Search Results - "Duchenne muscular dystrophy"

Aminoglycoside Enhances the Delivery of Antisense Morpholino Oligonucleotides In Vitro and in mdx Mice by Mingxing Wang, Bo Wu, Sapana N. Shah, Peijuan Lu, Qilong Lu

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THE IMPORTANCE OF SEVERE CYTOLYSIS SYNDROME IN HYPERTROPHIC CARDIOMYOPATHY IN CHILDREN by Flavia-Crist, Amalia Fagarasan

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Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System by Annalisa Lattanzi, Stephanie Duguez, Arianna Moiani, Araksya Izmiryan, Elena Barbon, Samia Martin, Kamel Mamchaoui, Vincent Mouly, Francesco Bernardi, Fulvio Mavilio, Matteo Bovolenta

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Prevention of Tracheo-Innominate Artery Fistula Formation as a Complication of Tracheostomy: Two Case Reports by Byungsun Yoo, Bongjin Lee, June Dong Park, Seong Keun Kwon, Jae Gun Kwak

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The Dual Nature of Onuf's Nucleus: Neuroanatomical Features and Peculiarities, in Health and Disease by Roberta Schellino, Roberta Schellino, Marina Boido, Marina Boido, Marina Boido, Alessandro Vercelli, Alessandro Vercelli, Alessandro Vercelli

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Osteopontin deficiency delays inflammatory infiltration and the onset of muscle regeneration in a mouse model of muscle injury by Kitipong Uaesoontrachoon, Dimuthu K. Wasgewatte Wijesinghe, Eleanor J. Mackie, Charles N. Pagel

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Can Human Embryonic Stem Cell-Derived Stromal Cells Serve a Starting Material for Myoblasts? by Yu Ando, Marie Saito, Masakazu Machida, Chikako Yoshida-Noro, Hidenori Akutsu, Masataka Takahashi, Masashi Toyoda, Akihiro Umezawa

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Prenatal diagnosis of de novo DMD duplication by multiplex ligation-dependent probe amplification (MLPA) after noninvasive prenatal screening (NIPS) at 11 gestational weeks by Soo Hyun Kim, So Yeon Hong, Min Jin Lee, Kyung Min Kang, Ji Eun Park, Sung Han Shim, Dong Hyun Cha

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Genetically engineered pigs as models for human disease by Carolin Perleberg, Alexander Kind, Angelika Schnieke

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Manifesting Pediatric Carrier of Isolated Dystrophinopathy with Initial Presentation of Myalgia and Persistent HyperCKemia by Chien-Hua Wang, Wen-Chen Liang, Yi-Ning Su, Wen-Chieh Lee, Ching-Chyuan Su, Yuh-Jyh Jong

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Beware of missed diagnosis in patients with multiple genetic diseases: a case report by Detong Guo, Xuemei Li, Nan Liu, Xiaoli Yu, Jianbo Shu, Wenchao Sheng, Dong Li, Chunquan Cai

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Hypoglycemia detected during cardiac arrest of a non-diabetic patient with heart failure by İnci Tuğçe Çöllüoğlu, Hüseyin Dursun, Mete Yılmaz, Asım Oktay Ergene

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Identifying inversions with breakpoints in the Dystrophin gene through long-read sequencing: report of two cases by Liqing Chen, Xiaoping Luo, Hongling Wang, Yu Tian, Yan Liu

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Rational Design of Short Locked Nucleic Acid-Modified 2'-O-Methyl Antisense Oligonucleotides for Efficient Exon-Skipping In Vitro by Bao T. Le, Abbie M. Adams, Susan Fletcher, Stephen D. Wilton, Rakesh N. Veedu

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Polyquaternium-mediated delivery of morpholino oligonucleotides for exon-skipping in vitro and in mdx mice by Mingxing Wang, Bo Wu, Sapana N Shah, Peijuan Lu, Qilong Lu

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Abscesso renal em pediatria - desafios para o diagnóstico e manejo: relato de caso by Alexandre Neves da Rocha Santos, Maria Cristina Andrade, Eduardo Freitas Hatanaka

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Gene and Cellular Therapies for Leukodystrophies by Fatima Aerts-Kaya, Niek P. van Til

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Muscle Mass as a Biomarker for Health Status and Function in Pediatric Individuals with Neuromuscular Disabilities: A Systematic Review by Isabella R. Ferrara, Cristina L. Sadowsky

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Taurine and Methylprednisolone Administration at Close Proximity to the Onset of Muscle Degeneration Is Ineffective at Attenuating Force Loss in the Hind-Limb of 28 Days Mdx Mice by Robert G. Barker, Chris van der Poel, Deanna Horvath, Robyn M. Murphy

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Autophagy increase in Merosin-Deficient Congenital Muscular Dystrophy type 1A by Mariangela Mastrapasqua, Roberta Rossi, Lucrezia De Cosmo, Annalisa Resta, Mariella Errede, Antonella Bizzoca, Stefania Zampatti, Nicoletta Resta, Emiliano Giardina, Maddalena Ruggieri, Daniela Virgintino, Tiziana Annese, Nicola Laforgia, Francesco Girolamo

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