Results 61 to 70 of about 13,368 (153)

Novel NOTCH3 mutation c.1564 T > A (p.Cys522Ser) presenting with early-onset Parkinsonism and white matter lesions

Clinical Parkinsonism & Related Disorders
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a hereditary small vessel disease caused by mutations in the NOTCH3 gene, characterized by recurrent strokes, cognitive decline, and psychiatric ...
Nicola Rifino, Silvia Baratta, Esteban Zacarias, Isabella Canavero, Benedetta Storti, Mario Stanziano, Emanuela Maderna, Gianluca Marucci, Franco Taroni, Anna Bersano   +9 more
doaj   +1 more source

Spatial discrimination in patients with MSA, PSP, DIP, and VP with pain

Scientific Reports
Pain is common in Parkinson’s disease and frequently observed in other diseases involving parkinsonism. Abnormal scaling function in PD has been reportedly associated with pain, but the role of this function in pain in other parkinsonism-related diseases
Min Seung Kim, Jaeho Kim, Suk Yun Kang
doaj   +1 more source

BACK PAIN IN PARKINSONISM: EXPLORING PAIN GENERATORS AND INTERVENTIONAL MANAGEMENT: A CASE SERIES

Jurnal Kedokteran dan Kesehatan
Pain is a common non-motor symptom in parkinsonism, often overlooked despite its significant clinical impact. The most common form is Parkinson's disease (PD), followed by secondary and atypical parkinsonisms such as PSP.
Ismi Hamdani, Lie Anto, Irma Savitri, Tiara Aninditha, Nurul Fadli, Yusak Mangara Tua Siahaan, Dyah Tunjungsari, Henry Riyanto Sofyan   +7 more
doaj   +1 more source

Luxembourg Parkinson's study -comprehensive baseline analysis of Parkinson's disease and atypical parkinsonism. [PDF]

Front Neurol, 2023
Pavelka L, Rawal R, Ghosh S, Pauly C, Pauly L, Hanff AM, Kolber PL, Jónsdóttir SR, Mcintyre D, Azaiz K, Thiry E, Vilasboas L, Soboleva E, Giraitis M, Tsurkalenko O, Sapienza S, Diederich N, Klucken J, Glaab E, Aguayo GA, Jubal ER, Perquin M, Vaillant M, May P, Gantenbein M, Satagopam VP, Krüger R, NCER-PD Consortium.   +27 more
europepmc   +1 more source

Diagnostic accuracy of cerebral [¹⁸F]FDG PET in atypical parkinsonism. [PDF]

EJNMMI Res, 2023
Houssein NJ, Henriksen AC, Hejl AM, Marner L.   +3 more
europepmc   +1 more source

Retinal Structure Abnormalities in Parkinson's Disease and Atypical Parkinsonism. [PDF]

Biomolecules, 2023
Ma X, Li S, Zheng B, Hu L, Liu H, Wang Z, Wang Z, Chen H, Su W.   +8 more
europepmc   +1 more source

Atypical Parkinsonism as a Manifestation of Central Nervous System Lymphoma. [PDF]

Cureus
Gomes S, Lopes S, Moreira S, Araújo JM, Freitas E.   +4 more
europepmc   +1 more source

Case report: Atypical Parkinsonism following SARS-CoV-2 infection. [PDF]

Front Neurol, 2023
Polverino P, De Santis T, Perdixi E, Chiò A, Albanese A.   +4 more
europepmc   +1 more source

Homozygous <i>PTRHD1</i> Mutation in Intellectual Disability and Atypical Parkinsonism. [PDF]

Yale J Biol Med
Bölükbaşı EY, Mumtaz S, Afzal M, Shabbir RMK, Tolun A, Malik S.   +5 more
europepmc   +1 more source

Rapidly Progressive Atypical Parkinsonism as a Presenting Feature of ATX-CACNA1G (SCA42). [PDF]

Mov Disord Clin Pract, 2023
Martínez-Villota VA, Castillo-Torres SA, Rossi M, Merello M.   +3 more
europepmc   +1 more source