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High levels of LIGHT/TNFSF14 in patients with Prader-Willi syndrome.
Faienza, M F; Brunetti, G; Fintini, D; Grugni, G; Wasniewska, M G; Crinò, A; D'Amato, G; Piacente, L; Oranger, A; Dicarlo, M; Colucci, S; Grano, M.
  • Faienza MF; Department of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
  • Brunetti G; Department of Biosciences, Biotechnologies and Environment, University of Bari Aldo Moro, Via Orabona, 4, 70125, Bari, Italy. giacomina.brunetti@uniba.it.
  • Fintini D; Endocrinology Unit, Pediatric University Department, Bambino Gesù Children's Hospital, Rome, Italy.
  • Grugni G; Division of Auxology, Istituto Auxologico Italiano, Research Institute, Verbania, Italy.
  • Wasniewska MG; Pediatric Unit, Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.
  • Crinò A; Reference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Rome, Italy.
  • D'Amato G; Neonatal Intensive Care Unit, Di Venere Hospital, Bari, Italy.
  • Piacente L; Department of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
  • Oranger A; Department of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
  • Dicarlo M; Department of Translational Biosciences and Neurosciences, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
  • Colucci S; Department of Translational Biosciences and Neurosciences, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
  • Grano M; Department of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
J Endocrinol Invest ; 46(9): 1901-1909, 2023 Sep.
Article en En | MEDLINE | ID: mdl-36917420
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi Tipo de estudio: Prognostic_studies Límite: Adult / Child / Humans Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi Tipo de estudio: Prognostic_studies Límite: Adult / Child / Humans Idioma: En Año: 2023 Tipo del documento: Article