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Magazine 2.21

Social cognition deficit and genetic vulnerability to schizophrenia in 22q11 deletion syndrome.

Authors: Frascarelli M, Padovani G, Buzzanca A, Accinni T, Carlone L, Ghezzi F, Lattanzi GM, Fanella M, Putotto C, Di Bonaventura C, Girardi N, Pasquini M, Biondi M, Di F.

Date: 2020

Scope of interest: Psychiatric disorders/rare diseases




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Magazine 9.54

High rates of early remission pattern in adult-onset compared with earlier-onset idiopathic generalized epilepsy: A long-term follow-up study.

Authors: Cerulli Irelli E, Orlando B, Salamone EM, Fisco G, Barone FA, Morano A, Fanella M, Fattouch J, Manfredi M, Giallonardo AT, Di Bonaventura C.

Date: 2022

Scope of interest: Epilepsy


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Magazine 15.26

ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.

Authors: Montecchiani C, Pedace L, Lo Giudice T, Casella A, Mearini M, Gaudiello F, Pedroso JL, Terracciano C, Caltagirone C, et al

Date: 2016

Scope of interest: Neurogenetics


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Magazine 7,802

Severe hypoglycemia is associated with antidiabetic oral treatment compared with insulin analogs in nursing home patients with type 2 diabetes and dementia: results from the HOME study.

Authors: Abbatecola AM, Bo M, Barbagallo M, Incalzi RA, Pilotto A, Bellelli G, Maggi S, Paolisso G; Italian Society of Gerontology and Geriatrics (SIGG), Florence, Italy

Date: 2015

Scope of interest: long term care


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