter, Eugeny K

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The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation von Kovalskaia, Valeriia A, Kungurtseva, Anastasiia L, Bostanova, Fatima M, Vasiliev, Peter A, Tabakov, Vyacheslav Y, Orlova, Mariia D, Povolotskaya, Inna S, Novoselova, Olga G, Bikanov, Roman A, Akhyamova, Mariia A, Tikhonovich, Yulia V, Popovich, Anastasiia V, Vitebskaya, Alisa V, Dadali, Elena L, Ryzhkova, Oxana P

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GABRA1‐Related Disorders: From Genetic to Functional Pathways von Musto, Elisa, Liao, Vivian W. Y., Johannesen, Katrine M., Fenger, Christina D., Lederer, Damien, Kothur, Kavitha, Fisk, Katrina, Bennetts, Bruce, Vrielynck, Pascal, Delaby, Delphine, Ceulemans, Berten, Weckhuysen, Sarah, Sparber, Peter, Bouman, Arjan, Ardern‐Holmes, Simone, Troedson, Christopher, Battaglia, Domenica I., Goel, Himanshu, Feyma, Timothy, Bakhtiari, Somayeh, Tjoa, Linda, Boxill, Martin, Demina, Nina, Shchagina, Olga, Dadali, Elena, Kruer, Michael, Cantalupo, Gaetano, Contaldo, Ilaria, Polster, Tilman, Isidor, Bertrand, Bova, Stefania M., Fazeli, Walid, Wouters, Leen, Miranda, Maria J., Darra, Francesca, Pede, Elisa, Le Duc, Diana, Jamra, Rami Abou, Küry, Sébastien, Proietti, Jacopo, McSweeney, Niamh, Brokamp, Elly, Andrews, Peter Ian, Gouray Garcia, Marie, Chebib, Mary, Møller, Rikke S., Ahring, Philip K., Gardella, Elena

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Cardiomyopathy of Friedreich's Disease. Modern Methods of Diagnostic von Fomicheva, E. I., Myasnikov, R. P., Selivyorstov, Y. A., Illarioshkin, S. N., Dadali, E. L., Drapkina, O. M.

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Сlinical and genetic characteristics of skeletal cyliopathies – short-rib thoracic dysplasia von Markova, Tatiana V., Kenis, Vladimir M., Melchenko, Evgeniy V., Komolkin, Igor A., Nagornova, Tatiana S., Osipova, Darya V., Semenova, Natalia A., Petukhova, Marina S., Demina, Nina A., Zakharova, Ekaterina Y., Dadali, Elena L., Kutsev, Sergey I.

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Elevated levels of mitochondrial CoQ 10 induce ROS-mediated apoptosis in pancreatic cancer von Dadali, Tulin, Diers, Anne R, Kazerounian, Shiva, Muthuswamy, Senthil K, Awate, Pallavi, Ng, Ryan, Mogre, Saie, Spencer, Carrie, Krumova, Katerina, Rockwell, Hannah E, McDaniel, Justice, Chen, Emily Y, Gao, Fei, Diedrich, Karl T, Vemulapalli, Vijetha, Rodrigues, Leonardo O, Akmaev, Viatcheslav R, Thapa, Khampaseuth, Hidalgo, Manuel, Bose, Arindam, Vishnudas, Vivek K, Moser, A James, Granger, Elder, Kiebish, Michael A, Gesta, Stephane, Narain, Niven R, Sarangarajan, Rangaprasad

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Erratum: Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Züchner, S, Mersiyanova, I V, Muglia, M, Bissar-Tadmouri, N, Rochelle, J, Dadali, E L, Zappia, M, Nelis, E, Patitucci, A, Senderek, J, Parman, Y, Evgrafov, O, Jonghe, P De, Takahashi, Y, Tsuji, S, Pericak-Vance, M A, Quattrone, A, Battologlu, E, Polyakov, A V, Timmerman, V, Schröder, J M, Vance, J M

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Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Zuchner, S, Mersiyanova, I V, Muglia, M, Bissar-Tadmouri, N, Rochelle, J, Dadali, E L, Zappia, M, Nelis, E, Patitucci, A, Senderek, J, Parman, Y, Evgrafov, O, Jonghe, P De, Takahashi, Y, Tsuji, S, Pericak-Vance, M A, Quattrone, A, Battologlu, E, Polyakov, A V, Timmerman, V, Schroder, J M, Vance, J M

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Correction: Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Züchner, S, Mersiyanova, I V, Muglia, M, Bissar-Tadmouri, N, Rochelle, J, Dadali, E L, Zappia, M, Nelis, E, Patitucci, A, Senderek, J, Parman, Y, Evgrafov, O, Jonghe, P De, Takahashi, Y, Tsuji, S, Pericak-Vance, M A, Quattrone, A, Battologlu, E, Polyakov, A V, Timmerman, V, Schröder, J M, Vance, J M

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Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features von Scala, M, Chua, GL, Chin, CF, Alsaif, HS, Borovikov, A, Riazuddin, S, Manzini, MC, Severino, M, Kuk, A, Fan, H, Jamshidi, Y, Toosi, MB, Doosti, M, Karimiani, EG, Salpietro, V, Dadali, E, Baydakova, G, Konovalov, F, Lozier, E, O'Connor, E, Sabr, Y, Alfaifi, A, Ashrafzadeh, F, Striano, P, Zara, F, Alkuraya, FS, Houlden, H, Maroofian, R, Silver, DL

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N78 Endoscopic versus open hydrocelectomy for the treatment of adult hydroceles von Emir, L, Sunay, M, Karakaya, Y, Dadalı, M, Erol, D

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