Results 121 to 130 of about 1,812,494 (311)
Advances in Digestive Medicine, EarlyView.Abstract Pharyngeal high‐resolution manometry with impedance (P‐HRM‐I) is an established assessment method used to evaluate pharyngeal swallowing. It provides precise quantification of swallowing biomechanics that enable the detection of alterations in swallowing physiology.
Mistyka Schar +5 more
wiley +1 more source
, 2018 Light blue and white hat with a cartoon bear head next to the words George Fox Spirit in light blue.https://digitalcommons.georgefox.edu/museum_gfu/1149/thumbnail ...
George Fox University Archives
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Journal of Optimization Theory and Applications, 2021 Mauro Pontani, Jason L. Speyer
openaire +1 more source
A Critical Assessment of Bonding Descriptors for Predicting Materials Properties
Advanced Intelligent Discovery, EarlyView.The impact of new bonding descriptors in machine learning models for predicting material properties is assessed. Improvements are validated using significance tests, and new, intuitive descriptors for screening lattice thermal conductivity and projected force constants are introduced.
Aakash Ashok Naik +6 more
wiley +1 more source
Letter from George Olcott to his son George Olcott, 26 November 1852 [PDF]
Sends items to George by express.Transcriptions may be subject to ...
Olcott, George, 1785-1864
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, 2018 Navy blue pennant with Gold trim and lettering. Has clocktower logo and George Fox University written in gold.https://digitalcommons.georgefox.edu/museum_gfu/1104/thumbnail ...
George Fox University Archives
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George Fox Life, March 1999 [PDF]
, 1998 Alumni newspaper of George Fox University.https://digitalcommons.georgefox.edu/gfc_life/1150/thumbnail ...
George Fox University Archives
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An Adult Presentation of KIF11‐Related MCLID Syndrome: Case Report and 40‐Year Follow‐Up
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Pathogenic variants in KIF11 are linked to autosomal dominant syndromes with microcephaly, chorioretinopathy, lymphedema, and intellectual disability (MCLID), though adult presentations remain underreported. We report a 42‐year‐old female presenting with a de novo single‐amino acid in‐frame deletion in the KIF11 gene (c.1294_1296del; p ...
Thrishna Chathurvedula +8 more
wiley +1 more source
George Fox Life, January 2000 [PDF]
, 2000 Alumni newspaper of George Fox University.https://digitalcommons.georgefox.edu/gfc_life/1154/thumbnail ...
George Fox University Archives
core +1 more source
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena +13 more
wiley +1 more source