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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2016 | 1 |
2019 | 2 |
2020 | 1 |
2021 | 2 |
2022 | 1 |
2023 | 0 |
Search Results
6
results
Results by year
Page 1
Ketogenic Diet in Patients with GLUT1 Deficiency Syndrome.
Maedica (Bucur). 2019 Jun;14(2):93-97. doi: 10.26574/maedica.2019.14.2.93.
Maedica (Bucur). 2019.
PMID: 31523287
Free PMC article.
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries.
Selvatici R, Rossi R, Fortunato F, Trabanelli C, Sifi Y, Margutti A, Neri M, Gualandi F, Szabò L, Fekete B, Angelova L, Litvinenko I, Ivanov I, Vildan Y, Iuhas OA, Vintan M, Burloiu C, Lacramioara B, Visa G, Epure D, Rusu C, Vasile D, Sandu M, Vlodavets D, Mager M, Kyriakides T, Delin S, Lehman I, Fureš JS, Bojinova V, Militaru M, Guergueltcheva V, Burnyte B, Molnar MJ, Butoianu N, Bensemmane SD, Makri-Mokrane S, Herczegfalvi A, Panzaru M, Emandi AC, Lusakowska A, Potulska-Chromik A, Kostera-Pruszczyk A, Shatillo A, Khelladi DB, Dendane O, Fang M, Lu Z, Ferlini A.
Selvatici R, et al. Among authors: burloiu c.
Neurol Genet. 2020 Dec 24;7(1):e536. doi: 10.1212/NXG.0000000000000536. eCollection 2021 Feb.
Neurol Genet. 2020.
PMID: 33376799
Free PMC article.
Item in Clipboard
Neurofibromatosis type 1 associated with moyamoya syndrome. Case report and review of the literature.
Budişteanu M, Burloiu CM, Papuc SM, Focşa IO, Riga D, Riga S, Arghir A.
Budişteanu M, et al. Among authors: burloiu cm.
Rom J Morphol Embryol. 2019;60(2):713-716.
Rom J Morphol Embryol. 2019.
PMID: 31658349
Free article.
Review.
Item in Clipboard
Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies-Data from a Romanian Cohort.
Riza AL, Streață I, Roza E, Budișteanu M, Iliescu C, Burloiu C, Dobrescu MA, Dorobanțu S, Dragoș A, Grigorescu A, Tătaru T, Ioana M, Teleanu R.
Riza AL, et al. Among authors: burloiu c.
Genes (Basel). 2022 Jul 15;13(7):1253. doi: 10.3390/genes13071253.
Genes (Basel). 2022.
PMID: 35886038
Free PMC article.
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A case of Bardet-Biedl syndrome caused by a recurrent variant in BBS12: A case report.
Focșa IO, Budișteanu M, Burloiu C, Khan S, Sadeghpour A, Bohîlțea LC, Davis EE, Bălgrădean M.
Focșa IO, et al. Among authors: burloiu c.
Biomed Rep. 2021 Dec;15(6):103. doi: 10.3892/br.2021.1479. Epub 2021 Oct 21.
Biomed Rep. 2021.
PMID: 34760276
Free PMC article.
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Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea.
Bauché S, O'Regan S, Azuma Y, Laffargue F, McMacken G, Sternberg D, Brochier G, Buon C, Bouzidi N, Topf A, Lacène E, Remerand G, Beaufrere AM, Pebrel-Richard C, Thevenon J, El Chehadeh-Djebbar S, Faivre L, Duffourd Y, Ricci F, Mongini T, Fiorillo C, Astrea G, Burloiu CM, Butoianu N, Sandu C, Servais L, Bonne G, Nelson I, Desguerre I, Nougues MC, Bœuf B, Romero N, Laporte J, Boland A, Lechner D, Deleuze JF, Fontaine B, Strochlic L, Lochmuller H, Eymard B, Mayer M, Nicole S.
Bauché S, et al. Among authors: burloiu cm.
Am J Hum Genet. 2016 Sep 1;99(3):753-761. doi: 10.1016/j.ajhg.2016.06.033. Epub 2016 Aug 25.
Am J Hum Genet. 2016.
PMID: 27569547
Free PMC article.
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