Zobrazeno 1 - 10 of 227 pro vyhledávání: '"pyramidal signs"'
1
Akademický článek
Infantile-Onset Charcot–Marie–Tooth Disease With Pyramidal Features and White Matter Abnormalities Due to a De novo MORC2 Gene Variant: A Case Report and Brief Review of the Literature
Autor: Ivana Frongia, Susanna Rizzi, Margherita Baga, Laura Maria Ceteroni, Carlotta Spagnoli, Grazia Gabriella Salerno, Daniele Frattini, Milja Kaare, Francesco Pisani, Carlo Fusco
Publikováno v: Frontiers in Neurology, Vol 12 (2021)
Background: Charcot–Marie–Tooth (CMT) is the most frequent group of inherited neuropathies and includes several heterogeneous phenotypes. Over 80 causative genes have been described so far. Variants in the microrchidia family CW-type zinc finger
Externí odkaz: https://doaj.org/article/40e0a2cf747a4aa68375f72fb1d55448
Zobrazit plný text záznamu
2
Akademický článek
Sensitivity of Pyramidal Signs in Patients with Cervical Spondylotic Myelopathy
Autor: Hossam Elnoamany
Publikováno v: Asian Spine Journal, Vol 10, Iss 1, Pp 65-69 (2016)
Study DesignThis was a retrospective study.PurposeThe purpose of this study was to study the relationship between prevalence of pyramidal signs and the severity of cervical myelopathy. The study is focused on patients having increased signal intensit
Externí odkaz: https://doaj.org/article/7de9e6a7bc87413d9aaf94827002115f
Zobrazit plný text záznamu
3
Akademický článek
TMS Correlates of Pyramidal Tract Signs and Clinical Motor Status in Patients with Cervical Spondylotic Myelopathy
Autor: Giuseppe Lanza, Valentina Puglisi, Luisa Vinciguerra, Francesco Fisicaro, Carla Vagli, Mariagiovanna Cantone, Giovanni Pennisi, Manuela Pennisi, Rita Bella
Publikováno v: Brain Sciences, Vol 10, Iss 11, p 806 (2020)
Background: While the association between motor-evoked potential (MEP) abnormalities and motor deficit is well established, few studies have reported the correlation between MEPs and signs of pyramidal tract dysfunction without motor weakness. We ass
Externí odkaz: https://doaj.org/article/420d11b4583646f3add281576ed5616a
Zobrazit plný text záznamu
5
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
6
Two cases of neuronopathic form of Gaucher disease – diagnostic difficulties
Autor: Kleinotienė, Gražina, Ivaškevičienė, Austėja, Tylki-Szymanska, Anna
Publikováno v: Acta Biochimica Polonica, Warszawa : Polskie Towarzystwo Biochemiczne (Polish Biochemical Society), 2022, vol. 69, no. 1, p. 119-122
Acta Biochimica Polonica, Warszawa : Polskie Towarzystwo Biochemiczne (Polish Biochemical Society), 2021, first published online, p. [1-4]
Background: Gaucher disease is one of the most common inherited lysosomal storage diseases caused by the deficiency of the enzyme β-glucocerebrosidase, leading to the accumulation of glucocerebroside. Depending on the clinical manifestations, two di
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c2d6332c683013c8d8855d1ce1e1934
https://doi.org/10.18388/abp.2020_5760
Zobrazit plný text záznamu
7
Infantile-Onset Charcot–Marie–Tooth Disease With Pyramidal Features and White Matter Abnormalities Due to a De novo MORC2 Gene Variant: A Case Report and Brief Review of the Literature
Autor: Carlotta Spagnoli, Daniele Frattini, Laura Maria Ceteroni, Milja Kaare, Ivana Frongia, Grazia Gabriella Salerno, Carlo Fusco, Francesco Pisani, Susanna Rizzi, Margherita Baga
Publikováno v: Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Background: Charcot–Marie–Tooth (CMT) is the most frequent group of inherited neuropathies and includes several heterogeneous phenotypes. Over 80 causative genes have been described so far. Variants in the microrchidia family CW-type zinc finger
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c431b3d44a42c01cf7f3620de02e46a7
https://www.frontiersin.org/articles/10.3389/fneur.2021.718808/full
Zobrazit plný text záznamu
8
Study on Primary Angiitis of Central Nervous System
Autor: Radhakrishna Hari, Bimal Prasad Padhy
Objective: To study the clinical features of primary central nervous system angiitis (PACNS) with case illustration and to review the current literature. Background: Primary angiitis is a rare disorder and is difficult to diagnose and there are many
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f1f478ad94b9372df1ace106a43ccab
https://doi.org/10.9734/bpi/nfmmr/v3/3389f
Zobrazit plný text záznamu
9
Surgical management of traumatic extradural hematomas in children: an analysis of 201 patients at a tertiary neurosurgical center
Autor: Subhas Konar, Bhagavatula Indira Devi, Dhananjaya I Bhat, Nishanth Sadashiva, Sandeep Kandregula, Dhaval Shukla, Kannepalli Narasingha Rao
Publikováno v: Child's Nervous System. 35:807-813
The effects of traumatic extradural hematoma (EDH) are potentially reversible if treated early. Pediatric EDH differs from its adult counterpart because of the differential elastic and adherence properties of skull bone and dura respectively. There i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f029199a8620d306a9159166a27fdfb1
https://doi.org/10.1007/s00381-019-04088-1
Zobrazit plný text záznamu
10
Atypical Childhood-onset Neuroaxonal Dystrophy in an Indian Girl
Autor: Marta Romani, Enza Maria Valente, Suvasini Sharma, Himani Bhasin, Sakshi Jain
Publikováno v: Journal of Pediatric Neurosciences
A 7-year-old girl presented with progressive walking difficulties, spasticity, and cognitive decline with onset at 3 years of age. No seizures, vision, or hearing impairment were reported. The magnetic resonance imaging of the brain revealed cerebell
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4621ce17c7ecd574f811e21d7c6bb63e
http://europepmc.org/articles/PMC6712922
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje