Maria J. Miranda
Clinical Associate Professor
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Validation of Pediatric Idiopathic Generalized Epilepsy Diagnoses from the Danish National Patient Register During 1994‒2019
Boesen, M. S., Hribljan, M. C., Christensen, S. K., Klein-Petersen, A. W., Mahdaoui, S. E., Sagar, M. V., Schou, E., Eltvedt, A. K., Børresen, M. L., Miranda, Maria J., Born, A. P., Uldall, P. V. & Thygesen, L. C., 2022, In: Clinical Epidemiology. 14, p. 501-509 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort study
Boesen, M. S., Børresen, M. L., Christensen, S. K., Klein-Petersen, A. W., El Mahdaoui, S., Sagar, M. V., Schou, E., Eltvedt, A. K., Cacic Hribljan, M., Born, A. P., Uldall, P. V., Thygesen, L. C. & Miranda, Maria J., 2023, In: European Journal of Paediatric Neurology. 42, p. 75-81 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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School performance and psychiatric comorbidity in juvenile absence epilepsy and juvenile myoclonic epilepsy: a Danish population-based cohort study
Boesen, M. S., Børresen, M. L., Christensen, S. K., Klein-Petersen, A. W., El Mahdaoui, S., Sagar, M. V., Schou, E., Eltvedt, A. K., Miranda, Maria J., Born, A. P., Uldall, P. V., Thygesen, L. C. & Cacic Hribljan, M., 2022, In: Journal of Neurology. 269, 9, p. 4997-5007 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
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The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant
Chatron, N., Møller, R. S., Champaigne, N. L., Schneider, A. L., Kuechler, A., Labalme, A., Simonet, T., Baggett, L., Bardel, C., Kamsteeg, E., Pfundt, R., Romano, C., Aronsson, J., Alberti, A., Vinci, M., Miranda, M. J., Lacroix, A., Marjanovic, D., Des Portes, V., Edery, P. & 7 others, , 2018, In: Annals of Neurology. 83, 5, p. 926-934 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Pontocerebellar hypoplasi er en sjælden årsag til slapt spædbarn
Christiansen, S., Roos, L. K. S. & Miranda, Maria J., 28 Sep 2015, In: Ugeskrift for Laeger. 177, 40, p. V05150380Research output: Contribution to journal › Journal article › Research › peer-review
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Algoritme til diagnosticering af slapt spædbarn
Christiansen, S. & Miranda, Maria J., 2 May 2016, In: Ugeskrift for Laeger. 178, 9, p. 867-71 5 p., V05150378.Research output: Contribution to journal › Journal article › Research › peer-review
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TARGETED NEXT GENERATION SEQUENCING AS A DIAGNOSTIC TOOL IN 163 PATIENTS WITH EPILEPTIC ENCEPHALOPATHIES
Dahl, H. A., Larsen, L. H. G., Olofsson, K., Miranda, M., Nielsen, J. E. K., Lavard, L., Linnet, K., Uldall, P., Talvik, T., Talvik, I., Frangu, M., Born, P., Gellert, P., Nikanorova, M., Jepsen, B., Marjanovic, D., Kragh-Olsen, B., Mosbech, M. -B., Hao, Q., Brusgaard, K. & 2 others, , Dec 2015, In: Epilepsia. 56, Supplement S1, p. 72-73Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
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Hovedpine hos børn og unge
Gren, C., Vogler, K., Miranda, Maria J. & Debes, Nanette M Monique Mol, 2018, In: Ugeskrift for Laeger. 180, 7, 5 p., V06170483.Research output: Contribution to journal › Journal article › Research › peer-review
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Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling
Grønborg, S., Darin, N., Miranda, Maria J., Damgaard, B., Cayuela, J. A., Oldfors, A., Kollberg, G., Hansen, T. V. O., Ravn, K., Wibrand, F. & Østergaard, Elsebet, 2016, JIMD Reports. Vol. 33. p. 69-77 9 p. (JIMD Reports).Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
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Effectiveness of the ketogenic diet used to treat resistant childhood epilepsy in Scandinavia
Hallböök, T., Sjölander, A., Åmark, P., Miranda, Maria J., Bjurulf, B. & Dahlin, M., Jan 2015, In: European Journal of Paediatric Neurology. 19, 1, p. 29-36 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 44652539
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Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development
Research output: Contribution to journal › Journal article › Research › peer-review
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Validation of Pediatric Idiopathic Generalized Epilepsy Diagnoses from the Danish National Patient Register During 1994‒2019
Research output: Contribution to journal › Journal article › Research › peer-review
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23
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The spectrum of intermediate SCN8A-related epilepsy
Research output: Contribution to journal › Journal article › Research › peer-review
Published