Vilma Mantovani
Overview
Explore the profile of Vilma Mantovani including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
54
Citations
831
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ollila H, Sharon E, Lin L, Sinnott-Armstrong N, Ambati A, Yogeshwar S, et al.
Nat Commun
. 2023 May;
14(1):2709.
PMID: 37188663
Narcolepsy type 1 (NT1) is caused by a loss of hypocretin/orexin transmission. Risk factors include pandemic 2009 H1N1 influenza A infection and immunization with Pandemrix®. Here, we dissect disease mechanisms...
2.
Maltoni G, Franceschi R, Di Natale V, Al-Qaisi R, Greco V, Bertorelli R, et al.
J Pers Med
. 2022 Oct;
12(10).
PMID: 36294752
Background: Classic criteria for a maturity-onset diabetes of the young (MODY) diagnosis are often unable to identify all subjects, and traditional Sanger sequencing, using a candidate gene approach, leads to...
3.
Brodosi L, Baracco B, Mantovani V, Pironi L
BMC Endocr Disord
. 2021 Oct;
21(1):202.
PMID: 34654408
Background: Maturity Onset Diabetes of the Young (MODY) is a monogenic, autosomal, dominant disease that results in beta-cells dysfunction with consequent hyperglycaemia. It represents a rare form of diabetes (1-2%...
4.
Mantovani V, Bin S, Graziano C, Capelli I, Minardi R, Aiello V, et al.
Front Genet
. 2020 May;
11:464.
PMID: 32457805
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common inherited disorders in humans and the majority of patients carry a variant in either or . Genetic testing...
5.
Calabro M, Porcelli S, Crisafulli C, Albani D, Kasper S, Zohar J, et al.
Neurosci Lett
. 2020 Jan;
720:134754.
PMID: 31945448
Background: Recent evidence suggests that psychiatric symptoms share a common genetic liability across diagnostic categories. The present study investigated the effects of variants within previously identified relevant genes on specific...
6.
Mosheva M, Serretti A, Stukalin Y, Fabbri C, Hagin M, Horev S, et al.
J Affect Disord
. 2019 Oct;
261:181-186.
PMID: 31634677
Introduction: Bipolar disorder (BD) is a highly heritable and disabling mental illness, commonly associated with substance abuse, being alcohol abuse the most frequent. Comorbid BD and substance abuse disorders are...
7.
Cimatti A, Martini S, Munarini A, Zioutas M, Vitali F, Aceti A, et al.
Front Pediatr
. 2019 Jan;
6:407.
PMID: 30622936
Docosahexaenoic acid (DHA) is a major constituent of neuronal and retinal membranes and plays a crucial role in brain and visual development within the first months of life. Dietary intakes...
8.
Martini S, Aceti A, Furini M, Munarini A, La Riccia C, Mantovani V, et al.
JPEN J Parenter Enteral Nutr
. 2018 Sep;
43(4):550-556.
PMID: 30260487
Background: Arachidonic acid (AA) and docosahexaenoic acid (DHA) are crucial for neural and visual development after premature birth. Preterm infants usually require tube feeding (TF) until the achievement of adequate...
9.
Delvecchio M, Salzano G, Bonura C, Cauvin V, Cherubini V, DAnnunzio G, et al.
Acta Diabetol
. 2018 Jun;
55(9):981-983.
PMID: 29948406
No abstract available.
10.
Vitale G, Gitto S, Raimondi F, Mattiaccio A, Mantovani V, Vukotic R, et al.
J Gastroenterol
. 2017 Dec;
53(8):945-958.
PMID: 29238877
Background: Mutations in ATP-transporters ATPB81, ABCB11, and ABCB4 are responsible for progressive familial intrahepatic cholestasis (PFIC) 1, 2 and 3, and recently the gene for tight junction protein-2 (TJP2) has...