PRATICO', ANDREA DOMENICO
PRATICO', ANDREA DOMENICO
CHIRURGIA GENERALE E SPECIALITA' MEDICO-CHIRURGICHE
A child with congenital heart disease and situs viscerum inversus
file da validare2008-01-01 Pavone, P; Praticò, Ad; DI GIORGIO, A; Incorpora, G; Ruggieri, Martino
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia?
2020-01-01 Sullo, F.; Palmucci, S.; Polizzi, A.; Ruggieri, M.; Pratico, A. D.
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment
2017-01-01 Pavone, Piero; Praticò, Andrea Domenico; Rizzo, Renata; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Falsaperla, Raffaele
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review
2016-01-01 Pavone, P; Praticò, Ad; Falsaperla, R; Ruggieri, Martino; Neri, G; Pavone, Vito; Zollino, M.
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature
file da validare2016-01-01 Pavone, Piero; Praticò, Andrea D.; Campisi, Corrado; Falsaperla, Raffaele
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas
2017-01-01 Caltabiano, Rosario; Magro, Gaetano; Polizzi, Agata; Praticó, Andrea Domenico; Ortensi, Andrea; D’Orazi, Valerio; Panunzi, Andrea; Milone, Pietro; Maiolino, Luigi; Nicita, Francesco; Capone, Gabriele Lorenzo; Sestini, Roberta; Paganini, Irene; Muglia, Mariella; Cavallaro, Sebastiano; Lanzafame, Salvatore; Papi, Laura; Ruggieri, Martino
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features
2016-01-01 Pavone, P; Praticò, Ad; Gentile, G; Falsaperla, R; Iemmolo, R; Guarnaccia, M; Cavallaro, S; Ruggieri, Martino
A New Patient with Potocki-Lupski Syndrome: A Literature Review
file da validare2018-01-01 Praticò, Andrea Domenico; Falsaperla, Raffaele; Rizzo, Renata; Ruggieri, Martino; Verrotti, Alberto; Pavone, Piero
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion
2018-01-01 Pratico, Andrea Domenico; Ruggieri, Martino; Falsaperla, Raffaele; Pavone, Piero
A Retrospective Study on Standard Regimen for Vaccination in Celiac Children
file da validare2011-01-01 Leonardi, Salvatore; Vitaliti, Giovanna; Pratico’, Andrea; Pecoraro, Rossella; Rosa, Mario La
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report
file da validare2012-01-01 Vitaliti, G.; Garozzo, Mt; Tomarchio, S.; Pecoraro, S.; Praticò, Ad; Leonardi, Salvatore; La Rosa, M.
Acquired peripheral neuropathy: a report on 20 children.
2012-01-01 Pavone, P; Praticò, Ad; Ruggieri, Martino; Verrotti, A; Castellano Chiodo, D; Greco, F; Falsaperla, R; Pavone, L.
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy
file da validare2010-01-01 Distefano, Giuseppe; Praticò, Andrea D
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations
file da validare2020-01-01 Portale, A.; Mazzurco, M.; Portale, L.; Pavone, P.; Bertini, E.; Polizzi, A.; Pratico, A. D.; Ruggieri, M.
Allergia agli insetti
file da validare2013-01-01 Praticò, Andrea D.; Papale, Maria; Castro, Agnese; Lanzafame, ANGELA MARIA; LA ROSA, Mario
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
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis
2021-01-01 Fontana, A.; Greco, F.; Smilari, P.; Pratico, A. D.; Fiumara, A.; Ruggieri, M.; Pavone, P.
Anti-mog associated encephalitis: when steroid therapy is not enough
2022-01-01 Arrabito, M.; Pratico, A. D.; Smilari, P.; Greco, F.; Oliva, C. F.; Ruggieri, M.; Pavone, P.; Fiumara, A.
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders
file da validare2018-01-01 Ruggieri, Martino; Praticò, Andrea D.; Lacarrubba, Francesco; Micali, Giuseppe; Schepis, Carmelo; Polizzi, Agata
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations
file da validare2021-01-01 Scalia, B.; Venti, V.; Ciccia, L. M.; Criscione, R.; Bianco, M. L.; Sciuto, L.; Falsaperla, R.; Zanghi, A.; Pratico, A. D.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A child with congenital heart disease and situs viscerum inversus | 1-gen-2008 | Pavone, P; Praticò, Ad; DI GIORGIO, A; Incorpora, G; Ruggieri, Martino | file da validare |
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? | 1-gen-2020 | Sullo, F.; Palmucci, S.; Polizzi, A.; Ruggieri, M.; Pratico, A. D. | |
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment | 1-gen-2017 | Pavone, Piero; Praticò, Andrea Domenico; Rizzo, Renata; Corsello, Giovanni; Ruggieri, Martino; Parano, Enrico; Falsaperla, Raffaele | |
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review | 1-gen-2016 | Pavone, P; Praticò, Ad; Falsaperla, R; Ruggieri, Martino; Neri, G; Pavone, Vito; Zollino, M. | |
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature | 1-gen-2016 | Pavone, Piero; Praticò, Andrea D.; Campisi, Corrado; Falsaperla, Raffaele | file da validare |
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas | 1-gen-2017 | Caltabiano, Rosario; Magro, Gaetano; Polizzi, Agata; Praticó, Andrea Domenico; Ortensi, Andrea; D’Orazi, Valerio; Panunzi, Andrea; Milone, Pietro; Maiolino, Luigi; Nicita, Francesco; Capone, Gabriele Lorenzo; Sestini, Roberta; Paganini, Irene; Muglia, Mariella; Cavallaro, Sebastiano; Lanzafame, Salvatore; Papi, Laura; Ruggieri, Martino | |
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features | 1-gen-2016 | Pavone, P; Praticò, Ad; Gentile, G; Falsaperla, R; Iemmolo, R; Guarnaccia, M; Cavallaro, S; Ruggieri, Martino | |
A New Patient with Potocki-Lupski Syndrome: A Literature Review | 1-gen-2018 | Praticò, Andrea Domenico; Falsaperla, Raffaele; Rizzo, Renata; Ruggieri, Martino; Verrotti, Alberto; Pavone, Piero | file da validare |
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion | 1-gen-2018 | Pratico, Andrea Domenico; Ruggieri, Martino; Falsaperla, Raffaele; Pavone, Piero | |
A Retrospective Study on Standard Regimen for Vaccination in Celiac Children | 1-gen-2011 | Leonardi, Salvatore; Vitaliti, Giovanna; Pratico’, Andrea; Pecoraro, Rossella; Rosa, Mario La | file da validare |
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report | 1-gen-2012 | Vitaliti, G.; Garozzo, Mt; Tomarchio, S.; Pecoraro, S.; Praticò, Ad; Leonardi, Salvatore; La Rosa, M. | file da validare |
Acquired peripheral neuropathy: a report on 20 children. | 1-gen-2012 | Pavone, P; Praticò, Ad; Ruggieri, Martino; Verrotti, A; Castellano Chiodo, D; Greco, F; Falsaperla, R; Pavone, L. | |
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy | 1-gen-2010 | Distefano, Giuseppe; Praticò, Andrea D | file da validare |
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations | 1-gen-2020 | Portale, A.; Mazzurco, M.; Portale, L.; Pavone, P.; Bertini, E.; Polizzi, A.; Pratico, A. D.; Ruggieri, M. | file da validare |
Allergia agli insetti | 1-gen-2013 | Praticò, Andrea D.; Papale, Maria; Castro, Agnese; Lanzafame, ANGELA MARIA; LA ROSA, Mario | file da validare |
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 | |
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis | 1-gen-2021 | Fontana, A.; Greco, F.; Smilari, P.; Pratico, A. D.; Fiumara, A.; Ruggieri, M.; Pavone, P. | |
Anti-mog associated encephalitis: when steroid therapy is not enough | 1-gen-2022 | Arrabito, M.; Pratico, A. D.; Smilari, P.; Greco, F.; Oliva, C. F.; Ruggieri, M.; Pavone, P.; Fiumara, A. | |
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders | 1-gen-2018 | Ruggieri, Martino; Praticò, Andrea D.; Lacarrubba, Francesco; Micali, Giuseppe; Schepis, Carmelo; Polizzi, Agata | file da validare |
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations | 1-gen-2021 | Scalia, B.; Venti, V.; Ciccia, L. M.; Criscione, R.; Bianco, M. L.; Sciuto, L.; Falsaperla, R.; Zanghi, A.; Pratico, A. D. | file da validare |