Robertino Dilena

Robertino Dilena

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Robertino Dilena

Robertino Dilena

Publications by authors named "Robertino Dilena"

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Acute flaccid paralysis due to Echovirus 30 in an immunosuppressed transplant recipient.

J Neurovirol 2019 Oct 22. Epub 2019 Oct 22.

Clinical Neurophysiology Unit, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://link.springer.com/10.1007/s13365-019-00812-4
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http://dx.doi.org/10.1007/s13365-019-00812-4DOI Listing
October 2019

Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.

Parkinsonism Relat Disord 2019 06 1;63:66-72. Epub 2019 Mar 1.

Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy; Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S13538020193009
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http://dx.doi.org/10.1016/j.parkreldis.2019.02.045DOI Listing
June 2019

Pseudotumour cerebri associated with mycoplasma pneumoniae infection and treatment with levofloxacin: a case report.

BMC Pediatr 2019 01 5;19(1). Epub 2019 Jan 5.

Pediatric Highly Intensive Care Unit, Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico, and a Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.

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https://bmcpediatr.biomedcentral.com/articles/10.1186/s12887
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http://dx.doi.org/10.1186/s12887-018-1371-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320575PMC
January 2019

Familial dominant epilepsy and mild pachygyria associated with a constitutional LIS1 mutation.

Am J Med Genet A 2018 12 25;176(12):2808-2812. Epub 2018 Aug 25.

Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Neuroscience Department, A. Meyer Children's Hospital, University of Florence, Italy.

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http://doi.wiley.com/10.1002/ajmg.a.40503
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http://dx.doi.org/10.1002/ajmg.a.40503DOI Listing
December 2018

A de novo C19orf12 heterozygous mutation in a patient with MPAN.

Parkinsonism Relat Disord 2018 03 27;48:109-111. Epub 2017 Dec 27.

IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S13538020173086
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http://dx.doi.org/10.1016/j.parkreldis.2017.12.025DOI Listing
March 2018

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

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http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy.

Brain Dev 2017 Apr 19;39(4):345-348. Epub 2016 Nov 19.

NICU, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Università degli Studi di Milano, Milan, Italy.

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http://dx.doi.org/10.1016/j.braindev.2016.10.015DOI Listing
April 2017

Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation.

Brain Dev 2016 Jan 23;38(1):128-31. Epub 2015 Jul 23.

Pediatric Neurology and Muscular Diseases Unit, Laboratory of Neurogenetics, Institute "G. Gaslini", Genoa, Italy.

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http://dx.doi.org/10.1016/j.braindev.2015.07.002DOI Listing
January 2016

Locked-in-like fulminant infantile Guillain-Barré syndrome associated with herpes simplex virus 1 infection.

Muscle Nerve 2016 Jan 1;53(1):140-3. Epub 2015 Oct 1.

Pediatric Intensive Care Unit, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

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http://dx.doi.org/10.1002/mus.24908DOI Listing
January 2016

Fetal acetylcholine receptor inactivation syndrome: A myopathy due to maternal antibodies.

Neurol Neuroimmunol Neuroinflamm 2015 Feb 23;2(1):e57. Epub 2014 Dec 23.

Department of Pediatric Neurology (Y.H., S.B., D.C., M.L., H.J.), Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, United Kingdom; Department of Clinical Neurology (Y.H., L.W.J., A.V.), Oxford University, Oxford; Department of Neurology (F.N.), Department of Neonatology (A.L.), Randall Division for Cell and Molecular Biophysics (H.J.), Muscle Signaling Section, and Department of Basic and Clinical Neuroscience Division (H.J.), IoP, King's College, London, United Kingdom; Dubowitz Neuromuscular Centre (S.R.), Great Ormond Street Hospital for Children, London, United Kingdom; Unit of Clinical Neurophysiology (R.D.), Department of Neuroscience and Mental Health and Neonatal Intensive Care Unit (M.F.), IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano, Milan, Italy; and Department of Pediatrics (A.P.B.), Rigshospitalet, Copenhagen University Hospital, Denmark.

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http://dx.doi.org/10.1212/NXI.0000000000000057DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4277302PMC
February 2015

Midazolam Responsive Oculogyric Crisis, Oral Automatisms, Akinesia and Rigidity Induced by Sedation Withdrawal in a Child.

Mov Disord Clin Pract 2014 Sep 6;1(3):235-236. Epub 2014 Jun 6.

Centro Clinico per la Neurostimolazione le Neurotecnologie ed i Disordini del Movimento Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan Italy.

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http://dx.doi.org/10.1002/mdc3.12038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6183240PMC
September 2014

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis.

J Neurol 2014 Feb 13;261(2):373-81. Epub 2013 Dec 13.

Laboratory of Molecular Biology, Scientific Institute IRCCS Eugenio Medea, Via D. L. Monza 20, Bosisio Parini, 23842, Lecco, Italy.

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http://dx.doi.org/10.1007/s00415-013-7206-6DOI Listing
February 2014

Medulloblastoma presenting as dialysis disequilibrium syndrome.

Hemodial Int 2011 Oct;15 Suppl 1:S64-7

Department of Neurological Sciences, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://doi.wiley.com/10.1111/j.1542-4758.2011.00604.x
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http://dx.doi.org/10.1111/j.1542-4758.2011.00604.xDOI Listing
October 2011