Results 131 to 140 of about 1,764,054 (308)

Research of Personalized Recommendation Service of Coal Enterprises Web Site Based on Web Log

Gong-kuang zidonghua, 2012
In order to solve problem of difficult finding information for users of coal mine enterprise Web site, the paper put forward a personalized recommendation service model of coal enterprise Web site based on Web log.
GUO Xiao-yuan, HE Zhen
doaj  

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

DOMtegrity: ensuring web page integrity against malicious browser extensions. [PDF]

Int J Inf Secur, 2019
Toreini E, Shahandashti SF, Mehrnezhad M, Hao F.   +3 more
europepmc   +1 more source

No Pedagogical Advantage Found Between LibGuides and Other Web Page Information Literacy Tutorials

, 2015
Kimberly Miller
openalex   +1 more source

Morphing Web Pages to Preclude Web Page Tampering Threats

, 2016
O número de utilizadores da Internet continua a aumentar todos os anos e a Internet é cada vez mais uma ferramenta diária na vida de cada indivíduo, utilizada como instrumento de trabalho ou de entretenimento. Contudo, ao navegar na Internet, os utilizadores tornam-se possíveis alvos de ataques informáticos um vez que efetuam transações de dados ...
openaire   +2 more sources

Rüdin's Unpublished Family Study From the Early 1920s: “On the Inheritance of Manic‐Depressive Insanity”

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Ernst Rüdin, an important and controversial figure in the history of psychiatric genetics, published only one major empirical study on siblings of dementia praecox (DP) probands in 1916. He conducted a parallel study of siblings of probands with manic‐depressive insanity (MDI), but the resulting monograph, written in the early 1920s, was left ...
Kenneth S. Kendler, Astrid Klee
wiley   +1 more source

Web Page Design Recommendations for People with Down Syndrome Based on Users' Experiences. [PDF]

Sensors (Basel), 2018
Alonso-Virgós L, Rodríguez Baena L, Pascual Espada J, González Crespo R.   +3 more
europepmc   +1 more source

Psychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.
Julia M. Morales, Camille F. Villar, Beatriz Varman, Gianna M. Colombo, Danqi Li, Sarah J. Sadek, Marie‐Eve Robinson, Chaya N. Murali, Kara Ayers, Jocelyn Gomez, Brendan Lee, V. Reid Sutton, Eric A. Storch, Andrew D. Wiese   +13 more
wiley   +1 more source

Measurment of Web Usability: Web Page of Hacettepe University Department of Information Management

Türk Kütüphaneciliği, 2009
Today, information is produced increasingly in electronic form and retrieval of information is provided via web pages. As a result of the rise of the number of web pages, many of them seem to comprise similar contents but different designs.
Nazan Özenç Uçak, Tolga Çakmak
doaj  

Non‐Synaptic Function and Localization of Syntaxin‐Binding Protein 1 in a Mouse Model of STXBP1‐Related Epileptic Encephalopathy

Annals of Neurology, EarlyView.
Objective De novo mutations in the syntaxin‐binding protein 1 (STXBP1), encoded by STXBP1, are among the most prevalent causes of variable neurodevelopmental disorders, including epileptic encephalopathy, developmental delay, and movement disorders.
Tao Yang, Rajat Banerjee, Yamei Deng, Sheetal Jahagirdar1, Alexey I. Nesvizhskii, Michael D. Uhler, Jack M. Parent, Yu Wang   +7 more
wiley   +1 more source