Torthaí cuardaigh - Hikmat, Omar
- 1 - 7 toradh as 7 á dtaispeáint
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1
Understanding the Epilepsy in POLG Related Disease de réir Hikmat, Omar, Eichele, Tom, Tzoulis, Charalampos, Bindoff, Laurence A.
Foilsithe / Cruthaithe 2017Téacs -
2
CFS in Children and Adolescent: Ten Years of Retrospective Clinical Evaluation de réir Elgen, Irene, Hikmat, Omar, Aspevik, Tora N., Hagen, Ellen Merete
Foilsithe / Cruthaithe 2013Téacs -
3
Serum biomarkers in primary mitochondrial disorders de réir Varhaug, Kristin N, Hikmat, Omar, Nakkestad, Hanne Linda, Vedeler, Christian A, Bindoff, Laurence A
Foilsithe / Cruthaithe 2021Téacs -
4
Renal Phenotype in Mitochondrial Diseases: A Multicenter Study de réir Parasyri, Maria, Brandström, Per, Uusimaa, Johanna, Ostergaard, Elsebet, Hikmat, Omar, Isohanni, Pirjo, Naess, Karin, de Coo, I.F.M., Nascimento Osorio, Andrés, Nuutinen, Matti, Lindberg, Christopher, Bindoff, Laurence A., Tulinius, Már, Darin, Niklas, Sofou, Kalliopi
Foilsithe / Cruthaithe 2022Téacs -
5
The impact of gender, puberty, and pregnancy in patients with POLG disease de réir Hikmat, Omar, Naess, Karin, Engvall, Martin, Klingenberg, Claus, Rasmussen, Magnhild, Tallaksen, Chantal M. E., Samsonsen, Christian, Brodtkorb, Eylert, Ostergaard, Elsebet, de Coo, Rene, Pias‐Peleteiro, Leticia, Isohanni, Pirjo, Uusimaa, Johanna, Darin, Niklas, Rahman, Shamima, Bindoff, Laurence A.
Foilsithe / Cruthaithe 2020Téacs -
6
Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease de réir Hikmat, Omar, Isohanni, Pirjo, Keshavan, Nandaki, Ferla, Matteo P., Fassone, Elisa, Abbott, Mary‐Alice, Bellusci, Marcello, Darin, Niklas, Dimmock, David, Ghezzi, Daniele, Houlden, Henry, Invernizzi, Federica, Kamarus Jaman, Nazreen B., Kurian, Manju A., Morava, Eva, Naess, Karin, Ortigoza‐Escobar, Juan Darío, Parikh, Sumit, Pennisi, Alessandra, Barcia, Giulia, Tylleskär, Karin B., Brackman, Damien, Wortmann, Saskia B., Taylor, Jenny C., Bindoff, Laurence A., Fellman, Vineta, Rahman, Shamima
Foilsithe / Cruthaithe 2021Téacs -
7
Progressive deafness–dystonia due to SERAC1 mutations: A study of 67 cases de réir Maas, Roeltje R., Iwanicka‐Pronicka, Katarzyna, Kalkan Ucar, Sema, Alhaddad, Bader, AlSayed, Moeenaldeen, Al‐Owain, Mohammed A., Al‐Zaidan, Hamad I., Balasubramaniam, Shanti, Barić, Ivo, Bubshait, Dalal K., Burlina, Alberto, Christodoulou, John, Chung, Wendy K., Colombo, Roberto, Darin, Niklas, Freisinger, Peter, Garcia Silva, Maria Teresa, Grunewald, Stephanie, Haack, Tobias B., van Hasselt, Peter M., Hikmat, Omar, Hörster, Friederike, Isohanni, Pirjo, Ramzan, Khushnooda, Kovacs‐Nagy, Reka, Krumina, Zita, Martin‐Hernandez, Elena, Mayr, Johannes A., McClean, Patricia, De Meirleir, Linda, Naess, Karin, Ngu, Lock H., Pajdowska, Magdalena, Rahman, Shamima, Riordan, Gillian, Riley, Lisa, Roeben, Benjamin, Rutsch, Frank, Santer, Rene, Schiff, Manuel, Seders, Martine, Sequeira, Silvia, Sperl, Wolfgang, Staufner, Christian, Synofzik, Matthis, Taylor, Robert W., Trubicka, Joanna, Tsiakas, Konstantinos, Unal, Ozlem, Wassmer, Evangeline, Wedatilake, Yehani, Wolff, Toni, Prokisch, Holger, Morava, Eva, Pronicka, Ewa, Wevers, Ron A., de Brouwer, Arjan P., Wortmann, Saskia B.
Foilsithe / Cruthaithe 2017Téacs