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1Academic Journal
المؤلفون: Skelly, A, Taylor, N, Fasser, C, Malkowski, JP, Goswami, P, Downey, L
المصدر: Value in Health ; volume 25, issue 1, page S235-S236 ; ISSN 1098-3015
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2Academic Journal
المؤلفون: Petzold A., Albrecht P., Balcer L., Bekkers E., Brandt A. U., Calabresi P. A., Deborah O. G., Graves J. S., Green A., Keane P. A., Nij Bijvank J. A., Sander J. W., Paul F., Saidha S., Villoslada P., Wagner S. K., Yeh E. A., Aktas O., Antel J., Asgari N., Audo I., Avasarala J., Avril D., Bagnato F. R., Banwell B., Bar-Or A., Behbehani R., Manterola A. B., Bennett J., Benson L., Bernard J., Bremond-Gignac D., Britze J., Burton J., Calkwood J., Carroll W., Chandratheva A., Cohen J., Comi G., Cordano C., Costa S., Costello F., Courtney A., Cruz-Herranz A., Cutter G., Crabb D., Delott L., De Seze J., Diem R., Dollfuss H., El Ayoubi N. K., Fasser C., Finke C., Fischer D., Fitzgerald K., Fonseca P., Frederiksen J. L., Frohman E., Frohman T., Fujihara K., Cuellar I. G., Galetta S., Garcia-Martin E., Giovannoni G., Glebauskiene B., Suarez I. G., Jensen, G. P., Hamann S., Hartung H. -P., Havla J., Hemmer B., Huang S. -C., Imitola J., Jasinskas V., Jiang H., Kafieh R., Kappos L., Kardon R., Keegan D., Kildebeck E., Kim U. S., Klistorner S., Knier B., Kolbe S., Korn T., Krupp L., Lagreze W., Leocani L., Levin N., Liskova P., Preiningerova J. L., Lorenz B., May E., Miller D., Mikolajczak J., Said S. M., Montalban X., Morrow M., Mowry E., Murta J., Navas C., Nolan R., Nowomiejska K., Oertel F. C., Oh J., Oreja-Guevara C., Orssaud C., Osborne B., Outteryck O., Paiva C., Palace J., Papadopoulou A., Patsopoulos N., Pontikos N., Preising M., Prince J., Reich D., Rejdak R., Ringelstein M., Rodriguez de Antonio L., Sahel J. -A., Sanchez-Dalmau B., Sastre-Garriga J., Schippling S., Schuman J., Shindler K., Shin R., Shuey N., Soelberg K., Specovius S., Suppiej A., Thompson A., Toosy A., Torres R., Touitou V., Trauzettel-Klosinski S., van der Walt A., Vermersch P., Vidal-Jordana A., Waldman A. T., Waters C., Wheeler R., White O., Wilhelm H., Winges K. M., Wiegerinck N., Wiehe L., Wisnewski T., Wong S., Wurfel J., Yaghi S., You Y., Yu Z., Yu-Wai-Man P., Zemaitien≐ R., Zimmermann H.
المساهمون: Petzold, A., Albrecht, P., Balcer, L., Bekkers, E., Brandt, A. U., Calabresi, P. A., Deborah, O. G., Graves, J. S., Green, A., Keane, P. A., Nij Bijvank, J. A., Sander, J. W., Paul, F., Saidha, S., Villoslada, P., Wagner, S. K., Yeh, E. A., Aktas, O., Antel, J., Asgari, N., Audo, I., Avasarala, J., Avril, D., Bagnato, F. R., Banwell, B., Bar-Or, A., Behbehani, R., Manterola, A. B., Bennett, J., Benson, L., Bernard, J., Bremond-Gignac, D., Britze, J., Burton, J., Calkwood, J., Carroll, W., Chandratheva, A., Cohen, J., Comi, G., Cordano, C., Costa, S., Costello, F., Courtney, A., Cruz-Herranz, A., Cutter, G., Crabb, D., Delott, L., De Seze, J., Diem, R., Dollfuss, H., El Ayoubi, N. K., Fasser, C., Finke, C., Fischer, D., Fitzgerald, K., Fonseca, P., Frederiksen, J. L., Frohman, E., Frohman, T., Fujihara, K., Cuellar, I. G., Galetta, S., Garcia-Martin, E., Giovannoni, G., Glebauskiene, B., Suarez, I. G., Jensen, G. P., Hamann, S., Hartung, H. -P., Havla, J., Hemmer, B., Huang, S. -C., Imitola, J., Jasinskas, V., Jiang, H., Kafieh, R., Kappos, L., Kardon, R., Keegan, D., Kildebeck, E., Kim, U. S., Klistorner, S., Knier, B., Kolbe, S., Korn, T., Krupp, L., Lagreze, W., Leocani, L., Levin, N., Liskova, P., Preiningerova, J. L., Lorenz, B., May, E., Miller, D., Mikolajczak, J., Said, S. M., Montalban, X., Morrow, M., Mowry, E., Murta, J.
مصطلحات موضوعية: Artificial Intelligence, Big Data, Cohort Studie, Human, Nervous System Disease, Retina, Tomography, Optical Coherence, Algorithms
وصف الملف: STAMPA
Relation: info:eu-repo/semantics/altIdentifier/pmid/34008926; info:eu-repo/semantics/altIdentifier/wos/WOS:000651823300001; volume:8; issue:7; firstpage:1528; lastpage:1542; numberofpages:15; journal:ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY; http://hdl.handle.net/11392/2488769
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3Academic Journal
المؤلفون: Sergouniotis, Panagiotis I., Maxime, Emmanuel, Leroux, Dorothée, Olry, Annie, Thompson, Rachel, Rath, Ana, Robinson, Peter N., Dollfus, HélèneAshworth JL, Audo I, Balciuniene VJ, Banin E, Black GC, Böhringer D, Boon CJF, Bremond-Gignac D, Calvas P, Castela G, Dagnelie G, Dollfus H, Downes SM, Fasolo A, Fasser C, Gelzinis A, Goetz K, Hamann S, Héon E, Iarossi G, Kawasaki A, Keegan D, Kessel L, Khan K, Klett A, Köhler S, Leroux D, Leroy BP, Lisch W, Liskova P, Lorenz B, Maggi R, Maxime E, Meunier I, Mohand-Said S, Nowomiejska K, Perdomo Y, Petzold A, Preising M, Robinson PN, Scholl HPN, Sergouniotis PI, Sodi A, Stingl K, Studer F, Suppiej A, Thompson R, Touitou V, Traboulsi E, Trumpaitis J, Tuft SJ, Vaclavik V, Valeina S, Van Cauwenbergh C, Verloes A, Vighetto A, Wheeler R, Wheeler-Schilling T, Yu-Wai-Man P, Zobor D, Zrenner E.
المساهمون: Sergouniotis, Panagiotis I., Maxime, Emmanuel, Leroux, Dorothée, Olry, Annie, Thompson, Rachel, Rath, Ana, Robinson, Peter N., Dollfus, Hélèneashworth, Jl, Audo, I, Balciuniene, Vj, Banin, E, Black, Gc, Böhringer, D, Boon, Cjf, Bremond-Gignac, D, Calvas, P, Castela, G, Dagnelie, G, Dollfus, H, Downes, Sm, Fasolo, A, Fasser, C, Gelzinis, A, Goetz, K, Hamann, S, Héon, E, Iarossi, G, Kawasaki, A, Keegan, D, Kessel, L, Khan, K, Klett, A, Köhler, S, Leroux, D, Leroy, Bp, Lisch, W, Liskova, P, Lorenz, B, Maggi, R, Maxime, E, Meunier, I, Mohand-Said, S, Nowomiejska, K, Perdomo, Y, Petzold, A, Preising, M, Robinson, Pn, Scholl, Hpn, Sergouniotis, Pi, Sodi, A, Stingl, K, Studer, F, Suppiej, A, Thompson, R, Touitou, V, Traboulsi, E, Trumpaitis, J, Tuft, Sj, Vaclavik, V, Valeina, S, Van Cauwenbergh, C, Verloes, A, Vighetto, A, Wheeler, R, Wheeler-Schilling, T, Yu-Wai-Man, P, Zobor, D, Zrenner, E.
مصطلحات موضوعية: Evidence-based precision medicine, Rare eye disease, Human phenotype ontology, Orphanet rare disease ontology
وصف الملف: STAMPA
Relation: info:eu-repo/semantics/altIdentifier/pmid/30626441; info:eu-repo/semantics/altIdentifier/wos/WOS:000455361900003; volume:14; issue:1; firstpage:8-1; lastpage:8-5; numberofpages:5; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/11392/2400086; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85059797765; https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0980-6
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4Academic Journal
المؤلفون: Sergouniotis, PI, Maxime, E, Leroux, D, Olry, A, Thompson, R, Rath, A, Robinson, PN, Dollfus, H, Ashworth, JL, Audo, I, Balciuniene, VJ, Banin, E, Black, GC, Boehringer, D, Boon, CJF, Bremond-Gignac, D, Calvas, P, Castela, G, Dagnelie, G, Downes, SM, Fasolo, A, Fasser, C, Gelzinis, A, Goetz, K, Hamann, S, Heon, E, Iarossi, G, Kawasaki, A, Keegan, D, Kessel, L, Khan, K, Klett, A, Koehler, S, Leroy, BP, Lisch, W, Liskova, P, Lorenz, B, Maggi, R, Meunier, I, Mohand-Said, S, Nowomiejska, K, Perdomo, Y, Petzold, A, Preising, M, Scholl, HPN, Sodi, A, Stingl, K, Studer, F, Suppiej, A, Touitou, V, Traboulsi, E, Trumpaitis, J, Tuft, SJ, Vaclavik, V, Valeina, S, Van Cauwenbergh, C, Verloes, A, Vighetto, A, Wheeler, R, Wheeler-Schilling, T, Yu-Wai-Man, P, Zobor, D, Zrenner, E
المصدر: Orphanet Journal of Rare Diseases , 14 , Article 8. (2019)
مصطلحات موضوعية: Evidence-based precision medicine, Rare eye disease, Human phenotype ontology, Orphanet rare disease ontology
وصف الملف: text
Relation: https://discovery.ucl.ac.uk/id/eprint/10085217/1/An%20ontological%20foundation%20for%20ocular%20phenotypes%20and%20rare%20eye%20diseases.pdf; https://discovery.ucl.ac.uk/id/eprint/10085217/
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5Academic Journal
المؤلفون: Varma, D, Hutcheson, R, Fasser, C, Regnier, SA, Karcher, H, Finger, RP
المصدر: Value in Health ; volume 20, issue 9, page A807-A808 ; ISSN 1098-3015
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6
المؤلفون: Black G. C., Sergouniotis P., Sodi A., Leroy B. P., Van Cauwenbergh C., Liskova P., Gronskov K., Klett A., Kohl S., Taurina G., Sukys M., Haer-Wigman L., Nowomiejska K., Marques J. P., Leroux D., Cremers F. P. M., De Baere E., Dollfus H., Ashworth J., Audo I., Bacci G., Balciuniene V. J., Bargiacchi S., Bertelsen M., Black G., Boon C., Bremond-Gignac D., Buzzonetti L., Calvas P., Thomsen A. C., Chirita-Emandi A., Chokoshvili D., Cremers F., Daly A., Downes S., Fasolo A., Fasser C., Fischer D., Fortunato P., Gelzinis A., Hall G., Hamann S., Heon E., Iarossi G., Iberg C., Jouanjan G., Kaariainen H., Kahn K., Keegan D., Laengsfeld M., Leon A., Leroux B., Lorenz B., Maggi R., Mauring L., Melico P., Meunier I., Mohand-Said S., Monterosso C., Morandi P., Parmeggiani F., Passerini I., Pelletier V., Peluso F., Perdomo Y., Rapizzi E., Roos L., Roosing S., Rozet J. -M., Simonelli F., Sowden J., Stingl K., Suppiej A., Testa F., Tracewska A., Traficante G., Valeina S., Wheeler-Schilling T., Yu-Wai-Man P., Zeitz C., Zemaitiene R.
المساهمون: Leroux, Dorothée [0000-0002-1412-6611], Apollo - University of Cambridge Repository, Ophthalmology, ANS - Complex Trait Genetics, Black, G. C., Sergouniotis, P., Sodi, A., Leroy, B. P., Van Cauwenbergh, C., Liskova, P., Gronskov, K., Klett, A., Kohl, S., Taurina, G., Sukys, M., Haer-Wigman, L., Nowomiejska, K., Marques, J. P., Leroux, D., Cremers, F. P. M., De Baere, E., Dollfus, H., Ashworth, J., Audo, I., Bacci, G., Balciuniene, V. J., Bargiacchi, S., Bertelsen, M., Black, G., Boon, C., Bremond-Gignac, D., Buzzonetti, L., Calvas, P., Thomsen, A. C., Chirita-Emandi, A., Chokoshvili, D., Cremers, F., Daly, A., Downes, S., Fasolo, A., Fasser, C., Fischer, D., Fortunato, P., Gelzinis, A., Hall, G., Hamann, S., Heon, E., Iarossi, G., Iberg, C., Jouanjan, G., Kaariainen, H., Kahn, K., Keegan, D., Laengsfeld, M., Leon, A., Leroux, B., Lorenz, B., Maggi, R., Mauring, L., Melico, P., Meunier, I., Mohand-Said, S., Monterosso, C., Morandi, P., Parmeggiani, F., Passerini, I., Pelletier, V., Peluso, F., Perdomo, Y., Rapizzi, E., Roos, L., Roosing, S., Rozet, J. -M., Simonelli, F., Sowden, J., Stingl, K., Suppiej, A., Testa, F., Tracewska, A., Traficante, G., Valeina, S., Wheeler-Schilling, T., Yu-Wai-Man, P., Zeitz, C., Zemaitiene, R.
المصدر: Orphanet journal of rare diseases, 16(1):142. BioMed Central
ORPHANET JOURNAL OF RARE DISEASES
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Orphanet Journal of Rare Diseases, 16
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 16, 1مصطلحات موضوعية: 0301 basic medicine, Eye Diseases, lcsh:Medicine, CHILDREN, Position statement, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], MOLECULAR-GENETICS, 0302 clinical medicine, HISTORY, Health care, Medicine and Health Sciences, Genetics(clinical), Pharmacology (medical), Child, Genetics (clinical), medicine.diagnostic_test, General Medicine, Genomics, Europe, TRIALS, ERN-EYE, Rare eye diseases, medicine.symptom, Genetic and genomic testing, Human, medicine.medical_specialty, Visual impairment, LEBER CONGENITAL AMAUROSIS, Socio-culturale, DIAGNOSIS, 03 medical and health sciences, Rare Diseases, medicine, Humans, Genetic Testing, Intensive care medicine, Genetic testing, business.industry, CLINICAL-FEATURES, lcsh:R, Rare eye disease, Eye Disease, Human genetics, Clinical trial, 030104 developmental biology, Genomic, 030221 ophthalmology & optometry, Personalized medicine, business, Rare disease
وصف الملف: application/pdf
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7Academic Journal
المصدر: Value in Health ; volume 19, issue 7, page A566 ; ISSN 1098-3015
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8
المؤلفون: Leroux, D., Dollfus, H., Ashworth, J., Black, G., Bohringer, D., Boon, C.J., Cremers, F., Daly, A., Fasser, C., Fischer, D., Keegan, D., Khan, K., Larkin, F., Larsen, M., Leroy, B.P., Liskova, P., Lorenz, B., Martinho, C., Mohand-Said, S., Petzold, A., Preising, M., Reinhart, T., Wheeler-Schilling, T., Wong, S., Zrenner, E., All ERN-EYE Members
المصدر: European Journal of Human Genetics, 26, 804-805
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9Academic Journal
المؤلفون: Fasser, C E, Smith, Q W, Luchi, R J
المصدر: Academic Medicine ; volume 67, issue 10, page 696-8 ; ISSN 1040-2446
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10Academic Journal
المؤلفون: Holcomb, J. David, Mullen, Patricia D., Fasser, C. Emil, Smith, Quentin, Martin, Jeanne B., Parks, Linda A., Wente, Susan M.
المصدر: Journal of Allied Health, 1985 Nov 01. 14(4), 373-385.
URL الوصول: https://www.jstor.org/stable/45479632
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11Academic Journal
المصدر: Journal of Allied Health, 1986 Feb 01. 15(1), 23-31.
URL الوصول: https://www.jstor.org/stable/45445109
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12Academic Journal
المؤلفون: Fasser, C., Holcomb, J. D., Johnson, D.
المصدر: Journal of the American Academy of Physician Assistants ; volume 21, issue 6, page 1 ; ISSN 1547-1896
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13Academic Journal
المؤلفون: Turner, K., Fasser, C., Erdman, K.
المصدر: Journal of the American Academy of Physician Assistants ; volume 21, issue 6, page 1 ; ISSN 1547-1896
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14Academic Journal
المؤلفون: Fasser, C., Spence, L., McLaughlin, R., Holcomb, J. D.
المصدر: Journal of the American Academy of Physician Assistants ; volume 21, issue 6, page 1 ; ISSN 1547-1896
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15Academic Journal
المؤلفون: Fasser, C., Spence, L., Middleton, J., Holcomb, J. D.
المصدر: The Journal of Physician Assistant Education ; volume 19, issue 4, page 34 ; ISSN 1941-9430
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16Academic Journal
المؤلفون: Fasser, C., Spence, L., Young, C., McLaughlin, R., Holcomb, J. D.
المصدر: The Journal of Physician Assistant Education ; volume 19, issue 4, page 42-43 ; ISSN 1941-9430
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17Academic Journal
المؤلفون: Blair, L., Insull, W., Fasser, C.
المصدر: Journal of the American Academy of Physician Assistants ; volume 20, issue 7, page 57-58 ; ISSN 1547-1896
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18Academic Journal
المؤلفون: Fasser, C, Bottomley, G, Feins, A, Getler, A
المصدر: The Journal of Physician Assistant Education ; volume 13, issue 2, page 113 ; ISSN 1941-9430
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19Academic Journal
المؤلفون: Fasser, C., Munier, F.
المصدر: Journal - Giornale / Retina Suisse, no. 2, pp. 11-15
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20Academic Journal
المؤلفون: Fasser, C., Munier, F.
المصدر: Serveur académique Lausannois ; Journal - Giornale / Retina Suisse, no. 2, pp. 11-15
Relation: 10670/1.udnev9; https://serval.unil.ch/notice/serval:BIB_66972E0E2C12