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Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study.
Seizure. 2021 May;88:60-72. doi: 10.1016/j.seizure.2021.03.025. Epub 2021 Mar 30.
Seizure. 2021.
PMID: 33831796
Free article.
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease.
Saredi S, Ardissone A, Ruggieri A, Mottarelli E, Farina L, Rinaldi R, Silvestri E, Gandioli C, D'Arrigo S, Salerno F, Morandi L, Grammatico P, Pantaleoni C, Moroni I, Mora M.
Saredi S, et al. Among authors: gandioli c.
J Neurol Sci. 2012 Jul 15;318(1-2):45-50. doi: 10.1016/j.jns.2012.04.008. Epub 2012 May 2.
J Neurol Sci. 2012.
PMID: 22554691
Free PMC article.
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SEPN1-related myopathy in three patients: novel mutations and diagnostic clues.
Ardissone A, Bragato C, Blasevich F, Maccagnano E, Salerno F, Gandioli C, Morandi L, Mora M, Moroni I.
Ardissone A, et al. Among authors: gandioli c.
Eur J Pediatr. 2016 Aug;175(8):1113-8. doi: 10.1007/s00431-015-2685-3. Epub 2016 Jan 16.
Eur J Pediatr. 2016.
PMID: 26780752
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Double-trouble in pediatric neurology: myotonia congenita combined with charcot-marie-tooth disease type 1a.
Ardissone A, Brugnoni R, Gandioli C, Milani M, Ciano C, Uziel G, Moroni I.
Ardissone A, et al. Among authors: gandioli c.
Muscle Nerve. 2014 Jul;50(1):145-7. doi: 10.1002/mus.24205. Epub 2014 May 5.
Muscle Nerve. 2014.
PMID: 24515601
No abstract available.
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Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4).
Piscosquito G, Saveri P, Magri S, Ciano C, Gandioli C, Morbin M, Bella DD, Moroni I, Taroni F, Pareyson D.
Piscosquito G, et al. Among authors: gandioli c.
J Peripher Nerv Syst. 2016 Sep;21(3):142-9. doi: 10.1111/jns.12175.
J Peripher Nerv Syst. 2016.
PMID: 27231023
Free PMC article.
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Early neurodevelopmental assessment in Duchenne muscular dystrophy.
Pane M, Scalise R, Berardinelli A, D'Angelo G, Ricotti V, Alfieri P, Moroni I, Hartley L, Pera MC, Baranello G, Catteruccia M, Casalino T, Romeo DM, Graziano A, Gandioli C, Bianco F, Mazzone ES, Lombardo ME, Scoto M, Sivo S, Palermo C, Gualandi F, Sormani MP, Ferlini A, Bertini E, Muntoni F, Mercuri E.
Pane M, et al. Among authors: gandioli c.
Neuromuscul Disord. 2013 Jun;23(6):451-5. doi: 10.1016/j.nmd.2013.02.012. Epub 2013 Mar 25.
Neuromuscul Disord. 2013.
PMID: 23535446
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