Results 71 to 80 of about 503,606 (298)

Reduced Muscular Carnosine in Proximal Myotonic Myopathy—A Pilot 1H‐MRS Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Myotonic dystrophy type 2 (proximal myotonic myopathy, PROMM) is a progressive multisystem disorder with muscular symptoms (proximal weakness, pain, myotonia) and systemic manifestations such as diabetes mellitus, cataracts, and cardiac arrhythmias.
Alexander Gussew, Maryam Kargaran, Maik Rothe, Andreas Deistung, Dietrich Stoevesandt, Walter A. Wohlgemuth, David Strube, Thomas Kendzierski, Anna Katharina Kölsch, Maurits Gerhard Abraham Heuschen, Markus Otto, Alexander Mensch   +11 more
wiley   +1 more source

The effect of upper instrumented vertebra level (T9 vs T10) on radiologic and functional outcomes in the surgical treatment of adult spinal deformity in osteoporotic patients over 60 years of age

Brain and Spine, 2021
Sina Coskun, Sinan Kahraman, Mustafa Eltayep, Recep Dincer, Ahmet Ates, Tunay Sanli, Ayhan Mutlu, Seray Gur, Selhan Karadereler, Meric Enercan, Azmi Hamzaoglu   +10 more
doaj   +1 more source

Daratumumab Treatment for Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP): A Case Report

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an immune‐mediated neuropathy featuring progressive weakness, sensory deficits, and areflexia. While corticosteroids, intravenous immunoglobulin, and plasmapheresis are effective first‐line immunotherapies, a subset of patients remains treatment‐refractory.
Xueyu Zhang, Jianli Zhao, Xue Zhao, Xiaowei Hu, Zichun Xiao, Jie Wu, Xiaowen Li, Jing Xu, Yu‐Jing Li   +8 more
wiley   +1 more source

Pulmonary functions after self sliding growth guidance for early-onset scoliosis with minimum five (5-13) years of follow-up

Brain and Spine, 2021
Sinan Kahraman, Sina Coskun, Recep Dincer, Ahmet Ates, Mustafa Eltayep, Ayhan Mutlu, Tunay Sanli, Selhan Karadereler, Sanem Eryilmaz Polat, Meric Enercan, Azmi Hamzaoglu   +10 more
doaj   +1 more source

Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian, Peter Auguste, Amy Grove, Anna Brown, Janette Parr, Mubarak Patel, Furqan Butt, Jeremiah Donoghue, Mehdi Yousefi, Jo Parsons   +9 more
wiley   +1 more source

Clinical and radiologic outcomes and pulmonary functions after vertebral body tethering for immature adolescent idiopathic scoliosis: Minimum 2 years follow up

Brain and Spine, 2021
Mustafa Eltayep, Sinan Kahraman, Ahmet Ates, Recep Dincer, Sina Coskun, Ugur Tasci, Seray Gur, Ayhan Mutlu, Sanem Eryilmaz Polat, Tunay Sanli, Selhan Karadereler, Meric Enercan, Azmi Hamzaoglu   +12 more
doaj   +1 more source

Advanced Technique of Unilateral Biportal Endoscopy on Revision Surgery for Recurred Herniated Interverbral Disc: A Technical Note

Case Reports in Orthopedics
Conclusion: Lumbar UBE offers a promising option for safe and effective reoperation in spinal surgery. Our technique, emphasizing bone-centered manipulation and specific strategies for scar tissue management, provides excellent visibility and enables ...
Hun-Chul Kim, Jin Young Lee, Hyeon Guk Cho, Jeong Woo Park, Sang-Ho Han, Young-Il Ko   +5 more
doaj   +1 more source

Neuregulin1 signaling promotes dendritic spine growth through kalirin [PDF]

, 2013
Michael E. Cahill, Christine Remmers, Kelly A. Jones, Zhong Xie, Robert A. Sweet, Peter Penzes   +5 more
openalex   +1 more source

Evaluation of the Efficacy and Safety of Satralizumab in a Pregnant NMOSD Patient With AQP4/MOG‐IgG Dual Seropositive: A Case Report

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Neuromyelitis Optica Spectrum Disorder (NMOSD) is a chronic autoimmune neuroinflammatory disease, typically characterized by antibodies against aquaporin 4 (AQP4‐IgG) or myelin oligodendrocyte glycoprotein (MOG‐IgG). Simultaneous seropositivity for both antibodies in a single patient is exceedingly rare.
Yeting Luo, Shuhua Xie, Xianghong Liu
wiley   +1 more source

Epidemiology of Lumbar Spine Injuries in Men’s and Women’s National Collegiate Athletic Association Basketball Athletes [PDF]

, 2019
Justin L. Makovicka, David G. Deckey, Karan A. Patel, Jeffrey D. Hassebrock, Andrew S. Chung, Sailesh V. Tummala, Thomas C. Hydrick, Austin Pena, Anikar Chhabra   +8 more
openalex   +1 more source