1.
Szabo, Fruzsina ; Grosz, Zoltan ; Gezsi, Andras ; Suveges, Anna ; Jimoh, Idris J ; Zeke, Helga ; Gal, Aniko ; Molnár, Mária Judit
Analysis of the most common nuclear genome encoded mitochondrial gene in Hungarian patients with adult-onset mitochondrial disorders
EUROPEAN JOURNAL OF HUMAN GENETICS 30 : Suppl.1 pp. 286-286. Paper: P09.082.C , 1 p. (2022)
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Publication:34090032 Validated Core Journal Article (Abstract ) Scientific
Abstract (Journal Article) | Scientific[34090032] [Validated]
2.
István, Lilla ✉ ; Benyó, Fruzsina ; Csorba, Anita ; Jimoh, Idris János ; Gál, Anikó ; Molnár, Mária Judit ; Nagy, Zoltán Zsolt ; Szabó, Viktória
Cornealis polymegathismus és retinalis pigmenthám-eltérések MELAS-szindrómában
SZEMÉSZET 159 : 2 pp. 69-75. , 7 p. (2022)
DOI REAL Matarka MOB
Publication:32990409 Validated Core Journal Article (Article ) Scientific
Article (Journal Article) | Scientific[32990409] [Validated]
3.
Jimoh, IJ ; Molnár, MJ
A mitochondrialis betegségek diagnosztikai és kezelési lehetőségei 2021-ben
ORVOSTOVÁBBKÉPZŐ SZEMLE (2022)
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Publication:32587580 Admin approved Core Journal Article (Survey paper ) Scientific
Survey paper (Journal Article) | Scientific[32587580] [Admin approved]
4.
Jimoh, I. J. ; Balicza, P. ; Csaban, D. ; Grosz, Z. ; Varga, N. ; Molnar, V. ; Fekete, B. ; Illes, A. ; Boczan, J. ; Klivenyi, P. et al.
SPG7 mutations in Hungarian cohorts: new insights and possible genotype-phenotype correlations
EUROPEAN JOURNAL OF NEUROLOGY 28 pp. 845-845. Paper: EPO-650 , 1 p. (2021)
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Publication:32596517 Validated Core Journal Article (Abstract ) Scientific
Abstract (Journal Article) | Scientific[32596517] [Validated]
5.
Jimoh, Idris Janos ; Sebe, Barbara ; Balicza, Peter ; Fedor, Mariann ; Pataky, Ilona ; Rudas, Gabor ; Gal, Aniko ; Inczedy-Farkas, Gabriella ; Nemeth, Gyorgy ; Molnar, Maria Judit ✉
Wernicke–Korsakoff syndrome associated with mtDNA disease
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS 13 : January-December Paper: 1756286420938972 , 7 p. (2020)
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Publication:31409996 Validated Core Citing Journal Article (Article ) Scientific
Citing papers: 5 | Independent citation: 2 | Self citation: 3 | Unknown citation: 0 | Number of citations in WoS: 5 | Number of citations in Scopus: 5 | WoS/Scopus assigned: 5 | Number of citations with DOI: 5
Article (Journal Article) | Scientific[31409996] [Validated]
All citations+mentions: 5, External citations: 2, Self citations: 3, Unhandled citations: 0
6.
Molnar, Maria Judit ✉ ; Jimoh, Idris János ; Zeke, Helga ; Palásti, Ágnes ; Fedor, Marianna
Early-Onset Schizophrenia With Predominantly Negative Symptoms: A Case Study of a Drug-Naive Female Patient Treated With Cariprazine
FRONTIERS IN PHARMACOLOGY 11 Paper: 477 (2020)
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Publication:31293409 Validated Core Citing Journal Article (Article ) Scientific
Citing papers: 9 | Independent citation: 7 | Self citation: 2 | Unknown citation: 0 | Number of citations in WoS: 8 | Number of citations in Scopus: 9 | WoS/Scopus assigned: 9 | Number of citations with DOI: 9
Article (Journal Article) | Scientific[31293409] [Validated]
All citations+mentions: 9, External citations: 7, Self citations: 2, Unhandled citations: 0
7.
Molnar, V. ; Gezsi, A. ; Illes, A. ; Balicza, P. ; Berta, B. ; Csaban, D. ; Jimoh, I. J. ; Gal, A. ; Molnar, M. J.
Sequential approach to identify disease causing variants in patients with mitochondrial dysfunction of a Hungarian cohort
EUROPEAN JOURNAL OF HUMAN GENETICS 27 : Supplement: 1 pp. 191-192. , 2 p. (2019)
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Publication:32686652 Validated Core Journal Article (Abstract ) Scientific
Abstract (Journal Article) | Scientific[32686652] [Validated]
8.
Fekete, Bálint ✉ ; Pentelényi, Klára ; Rudas, Gabor ; Gál, Anikó ; Grosz, Zoltán ; Illés, Anett ; Idris, Jimoh ; Csukly, Gabor ; Domonkos, Andor ; Molnar, Maria Judit
Broadening the phenotype of the TWNK gene associated Perrault syndrome
BMC MEDICAL GENETICS 20 : 1 Paper: 198 , 8 p. (2019)
DOI WoS SE Repozitórium Scopus PubMed
Publication:31032708 Validated Core Citing Journal Article (Article ) Scientific
Citing papers: 13 | Independent citation: 13 | Self citation: 0 | Unknown citation: 0 | Number of citations in WoS: 13 | Number of citations in Scopus: 13 | WoS/Scopus assigned: 13 | Number of citations with DOI: 13
Article (Journal Article) | Scientific[31032708] [Validated]
All citations+mentions: 13, External citations: 13, Self citations: 0, Unhandled citations: 0
9.
Molnár, V ; Gézsi, A ; Illés, A ; Balicza, P ; Berta, B ; Csabán, D ; Jimoh, IJ ; Gál, A ; Molnár, MJ.
Sequential approach to identify disease causing variants in patients with mitochondrial dysfunction of a Hungarian cohort (2018)
European Society of Human Genetics. ESHG Milan, Italy, 2018.06.16-2018.06.19. P06.55C / C,
Publication:31796560 Admin approved Core Miscellaneous (Not classified ) Scientific
Not classified (Miscellaneous) | Scientific[31796560] [Admin approved]
2025-01-22 01:26