Atypical Fibroxanthoma/Pleomorphic Dermal Sarcoma With Osseous Metaplasia: A Series of Three Cases
ABSTRACT Atypical fibroxanthoma (AFX) and pleomorphic dermal sarcoma (PDS) are rare mesenchymal tumors typically arising on sun‐damaged skin of the head and neck in elderly patients. PDS is a more aggressive tumor but with similar demographics, cellular morphology, immunohistochemical features, and genetic findings.
Taylor Novice +3 more
wiley +1 more source
Creating a diagnostic assessment model for autism spectrum disorder by differentiating lexicogrammatical choices through machine learning. [PDF]
Kato S, Hanawa K, Saito M, Nakamura K.
europepmc +1 more source
Processing Chinese relative clauses: evidence for the subject-relative advantage. [PDF]
Vasishth S, Chen Z, Li Q, Guo G.
europepmc +1 more source
Review of Susan Brown (1999) Sentential negation in Russian. (Stanford: Center for the Study of Language and Information.) [PDF]
Rowlett, PA
core +2 more sources
Abstract In the Jaru community of northern Western Australia, certain in‐laws and relatives are categorized as being in a highly respectful relationship in which they are expected to pay deference to one another. This conversation‐analytic study closely examines the deferential practices that are used among three Jaru siblings in an ordinary multi ...
Josua Dahmen
wiley +1 more source
Subject/object processing asymmetries in Korean relative clauses: Evidence from ERP data. [PDF]
Kwon N, Kluender R, Kutas M, Polinsky M.
europepmc +1 more source
We investigated the roles of PKM2, PKM1, and LDHA in retinal metabolism and structural integrity. In the normal retina, these enzymes are maintained at defined levels that support photoreceptor function. Rod‐specific deletion of LDHA, alone or with PKM2, caused age‐dependent degeneration, as PKM1 induction did not reach levels comparable to PKM2.
Ammaji Rajala +3 more
wiley +1 more source
<i>Ya</i><sup>33</sup> 'give' as a valency increaser in Jinghpo nuclear serialization: from benefactive to malefactive. [PDF]
Peng G, Chappell H.
europepmc +1 more source
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
Zooming in and out of semantics: proximal-distal construal levels and prominence hierarchies. [PDF]
Lobben M, Laeng B.
europepmc +1 more source

