Results 121 to 130 of about 9,338,478 (297)

Aquaporin-4 immunofluorescence of moderate (Figure 5A

open access: yes, 2013
with a–e at 2× magnification, a1–e1 at 4× magnification, and quantified in C) and severe (Figure 5Bwith a–e at 2× magnification, a1–e1 at 4× magnification, and quantified in C) TBI brains.
Yuji Kaneko (106226)   +5 more
core   +1 more source

MRI Diffusion Tensor Image Analysis Along the Perivascular Space: Effects of Mean Tract Orientation Divergence

open access: yesJournal of Magnetic Resonance Imaging, EarlyView.
ABSTRACT Background The diffusion tensor image analysis along the perivascular space (DTI‐ALPS) index is an established term, and ongoing research aims to explore underlying mechanisms. Hypothesis DTI‐ALPS measures are influenced by subject‐specific orientational differences of the projection and association fibers. Study Type Prospective.
Dávid Bognár   +9 more
wiley   +1 more source

Detection and clinical value of NMO-IgG in neuromyelitis optica

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2014
Neuromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system (CNS) of autoimmune etiology which predominantly affects the optic nerves and spinal cord.
De-hui HUANG, Wei-ping WU
doaj  

Repeated moderate hypothermia leads to sustained glymphatic dysfunction and loss of vascular AQP4 polarization

open access: yesFluids and Barriers of the CNS
Cerebrospinal fluid (CSF) enters the brain along perivascular spaces in a manner that depends on aquaporin-4 (AQP4) polarization, facilitating brain clearance and is called the glymphatic system.
Chenchen Liu   +8 more
doaj   +1 more source

The effects of royal jelly on human health: A narrative review of clinical studies

open access: yesJSFA reports, EarlyView.
Abstract Royal jelly (RJ) is a natural bioactive substance with documented effects on human health. This narrative review synthesizes evidence from clinical and clinically relevant experimental studies evaluating the therapeutic potential of RJ.
Georgios Goras   +2 more
wiley   +1 more source

Anti-aquaporin-4 antibody-positive dorsal midbrain syndrome

open access: yes, 2015
Neuromyelitis optica spectrum disorders (NMOSD) can cause various ocular motor disorders in addition to optic neuritis. Ocular motor findings associated with NMOSD include spontaneous vertical and gaze-evoked nystagmus, wall-eyed bilateral internuclear ...
Lee, Juyoun   +8 more
core   +1 more source

Personalized Treatment of Patients With Multiple Sclerosis: A Case Report and Literature Review

open access: yesMedicine Bulletin, EarlyView.
ABSTRACT Managing multiple sclerosis (MS) with a highly active disease course presents significant challenges, particularly regarding the timing of therapeutic escalation and the preservation of brain volume. We present a personalized management strategy for a 36‐year‐old male with relapsing‐remitting MS (RRMS) who experienced initial misdiagnosis ...
Fengjun Wang   +3 more
wiley   +1 more source

Co‐ and Multi‐Pathologies in Parkinson's Disease: An International Parkinson and Movement Disorder Society Scientific Issues Committee Review

open access: yesMovement Disorders, EarlyView.
Abstract Parkinson's disease (PD) has been historically defined as a disease of striatal dopamine deficiency secondary to degeneration of dopaminergic neurons in the substantia nigra pars compacta, related to the presence of Lewy bodies and Lewy neurites.
Michele Matarazzo   +10 more
wiley   +1 more source

The developmental history of study on neuromyelitis optica

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2014
In 19th century, neuromyelitis optica (NMO) indicated optic neuritis and myelitis with simultaneous onset of both sides. Later studies proposed that the onset of right or left side optic neuritis could be separated by weeks, months even years.
Kai FENG, Xing-hu ZHANG, Xian-hao XU
doaj  

With Regard to the Expression Status of Sarcolemmal Aquaporin 4 in Human Muscular Dystrophies

open access: yesNeurology and Clinical Neuroscience, EarlyView.
ABSTRACT Human muscular dystrophies are inherited muscle‐wasting diseases caused by the various kinds of gene mutations. Among them, Duchenne muscular dystrophy (DMD) is a representative type. Before the discovery of the causative dystrophin gene of DMD, the fragile myofiber plasma membrane was thought to be the trigger of myofiber necrosis in DMD ...
Yoshihiro Wakayama, Takahiro Jimi
wiley   +1 more source

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