Results 61 to 70 of about 1,346,685 (174)

Oculogyric Crisis

open access: yes, 2020
Dr.
Andrew G. Lee, MD; Daniel Bailey
core  

Ocular Adverse Events Associated With Antidepressants: A Large‐Scale Data Analysis From the FAERS Database

open access: yesCNS Neuroscience &Therapeutics, Volume 32, Issue 6, June 2026.
This decadal FAERS study (2015–2024) identifies 62,020 ocular adverse events (AEs) across 39 antidepressants, highlighting ocular neuromuscular disorders as a key risk. NDDIs show the strongest associations, while SSRIs exhibit the broadest signal spectrum.
Yiming Peng   +4 more
wiley   +1 more source

Irish contraception and crisis pregnancy [ICCP] study: a survey of the general population - summary [PDF]

open access: yes, 2004
The aim of the present study was to establish nationally representative data on current attitudes, knowledge and experience of contraception, crisis pregnancy and related services in Ireland.
McGee, Hannah   +3 more
core  

Mixed methods research of crisis pregnancy counselling and support services [PDF]

open access: yes, 2005
This study aimed to examine women’s experiences of crisis pregnancy counselling using both qualitative and quantitative methods. The study group comprised women with a crisis pregnancy who either decided on abortion or were continuing the pregnancy ...
Conlon, Catherine
core  

Oculogyric Crisis in a patient with PURA Syndrome

open access: yesSão Paulo Medical Journal, 2021
Context: PURA syndrome is a neurodevelopmental disorder characterized by neonatal hypotonia, delayed psychomotor development, early-onset feeding difficulties and an epileptic encephalopathy. Case Report: A 3-month-old Brazilian boy presented with severe neonatal hypotonia associated with feeding difficulties due to serious dysphagia requiring ...
Icaro França Navarro Pinto   +11 more
openaire   +1 more source

Pharmacodynamics, Efficacy, and Safety of Intraputaminal Eladocagene Exuparvovec Administered to Pediatric Patients With Aromatic L‐Amino Acid Decarboxylase Deficiency Using an MR‐Compatible Cannula: 48 Weeks of Follow‐Up

open access: yesJournal of Inherited Metabolic Disease, Volume 49, Issue 2, March 2026.
ABSTRACT Aromatic ʟ‐amino acid decarboxylase (AADC) deficiency is a rare pediatric neurotransmitter disorder that typically necessitates lifelong care, and that carries a risk of childhood mortality. Eladocagene exuparvovec gene therapy is designed to restore AADC production.
Daniel J. Curry   +22 more
wiley   +1 more source

Adolf Hitler and His Parkinsonism

open access: yesAnnals of Indian Academy of Neurology, 2015
Research works have suggested almost incontrovertibly, that Adolf Hitler suffered from Parkinsonism. However, the precise nature of his illness had always been controversial and post-encephalitic and idiopathic varieties were the ones which were most ...
Kalyan B Bhattacharyya
doaj   +1 more source

Crisis pregnancy and pregnancy decision making: An outline of influencing factors [PDF]

open access: yes, 2004
This document aims to review research literature in order to: • outline and describe the factors that have been demonstrated to affect the level and incidence of crisis pregnancy • examine the factors that affect a woman’s decision when faced with a ...
O’Keeffe, Stephanie
core  

Pheochromocytoma Across the Perioperative Course: Current Concepts and Clinical Management

open access: yesAnesthesiology Research and Practice, Volume 2026, Issue 1, 2026.
Pheochromocytoma is an uncommon neuroendocrine tumor with myriad nonspecific clinical presentations. If not recognized and treated, it is associated with the development of target organ damage and complications such as myocarditis, cardiomyopathy, cerebrovascular accidents, and diabetes mellitus, among numerous others. The pheochromocytoma diagnosis is
Aibek E. Mirrakhimov   +2 more
wiley   +1 more source

Identification of a Novel SLC18A2 Splicing Variant in a Case of Infantile Parkinsonism–Dystonia Type 2

open access: yesCase Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.
Parkinsonism–dystonia Type 2 (PKDYS2) is a rare autosomal recessive disorder caused by SLC18A2 variants affecting the vesicular monoamine transporter 2 (VMAT2). We report the first genetically confirmed Iranian patient, an 18‐month‐old boy presenting with profound developmental delay, axial hypotonia, limb hypertonia, dystonia, oculogyric crises ...
Ali Nikkhah   +5 more
wiley   +1 more source

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