Results 21 to 30 of about 48,653 (304)

Striatal D1 Dopamine Neuronal Population Dynamics in a Rat Model of Levodopa-Induced Dyskinesia

Frontiers in Aging Neuroscience, 2022
BackgroundThe pathophysiology of levodopa-induced dyskinesia (LID) in Parkinson’s disease (PD) is not well understood. Experimental data from numerous investigations support the idea that aberrant activity of D1 dopamine receptor-positive medium spiny ...
Shasha Gao, Rui Gao, Lu Yao, Jie Feng, Wanyuan Liu, Yingqiong Zhou, Qiongchi Zhang, Yong Wang, Jian Liu   +8 more
doaj   +1 more source

Domiciliary High-Flow Nasal Therapy in Primary Ciliary Dyskinesia [PDF]

, 2023
We report the case of an adolescent with severe primary ciliary dyskinesia (PCD) phenotype associated with a rare genotype. His clinical condition deteriorated, with daily cough and breathlessness, hypoxemia, and lung function decline.
Gomes, Rita, Barbosa, Telma, Queirós, Joana, Borges, Joana, Cardoso, Ana Lúcia   +4 more
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Clinical care for primary ciliary dyskinesia: current challenges and future directions

European Respiratory Review, 2017
Primary ciliary dyskinesia (PCD) is a rare genetic disease that affects the motility of cilia, leading to impaired mucociliary clearance. It is estimated that the vast majority of patients with PCD have not been diagnosed as such, providing a major ...
Bruna Rubbo, Jane S. Lucas
doaj   +1 more source

The Relationship Between Electrical Energy Delivered by Deep Brain Stimulation and Levodopa-Induced Dyskinesias in Parkinson's Disease: A Retrospective Preliminary Analysis

Frontiers in Neurology, 2021
Background: Adaptive Deep Brain Stimulation (aDBS) is now considered as a new feasible and effective paradigm to deliver DBS to patients with Parkinson's disease (PD) in such a way that not only stimulation is personalized and finely tuned to the ...
Marco Prenassi, Mattia Arlotti, Linda Borellini, Tommaso Bocci, Filippo Cogiamanian, Marco Locatelli, Marco Locatelli, Marco Locatelli, Paolo Rampini, Sergio Barbieri, Alberto Priori, Sara Marceglia, Sara Marceglia   +12 more
doaj   +1 more source

Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis [PDF]

Journal of Movement Disorders, 2022
Movement disorders associated with glial fibrillary acidic protein (GFAP) autoantibodies have rarely been reported as ataxia or tremors. A 32-year-old man with headache and fever, initially diagnosed with viral meningoencephalitis, showed gradual ...
Jae Young Joo, Dallah Yoo, Tae-Beom Ahn
doaj   +1 more source

Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm. [PDF]

, 2013
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous ciliopathy disorder affecting cilia and sperm motility. A range of ultrastructural defects of the axoneme underlie the disease, which is characterised by chronic respiratory symptoms ...
Danke-Roelse, JE, Hart, S.L., Munye, Mustafa M., Scambler, PJ, Rosser, E.M., Hart, Stephen L, Beales, Philip L, Bacchelli, C, Moore, Anthony T., Chung, Eddie MK, Sloper, John J, Danke-Roelse, Jeannette E, Moore, A.T., Pals, Gerard, Beales, Philip L., Sloper, John J., Moore, Anthony T, Hogg, C, Hogg, C., Bacchelli, Chiara, Mitchison, Hannah M, Shoemark, A., Moore, AT, James, C.T., Scambler, Peter J, Chung, E.M.K., Rosser, Elisabeth M., Bacchelli, C., Shoemark, Amelia; id_orcid, Patel, M., Hogg, Claire, Onoufriadis, Alexandros, Schmidts, Miriam, Emes, R.D., Munye, Mustafa M, Hull, S., Sloper, JJ, Hull, Sarah, Beales, PL, Beales, P.L., Hart, Stephen L., Munye, MM, Schmidts, M, James, Chela T, Scambler, P.J., James, Chela T., Mitchison, H.M., nke-Roelse, J.E., Hull, S, Onoufriadis, A., Rosser, Elisabeth M, Emes, Richard D., Patel, Mitali, Pals, G., Mitchison, Hannah M., Patel, M, Pals, G, Emes, RD, Munye, M.M., James, CT, Schmidts, M., Danke-Roelse, Jeannette E., Chung, Eddie M.K., Shoemark, Amelia, Mitchison, HM, Emes, Richard D, Chung, EM, Shoemark, A, Onoufriadis, A, Sloper, J.J., Hart, SL, Rosser, EM, Scambler, Peter J.   +72 more
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A case of paroxysmal kinesigenic dyskinesia suspected to be reflex epilepsy [PDF]

, 2021
An 11-year-old male patient developed weakness or right arm elevation after sudden movement at the age of eight. Reflex epilepsy was initially suspected; however, magnetic resonance imaging and electroen-cephalography (EEG) revealed no abnormality. Video-
Fukumura, Shinobu, Nakayama-Kamada, Chie, Ochi, Satoko, Mikuni, Nobuhiro, Enatsu, Rei, Kuribara, Tomoyoshi   +5 more
core   +1 more source

Tardive dyskinesia [PDF]

Acta Psychiatrica Scandinavica, 1988
ABSTRACT— Tardive dyskinesia (TD) is a syndrome of involuntary movements that develops in predisposed individuals during neuroleptic drug treatment, with an average prevalence of 15%. Neuroleptic (antidopaminergic) drugs are the predominant etiological factor.
J, Gerlach, D E, Casey
openaire   +6 more sources

Proceedings of the 2nd BEAT-PCD conference and 3rd PCD training school: part 1

BMC Proceedings, 2018
Primary ciliary dyskinesia (PCD) is a rare heterogenous condition that causes progressive suppurative lung disease, chronic rhinosinusitis, chronic otitis media, infertility and abnormal situs.
Florian Halbeisen, Claire Hogg, Mikkel C. Alanin, Zuzanna Bukowy-Bieryllo, Francisco Dasi, Julie Duncan, Amanda Friend, Myrofora Goutaki, Claire Jackson, Victoria Keenan, Amanda Harris, Robert A. Hirst, Philipp Latzin, Gemma Marsh, Kim Nielsen, Dominic Norris, Daniel Pellicer, Ana Reula, Bruna Rubbo, Nisreen Rumman, Amelia Shoemark, Woolf T. Walker, Claudia E. Kuehni, Jane S. Lucas   +23 more
doaj   +1 more source

Focal epilepsy presenting as tongue tremor: A case report

Clinical Case Reports, 2022
Plenty of etiologies are reported to cause tongue tremor. Focal epilepsy presenting as isolated tongue tremor is a rare condition, suggesting how variable the focal seizure presentation may be.
Mehri Salari, Kamran Rezaei, Alimohammad Mirdehghan, Arya Behzadi, Masoud Etemadifar   +4 more
doaj   +1 more source