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Seizures as the first manifestation of chromosome 2q24.2-q24.3 in a two and a half years old girl: A case report

open access: yesGynecology and Obstetrics Clinical Medicine, 2021
Background: Mutations and/or duplications in the chromosome 2q24.3 region are known to be responsible for various epilepsy phenotypes. However, microdeletion in childhood epilepsy is rarely reported. Case presentation: A two-and-a-half-year-old girl with
Wen-cheng Dai   +6 more
doaj   +1 more source

Diabetes mellitus – Definition, Klassifikation, Diagnose, Screening und Prävention (Update 2023)

open access: yesWiener Klinische Wochenschrift, 2023
Diabetes mellitus bezeichnet eine Gruppe von heterogenen Erkrankungen, deren gemeinsamer Befund die Erhöhung der Blutglukosekonzentration ist. Die gegenwärtige Klassifikation des Diabetes mellitus wird dargestellt und die wesentlichen Merkmale von Typ 1 ...
J. Harreiter, Michael Roden
semanticscholar   +1 more source

Use of GPT-4 to Diagnose Complex Clinical Cases

open access: yesNEJM AI, 2023
We assessed the performance of the newly released AI GPT-4 in diagnosing complex medical case challenges and compared the success rate to that of medical-journal readers.
A. V. Eriksen, S. Möller, J. Ryg
semanticscholar   +1 more source

Deep Learning Techniques to Diagnose Lung Cancer

open access: yesCancers, 2022
Simple Summary This study investigates the latest achievements, challenges, and future research directions of deep learning techniques for lung cancer and pulmonary nodule detection. Hopefully, these research findings will help scientists, investigators,
Lu-Lu Wang
semanticscholar   +1 more source

Profiling Early Humoral Response to Diagnose Novel Coronavirus Disease (COVID-19)

open access: yesClinical Infectious Diseases, 2020
Background The emergence of coronavirus disease 2019 (COVID-19) is a major healthcare threat. The current method of detection involves a quantitative polymerase chain reaction (qPCR)–based technique, which identifies the viral nucleic acids when present ...
Li Guo   +21 more
semanticscholar   +1 more source

Attend and Diagnose: Clinical Time Series Analysis using Attention Models [PDF]

open access: yesAAAI Conference on Artificial Intelligence, 2017
With widespread adoption of electronic health records, there is an increased emphasis for predictive models that can effectively deal with clinical time-series data. Powered by Recurrent Neural Network (RNN) architectures with Long Short-Term Memory (
Huan-Zhi Song   +3 more
semanticscholar   +1 more source

Clinical and Laboratory Approach to Diagnose COVID-19 Using Machine Learning

open access: yesInterdisciplinary Sciences Computational Life Sciences, 2022
Coronavirus 2 (SARS-CoV-2), often known by the name COVID-19, is a type of acute respiratory syndrome that has had a significant influence on both economy and health infrastructure worldwide.
K. Chadaga   +5 more
semanticscholar   +1 more source

A national strategy to diagnose COVID-19 associated invasive fungal disease in the ICU

open access: yesClinical Infectious Diseases, 2020
Background Fungal co-infection is a recognised complication of respiratory virus infections, increasing morbidity and mortality, but can be readily treated if diagnosed early.
P. L. White   +23 more
semanticscholar   +1 more source

Osteoporosis in children and adolescents: when to suspect and how to diagnose it

open access: yesEuropean Journal of Pediatrics, 2022
Early recognition of osteoporosis in children and adolescents is important in order to establish an appropriate diagnosis of the underlying condition and to initiate treatment if necessary.
Silvia Ciancia   +6 more
semanticscholar   +1 more source

Prevalência de mosaicismo cromossômico em 2.500 casos realizados em um laboratório de genética no Estado do Rio de Janeiro, Brasil

open access: yesVértices, 2020
Mosaicismo cromossômico é definido como a existência de duas ou mais linhagens celulares com diferentes constituições cromossômicas em um mesmo indivíduo. Este trabalho tem como objetivo analisar a prevalência de mosaicismo cromossômico a partir de 2.500
Mauricio Assis Rodrigues   +4 more
doaj   +1 more source

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