Results 161 to 170 of about 1,157,477 (291)

Correction: Clinical manifestations and outcomes of HSK following corneal transplantation. [PDF]

Front Med (Lausanne)
Wu D, Huang H, Zheng M, Chen Q, Zhou Z, Jiang L, Li Y, Liu Y, Ma B, Chen G, Huang Y, Cen F, Chen B, Li F, Qi H, Xu F, Lan Q.   +16 more
europepmc   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza, Arun Meyyazhagan, Eliseo Picchi, Gustavo Ribas, Ingrid Faber, Ryosuke Miyamoto, Preethi Basavaraju, Paolo Eusebi, Haripriya Kuchi Bhotla, Mario Stasi, Fabrizio Gaudiello, Francesco Patti, Filippo Maria Santorelli, Marcondes Cavalcante França Jr, José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Hélio Afonso Ghizoni Teive, Peter Henry St George‐Hyslop, Toshitaka Kawarai, Antonio Orlacchio   +19 more
wiley   +1 more source

Behçet's disease unraveled: Insights into clinical manifestations, diagnosis, and management. [PDF]

Medicine (Baltimore)
Alghamdi M, Lindsey S.
europepmc   +1 more source

The Case of a 19‐Year‐Old Woman Presenting With Headache and Transient Loss of Consciousness

Annals of Clinical and Translational Neurology, EarlyView.
Yan Lin, Xiaoyu Zhou, Lin Shen, Kunqian Ji, Yuying Zhao, Chuanzhu Yan, Yiming Liu, Wei Li   +7 more
wiley   +1 more source

ALDOA Promotes Glycolysis and NLRP3/GSDMD Pyroptosis to Accelerate ALS Progression

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Amyotrophic lateral sclerosis (ALS) is characterized by progressive motor neuron degeneration. Glycolytic dysregulation is implicated in disease progression, yet the underlying mechanisms remain unclear. This study investigates how Aldolase A (ALDOA) drives ALS progression through glycolysis‐mediated motor neuron pyroptosis.
Kaixin Yan, Yan Jiang, Yuxuan Yong, Tianshuo Zhang, Niannian Zhang, Qianqian Zeng, Xue Gong, Li Meng, Fangfang Bi, Yongmin Liu   +9 more
wiley   +1 more source

Clinical Manifestations of Emerging Trichosporon spp. Infections, France. [PDF]

Emerg Infect Dis
Desnos-Ollivier M, Alanio A, Gits-Muselli M, Boukris-Sitbon K, Bertho A, Sturny-Leclère A, Guemas E, Poirier P, Bonnal C, Bougnoux ME, Brun S, Chouaki T, Desbois-Nogard N, Chachaty E, Persat F, Pihet M, Paugam A, Botterel F, Demar M, Favennec L, Morio F, Gabriel F, Fekkar A, Gangneux JP, Mahinc C, Letscher-Bru V, Millon L, Dalle F, Bonhomme J, Nicolas M, Sendid B, Sasso M, Courtellemont L, Roux AL, Perraud-Cateau E, Guitard J, Mazars E, Lortholary O, Lanternier F.   +38 more
europepmc   +1 more source

Clinical Outcomes of SEEG‐Guided Radiofrequency Thermocoagulation in Children With Focal Drug‐Resistant Epilepsy: A Multicenter Real‐World Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Stereoelectroencephalography‐guided radiofrequency thermocoagulation (SEEG‐RFTC) has emerged as a safe and effective minimally invasive treatment for children with drug‐resistant focal epilepsy. Although evidence from real‐world studies remains limited, numerous pediatric cases have demonstrated promising outcomes. This retrospective
Weitao Chen, Stéphane Jean, Weihong Liu, Yihai Dai, Xinrong Fang, Xiaoqiang Wei, Shan Chen, Shiwei Song   +7 more
wiley   +1 more source

Clinical Manifestations of Lyme Borreliosis in Europe: Burden of Lyme Disease Study (BOLD), 2021-2022. [PDF]

Pathogens
Halsby K, Loew-Baselli A, Strle F, Moniuszko-Malinowska A, Berglund JS, Cibik V, Zakova D, Tan Y, Angulo FJ, Edwards J, Pilz A, Gessner BD, Begier E, Stark JH, On Behalf Of The Bold Study Group.   +14 more
europepmc   +1 more source

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone, Freddy Chafota, Miguel E. Rentería, Randi J. Hagerman, Ellery Santos, Anna Atkinson, Nicholas G. Martin, Elsdon Storey, Danuta Z. Loesch   +8 more
wiley   +1 more source

Clinical manifestations and cross-reactions between cockroaches and termites and identification of termites' major allergens. [PDF]

PLoS One
Lee MF, Wu CS, Lin TM, Li HF, Chen YH.
europepmc   +1 more source