M. Mastrangelo

P. Striano, F. Zara, D. Cassandrini, 2011, 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.

Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR)

R. Guerrini, D. Mei, E. Antelmi, 2012, Epileptic disorders : international epilepsy journal with videotape.

Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome

D. Montanaro, R. Borgatti, F. Zara, 2020, Neurology.

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

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

Ictal EEG patterns in epilepsy with centro-temporal spikes

P. Striano, A. Vignoli, P. Veggiotti, 2011, Brain and Development.

Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates

G. Cantalupo, L. Tadini, M. Fumagalli, 2021, Clinical Neurophysiology.

Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndrome.

R. Happle, P. Marchettini, M. Mastrangelo, 1998, Archives of dermatology.

Encephalocraniocutaneous lipomatosis: complete neuroradiologic evaluation and follow-up of two cases.

G. Scotti, C. Parazzini, F. Triulzi, 1999, AJNR. American journal of neuroradiology.

Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study

G. Cantalupo, C. Barba, A. Vignoli, 2016, Epilepsia.

The Milan Project: A newborn hearing screening programme

M. Parazzini, P. Ravazzani, F. Grandori, 2005, Acta paediatrica.

Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathy

O. Zuffardi, F. Novara, M. Mastrangelo, 2013, Epileptic disorders : international epilepsy journal with videotape.

Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series

P. Striano, R. Brugada, C. Tassinari, 2015, International Journal of Legal Medicine.

Abnormal Neonatal Patterns

F. Pisani, M. Mastrangelo, B. Scelsa, 2019, Clinical Electroencephalography.

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

H. Mefford, E. Bacchelli, P. Striano, 2019, Annals of clinical and translational neurology.

Natural history and long‐term outcome of cardiac rhabdomyomas detected prenatally

F. Mosca, M. Mastrangelo, L. Villa, 2004, Prenatal diagnosis.

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

Ethan M. Goldberg, S. Scherer, J. Howe, 2021, medRxiv.

Cumulative Contents to Volume 38

V. S. Gupta, Japan., F. Pidcock, 2016, Brain and Development.

Epilepsy in ring chromosome 20 syndrome

C. Barba, I. Naldi, A. Vignoli, 2016, Epilepsy Research.

Familial trigeminal neuralgia in charcot-marie-tooth disease

P. Crenna, M. Mastrangelo, D. Testa, 2004, Journal of Neurology.

Epileptic seizures, epilepsy and epileptic syndromes in newborns: A nosological approach to 94 new cases by the 2001 proposed diagnostic scheme for people with epileptic seizures and with epilepsy

F. Mosca, M. Mastrangelo, A. Marini, 2005, Seizure.

Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.

M. Fichera, C. Romano, J. Clayton-Smith, 2009, American journal of human genetics.

N8-acetylspermidine as a potential plasma biomarker for Snyder-Robinson syndrome identified by clinical metabolomics

Heinrich Sticht, Barbara Plecko, Bernhard Schmitt, 2016, Journal of Inherited Metabolic Disease.

Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study

P. Striano, A. Vignoli, P. Parisi, 2013, Epilepsia.

Infantile Spasms Secondary to the Surgical Excision of a Brain Tumor

A. Romeo, M. Mastrangelo, F. Viani, 1994, Journal of child neurology.

Early myoclonic encephalopathy and nonketotic hyperglycinemia.

M. Mastrangelo, G. Lista, I. Daniele, 2009, Pediatric neurology.

Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study

P. Striano, R. Møller, E. Gardella, 2021, Seizure.

Premature birth: complexities and difficulties in building the mother–child relationship

A. Bonanomi, S. Bova, M. Mastrangelo, 2017, Journal of reproductive and infant psychology.

Pediatric epilepsy following neonatal seizures symptomatic of stroke

A. Suppiej, B. Bernardina, G. Casara, 2016, Brain and Development.

Epilepsy Course and Developmental Trajectories in STXBP1-DEE

P. Striano, A. Coppola, G. Cantalupo, 2022, Neurology: Genetics.

KETASER01 protocol: What went right and what went wrong

D. Catelan, A. Biggeri, P. Biban, 2022, Epilepsia open.

Mild ventriculomegaly from fetal consultation to neurodevelopmental assessment: A single center experience and review of the literature.

A. Righini, G. Zuccotti, P. Veggiotti, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Snyder–Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype

A. Selicorni, S. Bova, Joy W. Norris, 2013, American journal of medical genetics. Part A.

Development of layer I of the human cerebral cortex after midgestation: Architectonic findings, immunocytochemical identification of neurons and glia, and in situ labeling of apoptotic cells

C. Frassoni, R. Spreafico, M. Bentivoglio, 1999, The Journal of comparative neurology.

P. Avanzini, G. Cantalupo, F. Benuzzi, 2014, Epilepsia.

Early-onset Hereditary Neuropathy with Liability to Pressure Palsy

M. Mastrangelo, P. Iannetti, G. Fabrizi, 2007, Neuropediatrics.

Spatio-temporal features of rhythmic cortical activity in epilepsy due to chromosome ring 20

P. Avanzini, F. Benuzzi, P. Nichelli, 2013 .

Definition of the neurological phenotype associated with dup (X)(p11.22–p11.23)

S. Buono, C. Romano, S. Reitano, 2011, Epileptic disorders : international epilepsy journal with videotape.

Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20

P. Avanzini, F. Benuzzi, P. Nichelli, 2014, Clinical Neurophysiology.

Fatal Status Epilepticus in Dravet Syndrome

R. Nabbout, D. Craiu, F. Vigevano, 2020, Brain sciences.

Reply to Dravet, C. Different Outcomes of Acute Encephalopathy after Status Epilepticus in Patients with Dravet Syndrome. How to Avoid Them? Comment on “De Liso et al. Fatal Status Epilepticus in Dravet Syndrome. Brain Sci. 2020, 10, 889”

R. Nabbout, D. Craiu, F. Vigevano, 2021, Brain sciences.

Acute neonatal encephalopathy and seizures recurrence: A combined aEEG/EEG study

Vincenzo Belcastro, Gianluca Lista, V. Belcastro, 2013, Seizure.

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

H. Mefford, E. Bacchelli, P. Striano, 2019, Annals of clinical and translational neurology.

PRRT2 Mutations are the major cause of benign familial infantile seizures

P. Striano, U. Stephani, P. Bauer, 2012, Human mutation.

Sleep in ring chromosome 20 syndrome: a peculiar electroencephalographic pattern.

A. Vignoli, L. Nobili, G. Didato, 2013, Functional neurology.