R. Pajno

First Occurrence of Plasmablastic Lymphoma in Adenosine Deaminase-Deficient Severe Combined Immunodeficiency Disease Patient and Review of the Literature

C. Doglioni, M. Roncarolo, A. Aiuti, 2018, Front. Immunol..

In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells

C. Cancrini, L. Biasco, M. Roncarolo, 2015, Science Translational Medicine.

Guided Growth in Leg Length Discrepancy in Beckwith-Wiedemann Syndrome: A Consecutive Case Series

G. Barera, S. Russo, R. Pajno, 2021, Children.

Anthropometric characteristics of newborns with Prader–Willi syndrome

A. Salvatoni, A. Crinò, S. Salvatore, 2019, American journal of medical genetics. Part A.

Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study

L. Biasco, S. Galimberti, M. Valsecchi, 2019, The Lancet. Haematology.

Urogenital Abnormalities in Adenosine Deaminase Deficiency

A. Salonia, C. Cancrini, A. Aiuti, 2020, Journal of Clinical Immunology.

Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency.

J. Puck, I. Tezcan, M. Roncarolo, 2016, Blood.

Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment.

A. Salvatoni, A. Franzese, F. Macchi, 2019, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Multicentric Italian case–control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome

M. Cappa, A. Crinò, G. Grugni, 2023, Journal of Endocrinological Investigation.

[Acute liver failure due to human herpesvirus 6 in an infant].

L. Cococcioni, P. Corsin, M. Fomasi, 2012, La Pediatria medica e chirurgica : Medical and surgical pediatrics.

La sindrome di Prader Willi: dal neonato all’adulto

R. Pajno, 2021, L'Endocrinologo.

Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency.

C. Cancrini, P. Rancoita, C. Di Serio, 2024, Nature medicine.

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation

A. Salvatoni, A. Crinò, G. Grugni, 2024, Frontiers in endocrinology.