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Peer-reviewedCC BYJournal of clinical medicine

Case Series: ADHD Phenotype in a Family with NPY Gene Microduplication

  • Paolo Alfieri1
  • Elisa Rolleri1
  • Cristina Caciolo1
  • Antonio Novelli2
  • Giusy Viscogliosi2
  • Silvia Genovese2
  • Francesca Cumbo3
  • Marco Cappa4
  • Deny Menghini1
  • Maria Cristina Digilio5
  • Floriana Costanzo1
  • Stefano Vicari1
5 affiliations
  1. 1Child and Adolescent Neuropsychiatry Unit, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy (F.C.); (S.V.)
  2. 2Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy
  3. 3Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy
  4. 4Research Unit for Innovative Therapies in Endocrinopathies, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy;
  5. 5Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy
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Cite

BibTeXRIS
BibTeX
@article{alfieri2026case,
  title = {{Case Series: ADHD Phenotype in a Family with NPY Gene Microduplication}},
  author = {Paolo Alfieri and Elisa Rolleri and Cristina Caciolo and Antonio Novelli and Giusy Viscogliosi and Silvia Genovese and Francesca Cumbo and Marco Cappa and Deny Menghini and Maria Cristina Digilio and Floriana Costanzo and Stefano Vicari},
  journal = {Journal of clinical medicine},
  year = {2026},
  month = sep,
  url = {https://europepmc.org/article/PMC/PMC13665950},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Case Series: ADHD Phenotype in a Family with NPY Gene Microduplication
AU  - Paolo Alfieri
AU  - Elisa Rolleri
AU  - Cristina Caciolo
AU  - Antonio Novelli
AU  - Giusy Viscogliosi
AU  - Silvia Genovese
AU  - Francesca Cumbo
AU  - Marco Cappa
AU  - Deny Menghini
AU  - Maria Cristina Digilio
AU  - Floriana Costanzo
AU  - Stefano Vicari
PY  - 2026
DA  - 2026/09/29
JO  - Journal of clinical medicine
UR  - https://europepmc.org/article/PMC/PMC13665950
SN  - 2077-0383
ER  -