المؤلفون: Elena Fea, Ida Colantonio, Ornella Garrone, G. Cento, G.G. Di Costanzo, Elvio G. Russi, Gianmauro Numico, Gianfilippo Bertelli, Milena Gasco, Cristina Granetto, Marco Merlano, M. Anfossi, Nicola Silvestris, Marcella Occelli

المصدر: Annals of Oncology. 20:941-945

مصطلحات موضوعية: Adult, Male, Health Knowledge, Attitudes, Practice, medicine.medical_specialty, Palliative care, Adolescent, Referral, Attitude of Health Personnel, Medical Oncology, Truth Disclosure, Young Adult, Level of consciousness, Patient Education as Topic, Neoplasms, Surveys and Questionnaires, medicine, Humans, In patient, Referral and Consultation, Aged, Aged, 80 and over, Physician-Patient Relations, business.industry, Age Factors, Cancer, Hematology, Awareness, Middle Aged, Prognosis, medicine.disease, Surgery, Patient Rights, Oncology, Health Care Surveys, Family medicine, Workforce, Female, Empathy, Communication skills, Comprehension, Training program, business, Program Evaluation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::274cbba9e331f0df27fe457b84ce139aTest
https://doi.org/10.1093/annonc/mdn709Test

المؤلفون: Sandro Sorbi, Orso Bugiani, Lorenzo Pinessi, Innocenzo Rainero, Carmine Tomaino, Livia Bernardi, B. Terni, Alfredo Postiglione, Alessandra Clodomiro, Sabina Pappatà, J. F. Foncin, R. Di Lorenzo, N. Abbamondi, Raffaele Maletta, M. Anfossi, L. Nee, Francesca Frangipane, P H St George Hyslop, A. Leotta, M. G. Muraca, Sabrina A.M. Curcio, Graziella Milan, Giorgio Giaccone, Gianfranco Puccio, Elisa Rubino, Amalia C. Bruni, Ekaterina Rogaeva, Silvana Geracitano, Rosanna Colao, Maura Gallo, Maria Grazia Spillantini, Gianluigi Forloni, Maria Mirabelli, Nicoletta Smirne, S Lio

المصدر: Neurology 74 (2010): 798–806. doi:10.1212/WNL.0b013e3181d52785
info:cnr-pdr/source/autori:Bruni AC;Bernardi L;Colao R;Rubino E;Smirne N;Frangipane F;Terni B;Curcio SA;Mirabelli M;Clodomiro A;Di Lorenzo R;Maletta R;Anfossi M;Gallo M;Geracitano S;Tomaino C;Muraca MG;Leotta A;Lio SG;Pinessi L;Rainero I;Sorbi S;Nee L;Milan G;Pappatà S;Postiglione A;Abbamondi N;Forloni G;St George Hyslop P;Rogaeva E;Bugiani O;Giaccone G;Foncin JF;Spillantini MG;Puccio G./titolo:Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation./doi:10.1212%2FWNL.0b013e3181d52785/rivista:Neurology/anno:2010/pagina_da:798/pagina_a:806/intervallo_pagine:798–806/volume:74

مصطلحات موضوعية: Adult, Male, Alzheimer disease, presenilin 1, Genotype, International Cooperation, Population, Biology, Global Health, PSEN1 mutation, History, 21st Century, Presenilin, History, 17th Century, Methionine, Gene Frequency, Alzheimer Disease, Fluorodeoxyglucose F18, Leucine, Presenilin-1, PSEN1, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, education, Prefrontal cortex, Family Health, Genetics, Memory Disorders, education.field_of_study, Brain, Articles, Middle Aged, Alzheimer's disease, medicine.disease, founder effect, Phenotype, Dorsolateral prefrontal cortex, medicine.anatomical_structure, Italy, Positron-Emission Tomography, Mutation, Mutation (genetic algorithm), Female, Neurology (clinical), Cognition Disorders

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f79a5059afdc1cd6987baed55d02717Test
http://hdl.handle.net/2318/152288Test

المؤلفون: John Hardy, Francesca Frangipane, Ekaterina Rogaeva, Silvana Geracitano, Gianfranco Puccio, Carmine Tomaino, Yosuke Wakutani, S. Pradella, Livia Bernardi, M. Anfossi, Amalia C. Bruni, Christine Sato, P. St. George-Hyslop, Parastoo Momeni, Rosanna Colao, Raffaele Maletta, T. Kawarai, Maria Mirabelli, Nicoletta Smirne, Andrew Kertesz, Joshua W. Elder, A. Costanzo, Sabrina A.M. Curcio, Maura Gallo

المصدر: Neurology. 69(2)

مصطلحات موضوعية: Proband, Adult, Genetic Markers, Male, Heterozygote, Genotype, DNA Mutational Analysis, Biology, Cohort Studies, Progranulins, Gene Frequency, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Allele, Age of Onset, Allele frequency, Aged, Phenocopy, Genetics, Aged, 80 and over, Genetic heterogeneity, Genetic Carrier Screening, Haplotype, Middle Aged, medicine.disease, Pedigree, Italy, Mutation (genetic algorithm), Mutation, Intercellular Signaling Peptides and Proteins, Dementia, Female, Neurology (clinical), Frontotemporal dementia, Chromosomes, Human, Pair 17

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f03ecc110fc922bde08a3aeab258c89eTest
https://pubmed.ncbi.nlm.nih.gov/17620543Test