Results 241 to 250 of about 1,301,558 (327)

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron, Nicholas E. Clifton, Daniel Cabezas de la Fuente, Peter Holmans, Nicholas J. Bray, Kathryn J. Peall   +5 more
wiley   +1 more source

Bidirectional Mendelian randomization analysis of the causal association between obesity and hepatocellular carcinoma in a European population. [PDF]

Medicine (Baltimore)
Ding X, Zhou X, Tang N, Wang X, Jin X, Ma X, Wu B, Wu C, Yang X, Yang J, Wu T, Liang Q, Yin L.   +12 more
europepmc   +1 more source

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi, Lara Basovic, Christopher Michael McGraw   +2 more
wiley   +1 more source

b -Hurwitz numbers from refined topological recursion. [PDF]

Math Ann
Kumar Chidambaram N, Dołęga M, Osuga K.   +2 more
europepmc   +1 more source

Modeling of radiative properties of an Oxyfuel atmosphere with a weighted sum of gray gases for variable carbon dioxide and water vapor concentrations

, 2011
Sebastian Rehfeldt, Christian Kuhr, Martin Ehmann, Christian Bergins   +3 more
openalex   +1 more source

ALS With and Without Upper Motor Neuron Signs: A Comparative Study Supporting the Gold Coast Criteria

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The Gold Coast criteria permit diagnosis of amyotrophic lateral sclerosis (ALS) even without upper motor neuron (UMN) signs. However, whether ALS patients with UMN signs (ALSwUMN) and those without (ALSwoUMN) share similar characteristics and prognoses remains unclear.
Hee‐Jae Jung, E‐nae Cheong, Jungmin So, Heung‐Won Kang, Yangsean Choi, Eun‐Jae Lee, Hyunjin Kim, Young‐Min Lim   +7 more
wiley   +1 more source

Multi-agent systems and credibility-based advanced scoring mechanism in fact-checking. [PDF]

Sci Rep
Dong Y, Ito T.
europepmc   +1 more source

Shared Genetic Effects and Antagonistic Pleiotropy Between Multiple Sclerosis and Common Cancers

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epidemiologic studies have reported inconsistent altered cancer risk in individuals with multiple sclerosis (MS). Factors such as immune dysregulation, comorbidities, and disease‐modifying therapies may contribute to this variability.
Asli Buyukkurt, Marius Ygonia, Ali Manouchehrinia, Philippe Lefrançois, Ingrid Kockum, Adil Harroud   +5 more
wiley   +1 more source

Modified prioritized DDPG algorithm for joint beamforming and RIS phase optimization in MISO downlink systems. [PDF]

Sci Rep
Shukry S, Fahmy Y.
europepmc   +1 more source

Almost absolute weighted summability with index k [PDF]

, 2019
Mehmet Ali Sarıgöl, M. Mursaleen
openalex