Results 171 to 180 of about 938,523 (305)

Baseline Regional Cholinergic Denervation Predicts Cognitive Trajectories in Moderate Parkinson Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cognitive decline is a disabling and variable feature of Parkinson disease (PD). While cholinergic system degeneration is linked to cognitive impairments in PD, most prior research reported cross‐sectional associations. We aimed to fill this gap by investigating whether baseline regional cerebral vesicular acetylcholine transporter ...
Taylor Brown, Giulia Carli, Prabesh Kanel, Stiven Roytman, Jaimie Barr, Nicolaas I. Bohnen, Roger L. Albin   +6 more
wiley   +1 more source

The Japanese Catheter Ablation Registry (J-AB): Annual Report in 2023. [PDF]

J Arrhythm
Kusano K, Inoue K, Kanaoka K, Miyamoto K, Okumura Y, Iwasaki YK, Satomi K, Takatsuki S, Nakamura K, Yamashita S, Masuda M, Iwanaga Y, Chishaki-Kawabata S, Yamane T, Shimizu W, Tada H, J‐AB registry investigators.   +16 more
europepmc   +1 more source

A Prospective Study of Individuals at Risk of Multiple Sclerosis Informs the Design of Primary Prevention Studies

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective In multiple sclerosis, the optimal time for deploying a therapeutic intervention is before the central nervous system is damaged; given the success of trials treating the earliest stage of MS, the radiologically isolated syndrome, developing primary prevention strategies is an important next challenge.
Amy W. Laitinen, Ceren Tozlu, Tina Roostaei, Fatoumata Diallo, Kaho Onomichi, Jiyeon Son, Zongqi Xia, Philip L. De Jager   +7 more
wiley   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina, Anna Marcé‐Grau, Barbara Masotto, Marta Codina, Lamia BenJemaa, Yasmina Elaribi, Mónica Martinez‐Gallo, Roger Colobran, Angel Sanchez‐Montañez, Irene Valenzuela, Yoshiko Murakami, Alfons Macaya   +11 more
wiley   +1 more source

The ERA Registry Annual Report 2023: epidemiology of kidney replacement therapy in Europe, with a focus on age comparisons. [PDF]

Clin Kidney J
Hoekstra MWF, Boenink R, Bonthuis M, Boerstra BA, Astley ME, Montez de Sousa IR, Gjorgjievski N, Resic H, Mitsides N, Hommel K, Guidotti R, Marín Sánchez I, Slon-Roblero MF, Artamendi M, Beckerman P, Buchwinkler L, Gellert R, Kuzema V, Okša A, Comas J, Heylen LMTJ, Lassalle M, Hernandez Ramirez S, Santhakumaran S, Seyahi N, Åsberg A, Weekers LE, Muñoz-Terol JM, Trujillo-Alemán S, Memeti Smaili F, Ots-Rosenberg M, Indridason OS, Komissarov KS, Ten Dam MAGJ, Stendahl M, Galvão AA, Ortiz A, Stel VS, Kramer A.   +38 more
europepmc   +1 more source

The President's Annual Report [PDF]

Occupational Health Nursing, 1970
openaire   +3 more sources

FDG‐PET Associations With Disease Severity and Outcomes in NMDA‐Receptor IgG Autoimmune Encephalitis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Patients with N‐methyl‐D‐aspartate (NMDA) receptor‐immunoglobulin G (IgG) autoimmune encephalitis (NMDAR‐IgG AE) demonstrate occipital lobe hypometabolism on baseline brain fluorodeoxyglucose‐positron emission tomography (bFDG‐PET).
Jonathan K. Lee, Jeffrey Lambe, Scott Johnson, Akua Abrah, Jennifer Bullen, Jeffrey A. Cohen, Tatchaporn Ongphichetmetha, Amy Kunchok   +7 more
wiley   +1 more source

Minimally invasive cardiac surgeries in 2022: annual report by Japanese Society of Minimally Invasive Cardiac Surgery. [PDF]

Gen Thorac Cardiovasc Surg
Shimokawa T, Kumamaru H, Motomura N, Nishi H, Nakajima H, Kamiya H, Okamoto K, Hosoba S, Saiki Y, Miura T, Tabata M, Shiose A, Sakaguchi T.   +12 more
europepmc   +1 more source

Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz, Christopher H. Thompson, Linda C. Laux, Alfred L. George Jr.   +3 more
wiley   +1 more source

Highlights of the 2024 American Joint Replacement Registry Annual Report. [PDF]

Arthroplast Today
Carender CN, Hegde V, Levine BR, Huddleston JI, Cohen-Rosenblum A.   +4 more
europepmc   +1 more source