Resultats de la cerca - Tal Ben‐Ami

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  1. 1
    Geographic Atrophy and Choroidal Neovascularization in the Same Eye: A Review

    Geographic Atrophy and Choroidal Neovascularization in the Same Eye: A Review per Patrick A. Kaszubski, Tal Ben Ami, Céline Saade, R. Theodore Smith

    Publicat 2016
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  2. 2
    HYPERSPECTRAL AUTOFLUORESCENCE IMAGING OF DRUSEN AND RETINAL PIGMENT EPITHELIUM IN DONOR EYES WITH AGE-RELATED MACULAR DEGENERATION

    HYPERSPECTRAL AUTOFLUORESCENCE IMAGING OF DRUSEN AND RETINAL PIGMENT EPITHELIUM IN DONOR EYES WITH AGE-RELATED MACULAR DEGENERATION per Yuehong Tong, Tal Ben Ami, Sung‐Min Hong, Rainer Heintzmann, Guido Gerig, Zsolt Ablonczy, Christine A. Curcio, Thomas Ach, R. Theodore Smith

    Publicat 2016
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  3. 3
    Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population

    Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population per Orna Steinberg‐Shemer, Tracie Goldberg, Joanne Yacobovich, Carina Levin, Ariel Koren, Shoshana Revel‐Vilk, Tal Ben‐Ami, Amir A. Kuperman, Vered Shkalim Zemer, Amos Toren, Joseph Kapelushnik, Ayelet Ben‐Barak, Hagit Miskin, Tanya Krasnov, Sharon Noy‐Lotan, Orly Dgany, Hannah Tamary

    Publicat 2019
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  4. 4
    Pleuropulmonary blastoma in children and adolescents: The EXPeRT/PARTNER diagnostic and therapeutic recommendations

    Pleuropulmonary blastoma in children and adolescents: The EXPeRT/PARTNER diagnostic and therapeutic recommendations per Gianni Bisogno, Sabine Sarnacki, Teresa Stachowicz‐Stencel, Veronique Minard Colin, Andrea Ferrari, Jan Godziński, Marion Gauthier Villars, Ewa Bień, Frédéric Hameury, Sylvie Helfré, Dominik T. Schneider, Yves Réguerre, Ricardo López Almaraz, Dragana Janić, Maja Česen, Alexandra Kolenová, Jelena Rascon, Ката Мартинова, Rodica Cosnarovici, Apostolos Pourtsidis, Tal Ben Ami, Jelena Roganović, Ewa Kościelniak, Kris Ann P. Schultz, Ines B. Brecht, Daniel Orbach

    Publicat 2021
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  5. 5
    Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases

    Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases per Celeste Bento, Melanie J. Percy, Betty Gardie, Tabita Maia, Richard van Wijk, Silverio Perrotta, Fulvio Della Ragione, Helena Almeida, Cédric Rossi, François Girodon, Maria Åström, Drorit Neumann, Susanne Schnittger, Britta Landin, Milen Minkov, Maria Luigia Randi, Richard J. Kahnoski, Nicole Casadevall, William Vainchenker, Susana Rives, Sylvie Hermouet, Letícia Ribeiro, Mary Frances McMullin, Holger Cario, Aurélie Chauveau, Anne‐Paule Gimenez‐Roqueplo, Brigitte Bressac–de Paillerets, Didem Altındirek, Felipe R. Lorenzo, Frédéric Lambert, Harlev Dan, Sophie Gad, Ana Catarina Oliveira, Cédric Rossi, Cristina Fraga, Gennadiy Taradin, Guillermo Martín–Núñez, Helena Vitória, Herrera Diaz Aguado, Jan Palmblad, Julia Vidán, Luís Relvas, Letícia Ribeiro, Maria Luigi Larocca, Maria Luigia Randi, Maria Pedro Silveira, Melanie J. Percy, Mor Gross, Ricardo Marques da Costa, Soheir Beshara, Tal Ben‐Ami, Valérie Ugo

    Publicat 2013
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  6. 6
    Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

    Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases per Alistair T. Pagnamenta, Carlos Camps, Edoardo Giacopuzzi, John Taylor, Mona Hashim, Eduardo Calpena, Pamela J. Kaisaki, Akiko Hashimoto, Jing Yu, Edward Sanders, Ron Schweßinger, Jim R. Hughes, Gerton Lunter, Hélène Dreau, Matteo P. Ferla, Lukas Lange, Yeşim Kesim, Vassilis Ragoussis, Dimitrios V. Vavoulis, Holger Allroggen, Olaf Ansorge, Christian Babbs, Siddharth Banka, Benito Banos‐Pinero, David Beeson, Tal Ben‐Ami, David Bennett, Celeste Bento, Edward Blair, Charlotte Brasch‐Andersen, Katherine R. Bull, Holger Cario, Deirdre Cilliers, Valerio Conti, E. Graham Davies, Fatima Dhalla, Beatriz Diez Dacal, Dong Yin, James E. Dunford, Renzo Guerrini, Adrian L. Harris, Jane Hartley, Georg A. Holländer, M K Javaid, Maureen A. Kane, Déirdre Kelly, Dominic F. Kelly, Samantha J.L. Knight, Alexandra Y. Kreins, Erika Kvikstad, Craig B. Langman, Tracy Lester, Kate E Lines, Simon Lord, Xin Lü, Sahar Mansour, Adnan Manzur, Reza Maroofian, Brian D. Marsden, Joanne Mason, Simon J. McGowan, Davide Mei, Hana Mlčochová, Yoshiko Murakami, Andrea H. Németh, Steven Okoli, Elizabeth Ormondroyd, Lilian Bomme Ousager, Jacqueline Palace, Smita Y. Patel, Melissa M. Pentony, Christopher W. Pugh, Abolfazl Rad, Archana Ramesh, Simone G. Riva, Irene Roberts, Noémi Roy, Outi Salminen, Kyleen D. Schilling, Caroline Scott, Arjune Sen, Conrad Smith, Mark Stevenson, Rajesh V. Thakker, Stephen R.F. Twigg, Holm H. Uhlig, Richard van Wijk, Barbara Vona, Steven A. Wall, Jing Wang, Hugh Watkins, Jaroslav Žák, Anna Schuh, Usha Kini, Andrew O.M. Wilkie, Niko Popitsch, Jenny C. Taylor

    Publicat 2023
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