Results 41 to 50 of about 116,541 (296)
Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte +13 more
wiley +1 more source
Migration and the Feminization of Power
In Nigeria and many other African countries, husbands are regarded as breadwinners and 'lords of the household'. When women get married, they are described as 'going to their husband's house' and in cases of separation or unresolved crisis within the ...
Elizabeth Olayiwola
doaj +1 more source
Isaiah’s Promise of the Restoration of Zion and Its Canonical Development [PDF]
For nearly three millennia, Isaiah’s prophecies of a peaceful kingdom centered in Zion have captured the human imagination and expressed the longings of the human heart.
Yates, Gary E
core
Cutaneous Phosphorylated Alpha‐Synuclein in Lewy Body Dementia
ABSTRACT Objective To determine the test performance of cutaneous phosphorylated alpha‐synuclein (P‐SYN) in dementia with Lewy bodies (DLB), individuals with reduced Montreal Cognitive Assessment (MoCA) and healthy controls. Methods This is the first subgroup analysis of the Synuclein‐One study, a prospective, blinded study evaluating P‐SYN detection ...
Christopher H. Gibbons +31 more
wiley +1 more source
Interactions between dietary supplements in hospitalized patients [PDF]
In this issue of the Journal, Levy et al. [1] report on the clinically relevant results of a cross-sectional prospective study, performed by a multidisciplinary team of researchers between 2009 and 2014, and aimed at detecting dietary and herbal ...
MUSCARITOLI, Maurizio
core +1 more source
Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein +13 more
wiley +1 more source
Introduction: Hypokalemic paralysis secondary to Conn’s syndrome is rare. The most common presentation of this condition is hypertension, which may be asymptomatic or range from mild to severe to refractory. Case Report: A 34-year-old hypertensive female
Dr. Samuel Noklang +7 more
doaj +1 more source
Digital Quantification of the Enzyme-Linked Immunospot (ELISPOT)
Enzyme-linked immunospot (ELISPOT) is a sensitive technique for the detection of cytokines released by immune cells. The technique is well established and correlates closely with the enzyme-linked immunosorbent assay (ELISA) technique. Here, we introduce
J.E. Vaquerano +4 more
doaj +1 more source
Things Never Change: Piecing Together College Life [PDF]
Sometimes you stumble on something on eBay you just can\u27t pass up. It\u27s that $6 buy that is awkward, odd and just a little out of your scope. But it\u27s only $6.
Rudy, John M.
core +1 more source
ABSTRACT Purpose Air pollution has been linked to several neurological conditions, including stroke and neurodegenerative diseases. Evidence regarding its association with multiple sclerosis (MS) remains conflicting, limited by small sample sizes. Methods PubMed, Embase, Scopus, and Cochrane controlled register of trials (CENTRAL) were searched on ...
Ahmad A. Toubasi, Thuraya N. Al‐Sayegh
wiley +1 more source

