Botulinum Toxin Effects and Its Association with Vitamin and Mineral Supplementation: A Narrative Review. [PDF]
Puizina E +7 more
europepmc +1 more source
Perspectives on ethnic and racial disparities in Alzheimer\u27s disease and related dementias: Update and areas of immediate need [PDF]
Babulal, Ganesh M +2 more
core +1 more source
Clinical‐grade HLA‐homozygous iPSC‐derived neural precursor cells restore motor function, rebuild striatal circuitry and reduce neuroinflammation in QA‐lesioned rats. These findings demonstrate robust neuronal replacement and microenvironment modulation, supporting their potential as a regenerative therapy for Huntington's disease.
Hyeonjoong Jeon +6 more
wiley +1 more source
Not All Ascending Weakness and Numbness Is Guillain-Barré Syndrome: A Report of Two Cases of Copper Deficiency Myelopathy. [PDF]
Albright NL, Pitter D, Benameur K.
europepmc +1 more source
SAMMENDRAG Introduksjon: Kroniske utbredte smerter (CWP) er ofte assosiert med nevrologiske symptomer som depresjon, angst og søvnløshet, og medfører betydelig funksjonsnedsettelse. Vitamin D-mangel er vanlig og har blitt foreslått som en mulig modifiserbar risikofaktor; imidlertid har tidligere studier gitt motstridende resultater.
openaire +1 more source
Summary This second part of the S3 guideline on the diagnosis and treatment of alopecia areata (AA), presents key recommendations on topical and systemic therapy, quality of life and support services. The first part of the guideline, published separately, covers the definition and content of epidemiology and diagnosis as well as comorbidities, risk and
Ulrike Blume‐Peytavi +13 more
wiley +1 more source
Alterations of fecal short-chain fatty acids solely in the course of multiple sclerosis: rethinking the gut-brain axis in the early stages of MS. [PDF]
Stögbauer J +6 more
europepmc +1 more source
Clinical and genetic characterization of intellectual disability
This study examines the etiological factors and comorbidities in a large cohort of Finnish patients with intellectual disability. Genetic causes—including chromosomal abnormalities and pathogenic gene variants—were more frequently identified in individuals with moderate to profound intellectual disability.
Aarni Venetvaara +14 more
wiley +1 more source
Unveiling the unexpected: refractory rickets as an uncommon presentation of tyrosinemia type I. [PDF]
Ramanna MB, Kamate M, Koppad B.
europepmc +1 more source
The cerebral palsy directed acyclic graph: A structural causal model of aetiology
The first international cerebral palsy directed acyclic graph (CP‐DAG) maps over 100 nodes and 370 links across biological, clinical, and social domains, offering a unified causal framework to guide research and identify knowledge gaps. Abstract Aim To describe the development of the initial version of the cerebral palsy (CP) directed acyclic graph ...
Shona Goldsmith +9 more
wiley +1 more source

