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Year Number of Results
2013 1
2017 4
2018 3
2019 2
2020 5
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Page 1
Understanding the Epilepsy in POLG Related Disease.
Hikmat O, Eichele T, Tzoulis C, Bindoff LA. Hikmat O, et al. Int J Mol Sci. 2017 Aug 24;18(9):1845. doi: 10.3390/ijms18091845. Int J Mol Sci. 2017. PMID: 28837072 Free PMC article. Review.
Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases.
Maas RR, Iwanicka-Pronicka K, Kalkan Ucar S, Alhaddad B, AlSayed M, Al-Owain MA, Al-Zaidan HI, Balasubramaniam S, Barić I, Bubshait DK, Burlina A, Christodoulou J, Chung WK, Colombo R, Darin N, Freisinger P, Garcia Silva MT, Grunewald S, Haack TB, van Hasselt PM, Hikmat O, Hörster F, Isohanni P, Ramzan K, Kovacs-Nagy R, Krumina Z, Martin-Hernandez E, Mayr JA, McClean P, De Meirleir L, Naess K, Ngu LH, Pajdowska M, Rahman S, Riordan G, Riley L, Roeben B, Rutsch F, Santer R, Schiff M, Seders M, Sequeira S, Sperl W, Staufner C, Synofzik M, Taylor RW, Trubicka J, Tsiakas K, Unal O, Wassmer E, Wedatilake Y, Wolff T, Prokisch H, Morava E, Pronicka E, Wevers RA, de Brouwer AP, Wortmann SB. Maas RR, et al. Among authors: hikmat o. Ann Neurol. 2017 Dec;82(6):1004-1015. doi: 10.1002/ana.25110. Ann Neurol. 2017. PMID: 29205472 Free PMC article.
The doctors' role in cases of suspected child abuse.
Stray-Pedersen A, Møller C, de Lange C, Due-Tønnessen BJ, Grøgaard JB, Haugen OH, Hikmat O, Mahesparan R, Müller LO, Myhre AK, Myhre MC, Nedregaard B, Nordhov SM, Rognum TO, Rosendahl K, Sørbø T, Vollmer-Sandholm MJ, Aukland SM. Stray-Pedersen A, et al. Among authors: hikmat o. Tidsskr Nor Laegeforen. 2018 Dec 21;138(2). doi: 10.4045/tidsskr.18.0922. Print 2019 Jan 29. Tidsskr Nor Laegeforen. 2018. PMID: 30698400 Free article. English, Norwegian. No abstract available.
Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications.
Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Tallaksen CME, Brodtkorb E, Fiskerstrand T, Isohanni P, Uusimaa J, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. Epilepsia. 2018 Aug;59(8):1595-1602. doi: 10.1111/epi.14459. Epub 2018 Jun 19. Epilepsia. 2018. PMID: 29920680 Free article.
Erratum to: The presence of anaemia negatively influences survival in patients with POLG disease.
Hikmat O, Tzoulis C, Klingenberg C, Rasmussen M, Tallaksen CME, Brodtkorb E, Fiskerstrand T, McFarland R, Rahman S, Bindoff LA. Hikmat O, et al. J Inherit Metab Dis. 2018 Jan;41(1):153. doi: 10.1007/s10545-017-0092-9. J Inherit Metab Dis. 2018. PMID: 28952135 No abstract available.
Correction: The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.
Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman JW, Bindoff LA, Rahman S. Hikmat O, et al. Genet Med. 2019 Apr;21(4):1027. doi: 10.1038/s41436-018-0098-1. Genet Med. 2019. PMID: 30228318 Free article.
The presence of anaemia negatively influences survival in patients with POLG disease.
Hikmat O, Tzoulis C, Klingenberg C, Rasmussen M, Tallaksen CME, Brodtkorb E, Fiskerstrand T, McFarland R, Rahman S, Bindoff LA. Hikmat O, et al. J Inherit Metab Dis. 2017 Nov;40(6):861-866. doi: 10.1007/s10545-017-0084-9. Epub 2017 Sep 1. J Inherit Metab Dis. 2017. PMID: 28865037
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.
Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman JW, Bindoff LA, Rahman S. Hikmat O, et al. Genet Med. 2017 Nov;19(11):1217-1225. doi: 10.1038/gim.2017.35. Epub 2017 Apr 27. Genet Med. 2017. PMID: 28471437 Free article.
[Polymerase gamma-related mitochondrial disorder].
Hikmat O, Varhaug KN, Bindoff LA. Hikmat O, et al. Tidsskr Nor Laegeforen. 2020 Jan 13;140(1). doi: 10.4045/tidsskr.19.0368. Print 2020 Jan 14. Tidsskr Nor Laegeforen. 2020. PMID: 31948198 Free article. Norwegian.
Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases.
Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Tallaksen CM, Brodtkorb E, Ostergaard E, de Coo IFM, Pias-Peleteiro L, Isohanni P, Uusimaa J, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. J Inherit Metab Dis. 2020 Jul;43(4):726-736. doi: 10.1002/jimd.12211. Epub 2020 Jan 23. J Inherit Metab Dis. 2020. PMID: 32391929
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