Rezultati - Yanick J. Crow

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  1. 1
    Cree encephalitis is allelic with Aicardi-Goutieres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

    Cree encephalitis is allelic with Aicardi-Goutieres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism od Yanick J. Crow

    Izdano 2003
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  2. 2
    Aicardi-Goutieres syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity

    Aicardi-Goutieres syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity od Yanick J. Crow, Jan Rehwinkel

    Izdano 2009
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  3. 3
    Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi–Goutières Syndrome and Beyond

    Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi–Goutières Syndrome and Beyond od Yanick J. Crow, John H. Livingston

    Izdano 2016
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  4. 4
    Type I interferon–mediated monogenic autoinflammation: The type I interferonopathies, a conceptual overview

    Type I interferon–mediated monogenic autoinflammation: The type I interferonopathies, a conceptual overview od Mathieu P. Rodero, Yanick J. Crow

    Izdano 2016
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  5. 5
    STING-Mediated Lung Inflammation and Beyond

    STING-Mediated Lung Inflammation and Beyond od Marie‐Louise Frémond, Yanick J. Crow

    Izdano 2021
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  6. 6
    The type I interferonopathies: 10 years on

    The type I interferonopathies: 10 years on od Yanick J. Crow, Daniel B. Stetson

    Izdano 2021
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  7. 7
    Self-Awareness: Nucleic Acid–Driven Inflammation and the Type I Interferonopathies

    Self-Awareness: Nucleic Acid–Driven Inflammation and the Type I Interferonopathies od Carolina Uggenti, Alice Lepelley, Yanick J. Crow

    Izdano 2019
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  8. 8
    Treatments in Aicardi–Goutières syndrome

    Treatments in Aicardi–Goutières syndrome od Yanick J. Crow, Jay Shetty, John H. Livingston

    Izdano 2019
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  9. 9
    Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes

    Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes od John H. Livingston, Stavros Stivaros, Dan Warren, Yanick J. Crow

    Izdano 2013
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  10. 10
    Autosomal dominant inheritance of a heterozygous mutation in <i>SAMHD1</i> causing familial chilblain lupus

    Autosomal dominant inheritance of a heterozygous mutation in <i>SAMHD1</i> causing familial chilblain lupus od Jane Ravenscroft, Mohnish Suri, Gillian Rice, Marcin Szynkiewicz, Yanick J. Crow

    Izdano 2010
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  11. 11
    Therapies in Aicardi–Goutières syndrome

    Therapies in Aicardi–Goutières syndrome od Yanick J. Crow, Adeline Vanderver, Simona Orcesi, Taco W. Kuijpers, Gillian Rice

    Izdano 2013
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  12. 12
    Recognizable phenotypes associated with intracranial calcification

    Recognizable phenotypes associated with intracranial calcification od John H. Livingston, Stavros Stivaros, Marjo S. van der Knaap, Yanick J. Crow

    Izdano 2012
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  13. 13
    Aicardi-Goutières Syndrome: Neuroradiologic Findings and Follow-Up

    Aicardi-Goutières Syndrome: Neuroradiologic Findings and Follow-Up od C. Uggetti, Roberta La Piana, Simona Orcesi, Maria Grazia Egitto, Yanick J. Crow, Elisa Fazzi

    Izdano 2009
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  14. 14
    Baricitinib Treatment in <scp>RNU7</scp>‐1‐Associated Aicardi–Goutières Syndrome in a South African Child: A Case Report

    Baricitinib Treatment in <scp>RNU7</scp>‐1‐Associated Aicardi–Goutières Syndrome in a South African Child: A Case Report od Timothy F. Spracklen, Shehnaaz Akhalwaya, Sally Ackermann, Carolina Uggenti, Luís Seabra, Yanick J. Crow, Kate Webb

    Izdano 2025
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  15. 15
    SAMHD1 is a nucleic-acid binding protein that is mislocalized due to aicardi-goutières syndrome-associated mutations

    SAMHD1 is a nucleic-acid binding protein that is mislocalized due to aicardi-goutières syndrome-associated mutations od Adriana Gonçalves, Evren Karayel, Gillian Rice, Keiryn L. Bennett, Yanick J. Crow, Giulio Superti‐Furga, Tilmann Bürckstümmer

    Izdano 2012
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  16. 16
    The SKIV2L RNA exosome limits activation of the RIG-I-like receptors

    The SKIV2L RNA exosome limits activation of the RIG-I-like receptors od Sterling Eckard, Gillian Rice, Alexandre Fabre, Catherine Badens, Elizabeth Gray, Jane Hartley, Yanick J. Crow, Daniel B. Stetson

    Izdano 2014
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  17. 17
    Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3

    Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3 od Siddharth Banka, Elena Chervinsky, William G. Newman, Yanick J. Crow, Shay Yeganeh, Joanne Yacobovich, Dian Donnai, Stavit A. Shalev

    Izdano 2010
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  18. 18
    Degos Disease

    Degos Disease od Cynthia M. Magro, Jonathan C. Poe, Connie Kim, Lee Shapiro, Gerard J. Nuovo, Mary K. Crow, Yanick J. Crow

    Izdano 2011
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  19. 19
    Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype

    Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype od Sarah L. N. Clarke, Lindsay Robertson, Grace E. Rice, Luís Seabra, Tom Hilliard, Yanick J. Crow, Athimalaipet V Ramanan

    Izdano 2020
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  20. 20
    Type I interferon–related kidney disorders

    Type I interferon–related kidney disorders od Lorenzo Lodi, Maria Vincenza Mastrolia, Federica Bello, Giovanni Maria Rossi, Maria Lucia Angelotti, Yanick J. Crow, Paola Romagnani, Augusto Vaglio

    Izdano 2022
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