Výsledky vyhledávání - Mounif El‐Youssef

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  1. 1
    Wilson Disease

    Wilson Disease Autor Mounif El‐Youssef

    Vydáno 2003
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  2. 2
    The natural history of familial adenomatous polyposis syndrome: A 24year review of a single center experience in screening, diagnosis, and outcomes

    The natural history of familial adenomatous polyposis syndrome: A 24year review of a single center experience in screening, diagnosis, and outcomes Autor Raelene Kennedy, D. Dean Potter, Christopher R. Moir, Mounif El‐Youssef

    Vydáno 2013
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  3. 3
    Chronic Intestinal Pseudoobstruction Associated With Altered Interstitial Cells of Cajal Networks

    Chronic Intestinal Pseudoobstruction Associated With Altered Interstitial Cells of Cajal Networks Autor Ariel E. Feldstein, Steven Miller, Mounif El‐Youssef, David A. Rodeberg, Noralane M. Lindor, Lawrence J. Burgart, Joseph H. Szurszewski, Gianrico Farrugia

    Vydáno 2003
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  4. 4
    A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees

    A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees Autor Sandro Rossetti, Roser Torrá, Eliécer Coto, Mark Consugar, Vickie Kubly, S Málaga, Mercedes Navarro, Mounif El‐Youssef, Vicente E. Torres, Peter C. Harris

    Vydáno 2003
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  5. 5
    Prospective Clinical Trial of Rifaximin Therapy for Patients With Primary Sclerosing Cholangitis

    Prospective Clinical Trial of Rifaximin Therapy for Patients With Primary Sclerosing Cholangitis Autor James H. Tabibian, Andrea A. Gossard, Mounif El‐Youssef, John E. Eaton, Jan Petz, Roberta A. Jorgensen, Felicity Enders, Anilga Tabibian, Keith D. Lindor

    Vydáno 2014
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  6. 6
    A population-based study of the frequency of corticosteroid resistance and dependence in pediatric patients with Crohnʼs disease and ulcerative colitis

    A population-based study of the frequency of corticosteroid resistance and dependence in pediatric patients with Crohnʼs disease and ulcerative colitis Autor Jeanne Tung, Edward V. Loftus, Deborah K. Freese, Mounif El‐Youssef, Alan R. Zinsmeister, Joseph L. Melton, Scott Harmsen, William J. Sandborn, William A. Faubion

    Vydáno 2006
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  7. 7
    Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD)

    Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD) Autor Magdalena Adeva, Mounif El‐Youssef, Sandro Rossetti, Patrick S. Kamath, Vickie Kubly, Mark Consugar, Dawn M. Milliner, Bernard F. King, Vicente E. Torres, Peter C. Harris

    Vydáno 2006
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  8. 8
    Predictors of Family Risk for Celiac Disease: A Population-Based Study

    Predictors of Family Risk for Celiac Disease: A Population-Based Study Autor Alberto Rubio‐Tapia, Carol T. Van Dyke, Brian D. Lahr, Alan R. Zinsmeister, Mounif El‐Youssef, S. Breanndan Moore, Martha Bowman, Lawrence J. Burgart, L. Joseph Melton, Joseph A. Murray

    Vydáno 2008
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  9. 9
    Celiac Disease in Type 1 Diabetes Mellitus in a North American Community: Prevalence, Serologic Screening, and Clinical Features

    Celiac Disease in Type 1 Diabetes Mellitus in a North American Community: Prevalence, Serologic Screening, and Clinical Features Autor Farid H. Mahmud, Joseph A. Murray, Yogish C. Kudva, Alan R. Zinsmeister, Ross Dierkhising, Brian D. Lahr, P. James B. Dyck, Robert A. Kyle, Mounif El‐Youssef, Lawrence J. Burgart, Carol T. Van Dyke, Deanna L. Brogan, L. Joseph Melton

    Vydáno 2005
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  10. 10
    RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities

    RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities Autor Margot A. Cousin, Erin Conboy, Jian‐She Wang, Dominic Lenz, Tanya L. Schwab, Monique Williams, Roshini S. Abraham, Sarah Barnett, Mounif El‐Youssef, Rondell P. Graham, Luz Helena Gutierrez Sanchez, Linda Hasadsri, Georg F. Hoffmann, Nathan C. Hull, Robert Kopajtich, Réka Kovács-Nagy, Jiaqi Li, Daniela Marx-Berger, Valérie A. McLin, Mark A. McNiven, Taofic Mounajjed, Holger Prokisch, Daisy Rymen, Ryan J. Schulze, Christian Staufner, Ye Yang, Karl J. Clark, Brendan C. Lanpher, Eric W. Klee

    Vydáno 2019
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  11. 11
    Gamma Glutamyltransferase Reduction Is Associated With Favorable Outcomes in Pediatric Primary Sclerosing Cholangitis

    Gamma Glutamyltransferase Reduction Is Associated With Favorable Outcomes in Pediatric Primary Sclerosing Cholangitis Autor Mark Deneau, Cara L. Mack, Reham Abdou, Mansi Amin, Achiya Amir, Marcus Auth, Fateh Bazerbachi, A Broderick, Albert C. Y. Chan, Matthew DiGuglielmo, Wael El‐Matary, Mounif El‐Youssef, Federica Ferrari, Katryn N. Furuya, Frédèric Gottrand, Nitika Gupta, Matjaž Homan, M. Kyle Jensen, Binita M. Kamath, Kyung Mo Kim, Kaija‐Leena Kolho, Anastasia Konidari, Bart G.P. Koot, Raffaele Iorio, Mercedes Martínez, Parvathi Mohan, Sirish Palle, Alexandra Papadopoulou, Amanda Ricciuto, Lawrence J. Saubermann, Pushpa Sathya, Eyal Shteyer, Vratislav Smolka, Atsushi Tanaka, Pamela L. Valentino, Raghu Varier, Veena Venkat, Bernadette Vitola, Miriam B. Vos, Marek Woynarowski, Jason Yap, Tamir Miloh

    Vydáno 2018
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  12. 12
    The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration

    The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration Autor Mark Deneau, Wael El‐Matary, Pamela L. Valentino, Reham Abdou, Khaled Alqoaer, Mansi Amin, Achiya Amir, Marcus Auth, Fateh Bazerbachi, Annemarie Broderick, Albert C. Y. Chan, Jillian M. Cotter, Sylvia Doan, Mounif El‐Youssef, Federica Ferrari, Katryn N. Furuya, Madeleine Gottrand, F. Gottrand, Nitika Gupta, Matjaž Homan, Binita M. Kamath, Kyung Mo Kim, Kaija‐Leena Kolho, Anastasia Konidari, Bart G.P. Koot, Raffaele Iorio, Oren Ledder, Cara L. Mack, Mercedes Martínez, Tamir Miloh, Parvathi Mohan, Niamh O’Cathain, Alexandra Papadopoulou, Amanda Ricciuto, Lawrence J. Saubermann, Pushpa Sathya, Eyal Shteyer, Vratislav Smolka, Atushi Tanaka, Raghu Varier, Veena Venkat, Bernadette Vitola, Miriam B. Vos, Marek Woynarowski, Jason Yap, M. Kyle Jensen

    Vydáno 2017
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  13. 13
    Understanding the evolving phenotype of vascular complications in telomere biology disorders

    Understanding the evolving phenotype of vascular complications in telomere biology disorders Autor Cecilia Higgs, Yanick J. Crow, Denise M. Adams, Emmanuel Chang, Don Hayes, Utz Herbig, James N. Huang, Ryan Himes, Kunal Jajoo, F. Brad Johnson, Susan D. Reynolds, Yoshihiro Yonekawa, Mary Armanios, Farid Boulad, Courtney D. DiNardo, Carlo Dufour, Frederick D. Goldman, Shakila P. Khan, Christian P. Kratz, Kasiani C. Myers, Ganesh Raghu, Blanche P. Alter, Geraldine Aubert, Sonia Bhala, Edward W. Cowen, Yigal Dror, Mounif El‐Youssef, Bruce Friedman, Neelam Giri, Lisa Helms Guba, Payal P. Khincha, Tiffany Lin, Hilary Longhurst, Lisa J. McReynolds, Adam Nelson, Tim Olson, Anne Pariser, Rosario Perona, Ghadir Sasa, Kristen E. Schratz, Douglas A. Simonetto, Danielle Townsley, Michael F. Walsh, Kate Stevens, Suneet Agarwal, Alison A. Bertuch, Sharon A. Savage

    Vydáno 2018
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