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Mostrati risultati da 1 a 6 di 6
Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies
file da validare1998-01-01 Polizzi, A; Clover, L; Incorpora, G; Lang, B; Vincent, A
Callosal agenesis and interhemispheric cyst: expandign the phenotype
2005-01-01 Pavone, P; Barone, R; Baieli, S; Manfrè, L; Incorpora, Concetta Gemma; Ruggieri, M
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins
2012-01-01 Incorpora, G; Pavone, P; Cocuzza, M; Praticò, Ad; Polizzi, A; Privitera, M; Pavone, L; Ruggieri, Martino
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome
2012-01-01 Pavone, P.; Praticò, A. D.; Bianca, Innocenzo; Raffaele, R.; Vecchio, I.; Salafia, S.; Praticò, E. R.; Incorpora, G.
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2
2020-01-01 Pavone, P.; Pappalardo, X. G.; Incorpora, G.; Falsaperla, R.; Marino, S. D.; Corsello, G.; Parano, E.; Ruggieri, M.
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability
2022-01-01 Pavone, Piero; Pappalardo, XENA GIADA; Mustafa, Naira; Yoon Cho, Sung; Kyu Jin, Dong; Incorpora, Gemma; Falsaperla, Raffaele; Marino, SIMONA DOMENICA; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies | 1-gen-1998 | Polizzi, A; Clover, L; Incorpora, G; Lang, B; Vincent, A | file da validare |
| Callosal agenesis and interhemispheric cyst: expandign the phenotype | 1-gen-2005 | Pavone, P; Barone, R; Baieli, S; Manfrè, L; Incorpora, Concetta Gemma; Ruggieri, M | |
| An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins | 1-gen-2012 | Incorpora, G; Pavone, P; Cocuzza, M; Praticò, Ad; Polizzi, A; Privitera, M; Pavone, L; Ruggieri, Martino | |
| Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome | 1-gen-2012 | Pavone, P.; Praticò, A. D.; Bianca, Innocenzo; Raffaele, R.; Vecchio, I.; Salafia, S.; Praticò, E. R.; Incorpora, G. | |
| Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 | 1-gen-2020 | Pavone, P.; Pappalardo, X. G.; Incorpora, G.; Falsaperla, R.; Marino, S. D.; Corsello, G.; Parano, E.; Ruggieri, M. | |
| Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability | 1-gen-2022 | Pavone, Piero; Pappalardo, XENA GIADA; Mustafa, Naira; Yoon Cho, Sung; Kyu Jin, Dong; Incorpora, Gemma; Falsaperla, Raffaele; Marino, SIMONA DOMENICA; Corsello, Giovanni; Parano, Enrico; Ruggieri, Martino |
Mostrati risultati da 1 a 6 di 6
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