Resultados de procura - Emad B. Abboud

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  1. 1
    Fundus autofluorescence imaging in hereditary retinal diseases

    Fundus autofluorescence imaging in hereditary retinal diseases por Francesco Pichi, Emad B. Abboud, Nicola G. Ghazi, Arif O. Khan

    Publicado 2017
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    Revisão
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  2. 2
    Vitreous levels of placental growth factor correlate with activity of proliferative diabetic retinopathy and are not influenced by bevacizumab treatment

    Vitreous levels of placental growth factor correlate with activity of proliferative diabetic retinopathy and are not influenced by bevacizumab treatment por Eman Al Kahtani, Zhi Ping Xu, Saba Al Rashaed, Lin Wu, Atharva Mahale, Jie Tian, Emad B. Abboud, Nicola G. Ghazi, Igor Kozak, Vishali Gupta, J. Fernando Arévalo, Elia J. Duh

    Publicado 2016
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    Artigo
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  3. 3
    Whole-exome sequencing identifies<i>ALMS1, IQCB1, CNGA3</i>, and<i>MYO7A</i>mutations in patients with leber congenital amaurosis

    Whole-exome sequencing identifies<i>ALMS1, IQCB1, CNGA3</i>, and<i>MYO7A</i>mutations in patients with leber congenital amaurosis por Xia Wang, Hui Wang, Ming Cao, Zhe Li, Xianfeng Chen, Claire Patenia, Athurva Gore, Emad B. Abboud, Ali A. Al‐Rajhi, Richard A. Lewis, James R. Lupski, Graeme Mardon, Kun Zhang, Donna M. Muzny, Richard A. Gibbs, Rui Chen

    Publicado 2011
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    Artigo
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  4. 4
    Congenital Retinal Macrovessel and the Association of Retinal Venous Malformations With Venous Malformations of the Brain

    Congenital Retinal Macrovessel and the Association of Retinal Venous Malformations With Venous Malformations of the Brain por Francesco Pichi, K. Bailey Freund, Antonio P. Ciardella, Mariachiara Morara, Emad B. Abboud, Nicola G. Ghazi, Christine Dackiw, Netan Choudhry, Eduardo Cunha de Souza, Leonardo Provetti Cunha, J. Fernando Arévalo, T. Y. Alvin Liu, Adam S. Wenick, Lingmin He, Guadalupe Villarreal, Piergiorgio Neri, David Sarraf

    Publicado 2018
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  5. 5
    Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

    Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes por Leen Abu‐Safieh, May Alrashed, Shamsa Anazi, Hisham Alkuraya, Arif O. Khan, Mohammed Al‐Owain, Jawahir Al-Zahrani, Lama AlAbdi, Mais Hashem, Salwa Al-Tarimi, Mohammed-Adeeb Sebai, Ahmed Shamia, Mohamed D. Ray-Zack, Malik Nassan, Zuhair N. Al‐Hassnan, Zuhair Rahbeeni, Saad Waheeb, Abdullah S. Al-Kharashi, Emad B. Abboud, Selwa A.F. Al-Hazzaa, Fowzan S. Alkuraya

    Publicado 2012
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  6. 6
    Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies

    Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies por Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Shamsa Anazi, Hadeel Alsharif, Arif O. Khan, Asma Sunker, Saleh Al-mohsen, Emad B. Abboud, Sawsan R. Nowilaty, Mohammed Al‐Owain, Hamad Alzaidan, Bandar Al‐Saud, Ali Alasmari, Ghada M. H. Abdel‐Salam, Mohamed Abouelhoda, Firdous Abdulwahab, Niema Ibrahim, Ewa A. Naim, Banan Al‐Younes, Abeer Al‐Mostafa, Abdulelah AlIssa, Mais Hashem, Olga Buzovetsky, Yong Xiong, Dorota Monies, Nada Al Tassan, Ranad Shaheen, Selwa A.F. Al-Hazzaa, Fowzan S. Alkuraya

    Publicado 2015
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  7. 7
    Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling

    Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling por Moumita Chaki, Rannar Airik, Amiya K. Ghosh, Rachel H. Giles, Rui Chen, Gisela G. Slaats, Hui Wang, Toby W. Hurd, Weibin Zhou, Andrew Cluckey, Heon Yung Gee, Gokul Ramaswami, Chen‐Jei Hong, Bruce A. Hamilton, Igor Červenka, Ranjani Sri Ganji, Vı́tězslav Bryja, Heleen H. Arts, Jeroen van Reeuwijk, Machteld M. Oud, Stef J.F. Letteboer, Ronald Roepman, Hervé Husson, Oxana Ibraghimov‐Beskrovnaya, Takayuki Yasunaga, Gerd Walz, Lorraine Eley, John A. Sayer, Bernhard Schermer, Max C. Liebau, Thomas Benzing, Stéphanie Le Corre, Iain A. Drummond, Sabine Janssen, Susan J. Allen, S. Natarajan, John F. O’Toole, Massimo Attanasio, Sophie Saunier, Corinne Antignac, Robert K. Koenekoop, Huanan Ren, Irma López, Ahmet Nayır, Corinne Stoetzel, Hélène Dollfus, Rustin Massoudi, Joseph G. Gleeson, Sharon Andreoli, D Doherty, Anna Lindstrad, Christelle Golzio, Nicholas Katsanis, Lars Pape, Emad B. Abboud, Ali A. Al‐Rajhi, Richard A. Lewis, Heymut Omran, Eva Y.-H.P. Lee, Shaohui Wang, JoAnn Sekiguchi, Rudel A. Saunders, Colin A. Johnson, Elizabeth Garner, Katja Vanselow, Jens Andersen, Joseph Shlomai, Gudrun Nürnberg, Peter Nürnberg, Shawn Levy, Agata Smogorzewska, Edgar A. Otto, Friedhelm Hildebrandt

    Publicado 2012
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