المؤلفون: Maseroli, E., Comeglio, P., Corno, C., Cellai, I., Filippi, S., Mello, T., Galli, A., Rapizzi, E., Presenti, L., Truglia, M. C., Lotti, F., Facchiano, E., Beltrame, B., Lucchese, M., Saad, F., Rastrelli, G., Maggi, M.^{Aff4, Aff7}, Vignozzi, L.^{Aff1, Aff7}

المصدر: Journal of Endocrinological Investigation: Official Journal of Italian Society of Endocrinology (SIE). 44(4):819-842

المؤلفون: Rapizzi, E., Benvenuti, S., Deledda, C., Martinelli, S., Sarchielli, E., Fibbi, B., Luciani, P., Mazzanti, B., Pantaleo, M., Marroncini, G., Vannelli, G. B., Maggi, M.^{Aff2, Aff4}, Mannelli, M., Luconi, M.^{Aff2, Aff4}, Peri, A.

المصدر: Journal of Endocrinological Investigation: Official Journal of Italian Society of Endocrinology (SIE). 43(9):1259-1269

المؤلفون: Rapizzi, E., Benvenuti, S., Deledda, C., Martinelli, S., Sarchielli, E., Fibbi, B., Luciani, P., Mazzanti, B., Pantaleo, M., Marroncini, G., Vannelli, G. B., Maggi, M., Mannelli, M., Luconi, M., Peri, A.

المصدر: Journal of Endocrinological Investigation; 20240101, Issue: Preprints p1-11, 11p

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Lorenzi, U., Mehech, J., Caporossi, T., Romano, M. R., De Fazio, R., Parrat, E., Matonti, F., Mora, P., Sborgia, G., Forlini, M., Ventre, L., Soler, V., Sampo, M., Fiore, T., Van Overdam, K., Guigou, S., Rouhette, H., Rapizzi, E., Denion, E., Rebollo, O., Meyer, F., Uzzan, J., Mafrici, M., Bacherini, D., Favilla, S., Ricciotti, G., Tedesco, S. A., Gandolfi, S., Muraine, M.

مصطلحات موضوعية: Visual Acuity, Retinal Perforations, Sensory Systems, Basement Membrane, Retina, Cellular and Molecular Neuroscience, Ophthalmology, No internal limiting membrane, Vitrectomy, Reconstructive surgery, Humans, Full thickness macular hole, Prognostic variables, Tomography, Optical Coherence, Retrospective Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc8a2f72e5daec0c5305c2f6f4db580
https://hdl.handle.net/11391/1538814

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, 1

مصطلحات 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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e51c1f1b7c050a66d7033dd369699172
https://www.repository.cam.ac.uk/handle/1810/322429

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.