Istvan Bodi
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Explore the profile of Istvan Bodi including associated specialties, affiliations and a list of published articles.
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Articles
99
Citations
2174
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Recent Articles
1.
Lee K, Kalyal N, Mthunzi E, Marchi F, Elhag A, Bodi I, et al.
J Surg Case Rep
. 2025 Feb;
2025(2):rjaf066.
PMID: 39975844
Intracranial dermoid cysts are benign lesions that may be diagnosed incidentally or present symptomatically due to mass effect-focal neurological deficits, seizures and/or hydrocephalus-or chemical meningitis secondary to spontaneous rupture. The...
2.
Reisz Z, Pereira R, Nevis S, Mackay A, Bhaw L, Grabovska Y, et al.
Acta Neuropathol Commun
. 2025 Jan;
13(1):7.
PMID: 39815339
Histone mutations (H3 K27M, H3 G34R/V) are molecular features defining subtypes of paediatric-type diffuse high-grade gliomas (HGG) (diffuse midline glioma (DMG), H3 K27-altered, diffuse hemispheric glioma (DHG), H3 G34-mutant). The...
3.
Valentino R, Scotton W, Roemer S, Lashley T, Heckman M, Shoai M, et al.
Lancet Neurol
. 2024 Apr;
23(5):487-499.
PMID: 38631765
Background: Pick's disease is a rare and predominantly sporadic form of frontotemporal dementia that is classified as a primary tauopathy. Pick's disease is pathologically defined by the presence in the...
4.
Meinhardt A, Reilly L, Kaliakatsos M, Abdel-Aziz K, Alsharidah S, Bodi I, et al.
J Infect
. 2024 Mar;
88(5):106142.
PMID: 38527653
No abstract available.
5.
Topf A, Cox D, Zaharieva I, Di Leo V, Sarparanta J, Jonson P, et al.
Nat Genet
. 2024 Mar;
56(3):395-407.
PMID: 38429495
In digenic inheritance, pathogenic variants in two genes must be inherited together to cause disease. Only very few examples of digenic inheritance have been described in the neuromuscular disease field....
6.
Sanders M, Van der Wolf I, Jansen F, Aronica E, Helmstaedter C, Racz A, et al.
Neurology
. 2024 Jan;
102(4):e208007.
PMID: 38290094
Background And Objective: Patients with presumed nonlesional focal epilepsy-based on either MRI or histopathologic findings-have a lower success rate of epilepsy surgery compared with lesional patients. In this study, we...
7.
Garcia-Moreno H, Langbehn D, Abiona A, Garrood I, Fleszar Z, Manes M, et al.
Brain
. 2023 Dec;
146(12):5044-5059.
PMID: 38040034
Xeroderma pigmentosum (XP) results from biallelic mutations in any of eight genes involved in DNA repair systems, thus defining eight different genotypes (XPA, XPB, XPC, XPD, XPE, XPF, XPG and...
8.
Lichtblau N, Aliaga-Arias J, Kalaitzoglou D, Bodi I, Ashkan K, Bhangoo R, et al.
Pract Neurol
. 2023 Jul;
23(5):441-445.
PMID: 37460210
Hypertrophic pachymeningitis is a rare disorder of the dura mater of the spine or brain. It can be caused by inflammatory, infective or neoplastic conditions or can be idiopathic. We...
9.
Ashkan K, Baig Mirza A, Soumpasis C, Syrris C, Kalaitzoglou D, Sharma C, et al.
J Pers Med
. 2023 Jun;
13(6).
PMID: 37373988
MGMT promoter methylation is related to the increased sensitivity of tumour tissue to chemotherapy with temozolomide (TMZ) and thus to improved patient survival. However, it is unclear how the extent...
10.
Reisz Z, Radics B, Nemes P, Laxton R, Kaizer L, Gabor K, et al.
Pathol Oncol Res
. 2023 Jun;
29:1611231.
PMID: 37362245
Angiocentric gliomas (AG) in brainstem location are exceedingly rare and might cause differential diagnostic problems and uncertainty regarding the best therapeutic approach. Hereby, we describe the clinicopathological findings in a...