Results 201 to 210 of about 61,809 (286)

Cerebral blood flow regulation, central arterial stiffness and traumatic brain injury: Effects of aerobic exercise training

open access: yesExperimental Physiology, EarlyView.
Abstract Advanced age is the strongest risk factor for Alzheimer's disease and related dementias (ADRDs). Traumatic brain injury (TBI) has also been recognized as a risk factor for ADRD, potentially contributing to an earlier onset of the disease. Thus, elucidating the mechanisms underlying brain ageing and TBI is critical for developing strategies to ...
Tsubasa Tomoto   +3 more
wiley   +1 more source

Non-paraneoplastic limbic encephalitis associated with NMDAR and VGKC antibodies [PDF]

open access: yes, 2010
Derfuss, Tobias   +4 more
core   +1 more source

Early Detection of Neuroinflammation and White Matter Damage Following Dorsal Spinal Nerve Root Sectioning in a Nonhuman Primate Model

open access: yesMagnetic Resonance in Medicine, Volume 95, Issue 5, Page 2786-2796, May 2026.
ABSTRACT Purpose Dorsal rhizotomy, or spinal dorsal nerve root lesioning, is a surgical procedure used to treat intractable nerve pain by selectively severing sensory afferent nerve roots. This study aimed to evaluate whether multiparametric MRI, including diffusion tensor imaging (DTI), quantitative magnetization transfer (qMT), chemical exchange ...
Feng Wang, John C. Gore, Li Min Chen
wiley   +1 more source

Hepatic Alveolar Echinococcosis Mimicking Hepatic Malignancy. [PDF]

open access: yesRev Soc Bras Med Trop
Şimşek S, Karaca MS, Sağlam T.
europepmc   +1 more source

Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous ALS2 Exons 24–25 Deletion: Expanding the Genotypic Spectrum

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 929-936, April 2026.
ABSTRACT We describe a novel homozygous intragenic deletion in the ALS2 gene in an 8‐year‐old boy with Infantile‐onset Ascending Hereditary Spastic Paraplegia (IAHSP) and oculomotor apraxia, thereby contributing to the expanding genetic landscape of ALS2‐related disorders.
Vito Luigi Colona   +15 more
wiley   +1 more source

Longitudinal Behavior Phenotype Hallmarks in RNU4‐2 Syndrome: Implications for Clinical Management

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 201, Issue 3, Page 205-211, April 2026.
ABSTRACT Pathogenic variants in the non‐coding spliceosomal gene RNU4‐2 underlie ReNU syndrome, one of the most prevalent monogenic causes of neurodevelopmental disorders, accounting for ~0.4% of cases. Despite increasing recognition, little is known about the longitudinal behavioral and neuropsychiatric phenotype of affected individuals. We report two
Paola Francesca Ajmone   +8 more
wiley   +1 more source

Endoscopic Ultrasound‐Guided Fine‐Needle Aspiration for Diagnosing Late‐Stage Pelvic Recurrence of Uterine Leiomyosarcoma 15 Years After Total Hysterectomy

open access: yesDEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Endoscopic ultrasonography (EUS) facilitates high‐resolution visualization of lesions adjacent to the gastrointestinal tract. Uterine leiomyosarcoma (uLMS) is rare, aggressive, and difficult to diagnose. This report describes a rare case of pelvic recurrence of uLMS that occurred 15 years after hysterectomy, which was successfully diagnosed ...
Koichi Soga   +9 more
wiley   +1 more source

Multi‐Parametric MRI Approach at 3 T and 7 T for Assessing Skeletal Muscle Pathology in Myofibrillar Myopathies: A Pilot Study

open access: yesJournal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 2, April 2026.
ABSTRACT Background Myofibrillar myopathies (MFM) form a large group of clinically and genetically heterogeneous protein aggregate diseases. We investigated whether a novel quantitative MRI protocol can reveal new aspects of structural and biochemical muscle pathology in three classic MFM subtypes.
Claudius S. Mathy   +15 more
wiley   +1 more source

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