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The hyperkinetic movement disorder of FOXG1‐related epileptic–dyskinetic encephalopathy

Developmental medicine and child neurology, 2016-01, Vol.58 (1), p.93-97

2016

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Dravet syndrome and SCN1A gene mutation related‐epilepsies: cognitive impairment and its determinants

Developmental medicine and child neurology, 2011-04, Vol.53 (s2), p.11-15

2011

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Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI)

BMC pediatrics, 2012-09, Vol.12 (1), p.144-144, Article 144

2012

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Incidence of epilepsy in extremely low‐birthweight infants (<1,000 g): A population study of central and southern Sardinia

Epilepsia (Copenhagen), 2009-01, Vol.50 (s1), p.37-40

2009

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Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy

Developmental medicine and child neurology, 2016-10, Vol.58 (10), p.1085-1091

2016

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Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI): a feasibility study

The journal of maternal-fetal & neonatal medicine, 2018-04, Vol.31 (8), p.973-980

2018

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The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWS

Neurology, 2016-03, Vol.86 (13), p.1250

2016

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The hyperkinetic movement disorder of FOXG 1 ‐related epileptic–dyskinetic encephalopathy

Developmental medicine and child neurology, 2016-01, Vol.58 (1), p.93-97

2016

Volltextzugriff (PDF)

Rapid assay of rufinamide in dried blood spots by a new liquid chromatography–tandem mass spectrometric method

Journal of pharmaceutical and biomedical analysis, 2011-01, Vol.54 (1), p.192-197

2011

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Atypical face shape and genomic structural variants in epilepsy

Brain (London, England : 1878), 2012-10, Vol.135 (Pt 10), p.3101-3114

2012

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Hypothermia for neonatal hypoxic-ischemic encephalopathy: may an early amplitude-integrated EEG improve the selection of candidates for cooling?

The journal of maternal-fetal & neonatal medicine, 2012-11, Vol.25 (11), p.2171-2176

2012

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Megalencephaly, Polymicrogyria, and Hydrocephalus (MPPH) Syndrome: A New Case With Syndactyly

Journal of child neurology, 2008-08, Vol.23 (8), p.916-918

2008

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Contractions in the second polyA tract of ARX are rare, non‐pathogenic polymorphisms

American journal of medical genetics. Part A, 2011-01, Vol.155 (1), p.164-167

2011

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Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH

American journal of medical genetics. Part A, 2010-01, Vol.152A (1), p.234-236

2010

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Incidence of epilepsy in extremely low-birthweight infants (< 1,000 g) : A population study of central and southern Sardinia: Italian League Against Epilepsy (LICE). Official Reports 2007-2008 and Proceedings of the 29th and 30th National Congresses, Pisa, June, 2006 and Reggio-Calabra, May, 2007

Epilepsia (Copenhagen), 2009, Vol.50, p.37-40

2009

Volltextzugriff (PDF)

Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphisms

American Journal of Medical Genetics Part A, 2011, Vol.155A (1), p.164-167

2011

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NRF2 and PPAR-γ Pathways in Oligodendrocyte Progenitors: Focus on ROS Protection, Mitochondrial Biogenesis and Promotion of Cell Differentiation

International journal of molecular sciences, 2020-09, Vol.21 (19), p.7216

2020

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NRF2 and PPAR-y Pathways in Oligodendrocyte Progenitors: Focus on ROS Protection, Mitochondrial Biogenesis and Promotion of Cell Differentiation

International journal of molecular sciences, 2020-10, Vol.21 (19), p.1

2020

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The hyperkinetic movement disorder of FOXG1‐related epileptic–dyskinetic encephalopathy

Dravet syndrome and SCN1A gene mutation related‐epilepsies: cognitive impairment and its determinants

Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI)

Incidence of epilepsy in extremely low‐birthweight infants (<1,000 g): A population study of central and southern Sardinia

Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy

Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI): a feasibility study

The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWS

The hyperkinetic movement disorder of FOXG 1 ‐related epileptic–dyskinetic encephalopathy

Rapid assay of rufinamide in dried blood spots by a new liquid chromatography–tandem mass spectrometric method

Atypical face shape and genomic structural variants in epilepsy

Hypothermia for neonatal hypoxic-ischemic encephalopathy: may an early amplitude-integrated EEG improve the selection of candidates for cooling?

Megalencephaly, Polymicrogyria, and Hydrocephalus (MPPH) Syndrome: A New Case With Syndactyly

Contractions in the second polyA tract of ARX are rare, non‐pathogenic polymorphisms

Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH

Incidence of epilepsy in extremely low-birthweight infants (< 1,000 g) : A population study of central and southern Sardinia: Italian League Against Epilepsy (LICE). Official Reports 2007-2008 and Proceedings of the 29th and 30th National Congresses, Pisa, June, 2006 and Reggio-Calabra, May, 2007

Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphisms

NRF2 and PPAR-γ Pathways in Oligodendrocyte Progenitors: Focus on ROS Protection, Mitochondrial Biogenesis and Promotion of Cell Differentiation

NRF2 and PPAR-y Pathways in Oligodendrocyte Progenitors: Focus on ROS Protection, Mitochondrial Biogenesis and Promotion of Cell Differentiation

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