Results 41 to 50 of about 3,208,800 (253)

Iatrogenic Ulnar Nerve Injury post Laceration Suturing – An Unusual Presentation

open access: yesJournal of Orthopaedic Case Reports, 2013
Introduction: Nerve entrapment while suturing a lacerated wound is a complication that is easily avoidable. We report a case low ulnar nerve palsy due to nerve entrapment while suturing a lacerated wound.
Murali Mothilal   +3 more
doaj   +1 more source

Oculomotor Nerve Palsy as a Rare Presentation and First Sign of Multiple Myeloma [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Acquired oculomotor nerve palsy has varied aetiologies like vascular (diabetes, heart disease, atherosclerosis and posterior communicating artery aneurysm), space occupying lesions or tumours, inflammation, infection, trauma, demyelinating disease like ...
Bijnya Birajita Panda   +3 more
doaj   +1 more source

Oculomotor nerve palsy, an unusual onset of polyarteritis nodosa

open access: yes, 2023
Introduction Cranial nerve involvement in polyarteritis nodosa(PAN) is underrecognized and rarely reported. The aim of this article is to review the available literature and present an example of oculomotor nerve palsy in the course of PAN. Material and
Filipe Oliveira Pinheiro   +9 more
core   +1 more source

The psychosocial toll of Dublin III on asylum seekers in the Netherlands

open access: yesAmerican Journal of Community Psychology, EarlyView.
Abstract The Dublin III Regulation determines which EU Member State is responsible for examining asylum claims, but its implementation carries significant consequences for those subjected to it. This study examines how Dublin III, as implemented in the Netherlands, affects asylum seekers' psychosocial wellbeing using Silove′s Adaptation and Development
Imen El Amouri
wiley   +1 more source

Isolated Trochlear Nerve Palsy Associated with Carotid–Cavernous Sinus Fistula

open access: yesInternational Journal of Gerontology, 2009
Cranial nerve ophthalmoplegia linked with a cavernous sinus lesion usually involves the third, fourth and sixth cranial nerve. Isolated fourth nerve palsy caused by carotid–cavernous sinus fistula (CCSF) is rare, and related case reports are sporadic in ...
Chih-Ming Lin, I-Hung Hseu
doaj   +1 more source

Genetic Variants of Na+,K+‐ATPase Associated With Neurological Disorders: A Systematic Review

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Neurological disorders encompass a wide range of severe symptoms and manifestations, many of which are associated with genetic variants that affect ionic homeostasis. Na+,K+‐ATPase, a transmembrane enzyme responsible for maintaining electrochemical gradients in cells, plays a crucial role in neuronal excitability and brain function.
Giovana Kummer da Rosa   +3 more
wiley   +1 more source

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan   +13 more
wiley   +1 more source

Third Nerve Palsy

open access: yes, 1986
Patient with third nerve palsy (no ...
Kathleen B. Digre, MD
core   +1 more source

Contralateral eye surgery with adjustable suture for management of third nerve palsy with aberrant regeneration

open access: yesIndian Journal of Ophthalmology, 2017
Aberrant regeneration of the third nerve following its palsy is commonly seen after trauma and compressive lesions. This phenomenon is thought to result due to misdirection of the regenerating axons.
Phuong Thi Thanh Nguyen   +2 more
doaj   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena   +13 more
wiley   +1 more source

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