A Torroni
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Explore the profile of A Torroni including associated specialties, affiliations and a list of published articles.
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88
Citations
3767
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Recent Articles
1.
Park G, Jalkh E, Boczar D, Bergamo E, Kim H, Kurgansky G, et al.
Med Oral Patol Oral Cir Bucal
. 2022 Aug;
27(5):e468-e475.
PMID: 35975804
Background: We aimed to histomorphometrically evaluate the effects of Leucocyte-Platelet-Rich Fibrin (L-PRF), with and without the combination of a bone grafting material, for alveolar ridge preservation using an in vivo...
2.
Raveane A, Aneli S, Montinaro F, Athanasiadis G, Barlera S, Birolo G, et al.
Sci Adv
. 2019 Sep;
5(9):eaaw3492.
PMID: 31517044
European populations display low genetic differentiation as the result of long-term blending of their ancient founding ancestries. However, it is unclear how the combination of ancient ancestries related to early...
3.
Marianetti T, DallAsta L, Torroni A, Gasparini G, Pelo S
Eur J Paediatr Dent
. 2014 Aug;
15(2 Suppl):218-20.
PMID: 25101507
Background: Trismus-Pseudocamptodactyly Syndrome (TPS) is a rare autosomal syndrome characterised by the inability to open the mouth fully, pseudocamptodactyly, short stature and foot deformities. The maxillofacial feature entails hyperplasia of...
4.
Boniello R, Gasparini G, DAmato G, Torroni A, Marianetti T, Foresta E, et al.
Eur Rev Med Pharmacol Sci
. 2013 Jun;
17(10):1411-8.
PMID: 23740458
Objectives: Rehabilitation of maxillary edentulism with implant-supported prostheses has come into common clinical practice. Although autologous bone has osteoinductive, osteoconductive and osteogenetic properties, its use is subject to certain disadvantages...
5.
Coudray C, Olivieri A, Achilli A, Pala M, Melhaoui M, Cherkaoui M, et al.
Ann Hum Genet
. 2008 Dec;
73(2):196-214.
PMID: 19053990
The mitochondrial DNA variation of 295 Berber-speakers from Morocco (Asni, Bouhria and Figuig) and the Egyptian oasis of Siwa was evaluated by sequencing a portion of the control region (including...
6.
La Morgia C, Achilli A, Iommarini L, Barboni P, Pala M, Olivieri A, et al.
Neurology
. 2008 Jan;
70(10):762-70.
PMID: 18216301
Objective: To investigate the mechanisms underlying myoclonus in Leber hereditary optic neuropathy (LHON). Methods: Five patients and one unaffected carrier from two Italian families bearing the homoplasmic 11778/ND4 and 3460/ND1...
7.
Annesi G, Aguglia U, Tarantino P, Annesi F, De Marco E, Civitelli D, et al.
Clin Genet
. 2007 Feb;
71(3):288-9.
PMID: 17309654
No abstract available.
8.
Valentino M, Barboni P, Rengo C, Achilli A, Torroni A, Lodi R, et al.
J Med Genet
. 2006 Jul;
43(7):e38.
PMID: 16816025
Background: Overlapping phenotypes including LHON, MELAS, and Leigh syndrome have recently been associated with numerous mtDNA point mutations in the ND5 gene of complex I, now considered a mutational hot...
9.
Marjanovic D, Fornarino S, Montagna S, Primorac D, Hadziselimovic R, Vidovic S, et al.
Ann Hum Genet
. 2005 Nov;
69(Pt 6):757-63.
PMID: 16266413
The variation at 28 Y-chromosome biallelic markers was analysed in 256 males (90 Croats, 81 Serbs and 85 Bosniacs) from Bosnia-Herzegovina. An important shared feature between the three ethnic groups...
10.
Bandelt H, Herrnstadt C, Yao Y, Kong Q, Kivisild T, Rengo C, et al.
Ann Hum Genet
. 2003 Dec;
67(Pt 6):512-24.
PMID: 14641239
In this study, a detailed analysis of both previously published and new data was performed to determine whether complete, or almost complete, mtDNA sequences can resolve the long-debated issue of...