Canlyniadau Chwilio - Shelly Pathak

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  1. 1
    Autoinflammatory diseases: update on classification diagnosis and management

    Autoinflammatory diseases: update on classification diagnosis and management gan Shelly Pathak, Michael McDermott, Sinisa Savic

    Cyhoeddwyd 2016
    Cael y testun llawn
    Revisão
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  2. 2
    Cellular Senescence and Inflammaging in the Bone: Pathways, Genetics, Anti-Aging Strategies and Interventions

    Cellular Senescence and Inflammaging in the Bone: Pathways, Genetics, Anti-Aging Strategies and Interventions gan Merin Lawrence, Abhishek Goyal, Shelly Pathak, Payal Ganguly

    Cyhoeddwyd 2024
    Cael y testun llawn Cael y testun llawn
    Revisão
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  3. 3
    ENaC-mediated sodium influx exacerbates NLRP3-dependent inflammation in cystic fibrosis

    ENaC-mediated sodium influx exacerbates NLRP3-dependent inflammation in cystic fibrosis gan Thomas Scambler, Heledd Jarosz-Griffiths, Samuel Lara‐Reyna, Shelly Pathak, Chi Huey Wong, Jonathan Holbrook, Fabio Martinon, Sinisa Savic, D. Peckham, Michael McDermott

    Cyhoeddwyd 2019
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  4. 4
    Exploratory Study of <i><scp>MYD</scp>88</i> L265P, Rare <i><scp>NLRP</scp>3</i> Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome

    Exploratory Study of <i><scp>MYD</scp>88</i> L265P, Rare <i><scp>NLRP</scp>3</i> Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome gan Shelly Pathak, Dorota Rowczenio, Roger G. Owen, Gina M. Doody, Darren J. Newton, Claire Taylor, Jan Taylor, Catherine Cargo, Philip N. Hawkins, Karoline Krause, Helen J. Lachmann, Sinisa Savic

    Cyhoeddwyd 2019
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  5. 5
    Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome

    Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome gan Dorota Rowczenio, Shelly Pathak, Juan I. Aróstegui, Anna Mensa‐Vilaró, Ebun Omoyinmi, Paul Brogan, Dan Lipsker, Thomas Scambler, Roger G. Owen, Hadija Trojer, Anna Baginska, Julian D. Gillmore, Ashutosh Wechalekar, Thirusha Lane, René M. Williams, Taryn Youngstein, Philip N. Hawkins, Sinisa Savic, Helen J. Lachmann

    Cyhoeddwyd 2017
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:

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