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Displaying 56 - 60 of 216

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The Phase 3 RESILIENT Study: Taldefgrobep Alfa in Spinal Muscular Atrophy

Author:Lair, Lindsey   Qureshi, Irfan   Bechtold, Clifford   Durham, Susan   Campbell, Daniel   Marin, Jackie   Coric, Vladimir   

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Spinal Muscular Atrophy and Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.008  

Author Institution:Biohaven Pharmaceuticals, Inc, New Haven, CT  Biohaven Pharmaceuticals, Inc, New Haven , CT  

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Distinct Genetic Distribution of Distal Hereditary Motor Neuropathy in Turkey: A Single Centre Experience

Author:Cakar, Arman   Candayan, Ayse   Maroofian, Reza   Durmus, Hacer   Houlden, Henry   Battaloglu, Esra   Parman, Fatma Yesim   

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Spinal Muscular Atrophy and Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.009  

Author Institution:Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey  Bogazici University, Istanbul, Turkey, Istanbul, Turkey  UCL Queen Square Institute of Neurology, London, United Kingdom  

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Neurofilament Light Chain in Spinal Bulbar Muscle Atrophy and Amyotrophic Lateral Sclerosis 4

Author:Shahim, Pashtun-Poh   Kokkinis, Angela   Alqahtani, Abdullah   Grunseich, Christopher   

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Spinal Muscular Atrophy and Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.010  

Author Institution:National Institutes of Health, Bethesda, MD  National Institutes of Health, Derwood, MD  

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Expanding Spectrum of Charcot Marie Tooth Disease type 2U: Novel Variants of the MARS Gene

Author:Zakin, Elina   Singh, Baljinder   

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Spinal Muscular Atrophy and Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.011  

Author Institution:NYU School of Medicine, New York, NY  NYU Langone Health, New York, NY  

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Neurogenetic Intersection: A Fascinating CMT-CIDP Overlap in a Brazilian Family

Author:Pupe, Camila   Moura, Carolina   Azevedo, Helen   Marques, Lya   Machado, Flavia   Davidovich, Eduardo   Nascimento, Osvaldo   

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Spinal Muscular Atrophy and Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.012  

Author Institution:Universidade Federal Fluminense, Rio De Janeiro, Brazil  Universidade Federal Fluminense, Niterói, Brazil  Hospital Universitário Antônio Pedro, Niterói, Brazil  HUAP, Niterói, Brazil  Fluminense Federal University, Rio De Janeiro, Brazil  

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Displaying 56 - 60 of 216

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