Showing 1 - 7 results of 7 for search 'Xena Giada Pappalardo', query time: 0.04s
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Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures by Raffaele Falsaperla, Xena Giada Pappalardo, Xena Giada Pappalardo, Catia Romano, Simona Domenica Marino, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Piero Pavone
Published 2020Connect to this object online.
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PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? by Piero Pavone, Giovanni. Corsello, Sung Yoon Cho, Xena Giada Pappalardo, Martino Ruggieri, Simona Domenica Marino, Dong Kyu Jin, Silvia Marino, Raffaele Falsaperla
Published 2019Connect to this object online.
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Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review by Piero Pavone, Piero Pavone, Pasquale Striano, Pasquale Striano, Giovanni Cacciaguerra, Simona Domenica Marino, Enrico Parano, Xena Giada Pappalardo, Raffaele Falsaperla, Martino Ruggieri
Published 2023Connect to this object online.
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Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability by Piero Pavone, Xena Giada Pappalardo, Naira Mustafa, Sung Yoon Cho, Dong Kyu Jin, Gemma Incorpora, Raffaele Falsaperla, Simona Domenica Marino, Giovanni Corsello, Enrico Parano, Martino Ruggieri
Published 2022Connect to this object online.
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