Results 131 to 140 of about 26,412 (249)

Central nervous system. Sense organs [PDF]

, 2017
Навчальний посібник рекомендований для студентів вищих медичних навчальних закладів IV рівня акредитації, які вивчають анатомію людини англійською ...
Bumeister, Valentyna Ivanivna, Prykhodko, Olha Oleksiivna, Sulym, Liudmyla Hryhorivna, Yarmolenkо, Olha Serhiivna, Бумейстер, Валентина Ивановна, Бумейстер, Валентина Іванівна, Приходько, Ольга Алексеевна, Приходько, Ольга Олексіївна, Сулим, Людмила Григорьевна, Сулим, Людмила Григорівна, Ярмоленкo, Ольга Сергіївна, Ярмоленко, Ольга Сергеевна   +11 more
core  

The status of thegn in late Anglo‐Saxon England

Early Medieval Europe, Volume 34, Issue 2, Page 323-352, May 2026.
This article considers how the term ‘thegn’ was used in tenth‐ and eleventh‐century England. Although commonly thought to indicate members of a face‐to‐face service aristocracy with specific attributes, it has resisted close definition. Examination of references to anonymous thegns in administrative and legal texts suggests that the people meant were ...
Richard Purkiss
wiley   +1 more source

Macroscopical and histological characterization of the perineal membrane and deep perineal pouch

Journal of Anatomy, Volume 248, Issue 5, Page 755-765, May 2026.
The existence of the deep transverse perineal muscle remains controversial. While the macroscopic appearance of the tissue in the deep perineal pouch differs between men and women, the differences in the histological composition of this fibromuscular plate is still unclear.
Morten Kampelmann, Carina Grindley, Christian Mühlfeld, Andreas Schmiedl   +3 more
wiley   +1 more source

A double CYP27A1 gene mutation in spinal cerebrotendinous xanthomatosis in a patient presenting with spastic gait: a case report

Journal of Medical Case Reports
Background Cerebrotendinous xanthomatosis (CTX, OMIM #213700) is a rare inherited metabolic disease caused by the mutation in the CYP27A1 gene. Spinal CTX is a rare clinical subgroup of CTX which lacks typical symptoms seen in classical CTX.
Je Hong Min, Yoon Seob Kim, Myeong Jin Son, In Soo Joo   +3 more
doaj   +1 more source

Cortico-spinal reorganization in postanoxic conditions in children: a series of case reports [PDF]

РМЖ. Мать и дитя
D.S. Kan'shina1, M.V. Ublinskiy1, I.A. Mel'nikov1, S.A. Valliulina1, T.A. Akhadov1, S.S. Nikitin2, V.P. Zykov3, E.E. Drozhevskaya4 1Research Institute of Emergency Pediatric Surgery and Traumatology, Moscow,   Russian Federation ...
D.S. Kan'shina, M.V. Ublinskiy, I.A. Mel'nikov, S.A. Valliulina, T.A. Akhadov, S.S. Nikitin, V.P. Zykov, E.E. Drozhevskaya   +7 more
doaj  

Multiple system atrophy—cerebellar type: Diagnostic challenge in resource‐limited settings case report

Clinical Case Reports
Key Clinical Message This case report highlights the challenges of diagnosing MSA‐C in resource‐limited settings. MRI findings like the “hot cross bun” sign can be supportive, but the unavailability of advanced tools like seed amplification assay may ...
Gebeyehu Tessema Azibte, Bereket Abraha Molla, Sebhatleab Teju Mulate, Selam Kifelew Melkamu, Zekarias Seifu Ayalew   +4 more
doaj   +1 more source

Tailored keyhole surgery for basal ganglia cavernous malformation with preoperative three-dimensional pyramidal tracts assessment and intraoperative electrophysiological monitoring [PDF]

, 2015

core   +1 more source

Impulses in the pyramidal tract [PDF]

The Journal of Physiology, 1939
E D, Adrian, G, Moruzzi
openaire   +2 more sources

Wallerian degeneration of the pyramidal tract

Deutsches Ärzteblatt international, 2022
Robert, Forbrig, Adrian, Danek
openaire   +2 more sources

Autoimmune cerebellopyramidal syndrome as a complex form of autoimmune cerebellar ataxia: a cohort study. [PDF]

Front Immunol
Liu M, Ren H, Fan S, Zhang L, Guan H.
europepmc   +1 more source