All papers authored by Isabelle Meyts
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Ottavia M. Delmonte ,
Marita Bosticardo ,
Mana Momenilandi ,
Peyton E. Conrey ,
Bénédicte Charmeteau-De Muylder,
Clotilde Bravetti,
Rebecca Bellworthy ,
Axel Cederholm ,
Frederik Staels,
Christian A. Ganoza ,
Samuel Darko ,
Samir Sayed ,
Corentin Le Floc’h ,
Masato Ogishi
and 83 other authors
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants
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Alberto Iannuzzo ,
Tarin M. Bigley ,
Bram Mylemans ,
Ruchit R. Rana,
Pieter Baatsen,
Maria Cecilia Poli ,
Daisy Rymen,
Katrien Jansen,
Djalila Mekahli ,
Ingele Casteels,
Catherine Cassiman,
Philippe Demaerel,
Alice Lepelley ,
Marie-Louise Frémond
and 19 other authors
Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome
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Antoine Pinton,
Marjon Wouters,
Anneleen Hombrouck,
Kate Sauer,
Xavier Bossuyt,
Arnout Voet,
Stefaan J. Soenen,
Cecilia Dominguez Conde,
Giorgia Bucciol
and 7 other authors
Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome
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Lisa Ehlers ,
Marjon Wouters,
Katrien Jansen,
Rik Schrijvers ,
Lien De Somer ,
Steven Vanderschueren ,
Marco Baggio ,
Leen Moens,
Benjamin Verhaaren,
Rik Lories ,
Giorgia Bucciol ,
Isabelle Meyts
A Narrative Review of the Neurological Manifestations of Human Adenosine Deaminase 2 Deficiency
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Laurent Abel,
Salah Al-Muhsen,
Alessandro Aiuti,
Fahd Al-Mulla,
Evangelos Andreakos,
Novelli Antonio,
Andrés A. Arias,
Sophie Trouillet-Assant,
Alexandre Belot,
Catherine M. Biggs,
Ahmed A. Bousfiha,
Alex Bolze,
Alessandro Borghesi
and 60 other authors
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Daniel Leung ,
Mana Momenilandi ,
Lauren C. W. Jones ,
Lucia Pacillo ,
Alyssa E. James ,
Jill R. Murrell ,
Selket Delafontaine ,
Jesmeen Maimaris ,
Maryam Vaseghi-Shanjani ,
Kate L. Del Bel ,
Henry Y. Lu ,
Gilbert T. Chua ,
Silvia Di Cesare ,
Oriol Fornes
and 79 other authors
Human germline heterozygous gain-of-functionSTAT6variants cause severe allergic disease
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Paul Bastard ,
Pascal Chappert ,
Giovanna Barba-Spaeth ,
Slim Fourati ,
Alexis Vanderberghe ,
Pauline Lagouge-Roussey ,
Isabelle Meyts ,
Adrian Gervais ,
Magali Bouvier-Alias ,
Imane Azzaoui ,
Ignacio Fernández ,
Andréa de la Selle ,
Qian Zhang ,
Lucy Bizien
and 37 other authors
Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination
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Anna-Lena Neehus ,
Emmanuel Laplantine ,
Frederik Staels ,
Masato Ogishi ,
Yoann Seeleuthner,
Franck Rapaport ,
Keenan A. Lacey ,
Erika Van Nieuwenhove ,
Maya Chrabieh,
David Hum ,
Mélanie Migaud ,
Araksya Izmiryan ,
Lazaro Lorenzo ,
Tatiana Kochetkov
and 47 other authors
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
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,
W. Meersseman,
P. Stordeur ,
K. Willekens ,
S. Van Loo,
A. Corveleyn,
I. Meyts ,
G. Meyfroidt,
R. Schrijvers
Terminal Complement Pathway Deficiency in an Adult Patient with Meningococcal Sepsis
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Seza Ozen,
Sule Unal,
Ikbal Ok Bozkaya,
Nurten Akarsu ,
Mervi Taskinen,
Minna Koskenvuo,
Janna Saarela,
Dimana Dimitrova,
Dennis D. Hickstein,
Amy P. Hsu,
Steven M. Holland,
Robert Krance,
Ghadir Sasa
and 36 other authors
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Seza Ozen,
Sule Unal,
Ikbal Ok Bozkaya,
Nurten Akarsu ,
Mervi Taskinen,
Minna Koskenvuo,
Janna Saarela,
Dimana Dimitrova,
Dennis D. Hickstein,
Amy P. Hsu,
Steven M. Holland,
Robert Krance,
Ghadir Sasa
and 36 other authors
Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients
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,
Selket Delafontaine ,
Leen Moens,
Anniek Corveleyn,
Marie-Anne Morren,
Isabelle Meyts
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Isabelle Meyts
Recent advances in primary immunodeficiency: from molecular diagnosis to treatment
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