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Rosalia D’Angelo was born in Sant’Agata M.llo (Messina), Italy.
She obtained her degree in “Biological Sciences” (1991), magna cum laude, at the University of Messina, Italy. In 1992-1993 she obtained professional qualification and registration in the National Board of Biologists. Following a four years specialization course, she obtained in 1998 at the University of Messina, the Specialization degree in “Biochemistry and Clinical Chemistry”. Between November 1998 and May 1999 she provided professional work at the Institute of Multidisciplinary Biochemical Sciences and Clinical biochemistry, University of Messina. In 2003 she obtained PhD in “Human Cell Biology” at Department of Biomorphology and Biotechnologies, Division of Biology and Genetics, University of Messina. In this years she extended her experience on studies of genoma and gene expression. Beetween September –November 2004 she stayed in the laboratories of the Department of Oncology, Biology and Genetics of the University of Genoa, Italy, within the framework of a collaboration aimed at the molecular genetic analysis of genes involved in the pathogenesis of cerebral cavernous malformations. In year 2006 she partecipated to a selection for University Researcher at the Medical School of the University of Messina: she won the selection and became University Researcher, in the field of Applicated Biology (BIO/13), with teaching and research activities at the Biomorphology and Biotechnologies Department of the University of Messina. Currently, she teaches Biology and Genetics in the Degree in Medicine and Surgery and in other courses. Actually her main research field is related to molecular and genetics features of Cerebral Cavernous Malformations; identification of candidate genes and causative variants in different forms of Retinitis Pigmentosa and molecular genetic features and genotype-phenotype correlations in Trimethylaminuria.
She is member of Italian Association of Biology and Genetics and author of several papers in international journals with impact factor.
ACADEMIC TASKS AND ROLES
2007. Member of the Commission Committee on Area 05 (PRA 2005).
2012-2013. Participation to register of reviewers of programs and ministerial research products.
2009-2010. Member of the Academic Board of PhD in "Science of receptors and posture" XXV cycle, University of Messina, Messina, Italy.
2011-2013. Member of the Academic Board of PhD in “ Biology and Cellular Biotechnology" XXVII cycle, University of Messina, Messina, Italy.
A.A. 2012-2013. Member of the Committee for admission to the Triennial Degrees of health professions, Faculty of Medicine, University of Messina, Messina, Italy.
A.A. 2012-2013. Component of the Teaching Commission of the Degree in Medicine and Surgery, University of Messina, Messina, Italy.
Since January 2013 member of the Committee for Research and Advanced Training in the Department of Biomedical Sciences and Morphological and Functional Images, University of Messina, Messina, Italy.
Current Research
Currently the research activity is mainly focused:
• On the study of genetic and molecular mechanisms underlying the pathogenesis of Cerebral Cavernous Malformations both sporadic and familial;
• Identification of candidate genes and causative variants in different forms of Retinitis Pigmentosa;
• Molecular genetic features and genotype-phenotype correlations in Trimethylaminuria
Interested topics
FUNDED PROJECTS IN COLLABORATION
2003 - 2004. PRIN 2004 "Characterization of KRIT1 and its molecular interactions with RAP1 and ICAP1A: physiological functions and role in the pathogenesis of Cerebral Cavernous Malformations."
2012 PRIN 2010-11 "Sciences 'omics' as a tool for translational research in neuroncology".
Scientific Societies
Member of the Italian Association of Genetics and Molecular Biology (AIBG)
Member of the Italian Society of Neuroscience (SINS)
Member of the Italian Association of Neuropathology and Clinical Neurobiology (AINPeNC)
Member of the Federation of European Neurosciences Societies (FENS)
Member of the International Society of Neuropathology (ISN)
Collaborating Partners EPIRARE (European Platform for Rare Diseases Registries)
She is referee for:
Journal of Neurology, Neurosurgery, and Psychiatry
Journal of the Neurological Sciences
International Journal of Medical Sciences
BMC Neurology
European Journal of Medical Genetics
Membership
Member of the following associations and scientific societies:
Editorships
Conference Organization
Rinaldi C, Bramanti P, Scimone C, Donato L, Alafaci C, D’Angelo R, Sidoti A. (2017) Relevance of CCM genes polymorphisms for clinical management of sporadic cerebral cavernous malformations. Journal of the Neurological Sciences. 380:331-337.
D'Angelo R, Donato L, Venza I, Scimone C, Aragona P, Sidoti A. (2017) Possibleprotectiverole of the ABCA4 gene c.1268A>G missensevariant in Stargardtdisease and syndromicretinitis pigmentosa in a Sicilian family: Preliminary data. Int J Mol Med, 39: 1011-1020
Scimone C, Bramanti P, Alafaci C, Granata F, Piva F, Rinaldi C, Donato L, Greco F, Sidoti A, D'Angelo R. (2017) Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations. J Mol Neurosci. Feb;61(2):189-198.
Donato, L., Scimone, C., D'Angelo, R.,Sidoti, A. (2017). Predictive and personalized approaches towards retinitis pigmentosa and cerebral cavernous malformations. Life Safety And Security.doi: 10.12882/2283-7604.2017.5.2
Scimone C, Donato L, Rinaldi C, Sidoti A, D'Angelo R. (2016)First case of Currarino Syndrome and Trimethylaminuria: two rare diseases for a complex clinical presentation.J Dig Dis. Sep, 17(9):628-632.
Concetta Scimone; PlacidoBramanti; Alessia Ruggeri; Luigi Donato; Concetta Alafaci; Concetta Crisafulli; Massimo Mucciardi; Carmela Rinaldi; Antonina Sidoti; Rosalia D'Angelo (2016). CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. BMC Med Genet, 17(1), 74.
Rinaldi C, Bramanti P, Famà A, Scimone C, Donato L, Antognelli C, Alafaci C, Tomasello F, D'Angelo R, Sidoti A. (2015)GLYOXALASE I A111E, PARAOXONASE 1 Q192R AND L55M POLYMORPHISMS IN ITALIAN PATIENTS WITH SPORADIC CEREBRAL CAVERNOUS MALFORMATIONS: A PILOT STUDY.J Biol Regul Homeost Agents. Apr-Jun;29(2):493-500.
Scimone C, Bramanti P, Ruggeri A, Katsarou Z, Donato L, Sidoti A, D'Angelo R.(2015) Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations. J Mol Neurosci. Nov;57(3):400-3.
Rosalia D’Angelo, Carmela Rinaldi, Alessia Ruggeri, Giacomo Nicocia, Antonina Sidoti (2015).The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome. Ann. Clin Lab. Sci. Spring;45(2):202-5.
Rosalia D’Angelo, Concetta Scimone, Teresa Esposito, Daniele Bruschetta, Carmela Rinaldi, Alessia Ruggeri, Antonina Sidoti (2014). Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report. JOURNAL OF MEDICAL CASE REPORTS, vol. 8, p. 328-332
Carmela Rinaldi, Rosalia D'Angelo, Alessia Ruggeri, Marco Calabrò, Concetta Scimone, Antonina Sidoti (2014). PON I andGLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy. JOURNAL OF MOLECULAR BIOMARKERS & DIAGNOSIS, vol. 5, p. 170-175.
Esposito T, Varriale B, D'Angelo R, Amato A, Sidoti A (2014). Regulation of flavin-containing mono-oxygenase (Fmo3) gene expression by steroids in mice and humans. HORMONE MOLECULAR BIOLOGY AND CLINICAL INVESTIGATION, vol. 20, p. 99-109, ISSN: 1868-1891
Rosalia D’Angelo, Concetta Alafaci, Concetta Scimone, Alessia Ruggeri, Francesco Maria Salpietro, PlacidoBramanti, Francesco Tomasello, Antonina Sidoti (2013). Sporadic cerebral cavernous malformations: report of further mutations of CCM genes in 40 Italian patients.Biomed Research International. vol. 2013, p. 459253
D'Angelo R, Scimone C, Calabrò M, Schettino C, Fratta M, SidotiA.(2013). Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: a causative mutation?Gene. 25; 519(1):202-7
D'Angelo R, Esposito T, Calabro M, Rinaldi C, Robledo R, Varriale B, Sidoti A. (2013) FMO3 allelic variants in Sicilian and Sardinian populations: trimethylaminuria and absence of fish-like body odor.Gene. 25; 515 (2):410-5.
Rosalia D'Angelo, Concetta Scimone, Carmela Rinaldi, Giuseppe Trimarchi, Domenico Italiano, PlacidoBramanti, Aldo Amato and Antonina Sidoti.(2012) CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case control study. Int J Mol Med.29 (6):1113-20
Carmela Rinaldi, Natalia Maria Malara, Rosalia D’Angelo, Antonina Sidoti, Attilio Leotta, Santo Lio, Basilio Caparello, Alessia Ruggeri, Vincenzo Mollace and Aldo Amato.(2012) Age dependent switching role of ciclyn D1 in breast cancer. Analytical Cellular Pathology. 1; 35(3):179-85.
D'Angelo R, Marini V, Rinaldi C, Origone P, Dorcaratto A, Avolio M, Goitre L, Forni M, Capra V, Alafaci C, Mareni C, Garre C, Bramanti P, Sidoti A, Retta SF, Amato A. (2011) Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation. Brain Pathology. 21: 215- 224.
Rosalia D'Angelo, Concetta Crisafulli, Carmela Rinaldi, Alessia Ruggeri, Aldo Amato, and Antonina Sidoti. (2011) CCR5Δ32 Polymorphism Associated with a Slower Rate Disease Progression in a Cohort of RR-MS Sicilian Patients.Mult Scler Int.153282. Epub2011 Jun 23. Article ID 153282.
Concetta Crisafulli, Raffaella Calati, Diana De Ronchi, Antonina Sidoti, Rosalia D'Angelo, Aldo Amato, Alessandro Serretti. (2010) Genetics of suicide, from genes to behaviour. Clinical Neuropsychiatry. 7, 4/5, 141-148.Review. Issn: 1724-4935.
Sidoti A., Antognelli C., Rinaldi C, D’Angelo R., Dattola V., Girlanda P., Talesa V., Amato A.(2007) Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? Multiple Sclerosis. 13(4):446-53.
Anastasi G., Cutroneo G., Sidoti A., Rinaldi C., Bruschetta D., Rizzo G., D’Angelo R., Tarone G., Amato A., Favaloro A. (2007) Sarcoglycan subcomplex in normal human smooth muscle. J. Histochem. Cytochem.(8): 831-43.
MALARA NM, LEOTTA A, SIDOTI A, LIO S, D'ANGELO R, CAPARELLO B, MUNAO F, PINO F, AMATO A. (2006) Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas. THE BREAST, vol. 15, p. 81-89
SIDOTI A, ROBLEDO R, RINALDI A, D'ANGELO R, RINALDI C, AMATO A. (2006). Further data on a 9.1-kb insertion-deletion polymorphism: Survey of Mediterranean populations. HUMAN BIOLOGY, vol. 78, p. 371-378
SIDOTI A, D'ANGELO R, RINALDI C, DE LUCA G, PINO F, SALPIETRO DAMIANO C., GIUNTA DE, SALTALAMACCHIA F, AMATO A (2005). Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population. INTERNATIONAL JOURNAL OF IMMUNOGENETICS, vol. 32, p. 193-198
ANASTASI G, CUTRONEO G, SIDOTI A, SANTORO G, D'ANGELO R, RIZZO G, RINALDI C, GIACOBBE O, BRAMANTI P, NAVARRA G, AMATO A, FAVALORO A (2005). Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, vol. 16, p. 367-374
Allegra, A. Corsonello, M. Buemi, R. D’Angelo, A. Di Benedetto, S. Bonanzinga, D. Cucinotta, R. Ientile and F. Corica (1997). Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY, vol. 11, p. 154-157
Corica F, Allegra A, Ientile R, Buemi M, Corsonello A, D'Angelo R, Bonanzinga S, Cucinotta D, Ceruso D. (1997). Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). ARCHIVES OF GERONTOLOGY AND GERIATRICS, vol. 25, p. 255-262
Corica F, Allegra A, Buemi M, Ientile R, Corsonello A, Di Benedetto A, Bonanzinga S, Ruello A, D'Angelo R, Cucinotta D, Ceruso D. (1996). Altered platelet magnesium and plasma and urinary soluble form of intercellular adhesion molecule I (sICAM-1) concentrations in insulin dependent diabetes mellitus (IDDM) patients with microalbuminuria. MAGNESIUM RESEARCH, vol. 9, p. 307-312.
D’Angelo R., Calabrò M., Scimone C., Crisafulli C., Esposito T., Varriale B., Amato A,Sidoti A FMO3 allelic variants in a Mediterranean population frequency and linkage analysis.. Humane Genome Meeting 2001- 4th Pan Arab Human Genetics Conference; Genomics of Human Diversity and Heritable Disorders. Dubai 14-17 March 2011; HUGO J(2011)5:1–346.301 A. Sidoti , R. D’Angelo, T. Esposito, M. Calabrò, R. Robledo, B. Varriale , A. Amato FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis.. 4th ESF Conference on Functional Genomics and Disease Dresden, Germany, April 14-17, 2010; New Biotechnology Volume 27S April 2010; [P2.13] doi:10.1016/j.nbt.2010.01.176 - ISSN: 1871-6784.
PROCEEDINGS ACTS OF JOURNALS AND INTERNATIONAL CONFERENCES
Luigi Donato, Concetta Scimone, Carmela Rinaldi, Elvira Velardi, Ivan Anchesi, Rosalia D’Angelo, Antonina Sidoti, Non-coding RNAome of oxidative stressed and normal RPE cells suggests unknown regulative aspects of Retinitis pigmentosa etiopathogenesis. Mathematical Modelling of Self-Organizations in Medicine, biology and Ecology:from micro to macro, Giardini Naxo, Messina, Italy, 18-21 September 2017 (SUBMITTED)
Luigi Donato, Concetta Scimone, Simona Alibrandi, Carmela Rinaldi, Rosalia D’Angelo, Antonina Sidoti,Circadian rhythms and fatty acids metabolism in retinitis pigmentosa: oxidative stress alteredpathways by a RNA-Seq analysis. 15th International Congress on Vision Science and Eye (2017), London, August 10 -11. (SUBMITTED)
C. Scimone, L. Donato, C. Rinaldi, R. D'Angelo, A. Sidoti, Possible role of oxidative stress in retinitis pigmentosa: a gene expression study. Human Genome Meeting (HGM 2017), Barcelona, Spain, 5-7 February 2017. Scimone C., Donato L., Greco F., Rinaldi C., D'Angelo R., Sidoti A., CCM genetic test: Can some CCM genes SNPs in a homozygous condition be causative of Cerebral Cavernous Malformations?, 2° Neurological Disorders Summit, September 7-9, 2016, Baltimore (MD), USA
Scimone C., Rinaldi C., Nicocia G., Greco F., Donato L., D'Angelo R., Sidoti A., A rare case of TMAU associated with suspected Currarino triad, ESHG Conference, June 6-9, 2015 Glasgow, Scotland, UK.
Donato L., Rinaldi C., Ruggeri A., Greco F., Scimone C., D'Angelo R., Sidoti A., RP1 gene polymorphisms and Retinitis pigmentosa: a possible genotype – phenotype correlation? International Conference on Eye Disorders and Treatment, July 13-15, 2015 Baltimore, Maryland, USA
Luigi Donato, Concetta Scimone, Alessia Ruggeri, Federica Greco, Carmela Rinaldi, Rosalia D’Angelo, Antonina Sidoti Stargardt disease: a late – onset case study . Eye Disorders and Treatment Conference 2015, Baltimore, USA
L. Donato, C. Rinaldi , A. Ruggeri, E. Velardi, C. Scimone, R. D’Angelo, A. Sidoti RP1 gene polymorphisms in a Retinitis pigmentosa patient affected by Congenital adrenal hyperplasia: a genotype – phenotype correlation European Society of Human Genetics (Glasgow, June 6-9,2015).
Scimone C, Ruggeri A, Bruschetta D, Rinaldi C, D'Angelo R, Sidoti A. A molecular- genetic analysis of flavin-containing monooxygenase3 gene (fmo3) in an Italian child with a tmauria like-phenotype. Human Genome Meeting - Genome Variation and Human Health. Geneva 27 – 30 April 2014.
D’Angelo R., Calabrò M., Scimone C., Crisafulli C., Esposito T., Varriale B., Amato A,Sidoti A. FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. Humane Genome Meeting 2001- 4th Pan Arab Human Genetics Conference; Genomics of Human Diversity and Heritable Disorders. Dubai 14-17 March 2011; HUGO J(2011)5:1–346.301
A. Sidoti , R. D’Angelo, T. Esposito, M. Calabrò, R. Robledo, B. Varriale , A. Amato. FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis. 4th ESF Conference on Functional Genomics and Disease Dresden, Germany, April 14-17, 2010; New Biotechnology Volume 27S April 2010 ; [P2.13] doi:10.1016/j.nbt.2010.01.176 - ISSN: 1871-6784.
N.M. Malara, A. Leotta, A. Sidoti, S. Lio, R. D’Angelo, B. Caparello, F. Munao’, F. Pino and A. Amato. Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women. Fourth European Cytogenetics Conference. September 6-9, 2003 – Bologna, Italy. Annales de génétique 2003 ;46 (2-3):166.
Sidoti A, D’Angelo R, Pino F, De Luca G, Rinaldi C, Malara NM, Licata N and Amato A Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. Meeting on Genetic of complex disease in isolated population. May 23rd – May 30th 2003-Tortoli’, Sardinia, Italy.
PROCEEDINGS ACTS OF THE NATIONAL CONGRESSES
A. Sidoti, R. D’Angelo, F. Pino, G. De Luca, C. Rinaldi, N. Malara, A. Amato. Distribution Δ32 mutated allele of the CCR5 gene in the healthy population of the Mediterranean basin. Proceedings of the Fifth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Perugia, 1-4 October 2001;p.154.
Sidoti, C. Salpietro, G. De Luca, R. D’Angelo, F. Pino, C. Rinaldi, A. Amato Distribution Δ32 mutated allele of the CCR5 gene in the Sicilian population. Proceedings of the Fifth National Congress S.I.G.U. (Italian Society of Human Genetics)Verona, 24-27 September 2002; p. 374.
N.M. Malara, A. Leotta, A. Sidoti, S. Lio, R. D’Angelo, B. Caparello, F. Munao’, F. Pino and A. Amato. Hormone receptors, CCND1 and proliferation in postmenopausal women. Proceedings of the Sixth National Congress S.I.G.U. (Italian Society of Human Genetics) Verona, 24-27 September 2003; p. 157.
Sidoti A., D'Angelo R., Malara N.M.,Costa G., Pino F., Amato A. Chemokine receptor CCR5 and mobilization of intracellular calcium in human lymphocytes: genotype-phenotype correlation. Proceedings of the Sixth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Giardini Naxos (ME), 1-5 October 2003; p.110.
Malara N.M., Cesario A., Boninsegna A., Granone P., Sgambato, Galletta D., Flamini G., Sidoti A., D'Angelo R., Pino F., Amato A.and Cittadini A. p 53 Subcellular compartmentalization, cell cycle and apoptotic pattern in non-small cell lung cancer (NSLC). Proceedings of the Sixth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Giardini Naxos (ME), 1-5 Ottobre 2003; p.127
N.M. Malara, A. Leotta, A. Sidoti, S. Lio, R. D’Angelo, B. Caparello, F. Munao’, F. Pino and A. Amato. Hormone receptors, CCND1 and proliferation in postmenopausal women. Proceedings of the Sixth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Giardini Naxos (ME), 1-5 Ottobre 2003; p.131.
M. Avolio, F. Francalanci, S. Degani, F. Balzac, F. Fraioli, F.Velasco, R. D’Angelo, F. Pino, A. Sidoti, A. Amato, G.Tarone, L. Silengo, S. F. Retta. KRIT 1: A new protein on integrin signaling pathways. Proceedings of the Sixth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Giardini Naxos (ME), 1-5 Ottobre 2003; p.45.
A. Sidoti, R. Robledo, R. D’Angelo, F. Pino, N.M. Malara, A. Amato. A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population. Proceedings of the Sixth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Giardini Naxos (ME), 1-5 Ottobre 2003; p.22.
N.M. Malara, A. Leotta, A. Sidoti, S. Lio, R. D’Angelo, B. Caparello, F. Munao’, F. Pino and A. Amato. Hormone receptors, CCND1 and proliferation in postmenopausal women. Proceedings of the Italian Congress SIAPEC- IAP Genoa, 23 to 25 October 2003. Review of the Italian Society of Pathology and Anatomy Diagnostics Phytopathology. 95:384.
Anastasi, A. Amato, G. Cutroneo, A. Sidoti, R. D’Angelo, N. Licata, G. Rizzo, F. Trimarchi, A. Arco, G. Santoro. Sarcoglycans in human smooth muscle: a CLSM and molecular study. Proceedings of the 58 th Meeting of the Italian Society of Anatomy. 17-19 September 2004- Chieti, Italy. Italian Journal of Anatomy and Embryology 2004. Jul-Sept; 109 (Suppl.1):77.
A. Sidoti, R. D’Angelo, F. Pino, C. Rinaldi, N . Malara, A . Amato. Genetic and functional study of CCR5 gene in HIV-1 infection. Proceedings of the VII Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Grado (GO), 23-26 Settembre 2004.
Sidoti A, Cutroneo G, D’Angelo R, Rinaldi C, Licata N, Favaloro A, Trimarchi F, Santoro G, Anastasi G, Amato A. Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? Proceedings of the VII Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Grado (GO),23-26 Settembre 2004.
M. Forni, P. Peretta, V. Marini, R. D'Angelo, L.Ferrera, A. Dorcaratto, A. Sidoti, F. Retta, G. Viale, C. Alafaci, F. Squitieri, V. Capra, P. Origone, C. Mareni, A. Amato and C. Garrè . Krit-1 mutations in 100 patients with cerebral cavernomas. 41st Meeting of the Italian association of Neuropathology. 26 - 28 May 2005 Saluzzo. Clinical Neuropathology 2005. May- June; p. 140.
Rinaldi C. Sidoti A., Cutroneo G., D’Angelo R, Favaloro A., Rizzo G., Anastasi G., Amato A. Sarcoglycans and integrins in muscular inactivity. Acts of 'A.I.B.G. VIII Congress (Italian Association of General and Molecular Biology and Genetics) Sirolo (AN),15-17 Settembre 2005; p.100.
Sidoti A., Antognelli C., Rinaldi C., D’Angelo R., Girlanda P., Talesa V., Amato A. Polimorfismi della gliossalasi I e della paraoxonasi I in individui sani ed individui affetti da Sclerosi Multipla.
Fattori di suscettibilità? Acts of 'A.I.B.G. VIII Congress (Italian Association of General and Molecular Biology and Genetics) Sirolo (AN), 15-17 Settembre 2005; p.121.
R. D’Angelo, V. Marini, L. Ferrera, A. Dorcaratto, A. Sidoti, M. Forni, F. Retta, C. Alafaci, V. Maglione, F. Squitieri, V. Capra, P. Origine, C. Mareni, A. Amato, C. Garrè. Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale. Acts of 'A.I.B.G. VIII Congress (Italian Association of General and Molecular Biology and Genetics)Sirolo (AN), 15-17 Settembre 2005; p.118
Sidoti Antonina, Rinaldi Carmela, Cutroneo Giuseppina, D’Angelo Rosalia, Favaloro Angelo, Rizzo Giuseppina, Anastasi Giuseppe, Amato Aldo. Il Subcomplesso dei sarcoglicani nel muscolo liscio umano. Proceedings of the IX Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Massa Lubrense (NA), 11 - 14 Settembre 2006; p. 52.
V. Marini, R. D’Angelo, L. Ferrera, A. Dorcaratto, M. Forni, V. Capra, M. Torrini, C. Alafaci, A. Sidoti, F. Retta, A. Amato, C. Mareni, P. Origone, C. Garrè. Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. Proceedings of the IX National Congress SIGU (Italian Society of Human Genetics) Venezia, 8-10 Novembre 2006.
G. Cutroneo, A. Amato, G. Speranza, A. Sidoti, R. D’Angelo, A. Duca, D. Bruschetta, M. Righi, A. Soscia, L. Magaudda. Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle Proceedings of the 32 th National Congress of the Italian Society of Histochemistry.Messina, 31 Maggio- 2 Giugno 2007; European Journal of Histochemistry. ISSN 1121-760X volume 51/ supplement 2 p.26, 2007.
D’Angelo Rosalia, Sidoti Antonella, Rinaldi Carmela, Amato Aldo. Genetic Screening of CCM gene in Italian patients with cerebral cavernous angioma: a family case. Proceedings of the Tenth Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Torino, Molecular Biotecnology Center, 20-22 Settembre 2007; p. 50.
Varriale B., Esposito T., Sidoti A., D’Angelo R., Scimone C., Calabrò M., Amato A. Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regulation of FMO3 gene. Proceedings of the XI Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Palermo, 08-10 Ottobre 2009; p.41;
D’Angelo R., Sidoti A., Marini V., Origone P., Labate A., Retta F.S., Amato A. Analysis of genomic rearrangements in patients with cavernous angioma brain. Proceedings of the XI Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Palermo, 08-10 Ottobre 2009; p.23;
Bruno W., Amato A., Sidoti A., D’Angelo R., Cannavò S., Guarneri C., Adamo V., Zanghì M., Russo A., Calo V., Rinaldi G., Tumino R., Bianchi Scarra G. Preliminary data on the molecular characterization of cases of familial melanoma from Sicily. SIGU XII Congress (Italian Society of Human Genetics).Torino, 8-10 Novembre 2009.
Bruno W., Amato A., Sidoti A., D’Angelo R., Cannavò S., Guarneri C., Adamo V., Zanghì M., Russo A., Calo V., Rinaldi G., Tumino R., Bianchi Scarrà G. Preliminary data on the molecular characterization of cases of familial melanoma from Sicily. IMI XV Congress (Italian Melanoma Intergroup).Genova, 18-20 Ottobre 2009;
Varriale B., Esposito T., Sidoti A., D'Angelo R., Amato A. Trimethylaminuria TMAU (FISH ODOR SYNDROME): a rare disease, monogenic. Regulation of FMO3 gene involved in its manifestation. XIII National Congress S.I.G.U. (Italian Society of Human Genetics) Firenze, 14-17 Ottobre 2010; 418, p.86.
R. D’Angelo, C. Rinaldi, C. Scimone, M. Calabrò, A. Ruggeri, C. Crisafulli, , A. Sidoti, A. Amato. Molecular lysis of CCM genes promoter regions. Proceedings of the XI Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Padova, 30 Settembre-1 Ottobre 2011; p.18;
R. D’ Angelo, A. Ruggeri, C. Scimone, C. Crisafulli, M. Calabrò, C. Rinaldi, A. Sidoti (2012). NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUS MALFORMATIONS. Proceedings of the XII Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Assisi-Perugia , 28 – 29 Settembre 2012; p. 73.
C. Scimone, C. Rinaldi, A. Ruggeri, L. Donato, R. D’Angelo, A. Sidoti (2014). Two non-homologous co-regulated genes PDCD10 and SerpinI1: any possible related function? Proceedings of the XIV Congress A.I.B.G. (Italian Association of General and Molecular Biology and Genetics) Napoli , 26 – 27 Settembre 2014; p. 15.
Scimone C, Alafaci C, Ruggeri A, Donato L, Rinaldi C, D’Angelo R, Sidoti A. Can loss of heterozygosity explain Cerebral Cavernous Malformations’ development in patients with no CCM genes germline mutations? XVI SINS Congress, Cagliari, 8 – 11 ottobre 2015.
L. Donato, C. Scimone, C. Rinaldi, F. Greco, R. D'Angelo, A. Sidoti, Retinitis pigmentosa: a NGS approach towards personalized medicine, AIBG (Italian Association of General and Molecular Biology and Genetics) 2016, Cagliari.
L. Donato, C. Scimone, R. D'Angelo, A. Sidoti, NGS technologies: a valid approach to Retinitis pigmentosa genetic forms classification, Smart Science 2017, Catania, Italia, 26-27 January 2017.
L. Donato, C. Scimone, C. Rinaldi, R. D'Angelo, A. Sidoti, Role 0f oxidative stress in Retinitis Pigmentosa :new involved pathways by a RNA-Seq analysis, PdD Students Meeting: Life Sciences for a better future, Santa Margherita Ligure, Genoa, Italy 11-13 May 2017.