Results 131 to 140 of about 5,007,319 (296)
Grant Mudford with Max Dupain in Artarmon Studio, 1990 [picture] /
Title from inscription on reverse.; Condition: Good.; Inscription: "Grant Mudford with Max Dupain in Artarmon Studio, 1990.
White, Jill.
core
Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro +6 more
wiley +1 more source
White‐Matter Structural Connectivity and Alzheimer's Disease: A Mendelian Randomization Study
Background Alzheimer's disease (AD) and white‐matter structural connectivity have been linked in some observational studies, although it is unknown if this is a causal relationship.
Siyu Liu, Daoying Geng
doaj +1 more source
Portrait of Glenn Murcutt, 1983 [picture] /
Title from inscription on reverse.; Condition: Good.; Inscription: "Portrait of Glen [i.e. Glenn] Murcutt, 1983.
White, Jill.
core
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru +13 more
wiley +1 more source
Portrait of Glenn Murcutt, c 1980s [picture] /
Title from inscription on reverse.; Condition: Good.; Inscription: "Portrait of Glen [i.e. Glenn] Murcutt, c 80s.
White, Jill.
core
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li +11 more
wiley +1 more source
David Moore at Kilcare, [N.S.W.], c. 1985 [picture] /
Title from inscription on reverse.; Condition: Good.; Inscription: "David Moore at Kilcare c 1985.
White, Jill.
core
Screening Routine Clinical Notes for Epilepsy Surgery Candidates Using Large Language Models
ABSTRACT Objective Epilepsy surgery is severely underutilized despite proven efficacy, with substantial under‐referral of eligible patients in routine clinical practice. This study evaluated the potential role of large language models (LLMs) as decision‐support tools for screening unstructured clinical notes to identify epilepsy surgery candidates and ...
Uriel Fennig +9 more
wiley +1 more source
Proteomic networks of gray and white matter reveal tissue‐specific changes in human tauopathy
Objective To define tauopathy‐associated changes in the human gray and white matter proteome. Method We applied tandem mass tagged labeling and mass spectrometry, consensus, and ratio weighted gene correlation network analysis (WGCNA) to gray and white ...
Ashlyn G. Johnson +5 more
doaj +1 more source

