- Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel missense mutation in AVP gene in a large Italian kindred
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Lara L.I. Feldkamp et al, 2020, Hormone and Metabolic Research CrossRef - Disorders of the Posterior Pituitary
Abhinash Srivatsa et al, 2021, Sperling Pediatric Endocrinology CrossRef - A Partial Phenotype of adFNDI Related to the Signal Peptide c.55G>A Variant of the AVP Gene
Vera Tocci et al, 2021, Endocrines CrossRef - Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
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Maria Inês Alvelos et al, 2021, Pituitary CrossRef - Vasopressin-Dependent Disorders: What Is New in Children?
Jane E. Driano et al, 2021, Pediatrics CrossRef - Response to Letter to the Editor: “Forty-One Individuals with Mutations in the AVP-NPII Gene Associated with Familial Neurohypophyseal Diabetes Insipidus
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Giuseppa Patti et al, 2020, Best Practice & Research Clinical Endocrinology & Metabolism CrossRef - Letter to the Editor: “Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus.”
Giuseppa Patti et al, 2020, The Journal of Clinical Endocrinology & Metabolism CrossRef - Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel nonsense mutation in AVP‑NPII gene
Hongbo Yang et al, 2019, Experimental and Therapeutic Medicine CrossRef