Hasil Pencarian - Enrico Parano

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  1. 1
    A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report

    A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report oleh Piero Pavone, Raffaele Falsaperla, Martino Ruggieri, Simona Domenica Marino, Enrico Parano, Xena Giada Pappalardo

    Diterbitkan 2023-09-01
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  2. 2
    Early Life Stress (ELS) Effects on Fetal and Adult Bone Development

    Early Life Stress (ELS) Effects on Fetal and Adult Bone Development oleh Xena Giada Pappalardo, Gianluca Testa, Rosalia Pellitteri, Paola Dell’Albani, Margherita Rodolico, Vito Pavone, Enrico Parano

    Diterbitkan 2023-01-01
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  3. 3
    Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review

    Diagnostic Tools in the Detection of Physical Child Abuse: A Systematic Review oleh Vito Pavone, Andrea Vescio, Ludovico Lucenti, Mirko Amico, Alessia Caldaci, Xena Giada Pappalardo, Enrico Parano, Gianluca Testa

    Diterbitkan 2022-08-01
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  4. 4
    Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype–Phenotype Correlation

    Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype–Phenotype Correlation oleh Piero Pavone, Xena Giada Pappalardo, Claudia Parano, Enrico Parano, Antonio Corsello, Martino Ruggieri, Giovanni Cacciaguerra, Raffaele Falsaperla

    Diterbitkan 2023-12-01
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  5. 5
    Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases

    Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases oleh Piero Pavone, Giovanni Corsello, Umberto Raucci, Riccardo Lubrano, Enrico Parano, Martino Ruggieri, Filippo Greco, Silvia Marino, Raffaele Falsaperla

    Diterbitkan 2022-12-01
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  6. 6
    Klippel–Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review

    Klippel–Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review oleh Piero Pavone, Lidia Marino, Giovanni Cacciaguerra, Alessandra Di Nora, Enrico Parano, Giuseppe Musumeci, Martino Ruggieri, Agata Polizzi, Raffaele Falsaperla

    Diterbitkan 2023-08-01
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  7. 7
    Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions

    Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions oleh Piero Pavone, Xena Giada Pappalardo, Xena Giada Pappalardo, Enrico Parano, Raffaele Falsaperla, Simona Domenica Marino, John Kane Fink, Martino Ruggieri

    Diterbitkan 2022-04-01
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  8. 8
    A novel GABRB3 variant in Dravet syndrome: Case report and literature review

    A novel GABRB3 variant in Dravet syndrome: Case report and literature review oleh Piero Pavone, Xena Giada Pappalardo, Simona D. Marino, Laura Sciuto, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Maria Piccione, Raffaele Falsaperla

    Diterbitkan 2020-11-01
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  9. 9
    Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures

    Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures oleh Raffaele Falsaperla, Xena Giada Pappalardo, Xena Giada Pappalardo, Catia Romano, Simona Domenica Marino, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Piero Pavone

    Diterbitkan 2020-09-01
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  10. 10
    Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review

    Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review oleh Piero Pavone, Piero Pavone, Pasquale Striano, Pasquale Striano, Giovanni Cacciaguerra, Simona Domenica Marino, Enrico Parano, Xena Giada Pappalardo, Raffaele Falsaperla, Martino Ruggieri

    Diterbitkan 2023-09-01
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  11. 11
    Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four‐member family and an unrelated boy

    Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four‐member family and an unrelated boy oleh Piero Pavone, Martino Ruggieri, Simona D. Marino, Giovanni Corsello, Xena Pappalardo, Agata Polizzi, Enrico Parano, Catia Romano, Silvia Marino, Andrea Domenico Praticò, Raffaele Falsaperla

    Diterbitkan 2020-04-01
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  12. 12
    Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability

    Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability oleh 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

    Diterbitkan 2022-02-01
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