has been cited by the following article(s):
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[1]
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Disorders of Nucleotide Metabolism
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Kirsch, V Tüngler, S Orcesi, D Tonduti - Physician's Guide to the …,
2022 |
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[2]
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Aicardi–Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations
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2020 |
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[3]
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Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review
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2019 |
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[4]
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Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene
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European Journal of Paediatric Neurology,
2018 |
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[5]
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Cerebral palsy: not always what it seems
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2018 |
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[6]
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Type 1 Diabetes and Type 1 Interferonopathies: Localization of a Type 1 Common Thread of Virus Infection in the Pancreas
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EBioMedicine,
2017 |
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[7]
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Ribonuclease H2 mutations induce a cGAS/STING‐dependent innate immune response
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The EMBO journal,
2016 |
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[8]
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The Type I Interferonopathies
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2016 |
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[9]
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Type I interferonopathies—an expanding disease spectrum of immunodysregulation
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Seminars in immunopathology,
2015 |
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[10]
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Klinische Symptome und Pathogenese der Typ-1-Interferonopathien
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Monatsschrift Kinderheilkunde,
2015 |
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[11]
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Typ-1-Interferonopathien
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Arthritis und Rheuma,
2014 |
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[1]
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Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases
2022
DOI:10.1007/978-3-030-67727-5_14
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[2]
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Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review
Journal of Clinical Medicine,
2019
DOI:10.3390/jcm8050750
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[3]
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Cerebral palsy: not always what it seems
Archives of Disease in Childhood,
2019
DOI:10.1136/archdischild-2018-315633
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[4]
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The Type I Interferonopathies
Annual Review of Medicine,
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[5]
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Type 1 Diabetes and Type 1 Interferonopathies: Localization of a Type 1 Common Thread of Virus Infection in the Pancreas
EBioMedicine,
2017
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Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene
European Journal of Paediatric Neurology,
2017
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[7]
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Ribonuclease H2 mutations induce a
cGAS
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The EMBO Journal,
2016
DOI:10.15252/embj.201593339
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[8]
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Type I interferonopathies—an expanding disease spectrum of immunodysregulation
Seminars in Immunopathology,
2015
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[9]
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Klinische Symptome und Pathogenese der Typ-1-Interferonopathien
Monatsschrift Kinderheilkunde,
2015
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