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1
المؤلفون: Pellegrini, C., Raimondi, S., Di Nardo, L., Ghiorzo, P., Menin, C., Manganoni, M. A., Palmieri, G., Guida, G., Quaglino, P., Stanganelli, I., Massi, D., Pastorino, L., Elefanti, L., Tosti, G., Queirolo, P., Leva, A., Maurichi, A., Rodolfo, M., Fargnoli, M. C., Martinoli, C., Gandini, S., Vecchiato, A., Alaibac, M., Facchetti, F., Ferrari, A., Frigerio, S., Valeri, B., Guida, S., Giudice, G., Ribero, S., Astrua, C., Mazzoni, L.
مصطلحات موضوعية: Oncology, Adult, medicine.medical_specialty, Skin Neoplasms, Adolescent, Population, Context (language use), p16, Dermatology, Quantitative trait locus, CDKN2A, POT1, Internal medicine, MC1R, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, education, Child, neoplasms, Melanoma, MITF, education.field_of_study, business.industry, Genes, p16, Pediatric melanoma, medicine.disease, Penetrance, Receptor, Melanocortin, Type 1, Infectious Diseases, Genes, Cohort, Melanocortin, genetic susceptibility, business, Receptor, Type 1
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7f0e4cdd383a8503365b4d249a9e0dTest
https://hdl.handle.net/11380/1255741Test -
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المؤلفون: Anichini, A., Asero, S., Bersanelli, M., Caraco, C., De Giorgi, V., Di Giacomo, A. M., Feliciani, C., Ferraresi, V., Ghiorzo, P., Grimaldi, A. M., Guida, M., Mandala, M., Massi, D., Mocellin, S., Palmieri, G., Patuzzo, R., Pizzichetta, M. A., Ricci, R., Rossi, G., Quaglino, P., Queirolo, P., Senetta, R., Stanganelli, I., Tucci, M.
المساهمون: Anichini, A., Asero, S., Bersanelli, M., Caraco, C., De Giorgi, V., Di Giacomo, A. M., Feliciani, C., Ferraresi, V., Ghiorzo, P., Grimaldi, A. M., Guida, M., Mandala, M., Massi, D., Mocellin, S., Palmieri, G., Patuzzo, R., Pizzichetta, M. A., Ricci, R., Rossi, G., Quaglino, P., Queirolo, P., Senetta, R., Stanganelli, I., Tucci, M.
المصدر: Dermatology Reports, Vol 13, Iss 1 (2021)
Dermatology Reportsمصطلحات موضوعية: medicine.medical_specialty, Telemedicine, Coronavirus disease 2019 (COVID-19), business.industry, Melanoma, Sentinel lymph node, COVID-19, Italy, management, Dermatology, lcsh:RL1-803, medicine.disease, Article, Management, Health services, Pandemic, medicine, lcsh:Dermatology, Skin melanoma, Intensive care medicine, business, Melanoma diagnosis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab76b17c7d04caa2e783055b46cd0b90Test
https://hdl.handle.net/2318/1890616Test -
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المؤلفون: Dalmasso, B., Pastorino, L., Nathan, V., Shah, N.N., Palmer, J.M., Howlie, M., Johansson, P.A., Freedman, N.D., Carter, B.D., Beane-Freeman, L., Hicks, B., Molven, A., Helgadottir, H., Sankar, A., Tsao, H., Stratigos, A.J., Helsing, P., Doorn, R. van, Gruis, N.A., Visser, M., Wadt, K.A.W., Mann, G., Holland, E.A., Nagore, E., Potrony, M., Puig, S., Menin, C., Peris, K., Fargnoli, M.C., Calista, D., Soufir, N., Harland, M., Bishop, T., Kanetsky, P.A., Elder, D.E., Andreotti, V., Vanni, I., Bruno, W., Hoiom, V., Tucker, M.A., Yang, X.R., Andresen, P.A., Adams, D.J., Landi, M.T., Hayward, N.K., Goldstein, A.M., Ghiorzo, P., GenoMEL, MelaNostrum Consortia
المصدر: Genetics in Medicine, 23(11), 2087-2095. SPRINGERNATURE
Genetics in Medicine
Genetics in medicine : official journal of the American College of Medical Genetics, vol 23, iss 11مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Clinical Sciences, Ataxia Telangiectasia Mutated Proteins, MelaNostrum consortia, Article, Germline, Ataxia Telangiectasia, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Internal medicine, Genetics, medicine, 2.1 Biological and endogenous factors, Humans, Genetic Predisposition to Disease, Aetiology, Allele, Melanoma, Allele frequency, Exome, Genotyping, Germ-Line Mutation, Genetics (clinical), Cancer, Genetics & Heredity, business.industry, Human Genome, Australia, GenoMEL, medicine.disease, 030104 developmental biology, 030220 oncology & carcinogenesis, Ataxia-telangiectasia, Cohort, Settore MED/35 - MALATTIE CUTANEE E VENEREE, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51b0ef9606b12f87dff498e2a2603490Test
http://hdl.handle.net/1887/3280197Test -
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المؤلفون: Lesueur, F., Easton, D. F., Renault, A. -L., Tavtigian, S. V., Bernstein, J. L., Kote-Jarai, Z., Eeles, R. A., Plaseska-Karanfia, D., Feliubadalo, L., Moles-Fernandez, A., Santamarina-Pena, M., Sanchez, A. T., Lopez-Novo, A., Porras, L. -M., Blanco, A., Capella, G., de la Hoya, M., Molina, I. J., Osorio, A., Pineda, M., Rueda, D., de la Cruz, X., Diez, O., Ruiz-Ponte, C., Gutierrez-Enriquez, S., Vega, A., Lazaro, C., Arun, B., Herold, N., Versmold, B., Schmutzler, R. K., Nguyen-Dumont, T., Southey, M. C., Dorling, L., Dunning, A. M., Ghiorzo, P., Dalmasso, B. S., Cavaciuti, E., Le Gal, D., Roberts, N. J., Dominguez-Valentin, M., Rookus, M., Taylor, A. M. R., Goldstein, A. M., Goldgar, D. E., Couch, F., Kraft, P., Weitzel, J., Nathanson, K., Domchek, S., Laduca, H., Stoppa-Lyonnet, D., Andrieu, N.
المصدر: Fam Cancer
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, medicine.medical_specialty, Heterozygote, Variants classification, ATM, Cancer risk, Cancer spectrum, Tumor profiles, Population, Context (language use), Breast Neoplasms, Ataxia Telangiectasia Mutated Proteins, 030105 genetics & heredity, Article, 03 medical and health sciences, Ataxia Telangiectasia, 0302 clinical medicine, Neoplasms, Epidemiology, Genetics, medicine, Humans, Genetic Predisposition to Disease, education, Genetics (clinical), education.field_of_study, business.industry, Cancer, medicine.disease, Oncology, 030220 oncology & carcinogenesis, Family medicine, Female, France, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f15fec2bfdc6211ab4a9d904d906f28Test
https://europepmc.org/articles/PMC9969796Test/ -
5Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients
المؤلفون: Ciccarese, G., Dalmasso, B., Bruno, W., Queirolo, P., Pastorino, L., Andreotti, V., Spagnolo, F., Tanda, E., Ponti, G., Massone, C., Drago, F., Parodi, A., Ghigliotti, G., Pizzichetta, M. A., Ghiorzo, P.
المساهمون: Ciccarese, G., Dalmasso, B., Bruno, W., Queirolo, P., Pastorino, L., Andreotti, V., Spagnolo, F., Tanda, E., Ponti, G., Massone, C., Drago, F., Parodi, A., Ghigliotti, G., Pizzichetta, M. A., Ghiorzo, P.
المصدر: Journal of Translational Medicine
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-11 (2020)مصطلحات موضوعية: medicine.medical_specialty, Nevi and melanomas, Skin Neoplasms, lcsh:Medicine, Dermoscopy, Nodular melanoma, Melanocyte Inducing Transcription Factor, General Biochemistry, Genetics and Molecular Biology, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, CDKN2A, Dysplastic nevi, medicine, Humans, Genetic Predisposition to Disease, Melanoma, neoplasms, Cancer genetics, Retrospective Studies, E318K, Microphthalmia-Associated Transcription Factor, Germline variant, integumentary system, business.industry, Nevi, Research, lcsh:R, Cutaneous melanoma, Renal cell carcinoma, Susceptibility, General Medicine, medicine.disease, Microphthalmia-associated transcription factor, Penetrance, Dermatology, body regions, Phenotype, 030220 oncology & carcinogenesis, Dysplastic nevus, Cancer genetic, business
وصف الملف: ELETTRONICO
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cdbce6a7d062116beee14e6c68c07dTest
https://hdl.handle.net/11380/1201638Test -
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المؤلفون: Manca, A., Paliogiannis, P., Colombino, M., Casula, M., Lissia, A., Botti, G., Caraco, C., Ascierto, P. A., Sini, M. C., Palomba, G., Pisano, M., Dedola, M. F., Fedeli, M. A., Montesu, M. A., Rubino, C., Satta, R., Scotto, T., Sini, G., Maio, M., Massi, D., Anichini, A., Pfeffer, U., Doneddu, V., Cossu, A., Palmieri, G., Ghiorzo, P., Queirolo, P., Quaglino, P., Sileni, V. C., Di Giacomo, A. M.
المصدر: Journal of Translational Medicine
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-10 (2019)مصطلحات موضوعية: 0301 basic medicine, Neuroblastoma RAS viral oncogene homolog, Oncology, Male, Proto-Oncogene Proteins B-raf, medicine.medical_specialty, Concordance, BRAF, Cancer, Melanoma, Metastasis, Mutations, NRAS, Skin, lcsh:Medicine, General Biochemistry, Genetics and Molecular Biology, GTP Phosphohydrolases, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Medicine, Humans, Neoplasm Metastasis, business.industry, Research, lcsh:R, High-Throughput Nucleotide Sequencing, Membrane Proteins, General Medicine, Ion semiconductor sequencing, Amplicon, Middle Aged, medicine.disease, 3. Good health, Female, Mutation, 030104 developmental biology, 030220 oncology & carcinogenesis, Cohort, business, Cohort study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdb4f03ed55d6ce04c8b63327e43959Test
http://hdl.handle.net/2158/1177805Test -
7
المؤلفون: Borghesi, A, Mencarelli, Ma, Memo, L, Ferrero, Gb, Bartuli, A, Genuardi, M, Stronati, M, Villani, A, Renieri, A, Corsello, G, Their Respective Scientific Societies, Agostiniani, R, Staiano, A, Del Vecchio, A, Banderali, G, Peroni, D, Piazzolla, R, Turra, R, Bozzola, E, Vecchio, D, Rosati, Gv, Macrì, F, Romagnoli, C, De Curtis, M, Orfeo, L, Mangili, G, Mosca, F, Fanos, V, Paolillo, P, Raimondi, F, Rizzo, A, Chirico, G, Corvaglia, Lt, Cacace, Concetta, Poggiani, C, Zuppa, Aa, Pisano, D, Melis, D, Giuffrè, M, Carbone, Mt, Macchiaiolo, M, Tarani, L, Selicorni, A, Andria, G, Coviello, D, Gentile, M, Ghiorzo, P, Novelli, A, Ragusa, A, Scarano, G, Giardino, D.
المساهمون: Borghesi A, Mencarelli MA, Memo L, Ferrero GB, Bartuli A, Genuardi M, Stronati M, Villani A, Renieri A, Corsello G, Borghesi, Alessandro, Mencarelli, Maria Antonietta, Memo, Luigi, Ferrero, Giovanni Battista, Bartuli, Andrea, Genuardi, Maurizio, Stronati, Mauro, Villani, Alberto, Renieri, Alessandra, Corsello, Giovanni, Agostiniani R, Staiano A, Del Vecchio A, Banderali G, Peroni D, Piazzolla R, Turra R, Bozzola E, Vecchio D, Rosati GV, Macrì F, Romagnoli C, De Curtis M, Orfeo L, Mangili G, Mosca F, Fanos V, Paolillo P, Raimondi F, Rizzo A, Chirico G, Corvaglia LT, Cacace C, Poggiani C, Zuppa AA, Pisano D, Melis D, Giuffrè M, Carbone MT, Macchiaiolo M, Tarani L, Selicorni A, Andria G, Coviello D, Gentile M, Ghiorzo P, Novelli A, Ragusa A, Scarano G, Giardino D.
المصدر: Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-8 (2017)مصطلحات موضوعية: 0301 basic medicine, Male, Neonatal intensive care unit, Disease, Review, 030105 genetics & heredity, Pediatrics, Whole Exome Sequencing, Neonate, Neonatal, Outcome Assessment, Health Care, Diagnosis, Policy Making, Exome sequencing, Sanger sequencing, Genome, lcsh:RJ1-570, Perinatology and Child Health, Settore MED/38, Intensive Care Units, Italy, Whole-exome sequencing, Practice Guidelines as Topic, symbols, WES, Female, Human, Diagnosi, NICU, medicine.medical_specialty, Mendelian, 03 medical and health sciences, symbols.namesake, Outcome Assessment (Health Care), Neonatal Screening, Genetic, Intensive Care Units, Neonatal, Exome Sequencing, medicine, WGS, Pediatrics, Perinatology and Child Health, Humans, Genetic Testing, Intensive care medicine, Settore MED/06 - ONCOLOGIA MEDICA, Genetic heterogeneity, Critically ill, business.industry, Genome, Human, Infant, Newborn, Infant, lcsh:Pediatrics, Newborn, Infant newborn, 030104 developmental biology, Differential diagnosis, business
وصف الملف: ELETTRONICO
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3f5bb4c34c3e2ab8530519642fcb0dfTest
http://hdl.handle.net/10447/393781Test -
8
المؤلفون: Taylor, N.J., Handorf, E.A., Mitra, N., Avril, M.F., Azizi, E., Bergman, W., Bianchi-Scarra, G., Bishop, D.T., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L.A., Cuellar, F., Cust, A.E., Demenais, F., Elder, D.E., Friedman, E., Gerdes, A.M., Ghiorzo, P., Goldstein, A.M., Grazziotin, T.C., Hansson, J., Hayward, N.K., Hocevar, M., Hoiom, V., Holland, E.A., Ingvar, C., Landi, M.T., Landman, G., Larre-Borges, A., Leachman, S.A., Mann, G.J., Nagore, E., Olsson, H., Palmer, J., Peric, B., Pjanova, D., Puig, S., Schmid, H., Stoep, N. van der, Tucker, M.A., Wadt, K.A.W., Whitaker, L., Yang, X.H.R., Bishop, J.A.N., Gruis, N.A., Kanetsky, P.A., GenoMEL Consortium
المصدر: Journal of Investigative Dermatology, 136(5), 1066-1069
مصطلحات موضوعية: Oncology, Adult, Male, CDKN2A Mutation, medicine.medical_specialty, Skin Neoplasms, Databases, Factual, Dermatology, Bioinformatics, Biochemistry, Risk Assessment, Article, Cohort Studies, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Molecular Biology, 2708, Cell Biology, CDKN2A, Internal medicine, medicine, Cyclin-Dependent Kinase Inhibitor p18, Humans, Genetic Predisposition to Disease, Melanoma, Cyclin-Dependent Kinase Inhibitor p16, Aged, business.industry, Incidence, Biopsy, Needle, Middle Aged, medicine.disease, Prognosis, Phenotype, Immunohistochemistry, Pedigree, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Mutation, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97c3aa949b208844356c914f8333ed9Test
https://hdl.handle.net/1887/112521Test -
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المؤلفون: Bruno, W., Ghiorzo, P., Battistuzzi, L., Ascierto, P. A., Barile, M., Gargiulo, S., Gensini, Francesca, Gliori, S., Guida, M., Lombardo, M., Manoukian, S., Menin, C., Nasti, S., Origone, P., Pasini, B., Pastorino, . L., Peissel, B., Pizzichetta, M. A., Queirolo, P., Rodolfo, M., Romanini, A., Scaini, M. C., Testori, A., Tibiletti, M. G., Turchetti, D., Leachman, S. A., Bianchi Scarrà, G., Imi, Italian Melanoma Intergroup
المساهمون: Bruno, W, Ghiorzo, P, Battistuzzi, L, Ascierto, Pa, Barile, M, Gargiulo, S, Gensini, F, Gliori, S, Guida, M, Lombardo, M, Manoukian, S, Menin, C, Nasti, S, Origone, P, Pasini, B, Pastorino, L, Peissel, B, Pizzichetta, Ma, Queirolo, P, Rodolfo, M, Romanini, A, Scaini, Mc, Testori, A, Tibiletti, Mg, Turchetti, D, Leachman, Sa, Scarra, Gb, Bruno W., Ghiorzo P., Battistuzzi L., Ascierto P.A., Barile M., Gargiulo S., Gensini F., Gliori S., Guida M., Lombardo M., Manoukian S., Menin C., Nasti S., Origone P. Pasini B., Pastorino L., Peissel B., Pizzichetta M.A., Queirolo P., Rodolfo M., Romanini A., Scaini M.C., Testori A., Tibiletti M.G., Turchetti D., Leachman S.A., Bianchi Scarrà G., IMI, Italian Melanoma Intergroup.
مصطلحات موضوعية: Skin Neoplasms, cyclin-dependent kinase 4, cyclin-dependent kinase inhibitor 2A, familial melanoma, genetic testing, GENETIC COUNSELING, Genetic counseling, Dermatology, Neoplasms, Multiple Primary, CDKN2A, Gene Frequency, medicine, melanoma, Humans, Point Mutation, Hereditary Melanoma, Allele frequency, Cyclin-Dependent Kinase Inhibitor p16, Genetic testing, Family Health, Genetics, medicine.diagnostic_test, business.industry, Melanoma, medicine.disease, Human genetics, Italy, Mutation (genetic algorithm), business
وصف الملف: STAMPA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000ab7bd7179be8a5f9a95c98ff6a5b0Test
http://hdl.handle.net/11567/274207Test -
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المؤلفون: Zebary, A., Omholt, K., Doorn, R. van, Ghiorzo, P., Harbst, K., Johansson, C.H., Hoiom, V., Jonsson, G., Pjanova, D., Puig, S., Scarra, G.B., Harland, M., Olsson, H., Brage, S.E., Palmer, J., Kanter-Lewensohn, L., Vassilaki, I., Hayward, N.K., Newton-Bishop, J., Gruis, N.A., Hansson, J., Melanoma Genetics Consortium GenoM
المصدر: Journal of Investigative Dermatology
Journal of Investigative Dermatology, 134(1), 287-290مصطلحات موضوعية: Adult, Male, Proto-Oncogene Proteins B-raf, Neuroblastoma RAS viral oncogene homolog, Skin Neoplasms, Adolescent, Somatic cell, Dermatology, Biochemistry, Germline, GTP Phosphohydrolases, Young Adult, Germline mutation, CDKN2A, Humans, Medicine, Young adult, Melanoma, Molecular Biology, Cyclin-Dependent Kinase Inhibitor p16, Germ-Line Mutation, Aged, Aged, 80 and over, business.industry, Membrane Proteins, Cell Biology, Middle Aged, Cancer research, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e138464d40dad058a05ba18766d1dd3Test
https://hdl.handle.net/1887/103912Test