Results 81 to 90 of about 2,407,465 (287)

Genetic testing: A threat to privacy

open access: yes, 2001
This chapter summarises some of the problems associated with privacy and genetic information in the medical context of genetic testing. It outlines some of the major reasons why legislation is needed to protect our genetic privacy.
Gesche, Astrid H.
core  

Review : "Genetic Privacy: A challenge to Medico-Legal Norms" by Laurie, G

open access: yes, 2003
The discovery by Watson and Crick of the structure of DNA is one of the great scientific discoveries. In the period since that discovery new areas of genetic research have opened up which hold out the hope of developing treatments or cures for many ...
Bennett, Belinda
core   +1 more source

Comparative Effectiveness and Safety of Inebilizumab Versus Rituximab in AQP4‐IgG‐Positive NMOSD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Rituximab (anti‐CD20, RTX) and inebilizumab (anti‐CD19, INE) represent B‐cell‐depleting therapies used for aquaporin‐4 antibody‐positive (AQP4‐IgG+) neuromyelitis optica spectrum disorder (NMOSD); however, direct comparative evidence remains limited.
Jie Lin   +11 more
wiley   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru   +13 more
wiley   +1 more source

Greater consistency required for telecommunications privacy

open access: yes, 2007
In her detailed submission to the Australian Law Reform Commission\u27s Review of Privacy, the Privacy Commissioner, Karen Curtis, has called for changes to a number of laws to assist in clarifying privacy requirements in the telecommunications industry.
Karen Curtis   +1 more
core  

Essentially yours: the protection of human genetic information in Australia [PDF]

open access: yes, 2003
ALRC Report 96 (tabled May 2003)  was the product of a two-year inquiry by the ALRC and the Australian Health Ethics Committee (AHEC) of the NHMRC, involving extensive research and widespread public consultation.The inquiry was the most ...
Kerry Breen   +2 more
core  

Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon   +5 more
wiley   +1 more source

Submission to the Australian Law Reform Commission's review of privacy

open access: yes, 2007
In this detailed submission to the Australian Law Reform Commission\u27s review of privacy laws, the Privacy Commissioner, Karen Curtis, calls for changes to a number of laws.
Office of the Privacy Commissioner
core  

Screening Routine Clinical Notes for Epilepsy Surgery Candidates Using Large Language Models

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epilepsy surgery is severely underutilized despite proven efficacy, with substantial under‐referral of eligible patients in routine clinical practice. This study evaluated the potential role of large language models (LLMs) as decision‐support tools for screening unstructured clinical notes to identify epilepsy surgery candidates and ...
Uriel Fennig   +9 more
wiley   +1 more source

Disclosure to genetic relatives without consent – Australian genetic professionals’ awareness of the health privacy law

open access: yesBMC Medical Ethics, 2020
Background When a genetic mutation is identified in a family member (proband), internationally, it is usually the proband’s or another responsible family member’s role to disclose the information to at-risk relatives. However, both active and passive non-
Natalia Meggiolaro   +4 more
doaj   +1 more source

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