Adult spinal muscular atrophy: problems of early diagnosis by Yu. A. Shpilyukova, S. N. Illarioshkin

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Outcomes of genetic testing and prenatal diagnosis of spinal muscular atrophy in Jordan by Mohammad Shboul, Mohammed El-Khateeb, Rajaa Fathallah, Khadeeja Al-Rashed

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Biomarkers in spinal muscular atrophy by Liping Yan, Jinping Zhang, Jian Zheng, Hua Hao

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Insights into diagnostic difficulties in spinal muscular atrophy: a Case Report series by Kakha Bregvadze, Luka Abashishvili, Nana Nino Tatishvili, Nana Nino Tatishvili, Teona Shatirishvili, Teona Shatirishvili, Ana Bedoshvili, Ana Bedoshvili, Gocha Chikvinidze, Arndt Rolfs, Arndt Rolfs, Volha Skrahina, Tinatin Tkemaladze, Tinatin Tkemaladze

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Diagnostic criteria for spinal muscular atrophy 5q by I. V. Sharkova, E. L. Dadali, S. S. Nikitin

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Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy in Ningde City, Fujian Province by JiaoJiao Lu, Xian Zheng, Jing Yang, WenXu Dong, LuoYuan Cao, Xiaomei Zeng, Qinjuan Wu, Xunyan Chen, XianGuo Fu

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Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile by Karin ALVAREZ, Bernardita SUAREZ, María Angélica PALOMINO, Cecilia HERVIAS, Giancarlo CALCAGNO, Maripaz MARTÍNEZ-JALILIE, Andrés LOZANO-ARANGO, Susana LILLO, Mariana HARO, Fanny CORTÉS, Samuel PANTOJA, Andrés CHAHIN, Paulina ORELLANA, Jorge A BEVILACQUA, Enrico BERTINI, Claudia CASTIGLIONI

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The efficacy and safety of nusinersen within the expanded access program in Russia by S. B. Artemieva, L. M. Kuzenkova, E. S. Ilyina, Yu. A. Kursakova, L. M. Kolpakchi, E. Yu. Sapego, A. A. Golenko, S. G. Popovich, D. V. Parshin, O. A. Shidlovskaya, Yu. O. Papina, A. V. Monakhova, D. V. Vlodavets

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Common complications in spinal muscular atrophy (SMA) type 1 after nusinersen treatment by Yiğithan Güzin, Osman Büyükşen, Pınar Gençpınar, Nihal Olgaç Dündar, Figen Baydan

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Factors modifying the course of spinal muscular atrophy 5q by M. A. Akhkiamova, O. A. Shchagina, A. V. Polyakov

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Spinal Muscular Atrophy 5q under the Mask of Myopathy: 10 Clinical Cases by Sergei A. Kurbatov

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Characteristics of genetic changes in the <i>SMN1</i> gene in spinal muscular atrophy 5q by A. V. Dil, V. D. Nazarov, D. V. Sidorenko, S. V. Lapin, V. L. Emanuel

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Quantitative and structural features of the SMN1 and SMN2 genes in patients with spinal muscular atrophy 5q by A. I. Vlasenko, V. D. Nazarov, S. V. Lapin, A. V. Mazing, E. A. Surkova, T. V. Blinova, T. M. Alekseeva

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Outcomes of a Pilot Newborn Screening Program for Spinal Muscular Atrophy in the Valencian Community by Alba Berzal-Serrano, Belén García-Bohórquez, Elena Aller, Teresa Jaijo, Inmaculada Pitarch-Castellano, Dolores Rausell, Gema García-García, José M. Millán

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Molecular mechanism of neurodegeneration in spinal muscular atrophy by A. I. Vlasenko, V. D. Nazarov, S. V. Lapin, A. V. Mazing, E. A. Surkova, T. V. Blinova, M. P. Topuzova, T. M. Alekseeva

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Experience of using gene replacement therapy with Zolgensma® (onasemnogene abeparvovec) in real clinical practice in Russia by S. B. Artemyeva, Yu. O. Papina, O. A. Shidlovskaya, A. V. Monakhova, D. V. Vlodavets

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Unraveling the genetic mysteries of spinal muscular atrophy in Chinese families by Shanshan Gao, Duo Chen, Qianqian Li, Xuechao Zhao, Chen Chen, Lina Liu, Miao Jiang, Zhenhua Zhao, Yanhua Wang, Xiangdong Kong

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Approaches to pathogenetic therapy of spinal muscular atrophy in children and newborns by S. B. Artemyeva, O. A. Shidlovskaya, Yu. O. Papina, A. V. Monakhova, I. V. Shulyakova, E. D. Belousova, O. Yu. Germanenko, D. V. Vlodavets

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Spinal muscular atrophy type 1 in the Caribbean: the first case report from the Dominican Republic by María Belén Martín-Sanz, Delvis Lucas-Muñoz, Manuel Colomé-Hidalgo, Manuel Colomé-Hidalgo

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Assessment of social emotional, cognitive and communicative development and adaptive behavior in children with spinal muscular atrophy 5q by Yu. O. Papina, N. N. Zavadenko, E. A. Melnik, S. B. Artemyeva, I. A. Berdalina, D. V. Vlodavets

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