Results 111 to 120 of about 2,696,637 (307)

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen   +5 more
wiley   +1 more source

[Cranial nerve palsy caused by tumours of the head and neck]

open access: yes, 2013
Contains fulltext : 117970.pdf (Publisher’s version ) (Open Access)Cranial nerve palsy is a diagnostic guiding symptom, but often goes unrecognized.
Hoogen, F.J.A. van den   +2 more
core  

Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen   +13 more
wiley   +1 more source

North American Delphi Consensus Study on Sinonasal Malignancy Survivorship Care

open access: yesInternational Forum of Allergy &Rhinology, EarlyView.
ABSTRACT Background Survival for patients with sinonasal cancers has improved over the past decades, but there are no dedicated survivorship guidelines for this cohort. Objective To understand experts’ priorities and perspectives on key survivorship tenets (surveillance, second tumor screening, toxicity, and symptom management).
Matheus Sewastjanow‐Silva   +18 more
wiley   +1 more source

Familial Amyloid Polyneuropathy Type IV (FINNISH) with Rapid Clinical Progression in an Iranian Woman: A Case Report

open access: yesIranian Journal of Medical Sciences, 2016
Familial amyloid polyneuropathy (FAP) type IV (FINNISH) is a rare clinical entity with challenging neuropathy and cosmetic deficits. Amyloidosis can affect peripheral sensory, motor, or autonomic nerves.
Arash Babaei-Ghazani   +1 more
doaj  

Management Approach to Isolated Ocular Motor Nerve Palsies

open access: yes
Anatomy: Optic nerve; Oculomotor nerve; Trochlear nerve; Abducens nerve; Pupil. Disease/Diagnosis: Oculomotor nerve diseases; Trochlear nerve diseases; Oculomotor nerve paralysis; Fourth cranial nerve palsy; Abducens nerve diseases; Gradenigo\u27s ...
Alfredo A. Sadun, MD, PhD
core  

Microvascular Cranial Nerve Palsy_Russian

open access: yes, 2008
Microvascular cranial nerve palsy is one of the most common causes of double vision in the older poulation. They are often referred to as "diabetic" palsies.
NANOS
core  

Cranial Nerve Dysfunction Following Carotid Endarterectomy

open access: yes, 1987
In an effort to establish the true incidence of cranial nerve dysfunction after carotid endarterectomy, 50 consecutive carotid endarterectomy procedures were assessed by careful and objective preoperative and postoperative cranial nerve evaluations ...
Moody, James A.   +4 more
core   +1 more source

Animal stroke models and outcome evaluation: A review

open access: yesAnimal Models and Experimental Medicine, EarlyView.
Rodents are the preeminent stroke model species. Large animal models exist too, but are poorly standardized. Ischemic and hemorrhagic experimental models are available, with the intraluminal filament model being predominant. Outcomes are evaluated via quantifying subjects' sensorimotor impairment, cognitive memory faculties, degree of cellular ...
Solsa Cariba   +2 more
wiley   +1 more source

Malignant Disease of Temporal Bone with Involvement of Cranial Nerves [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1922
J S, Collier, L, Colledge
openaire   +2 more sources

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