Results 151 to 160 of about 2,756,091 (350)
Speech Recognition with Cochlea‐Inspired In‐Sensor Computing
Advanced Intelligent Systems, EarlyView.Traditional speech recognition methods rely on software‐based feature extraction that introduces latency and high energy costs, making them unsuitable for low‐power devices. A proof‐of‐concept demonstration is provided of a bioinspired tonotopic sensor for speech recognition that mimics the human cochlea, using a spiral‐shaped elastic metamaterial. The
Paolo H. Beoletto +4 more
wiley +1 more source
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 +3 more
wiley +1 more source
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 +6 more
wiley +1 more source
Carcinoma of the External Ear [PDF]
Proceedings of the Royal Society of Medicine, 1933 openaire +3 more sources
Prevalence of external ear disorders in Belgian stray cats
Journal of feline medicine and surgery, 2017 Anouck Bollez +3 more
semanticscholar +1 more source
The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley +1 more source
Australian Journal of Social Issues, EarlyView.ABSTRACT Hearing loss is a poignant issue in many Aboriginal and Torres Strait Islander communities and, without sufficient support, it can also contribute to disabling life experiences. The National Disability Insurance Scheme (NDIS) is intended to provide support to eligible people experiencing disability, however, to effectively serve this ...
Hannah Lack +4 more
wiley +1 more source
Fungal infections of external ear canal in patients with Otomycosis, Babol, 1991-2000
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2002 Background and Objective: Fungal infection of external ear canal is a common and chronic disease that causes some complications. The objective of this study was to survey the fungal infections of external ear canal in Babol during 1999-2000.
AA Sefidgar +3 more
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