Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians? by Modibo Sangare, Ilo Dicko, Cheick Oumar Guinto, Adama Sissoko, Kekouta Dembele, Youlouza Coulibaly, Siaka Y. Coulibaly, Guida Landoure, Abdallah Diallo, Mamadou Dolo, Housseini Dolo, Boubacar Maiga, Moussa Traore, Mamadou Karembe, Kadiatou Traore, Amadou Toure, Mariam Sylla, Arouna Togora, Souleymane Coulibaly, Sékou Fantamady Traore, Brant Hendrickson, Katherine Bricceno, Alice B. Schindler, Angela Kokkinis, Katherine G. Meilleur, Hammadoun Ali Sangho, Brehima Diakite, Yaya Kassogue, Yaya Ibrahim Coulibaly, Barrington Burnett, Youssoufa Maiga, Seydou Doumbia, Kenneth H. Fischbeck

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Mitochondrial defects in the respiratory complex I contribute to impaired translational initiation via ROS and energy homeostasis in SMA motor neurons by Maximilian Paul Thelen, Brunhilde Wirth, Min Jeong Kye

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Spinal muscular atrophy caused by a novel Alu‐mediated deletion of exons 2a‐5 in SMN1 undetectable with routine genetic testing by Ivana Jedličková, Anna Přistoupilová, Lenka Nosková, Filip Majer, Viktor Stránecký, Hana Hartmannová, Kateřina Hodaňová, Helena Trešlová, Michaela Hýblová, Peter Solár, Gabriel Minárik, Mária Giertlová, Stanislav Kmoch

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What could be the function of the spinal muscular atrophy-causing protein SMN in macrophages? by Ines Tapken, Ines Tapken, Nora T. Detering, Nora T. Detering, Peter Claus, Peter Claus

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Enhancement of SMN protein levels in a mouse model of spinal muscular atrophy using novel drug‐like compounds by Jonathan J. Cherry, Erkan Y. Osman, Matthew C. Evans, Sungwoon Choi, Xuechao Xing, Gregory D. Cuny, Marcie A. Glicksman, Christian L. Lorson, Elliot J. Androphy

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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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Studying carrier frequency of spinal muscular atrophy in the State of Qatar and comparison to other ethnic groups: Pilot study by Faisal Ibrahim, Dinesh Velayutham, Mohamed Alsharshani, Usama AlAlami, Manar AlDewik, Tala Abuarja, Hilal Al Rifai, Nader I. Al‐Dewik

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The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method by Sinem Yalcintepe, Yasemin Karal, Selma Demir, Emine Ikbal Atli, Engin Atli, Damla Eker, Cisem Mail, Drenushe Zhuri, Hazal Sezginer Guler, Hakan Gurkan

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The importance of SMA screening tests in newborns – review by Barbara Rusinowska

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MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13.2 genes with disease phenotype in Egyptian patients by Heba A. Hassan, Nagia A. Fahmy, Nagham M. El-Bagoury, Noura R. Eissa, Wessam E. Sharaf-Eldin, Mahmoud Y. Issa, Maha S. Zaki, Mona L. Essawi

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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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Genetic pattern of SMN1, SMN2, and NAIP genes in prognosis of SMA patients by Heba Amin Hassan, Maha Saad Zaki, Mahmoud Yousry Issa, Nagham Maher El-Bagoury, Mona Lotfi Essawi

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Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype by Drenushe Zhuri, Hakan Gurkan, Damla Eker, Yasemin Karal, Sinem Yalcintepe, Engin Atli, Selma Demir, Emine Ikbal Atli

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SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver DiseaseSummary by Marc-Olivier Deguise, Chantal Pileggi, Yves De Repentigny, Ariane Beauvais, Alexandra Tierney, Lucia Chehade, Jean Michaud, Maica Llavero-Hurtado, Douglas Lamont, Abdelmadjid Atrih, Thomas M. Wishart, Thomas H. Gillingwater, Bernard L. Schneider, Mary-Ellen Harper, Simon H. Parson, Rashmi Kothary

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Spinal muscular atrophy in Venezuela: quantitative analysis of SMN1 and SMN2 genes by Yuri Yépez, Irene Paradisi, Sergio Arias

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Atrofia muscular espinhal: diagnóstico, tratamento e perspectivas futuras by Mariana T. C. Baioni, Celia R. Ambiel

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Spinal muscular atrophy (Werdnig‑Hoffmann atrophy disease) by Mariana A. RYZNYCHUK, Mariana I. KRYVCHANSKA, Irina V. LASTIVKA, Tatiana V. KHMARA, Valentyna A. GONCHARENKO

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Comprehensive Modeling of Spinal Muscular Atrophy in Drosophila melanogaster by Ashlyn M. Spring, Amanda C. Raimer, Amanda C. Raimer, Christine D. Hamilton, Michela J. Schillinger, A. Gregory Matera, A. Gregory Matera, A. Gregory Matera, A. Gregory Matera, A. Gregory Matera

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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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The Need for SMN-Independent Treatments of Spinal Muscular Atrophy (SMA) to Complement SMN-Enhancing Drugs by Niko Hensel, Niko Hensel, Sabrina Kubinski, Sabrina Kubinski, Peter Claus, Peter Claus

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