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1.
Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy.
Am J Med Genet A
; 176(12): 2867-2871, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30462361
2.
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
3.
A novel mutation in COL4A1 gene: a possible cause of early postnatal cerebrovascular events.
Am J Med Genet A
; 167A(4): 810-5, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25706114
4.
Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy.
BMC Med Genet
; 14: 89, 2013 Sep 11.
Article
in English
| MEDLINE | ID: mdl-24024685
5.
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Epilepsia
; 54(3): 425-36, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23360469
6.
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.
Epilepsia
; 53(12): 2111-9, 2012 Dec.
Article
in English
| MEDLINE | ID: mdl-22946748
7.
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients.
Eur J Paediatr Neurol
; 28: 193-197, 2020 Sep.
Article
in English
| MEDLINE | ID: mdl-32651081
8.
The Conundrum of Cognitive Dysfunction in Children With Portal Hypertension: The Experience of Bergamo, Italy.
J Clin Exp Hepatol
; 12(2): 723-724, 2022.
Article
in English
| MEDLINE | ID: mdl-35535078
9.
A questionnaire on sleep behaviour in the first years of life: preliminary results from a normative sample.
Funct Neurol
; 21(3): 151-8, 2006.
Article
in English
| MEDLINE | ID: mdl-17049134
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