المؤلفون: Bancroft, E. K., Page, E. C., Brook, M. N., Thomas, S., Taylor, N., Pope, J., McHugh, J., Jones, A. B., Karlsson, Q., Merson, S., Ong, K. R., Hoffman, J., Huber, C., Maehle, L., Grindedal, E. M., Stormorken, A., Evans, D. G., Rothwell, J., Lalloo, F., Brady, A. F., Bartlett, M., Snape, K., Hanson, H., James, P., McKinley, J., Mascarenhas, L., Syngal, S., Ukaegbu, C., Side, L., Thomas, T., Barwell, J., Teixeira, M. R., Izatt, L., Suri, M., Macrae, F. A., Poplawski, N., Chen-Shtoyerman, R., Ahmed, M., Musgrave, H., Nicolai, N., Greenhalgh, L., Brewer, C., Pachter, N., Spigelman, A. D., Azzabi, A., Helfand, B. T., Halliday, D., Buys, S., Ramon, Y. Cajal T., Donaldson, A., Cooney, K. A., Harris, M., McGrath, J., Davidson, R., Taylor, A., Cooke, P., Myhill, K., Hogben, M., Aaronson, N. K., Ardern-Jones, A., Bangma, C. H., Castro, E., Dearnaley, D., Dias, A., Dudderidge, T., Eccles, D. M., Green, K., Eyfjord, J., Falconer, A., Foster, C. S., Gronberg, H., Hamdy, F. C., Johannsson, O., Khoo, V., Lilja, H., Lindeman, G. J., Lubinski, J., Axcrona, K., Mikropoulos, C., Mitra, A. V., Moynihan, C., Ni Raghallaigh, H., Rennert, G., Collier, R., Offman, J., Kote-Jarai, Z., Eeles, R. A.

مصطلحات موضوعية: Adult, Aged, Biomarkers, Tumor/blood, DNA Mismatch Repair/*genetics, DNA-Binding Proteins/genetics, Early Detection of Cancer, Germ-Line Mutation, Heterozygote, Humans, Incidence, Male, Middle Aged, MutS Homolog 2 Protein/genetics, Prospective Studies, Prostate-Specific Antigen/blood, Prostatic Neoplasms/*diagnosis/epidemiology/genetics

العلاقة: https://linkinghub.elsevier.com/retrieve/pii/S1470-2045Test(21)00522-2; Lancet Oncol. 2021 Nov;22(11):1618-1631. doi:10.1016/S1470-2045(21)00522-2. Epub 2021 Oct 19.; https://rde.dspace-express.com/handle/11287/622259Test; The Lancet. Oncology; PMC8576477 patent for a statistical method to detect prostate cancer licensed to Arctic Partners and commercialised by OPKO Health, and has stock in Arctic Partners and OPKO Health and receives royalties from sales of the 4Kscore test. RAE has received speaker honoraria from Genitourinary-American Society of Clinical Oncology, The University of Chicago, European Society for Medical Oncology (paid by Bayer and Ipsen), and The Royal Marsden NHS Foundation Trust (with support from Janssen), and is a member of the AstraZeneca UK Limited Prostate Dx Advisory Panel external expert committee. No organisation had any role in the decision to publish or in the writing of the manuscript. All other authors declare no competing interests.

الإتاحة: https://doi.org/10.1016/s1470-2045Test(21)00522-2
https://doi.org/10.1016/S1470-2045Test(21)00522-2
https://rde.dspace-express.com/handle/11287/622259Test

المؤلفون: Williams, F. M., Carter, A. M., Hysi, P. G., Surdulescu, G., Hodgkiss, D., Soranzo, N., Traylor, M., Bevan, S., Dichgans, M., Rothwell, P. M., Sudlow, C., Farrall, M., Silander, K., Kaunisto, M., Wagner, P., Saarela, O., Kuulasmaa, K., Virtamo, J., Salomaa, V., Amouyel, P., Arveiler, D., Ferrieres, J., Wiklund, P. G., Ikram, M. A., Hofman, A., Boncoraglio, G. B., Parati, E. A., Helgadottir, A., Gretarsdottir, S., Thorsteinsdottir, U., Thorleifsson, G., Stefansson, K., Seshadri, S., DeStefano, A., Gschwendtner, A., Psaty, B., Longstreth, W., Mitchell, B. D., Cheng, Y. C., Clarke, R., Bis, J. C., Levi, C., Attia, J., Holliday, E. G., Scott, R. J., Fornage, M., Sharma, P., Furie, K. L., Rosand, J., Nalls, M., Meschia, J., Mosely, T. H., Evans, A., Palotie, A., Markus, H. S., Grant, P. J., Spector, T. D., EuroCLOT Investigators, Wellcome Trust Case Control Consortium 2, MOnica Risk, Genetics, Archiving, Monograph, MetaStroke, International Stroke Genetics Consortium, FERRARIO, MARCO MARIO ANGELO

المساهمون: Williams, F. M., Carter, A. M., Hysi, P. G., Surdulescu, G., Hodgkiss, D., Soranzo, N., Traylor, M., Bevan, S., Dichgans, M., Rothwell, P. M., Sudlow, C., Farrall, M., Silander, K., Kaunisto, M., Wagner, P., Saarela, O., Kuulasmaa, K., Virtamo, J., Salomaa, V., Amouyel, P., Arveiler, D., Ferrieres, J., Wiklund, P. G., Ikram, M. A., Hofman, A., Boncoraglio, G. B., Parati, E. A., Helgadottir, A., Gretarsdottir, S., Thorsteinsdottir, U., Thorleifsson, G., Stefansson, K., Seshadri, S., Destefano, A., Gschwendtner, A., Psaty, B., Longstreth, W., Mitchell, B. D., Cheng, Y. C., Clarke, R., Ferrario, MARCO MARIO ANGELO, Bis, J. C., Levi, C., Attia, J., Holliday, E. G., Scott, R. J., Fornage, M., Sharma, P., Furie, K. L., Rosand, J., Nalls, M., Meschia, J., Mosely, T. H., Evans, A., Palotie, A., Markus, H. S., Grant, P. J., Spector, T. D., Euroclot, Investigator, Wellcome Trust Case Control Consortium, 2, Monica, Risk, Genetics, Archiving, Monograph, Metastroke, International Stroke Genetics, Consortium

مصطلحات موضوعية: ABO Blood-Group System, genetics, Adolescent, Adult, Aged, 80 and over, Blood Coagulation, Brain Ischemia, diagnosis/epidemiology/genetics, Cohort Studies, Europe, epidemiology, Female, Genetic Loci, Genetic Predisposition to Disease, epidemiology/genetics, Genetic Variation, Genome-Wide Association Study, methods, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide, Stroke, Young Adult

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23381943; info:eu-repo/semantics/altIdentifier/wos/WOS:000314660800007; volume:73; issue:1; firstpage:16; lastpage:31; numberofpages:16; journal:ANNALS OF NEUROLOGY; http://hdl.handle.net/11383/1850158Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84875299446; http://dx.doi.org/10.1002/ana.23838Test

الإتاحة: https://doi.org/10.1002/ana.23838Test
http://hdl.handle.net/11383/1850158Test

المؤلفون: Dario Gregori, Giulia Barbati, Michele Moretti, Bruno Pinamonti, Francesca Brun, Andrea Di Lenarda, Marco Merlo, Gianfranco Sinagra, Luisa Mestroni

المساهمون: Moretti, M, Merlo, M, Barbati, Giulia, Di Lenarda, A, Brun, F, Pinamonti, B, Gregori, D, Mestroni, L, Sinagra, Gianfranco

المصدر: European Journal of Heart Failure. 12:922-927

مصطلحات موضوعية: trends, Adult, Cardiomyopathy, Dilated, Male, Proband, medicine.medical_specialty, Cardiomyopathy, diagnosis/epidemiology/genetics, Early Diagnosis, Family, Female, Follow-Up Studies, Humans, Italy, Disease, Adult, Cardiomyopathy, Dilated, epidemiology, Male, Mass Screening, methods, Middle Aged, Prevalence, Prognosis, Retrospective Studies, Survival Rate, familial screening, methods, Internal medicine, Prevalence, medicine, Humans, Mass Screening, Family, cardiovascular diseases, Stage (cooking), Retrospective Studies, Ejection fraction, business.industry, diagnosis/epidemiology/genetics, Retrospective cohort study, Dilated cardiomyopathy, Middle Aged, Prognosis, medicine.disease, Surgery, Survival Rate, trend, Early Diagnosis, Italy, Heart failure, epidemiology, Female, Cardiology and Cardiovascular Medicine, business, Follow-Up Studies

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef069ec778e4bd955994d51ae0f6c8b3Test
https://doi.org/10.1093/eurjhf/hfq093Test

المؤلفون: Jensen, R. T., Rindi, G., Arnold, R., Lopes, J. M., Brandi, M. L., Bechstein, W. O., Christ, E., Taal, B. G., Knigge, U., Ahlman, Håkan, 1947, Kwekkeboom, D. J., O'Toole, D.

المصدر: Neuroendocrinology. 84(3):165-72

مصطلحات موضوعية: MEDICAL AND HEALTH SCIENCES, MEDICIN OCH HÄLSOVETENSKAP, Carcinoma/*diagnosis/epidemiology/genetics/*therapy, Duodenal Neoplasms/*diagnosis/epidemiology/genetics/*therapy, Humans

الوصول الحر: https://gup.ub.gu.se/publication/46434Test

المؤلفون: Jonathan Rosand, Matthew Traylor, Sudha Seshadri, Veikko Salomaa, Robert Clarke, Anita L. DeStefano, Rodney J. Scott, Steve Bevan, Braxton D. Mitchell, Alun Evans, Philippe Amouyel, Myriam Fornage, Hugh S. Markus, Olli Saarela, Peter Wagner, Dylan Hodgkiss, Angela M. Carter, Giorgio B. Boncoraglio, Catherine Sudlow, K. L. Furie, Will Longstreth, Nicole Soranzo, Peter M. Rothwell, Jean Ferrières, John Attia, Bruce M. Psaty, Martin Dichgans, Christopher Levi, M. Arfan Ikram, Jarmo Virtamo, Gudmar Thorleifsson, Frances M K Williams, Pankaj Sharma, Martin Farrall, Kari Kuulasmaa, Per-Gunnar Wiklund, Elizabeth G. Holliday, James F. Meschia, Anna Helgadottir, Unnur Thorsteinsdottir, Michael A. Nalls, Peter J. Grant, Marco M Ferrario, Dominique Arveiler, Tim D. Spector, Andreas Gschwendtner, Eugenio Parati, Mari A. Kaunisto, Gabriela L. Surdulescu, Joshua C. Bis, Solveig Gretarsdottir, Kaisa Silander, Kari Stefansson, Thomas H. Mosely, Albert Hofman, Pirro G. Hysi, Yu-Ching Cheng, Aarno Palotie

المساهمون: Radiology & Nuclear Medicine, Epidemiology

المصدر: Annals of Neurology; Vol 73
Annals of Neurology
Williams, F M K, Carter, A M, Hysi, P G, Surdulescu, G, Hodgkiss, D, Soranzo, N, Traylor, M, Bevan, S, Dichgans, M, Rothwell, P M W, Sudlow, C, Farrall, M, Silander, K, Kaunisto, M, Wagner, P, Saarela, O, Kuulasmaa, K, Virtamo, J, Salomaa, V, Amouyel, P, Arveiler, D, Ferrieres, J, Wiklund, P, Arfan Ikram, M, Hofman, A, Boncoraglio, G B, Parati, E A, Helgadottir, A, Gretarsdottir, S, Thorsteinsdottir, U, Thorleifsson, G, Stefansson, K, Seshadri, S, Destefano, A, Gschwendtner, A, Psaty, B, Longstreth, W, Mitchell, B D, Cheng, Y, Clarke, R, Ferrario, M, Bis, J C, Levi, C, Attia, J, Holliday, E G, Scott, R J, Fornage, M, Sharma, P, Furie, K L, Rosand, J, Nalls, M, Meschia, J, Mosely, T H, Evans, A, Palotie, A, Markus, H S, Grant, P J & Spector, T D 2013, ' Ischemic stroke is associated with the ABO locus: the EuroCLOT study. ', Annals of Neurology, vol. 73, no. 1, pp. 16-31 . https://doi.org/10.1002/ana.23838Test
Annals of Neurology, 73(1), 16-31. John Wiley & Sons Inc.

مصطلحات موضوعية: Male, Neurology, Genome-wide association study, 030204 cardiovascular system & hematology, Bioinformatics, Brain Ischemia, Brain ischemia, Coronary artery disease, Pathogenesis, Cohort Studies, 0302 clinical medicine, 80 and over, genetics, Genetics, Aged, 80 and over, biology, Atrial fibrillation, Single Nucleotide, Middle Aged, 3. Good health, Europe, Stroke, epidemiology, Female, Rapid Communication, Adult, medicine.medical_specialty, Adolescent, Polymorphism, Single Nucleotide, Fibrin, methods, ABO Blood-Group System, 03 medical and health sciences, Young Adult, ABO blood group system, medicine, Humans, Genetic Predisposition to Disease, Polymorphism, Blood Coagulation, Aged, epidemiology/genetics, diagnosis/epidemiology/genetics, genetics, Adolescent, Adult, Aged, Aged, 80 and over, Blood Coagulation, genetics, Brain Ischemia, diagnosis/epidemiology/genetics, Cohort Studies, Europe, epidemiology, Female, Genetic Loci, genetics, Genetic Predisposition to Disease, epidemiology/genetics, Genetic Variation, genetics, Genome-Wide Association Study, methods, Humans, Male, Middle Aged, Polymorphism, genetics, Stroke, diagnosis/epidemiology/genetics, Young Adult, Genetic Variation, medicine.disease, Genetic Loci, biology.protein, Neurology (clinical), 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6608414d9f9f00d9c383049e49fd4018Test
http://ora.ox.ac.uk/objects/uuid:273d54ad-f9b4-4bdc-bca6-7667a92c622dTest

المؤلفون: Olsson, Louise, Lööf, Lars, Ekbom, A

المصدر: Scand J Gastroenterol. 39(2):158-63

مصطلحات موضوعية: Barium Sulfate/diagnostic use, Colonoscopy, Colorectal Neoplasms/*diagnosis/epidemiology/genetics, Diagnosis, Differential, Enema, Humans, Medical History Taking, Occult Blood, Primary Health Care, Risk Assessment, Sweden/epidemiology

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-72796Test
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=15000278&dopt=CitationTest

المؤلفون: Maura Pugliatti, Carlo Casali, Roberto Di Fabio, Eugenia Storti, Alessandra Tessa, Virgilio Agnetti, Filippo M. Santorelli, Loretta Racis

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Pathology, age factors, Spastin, spastic paraplegia, Hereditary spastic paraplegia, disability evaluation, Population, prevalence, Neurological examination, sardinia, Autosomal dominant transmission, community health planning, NO, male, Epidemiology, middle aged, italy, medicine, genetics, Genetic variability, hereditary spastic paraplegia, education, humans, education.field_of_study, High prevalence, medicine.diagnostic_test, Spastic Paraplegia, Hereditary, business.industry, adult, diagnosis/epidemiology/genetics, Adenosine Triphosphatases, Adult, Age Factors, Aged, Community Health Planning, DNA Mutational Analysis, Disability Evaluation, Female, Humans, Italy, Male, Middle Aged, Mutation, Prevalence, Retrospective Studies, Young Adult, Mean age, adenosine triphosphatases, medicine.disease, aged, retrospective studies, female, Neurology, mutation, epidemiology, young adult, dna mutational analysis, hereditary, Neurology (clinical), business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0b3a20c75b9851531fe2c2030e5db8Test
http://hdl.handle.net/11573/678254Test

المؤلفون: Pasquale Striano, Francesca Madia, Salvatore Striano, Federico Zara, Carlo Minetti

المساهمون: Striano, P, Madia, F, Minetti, C, Striano, Salvatore, Zara, F.

مصطلحات موضوعية: Male, Myoclonus, Somatosensory, Epilepsies, Myoclonic, Neurological disorder, Comorbidity, Audiology, Epilepsies, Epilepsy, genetics, Child, Evoked Potentials, Adolescent, Adult, Child, Chromosome Mapping, Chromosomes, Human, Pair 2, genetics, Comorbidity, Electroencephalography, statistics /&/ numerical data, Electrophysiology, statistics /&/ numerical data, Epilepsies, Myoclonic, diagnosis/epidemiology/ethnology/genetics, Essential Tremor, diagnosis/ethnology/genetics, European Continental Ancestry Group, genetics, Evoked Potentials, Somatosensory, Female, Follow-Up Studies, Genetic Markers, Haplotypes, genetics, Humans, Italy, ethnology, Lod Score, Male, Middle Aged, Myoclonus, diagnosis/epidemiology/genetics, Pedigree, Syndrome, Chromosome Mapping, Electroencephalography, Syndrome, Middle Aged, Pathophysiology, statistics /&/ numerical data, Pedigree, Electrophysiology, diagnosis/ethnology/genetics, Neurology, Italy, Chromosomes, Human, Pair 2, Female, medicine.symptom, Psychology, Adult, Genetic Markers, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Adolescent, Essential Tremor, European Continental Ancestry Group, White People, Chromosomes, Central nervous system disease, Genetic linkage, Evoked Potentials, Somatosensory, Hand tremor, medicine, Humans, ethnology, diagnosis/epidemiology/genetics, medicine.disease, diagnosis/epidemiology/ethnology/genetics, nervous system diseases, Haplotypes, Long loop reflex, Neurology (clinical), Lod Score, Neuroscience, Follow-Up Studies

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e709dc73e3385bf9ba8575192a25b807Test
http://hdl.handle.net/11567/314998Test

المؤلفون: Moretti M, Merlo M, BARBATI, GIULIA, Di Lenarda A, Brun F, Pinamonti B, Gregori D, Mestroni L, SINAGRA, GIANFRANCO

المساهمون: Moretti, M, Merlo, M, Barbati, Giulia, Di Lenarda, A, Brun, F, Pinamonti, B, Gregori, D, Mestroni, L, Sinagra, Gianfranco

مصطلحات موضوعية: Adult, Cardiomyopathy, Dilated, diagnosis/epidemiology/genetics, Early Diagnosis, Family, Female, Follow-Up Studies, Humans, Italy, epidemiology, Male, Mass Screening, methods, Middle Aged, Prevalence, Prognosis, Retrospective Studies, Survival Rate, trend, familial screening

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/20525703; info:eu-repo/semantics/altIdentifier/wos/WOS:000282473600006; volume:12; firstpage:922; lastpage:927; numberofpages:6; journal:EUROPEAN JOURNAL OF HEART FAILURE; http://hdl.handle.net/11368/2440331Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-77955952904; http://dx.doi.org/10.1093/eurjhf/hfq093Test

الإتاحة: https://doi.org/10.1093/eurjhf/hfq093Test
http://hdl.handle.net/11368/2440331Test

المؤلفون: A, Bossi, F, Battistini, C, Braggion, E C, Magno, A, Cosimi, G, de Candussio, R, Gagliardini, L, Giglio, A, Giunta, G L, Grzincich, M, La Rosa, M, Lombardo, V, Lucidi, A, Manca, G, Mastella, P, Moretti, R, Padoan, F, Pardo, S, Quattrucci, V, Raia, L, Romano, D, Salvatore, G, Taccetti, M, Zanda

المساهمون: Bossi, F., Battistini, C., Braggion, Ec, Magno, A., Cosimi, G., Candusso, R., Gagliardini, L., Giglio, A., Giunta, Grzincich, G. L., M., La Rosa, M., Lombardo, V., Lucidi, A., Manca, G., Mastella, P., Moretti, R., Padoan, F., Pardo, Raia, Valeria, L., Romano, D., Salvatore, G., Taccetti, M. Zanda, .

مصطلحات موضوعية: Adult, Male, Time Factors, Adolescent, Cystic Fibrosis, diagnosis/epidemiology/genetics, Infant, Newborn, Age Distribution, Age of Onset, Child, Preschool, Female, Humans, Infant, Newborn, Italy, epidemiology, Registries, Child, Preschool

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a390a568bea963267fa7fd72fe6e43bbTest
http://hdl.handle.net/11573/417578Test