Results 231 to 240 of about 334,073 (319)

BASAL CELL LESIONS OF THE NOSE, CHEEK AND LIPS

, 1944
Warren B. Davis
openalex   +2 more sources

In‐Sensor Reservoir Computing Using Ferroelectric Optoelectronic Synapse for Near‐Infrared Face Recognition

Advanced Intelligent Systems, EarlyView.
Near‐infrared reservoir computing system has been realized by using α‐In2Se3 optoelectronic device with concise device and algorithm architecture, achieving high accuracy near 100% and noise robustness in face recognition tasks. These findings demonstrate 2D ferroelectric device‐based optoelectronic RC system as a compact and efficient computing ...
Wenyu Songlu, Quan Chen, Yi Cao, Han Wang, Han Chen, Weihui Sang, Yang Gan, Shijia Tian, Yuan Yu, Zhou Xin, Yukang Chen, Shuming Guo, Lin Wang, Xumeng Zhang, Tao Liu, Du Xiang   +15 more
wiley   +1 more source

Vibratory Angioedema Due to Vigorous Nose Blowing: A Case Report. [PDF]

Cureus
Truong T, Kaddis T, Wang V, Tsai M, Yusin J.   +4 more
europepmc   +1 more source

Expanding the Clinical Spectrum of Cousin Syndrome: A Novel Biallelic Missense Variant in TBX15 Causing a Milder Phenotype

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cousin syndrome is a rare skeletal dysplasia characterized by distinctive facial features, humeroradial synostosis, and hypoplasia of the ilia and scapula. Since the original description of the phenotype in two cases by Cousin in 1982, only three additional cases have been published.
Suzanne E. L. Detiger, Martijn V. Verhagen, Tuula Rinne, Hermine E. Veenstra‐Knol   +3 more
wiley   +1 more source

A Comprehensive Review on Sensor-Based Electronic Nose for Food Quality and Safety. [PDF]

Sensors (Basel)
Sanislav T, Mois GD, Zeadally S, Folea S, Radoni TC, Al-Suhaimi EA.   +5 more
europepmc   +1 more source

Novel Intragenic Duplication of GATAD2B in a Patient With GAND

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The nucleosome remodeling and deacetylation (NuRD) complex is a major chromatin regulator and plays a critical role in regulating gene transcription, genome integrity, and cell cycle progression. Heterozygous variants in GATAD2B, a core NuRD component, have been reported to cause GATAD2B‐Associated Neurodevelopmental Disorder (GAND), an ...
Mari Mori, Steven Estes, Swetha Ramadesikan, Betsy Schmalz, Shayne Plourde, Maria E. Hernandez Gonzalez, Anthony R. Miller, Bimal P. Chaudhari, Richard K. Wilson, Daniel C. Koboldt   +9 more
wiley   +1 more source

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil, Allison Daley, Emily R. Sites, Shayne M. Plourde, Jesse M. Hunter, Dennis W. Bartholomew, April N. Lehman, Daniel C. Koboldt, Rolf W. Stottmann   +8 more
wiley   +1 more source

Adverse Cardiovascular Risk Profile and Increased Diurnal Salivary Cortisol in Girls With Turner Syndrome: An Exploratory Study

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Patients with Turner Syndrome (TS) and those exposed to high concentrations of glucocorticoids have a number of characteristics in common, including an increased risk of cardiovascular disease. Pediatric TS patients underwent studies of salivary cortisol (SC) and cortisone (SCn), body composition, continuous glucose monitoring, vascular ...
Lily Jones, Julie Park, Silothabo Dliso, Daniel B. Hawcutt, Alena Shantsila, Gregory Y. H. Lip, Joanne Blair   +6 more
wiley   +1 more source