Results 111 to 120 of about 52,620 (298)

Clinical factors underlying a single surgery or repetitive surgeries to treat superior oblique muscle palsy [PDF]

open access: yes, 2015
The purpose of this study is to know clinical factors underlying either a single surgery or repetitive surgeries, required to treat superior oblique muscle palsy.
Aoba, Kana   +3 more
core   +1 more source

Identifying Common Disease Trajectories of Progressive Supranuclear Palsy with Electronic Health Records

open access: yesMovement Disorders Clinical Practice, Volume 12, Issue 10, Page 1528-1538, October 2025.
Abstract Background Progressive supranuclear palsy (PSP) is a rare neurodegenerative disorder characterized by parkinsonism and impairments in balance, language, and cognition. As an atypical parkinsonism, PSP progresses rapidly, lacks effective treatments, and poses significant caregiving burdens. While prior studies have identified risk factors, they
Mingzhou Fu   +3 more
wiley   +1 more source

Clinical Features, ARIX and PHOX2B Nucleotide Changes in Three Families with Congenital Superior Oblique Muscle Palsy [PDF]

open access: yes, 2008
We analyzed nucleotide changes in 3 genes, ARIX, PHOX2B, and KIF21A, in 6 patients of 3 families with congenital superior oblique muscle palsy. Three exons of ARIX, 3 exons of PHOX2B, and exons 8, 20, and 21 of KIF21A were amplified by polymerase chain ...
Imai, Sayuri   +3 more
core   +1 more source

Brain Networks Route Neurodegeneration Patterns in Patients with Progressive Supranuclear Palsy

open access: yesMovement Disorders, Volume 40, Issue 10, Page 2102-2115, October 2025.
Abstract Background Progressive supranuclear palsy (PSP) is a neurodegenerative disease driven by 4‐repeat τ pathology, which is thought to propagate across interconnected neurons. Objectives We hypothesized that interconnected brain regions exhibit correlated atrophy, and that atrophy propagates network‐like from fast‐declining epicenters to connected
Carla Palleis   +183 more
wiley   +1 more source

Chondroblastoma of the Clivus: Case Report and Review. [PDF]

open access: yes, 2015
Background and Importance Chondroblastoma is a benign primary bone tumor that typically develops in the epiphyses of long bones. Chondroblastoma of the craniofacial skeleton is extremely rare, with most cases occurring in the squamosal portion of the ...
Ahmadpour, Arjang   +5 more
core   +1 more source

Closing in on a Consensus in Identifying, Assessing and Diagnosing Children With Cerebral Visual Impairment

open access: yesActa Paediatrica, Volume 114, Issue 10, Page 2490-2498, October 2025.
ABSTRACT Aim Lack of global consensus regarding CVI makes assessment and research more difficult. Our aim is to describe current consensus and evident methods for how to identify, assess and diagnose CVI in children. Method Data‐based search on reviews and papers published 2014–2023. Result The seven reviews and 23 papers reviewed here jointly convey a
Barbro Lindquist, Christina Westerberg
wiley   +1 more source

Isolated oculomotor nerve palsy related to sinusitis? [PDF]

open access: yes, 2018
The association of sinusitis with ocular motility disorders is a seductive theory due to their close anatomical vicinity. Typically, sinusitis can influence ocular motility by affecting single muscles or a combination of muscles and/or cranial nerves due
Kordic, Helena   +3 more
core  

Evaluation of strain values of critical anatomic regions for two different pterygomaxillary approaches in Le Fort I osteotomy : an experimental study [PDF]

open access: yes, 2017
The purpose of this experimental study was to measure stresses both on the pterygoid plates and the skull base following two different pterygomaxillary approaches in Le Fort I osteotomy. The prepared skull models were randomly divided into 2 groups of 7.
Dolanmaz, Dogan   +4 more
core   +1 more source

Irreversible hypersomnolence after bilateral thalamic infarction [PDF]

open access: yes, 2018
info:eu-repo/semantics ...
Joaquim, Natércia   +5 more
core   +2 more sources

Autosomal Recessive Cerebellar Ataxias: Translating Genes to Therapies

open access: yesAnnals of Neurology, Volume 98, Issue 3, Page 448-470, September 2025.
[Color figure can be viewed at www.annalsofneurology.org] Autosomal recessive cerebellar ataxias are disabling neurodegenerative genetic conditions affecting balance and coordination. Advancements in genomic testing have improved diagnosis, leading to a new focus on the development of targeted precision therapeutics addressing cellular, biochemical ...
Brent L. Fogel   +10 more
wiley   +1 more source

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