Results 231 to 240 of about 217,018 (317)

Mitochondrial Disorders Should Be Considered as a Differential Diagnosis of Thiamine Deficiency. [PDF]

HCA Healthc J Med
Finsterer J.
europepmc   +1 more source

Myelitis‐Predominant Aggressive Phenotype: Unveiling Unique Patterns of Late‐Onset Neuromyelitis Optica Spectrum Disorders

Annals of Neurology, EarlyView.
Objective The objective of this study was to compare clinical features and prognosis of late‐onset neuromyelitis optica spectrum disorder (LO‐NMOSD, onset age ≥60 years) with adult‐onset NMOSD (AO‐NMOSD, onset age 18–59 years), and to provide insights for individualized management in elderly patients.
Ya‐Lan Pu, Jin‐Zhou Feng, Hua‐Xing Meng, Hai‐Bing Xiao, Xiao‐Ling Li, Jin Zhen, Wen‐Ying Lu, Xu‐Ming Xi, Ti Wu, Bao‐Shi Yuan, Mo‐Li Fan, Chao Zhang, De‐Cai Tian, Xia Meng, Fu‐Dong Shi, Tian Song   +15 more
wiley   +1 more source

Switch-Off response to mid-cingulate cortex stimulation: a video case report. [PDF]

Clin Neurophysiol Pract
Vassallo P, Poole O, Guan X, Giampiccolo D, Marques E, Vivekananda U, Duncan JS, Diehl B.   +7 more
europepmc   +1 more source

Neurochemical organization of cortical proteinopathy and neurophysiology along the Alzheimer's disease continuum [PDF]

Alex I. Wiesman, Jonathan Gallego‐Rudolf, Sylvia Villeneuve, Sylvain Baillet, Tony W. Wilson   +4 more
openalex   +1 more source

Brain Atrophy Associated With Risk Variant rs10191329 Extends Beyond Multiple Sclerosis

Annals of Neurology, EarlyView.
The risk allele rs10191329*A is associated with disease severity and brain atrophy in people with multiple sclerosis (MS). We investigated the association of rs10191329 with age‐related brain atrophy in a population‐based cohort using 10,308 magnetic resonance imaging (MRI) scans of 4,815 participants aged ≥ 45 years without MS in cross‐sectional and ...
Cato E. A. Corsten, Ana M. Marques, Elisabeth J. Vinke, C. Louk de Mol, Rinze F. Neuteboom, M. Kamran Ikram, Mohsen Ghanbari, Frank J. Wolters, Beatrijs Wokke, Meike W. Vernooij, Joost Smolders   +10 more
wiley   +1 more source

Peripheral Neuropathy in p.Val142Ile (Val122Ile) Variant Hereditary Transthyretin-Mediated Amyloidosis: United Kingdom Experience. [PDF]

Neurol Genet
Zhang VJW, O'Donnell LF, Skorupinska M, Carganillo R, Rossor AM, Fontana M, Rowczenio D, Gilbertson J, Gillmore JD, Reilly MM.   +9 more
europepmc   +1 more source

Clinical neurophysiology in the treatment of movement disorders: IFCN handbook chapter [PDF]

Jean‐Pascal Lefaucheur, Elena Moro, Yuichiro Shirota, Yoshikazu Ugawa, Talyta Grippe, Robert Chen, David Benninger, Bahman Jabbari, Sanaz Attaripour, Mark Hallett, Walter Paulus   +10 more
openalex   +1 more source

Probabilistic Lesion Mapping to Optimize Thalamotomy Targets for Focal Hand Dystonia

Annals of Neurology, EarlyView.
Objective Focal hand dystonia (FHD) severely impairs task‐specific motor control, yet the optimal surgical target for stereotactic intervention remains uncertain. This study aimed to identify the precise thalamic lesion site associated with symptomatic improvement and to clarify its network connectivity. Methods We retrospectively analyzed 164 patients
Masahiko Nishitani, Shiro Horisawa, Konstantin Butenko, Hiroki Togo, Arun Garimella, William Drew, Melissa Chua, Esraa Shaban, Takakazu Kawamata, Takaomi Taira, Andreas Horn, Michael D. Fox, Takashi Hanakawa   +12 more
wiley   +1 more source

Before depression in diabetes is attributed to polyneuropathy, all other causes must be ruled out. [PDF]

Future Sci OA
Finsterer J.
europepmc   +1 more source