Results 51 to 60 of about 12,044 (181)

Atypical tabes dorsalis: one case report

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2019
DOI: 10.3969/j.issn.1672-6731.2019.05 ...
Ai-jun FENG
doaj  

Effectiveness of Total Hip Arthroplasty Combined With Hip Braces for Hip Charcot Arthropathy

open access: yesOrthopaedic Surgery, Volume 17, Issue 3, Page 790-800, March 2025.
This study evaluates the efficacy of Total Hip Arthroplasty combined with Hip Braces in patients with Charcot arthropathy. Assessment indicators such as VAS score, Oxford Hip Score, and UCLA score demonstrate significant improvements in hip joint function post‐surgery. Key complications include hip dislocation and acetabular component loosening.
Long‐Teng Chao   +8 more
wiley   +1 more source

Tabes dorsalis und chronische Spinalmeningitis

open access: yes, 1902
TABES DORSALIS UND CHRONISCHE SPINALMENINGITIS Tabes dorsalis und chronische Spinalmeningitis ([1]) Binding ( - ) Title page ([1]) Dedication ([3]) Introduction ([5]) II. (10) III.
Edens, Ernst
core   +1 more source

Biomechanical modeling of musculoskeletal function related to the terrestrial locomotion of Riojasuchus tenuisceps (Archosauria: Ornithosuchidae)

open access: yesThe Anatomical Record, Volume 308, Issue 2, Page 369-393, February 2025.
Abstract Riojasuchus tenuisceps was a pseudosuchian archosaur from the Late Triassic period in Argentina. Like other ornithosuchids, it had unusual morphology such as a unique “crocodile‐reversed” ankle joint, a lesser trochanter as in dinosaurs and a few other archosaurs, robust vertebrae, and somewhat shortened, gracile forelimbs.
M. Belen von Baczko   +4 more
wiley   +1 more source

Abordagem Diagnóstica, Terapêutica e de Monitorização na Suspeita de Neurossífilis: Proposta de Protocolo Clínico

open access: yesActa Médica Portuguesa
O presente protocolo clínico foi desenhado para servir como um guia hospitalar na abordagem diagnóstica, terapêutica e de monitorização da neurossífilis, tendo em conta a positividade ou não para o vírus de imunodeficiência humana.
Bárbara Martins   +6 more
doaj   +1 more source

A new semi‐fossorial thescelosaurine dinosaur from the Cenomanian‐age Mussentuchit Member of the Cedar Mountain Formation, Utah

open access: yesThe Anatomical Record, Volume 307, Issue 12, Page 3717-3781, December 2024.
Abstract Thescelosaurines are a group of early diverging, ornithischian dinosaurs notable for their conservative bauplans and mosaic of primitive features. Although abundant within the latest Cretaceous ecosystems of North America, their record is poor to absent in earlier assemblages, leaving a large gap in our understanding of their evolution ...
Haviv M. Avrahami   +3 more
wiley   +1 more source

Ein Fall von Aorteninsufficienz bei Tabes dorsalis

open access: yes, 1900
EIN FALL VON AORTENINSUFFICIENZ BEI TABES DORSALIS Ein Fall von Aorteninsufficienz bei Tabes dorsalis ([1]) Binding ( - ) Title page ([1]) Dedication ([3]) Chapter ([5]) Lebenslauf. ( - ) Binding ( -
Simon, Otto
core   +1 more source

A neurosyphilis case presenting with cognitive dysfunction, epileptic seizures, high signal intensity and significant atrophy in left amygdala/ hipocampal region

open access: yesPsychiatry and Clinical Psychopharmacology, 2021
Syphilis is generally a sexually transmitted, chronic, multisystem disease caused by Treponema pallidum. Syphilis has 3 stages: primary, secondary and tertiary.
Özden Arısoy   +5 more
doaj  

Temporal changes in the composition of parasitoid assemblages associated with the invasive chestnut gall wasp

open access: yesEcological Entomology, Volume 49, Issue 6, Page 779-797, December 2024.
After 4‐year monitoring of Dryocosmus kuriphilus, we found that the abundance of each associated parasitoid species varied over time and that the number of species increased year after year. Changes in the number of parasitoid species associated with D.
Juan Luis Jara‐Chiquito   +3 more
wiley   +1 more source

Hereditary sensory neuropathy type I

open access: yesOrphanet Journal of Rare Diseases, 2008
Hereditary sensory neuropathy type I (HSN I) is a slowly progressive neurological disorder characterised by prominent predominantly distal sensory loss, autonomic disturbances, autosomal dominant inheritance, and juvenile or adulthood disease onset.
Auer-Grumbach Michaela
doaj   +1 more source

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