Results 61 to 70 of about 7,103 (220)

Severe neuropathic attack in a woman with acute intermittent porphyria: a case report

Journal of International Medical Research, 2021
Acute intermittent porphyria (AIP) is a rare autosomal dominant metabolic disease with a broad spectrum of clinical manifestations, and can be easily confused with other diseases.
Shiqian Huang, Ruiting Li, Yin Yuan
doaj   +1 more source

Clinical Validation of Plasma p‐217tau in Neurological Diseases

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi, Takumi Nakamura, Ryoma Takahashi, Tetsuya Ueda, Seiji Kinoshita, Chikage Uchida, Takashi Sugawara, Kentaro Hashimoto, Kunihiko Ishizawa, Masakuni Amari, Hiroo Kasahara, Yoshio Ikeda, Masamitsu Takatama, Mikio Shoji   +13 more
wiley   +1 more source

Motor Neurone Disease (MND/ALS) among Maltese in Malta and Australia : many sporadic cases were related [PDF]

, 2014
Objective: to look for genetic links between cases of MND. Method: to search for ancestors of Maltese cases dying in Malta and Australia and to record dispensations for consanguineous marriages.
Wyatt, H. V.
core  

Management of oral secretions in neurological disease. [PDF]

, 2017
Sialorrhoea is a common and problematic symptom that arises from a range of neurological conditions associated with bulbar or facial muscle dysfunction.
Abdelnour-Mallet, Alexander J McGeachan, Andersen, Arbouw, Banfi, Barbero, Bentivoglio, Chaléat-Valayer, Christopher J Mcdermott, Dressler, Dressler, Eiland, Erasmus, Faria, Foran, Garnock-Jones, Hadjikoutis, Hawkey, Hobson, Hockstein, Hyson, Intiso, Kasarskis, Khan, Layton, Marks, Mato, Miller, Mintzer, Moulding, Møller, Newall, Nicaretta, Norderyd, Parkes, Perez Lloret, Perry, Petracca, Proctor, Prommer, Rashnoo, Reed, Rodrigues, Rudney, Seppi, Sinha, Squires, Srivanitchapoom, Stone, Stuchell, Tahmassebi, Vandenberghe, Vashishta, Xu, Zeller   +54 more
core   +1 more source

The Spectrum of Abnormal Tongue Movements: Review of Phenomenology, Etiology, and Differential Diagnosis

Movement Disorders Clinical Practice, EarlyView.
ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan, Seyed‐Mohammad Fereshtehnejad, Christos Ganos, Emily Swinkin, Anthony E. Lang   +4 more
wiley   +1 more source

Isolated unilateral palatal and vocal cord palsy as an initial presentation of chronic inflammatory demyelinating polyradiculoneuropathy

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2019
Introduction Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an acquired autoimmune disease of the peripheral nervous system. Its clinical presentation and excellent response to steroids is a hallmark to the disease entity.
Madhavi Karri, Balakrishnan Ramasamy
doaj   +1 more source

Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale. [PDF]

PLoS ONE, 2011
The Natural History and Neuroprotection in Parkinson Plus Syndromes (NNIPPS) study was a large phase III randomized placebo-controlled trial of riluzole in Progressive Supranuclear Palsy (PSP, n = 362) and Multiple System Atrophy (MSA, n = 398).
Christine A M Payan, François Viallet, Bernhard G Landwehrmeyer, Anne-Marie Bonnet, Michel Borg, Franck Durif, Lucette Lacomblez, Frédéric Bloch, Marc Verny, Jacques Fermanian, Yves Agid, Albert C Ludolph, Peter N Leigh, Gilbert Bensimon, NNIPPS Study Group   +14 more
doaj   +1 more source

Striatal dopaminergic lesions contributed to the disease severity in progressive supranuclear palsy

Frontiers in Aging Neuroscience, 2022
BackgroundReduced dopamine transporter (DAT) binding in the striatum has been reported in patients with progressive supranuclear palsy (PSP). However, the relationship between striatal dopaminergic lesions and the disease severity of PSP remains to be ...
Ming-Jia Chen, Jia-Ying Lu, Xin-Yi Li, Fang-Yang Jiao, Chuan-Tao Zuo, Chuan-Tao Zuo, Jian Wang, Feng-Tao Liu, Yu-Jie Yang, Yu-Jie Yang   +9 more
doaj   +1 more source

Atypical MRI features in familial adult onset Alexander disease: case report [PDF]

, 2016
BACKGROUND: Alexander disease (AxD) is a rare neurological disease, especially in adults. It shows variable clinical and radiological features. CASE PRESENTATION: We diagnosed a female with AxD presenting with paroxysmal numbness of the limbs at the ...
Anna Zhou, Heng Zhou, Huabing Wang, Lin Zhao, Xiaoqing Gong, Xindi Li, Xinghu Zhang, Yonghong Liu   +7 more
core   +1 more source

Longitudinal Videofluorographic Dysphagia Measures in Progressive Supranuclear Palsy

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Dysphagia can lead to fatal aspiration pneumonia in progressive supranuclear palsy (PSP). Little is known about the longitudinal progression of dysphagia or whether it differs across PSP clinical variants. Objectives To characterize longitudinal changes in dysphagia across PSP variants and determine relationships with disease ...
Anna Chiara Cattani, Jerusha G. Bhaskaran, Farwa Ali, Julie Stierwalt, Federica Agosta, Massimo Filippi, Keith A. Josephs, Heather M. Clark, Jennifer L. Whitwell   +8 more
wiley   +1 more source