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1.
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.
Am J Hum Genet
; 2024 May 28.
Article
in English
| MEDLINE | ID: mdl-38815585
2.
HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication study.
Brain Behav Immun
; 79: 314-318, 2019 07.
Article
in English
| MEDLINE | ID: mdl-30763769
3.
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study.
Epilepsia
; 59(12): 2260-2271, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30451291
4.
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy.
Epilepsia
; 52(5): e40-4, 2011 May.
Article
in English
| MEDLINE | ID: mdl-21561445
5.
Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 cases.
Epilepsia
; 52(6): 1168-76, 2011 Jun.
Article
in English
| MEDLINE | ID: mdl-21320117
6.
Unexpected Neurological Symptoms of Ruxolitinib: A Case Report.
J Hematol
; 9(4): 137-139, 2020 Dec.
Article
in English
| MEDLINE | ID: mdl-33224394
7.
Preliminary evidence about irritability in patients with epilepsy treated by perampanel as first add-on therapy compared to levetiracetam and valproic acid.
CNS Neurosci Ther
; 25(5): 632-637, 2019 05.
Article
in English
| MEDLINE | ID: mdl-30675751
8.
First ultrastructural autoptic findings of SARS -Cov-2 in olfactory pathways and brainstem.
Minerva Anestesiol
; 86(6): 678-679, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32401000
9.
Ring chromosome 20.
Eur J Med Genet
; 55(5): 381-7, 2012 May.
Article
in English
| MEDLINE | ID: mdl-22406087
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