Search Results - "Papi, Laura"

In Vitro Assessment of Essential Oils as Sustainable Antifungal Agents Against Sclerotinia sclerotiorum Causing Lettuce Drop.

Authors: Tunç, Mehdiye Piancatelli, Simone Makau, Sarah Mojela et al.

Source: Molecules. Feb2026, Vol. 31 Issue 4, p682. 15p.

Alu–Mediated Duplication and Deletion of Exon 11 Are Frequent Mechanisms of PALB2 Inactivation, Predisposing Individuals to Hereditary Breast–Ovarian Cancer Syndrome.

Authors: Sidoti, Diletta Margotta, Valeria Calosci, Diletta et al.

Source: Cancers. Dec2024, Vol. 16 Issue 23, p4022. 13p.

A Magnetic Resonance Imaging‐Chemical Exchange Saturation Transfer (MRI‐CEST) Method for the Detection of Water Cycling across Cellular Membranes.

Authors: Di Gregorio, Enza Papi, Chiara Conti, Laura et al.

Source: Angewandte Chemie. Feb2024, Vol. 136 Issue 6, p1-10. 10p.

Breast cancer: the first comparative evaluation of oncobiome composition between males and females.

Authors: Niccolai, Elena Baldi, Simone Nannini, Giulia et al.

Source: Biology of Sex Differences. 6/5/2023, Vol. 14 Issue 1, p1-9. 9p.

Male bilateral risk‐reducing mastectomy: Report of a case.

Authors: Combi, Francesca Razzaboni, Elisabetta Toss, Angela et al.

Source: Breast Journal. Oct2020, Vol. 26 Issue 10, p2135-2136. 2p.

Economic and Political Determinants of Sovereign Default and IMF Credit Use: A Robustness Assessment Post 2010.

Authors: Maddah, Lina Sherry, Hassan Zeaiter, Hussein

Source: Economies. Jul2024, Vol. 12 Issue 7, p181. 36p.

MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.

Authors: Aretz, Stefan Tricarico, Rossella Papi, Laura et al.

Source: European Journal of Human Genetics. Jul2014, Vol. 22 Issue 7, p923-929. 7p.

Expanding the mutational spectrum of LZTR1 in schwannomatosis.

Authors: Paganini, Irene Chang, Vivian Y Capone, Gabriele L et al.

Source: European Journal of Human Genetics. Jul2015, Vol. 23 Issue 7, p963-968. 6p.

A Systematic Assessment of Accuracy in Detecting Somatic Mosaic Variants by Deep Amplicon Sequencing: Application to NF2 Gene.

Authors: Contini, Elisa Paganini, Irene Sestini, Roberta et al.

Source: PLoS ONE. Jun2015, Vol. 10 Issue 6, p1-15. 15p.

Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1.

Authors: Caleca, Laura Putignano, Anna Laura Colombo, Mara et al.

Source: PLoS ONE. Feb2014, Vol. 9 Issue 2, p1-9. 9p.

Somatic variants of potential clinical significance in the tumors of BRCA phenocopies.

Authors: Buckingham, Lela Mitchell, Rachel Maienschein-Cline, Mark et al.

Source: Hereditary Cancer in Clinical Practice. 7/16/2019, Vol. 17 Issue 1, pN.PAG-N.PAG. 1p.

GENE-08. SCHWANNOMATOSIS SCHWANNOMAS HARBOR DISTINCT DNA METHYLATION PROFILES.

Authors: Mansouri, Sheila Paganini, Irene Karimi, Shirin et al.

Source: Neuro-oncology 2018 Supplement; Vol. 20.

Journal Info: Publisher: Oxford University Press / USA ISSN: 1522-8517

Augmentative and Alternative Communication: Models and Applications, Second Edition

Authors: Loncke, Filip Lo

Resource Type: eBook.

Subjects: Nonverbal communication, Interpersonal relations, Communicative disorders--Prevention--Needs assessment, Communicative disorders--Rehabilitation, Communication devices for people with disabilities, Needs assessment

Categories: MEDICAL / Audiology & Speech Pathology

Augmentative and Alternative Communication: Models and Applications for Educators, Speech-Language Pathologists, Psychologists, Caregivers, and Users

Authors: Loncke, Filip

Resource Type: eBook.

Subjects: Needs assessment, Linguistics, Communicative disorders--Treatment, Communication devices for people with disabilities, Nonverbal communication

Categories: MEDICAL / Internal Medicine, HEALTH & FITNESS / Diseases & Conditions / General, MEDICAL / Clinical Medicine, MEDICAL / Diseases, MEDICAL / Evidence-Based Medicine

Early-onset malignant phyllodes breast tumor in a patient with germline pathogenic variants in NF1 and BRCA1 genes.

Authors: Gensini F Sestini R De Luca A et al.

Source: Familial cancer [Fam Cancer] 2021 Jul; Vol. 20 (3), pp. 195-199. Date of Electronic Publication: 2020 Nov 19.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE

Poster Presentations.

Source: Familial cancer 2005 Supplement; Vol. 4.

Journal Info: Publisher: Springer Nature ISSN: 1389-9600

Abstracts of the 1st Conference of InSiGHT, the International Society for Gastrointestinal Hereditary Tumors, Newcastle upon Tyne, United Kingdom, 14-17 June 2005.

Source: Familial cancer [Fam Cancer] 2005; Vol. 4 Suppl 1, pp. 25-140.

Publication Type: Conference Proceedings; Overall

Journal Info: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print Cited Medium: Print ISSN: 1389-9600 (Print) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE