L. Caffi

Neurodevelopmental outcome at 5-7 years in preterm infants with periventricular leukomalacia.

S. Orcesi, E. Fazzi, L. Caffi, 1994, Neuropediatrics.

Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene

G. Scarano, L. Caffi, A. Selicorni, 2015, Clinical genetics.

Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients.

F. Benfenati, P. Striano, F. Zara, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study

E. Bertini, P. Striano, R. Guerrini, 2018, Epilepsia.

Focal seizures with affective symptoms are a major feature of PCDH19 gene–related epilepsy

R. Guerrini, D. Mei, L. Parmeggiani, 2012, Epilepsia.

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

P. Striano, F. Zara, C. Minetti, 2013, Epilepsia.

Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy

L. Caffi, L. Pezzani, M. Iascone, 2018, American journal of medical genetics. Part A.

Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy

S. Maestrini, L. Morandi, F. Blàsevich, 2013, BMC Medical Genetics.

A novel mutation in COL4A1 gene: A possible cause of early postnatal cerebrovascular events

A. Pichiecchio, S. Orcesi, R. Giorda, 2015, American journal of medical genetics. Part A.

Novel PTRF-CAVIN mutation in a child with mild myopathy and very mild congenital lipodystrophy

L. Morandi, F. Blàsevich, M. Mora, 2012 .

The Conundrum of Cognitive Dysfunction in Children With Portal Hypertension: The Experience of Bergamo, Italy.

L. D’Antiga, P. Amodio, V. Casotti, 2021, Journal of Clinical and Experimental Hepatology.