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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Bucciol G" with an ORCID

Giorgia Bucciol
KU Leuven
16
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794
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Human ADA2 Deficiency: Ten Years Later.
Wouters M, Ehlers L, Dzhus M, Kienapfel V, Bucciol G, Delafontaine S, Hombrouck A, Pillay B, Moens L, Meyts I
Curr Allergy Asthma Rep, 24(9):477-484, 06 Jul 2024
Cited by: 0 articles | PMID: 38970744 | PMCID: PMC11364588
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Inborn errors of immunity: A field without frontiers.
Bucciol G, Delafontaine S, Meyts I, Poli C
Immunol Rev, 322(1):15-27, 08 Dec 2023
Cited by: 0 articles | PMID: 38062988
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Spotlight: "Human STAT2 deficiency: a severe defect of antiviral immunity".
Bucciol G, Meyts I
Genes Immun, 25(3):261-263, 25 Dec 2023
Cited by: 0 articles | PMID: 38146002
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Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinﬂammatory syndrome.
Delafontaine S, Iannuzzo A, Bigley TM, Mylemans B, Rana R, Baatsen P, Poli MC, Rymen D, Jansen K, Mekahli D, Casteels I, Cassiman C, Demaerel P, Lepelley A, Frémond ML, Schrijvers R, Bossuyt X, Vints K, Huybrechts W, [...] Meyts I
J Clin Invest, 134(4):e163604, 04 Jan 2024
Cited by: 2 articles | PMID: 38175705 | PMCID: PMC10866661
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Proposal for a Disease Activity Score and Disease Damage Score for ADA2 Deficiency: the DADA2AI and DADA2DI.
Bucciol G, Ombrello AK, Chambers EP, Meyts I
J Clin Immunol, 44(1):25, 22 Dec 2023
Cited by: 1 article | PMID: 38129740 | PMCID: PMC10739542
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Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.
Riestra MR, Pillay BA, Willemsen M, Kienapfel V, Ehlers L, Delafontaine S, Pinton A, Wouters M, Hombrouck A, Sauer K, Bossuyt X, Voet A, Soenen SJ, Conde CD, Bucciol G, Boztug K, Humblet-Baron S, Touzart A, Rieux-Laucat F, [...] Meyts I
J Clin Immunol, 44(1):2, 15 Dec 2023
Cited by: 0 articles | PMID: 38099988 | PMCID: PMC11252662
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Combined deficient response to polysaccharide-based and protein-based vaccines predicts a severe clinical phenotype.
Cockx M, Haerynck F, Hoste L, Schrijvers R, Van der Werff Ten Bosch J, Dillaerts D, Thomas D, Schaballie H, Bucciol G, Robberechts W, Patel D, Berbers G, Desombere I, Geukens N, Meyts I, Bossuyt X
Clin Chem Lab Med, 62(1):138-149, 21 Sep 2023
Cited by: 0 articles | PMID: 37731388
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Diagnosis of IRAK-4-deficiency by flow cytometric measurement of IκB-α degradation.
Frans G, Michiels B, Picard C, Ampofo L, Raes M, Toelen J, Bucciol G, van der Werff Ten Bosch J, Moens L, Wuyts G, Dillaerts D, Casanova JL, Schrijvers R, Meyts I, Bossuyt X
Clin Chem Lab Med, 62(4):e102-e105, 06 Nov 2023
Cited by: 0 articles | PMID: 37929815
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Human ADA2 deficiency is characterized by the absence of an intracellular hypoglycosylated form of adenosine deaminase 2
Ehlers L, Hombrouck A, Wouters M, Pillay B, Delafontaine S, Bucciol G, Baggio M, Dzhus M, Ebstein F, Ebstein F, Jacquemyn M, De Somer L, Schrijvers R, Vanderschueren S, Cassiman D, Kirchner M, Mertins P, Mashreghi M, Kallinich T, [...] Meyts I
bioRxiv, 29 Oct 2023
Cited by: 0 articles | PPR: PPR750039
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A Narrative Review of the Neurological Manifestations of Human Adenosine Deaminase 2 Deficiency.
Dzhus M, Ehlers L, Wouters M, Jansen K, Schrijvers R, De Somer L, Vanderschueren S, Baggio M, Moens L, Verhaaren B, Lories R, Bucciol G, Meyts I
J Clin Immunol, 43(8):1916-1926, 07 Aug 2023
Cited by: 2 articles | PMID: 37548813 | PMCID: PMC10661818
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Haploidentical Stem Cell Transplantation with Post-transplantation Cyclophosphamide in High-Risk Chronic Granulomatous Disease Patient with Invasive Mucormycosis.
Ruttens D, Philippet P, HSCT advisory team, Bucciol G, Meyts I
J Clin Immunol, 43(8):1758-1765, 14 Aug 2023
Cited by: 0 articles | PMID: 37578614
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An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia.
Nishimura A, Uppuluri R, Raj R, Swaminathan VV, Cheng Y, Abu-Arja RF, Fu B, Laberko A, Albert MH, Hauck F, Bucciol G, Bigley V, Elcombe S, Kharya G, Pronk CJH, Wehr C, Neven B, Warnatz K, Meyts I, [...] Kanegane H
J Clin Immunol, 43(8):1827-1839, 16 Jul 2023
Cited by: 1 article | PMID: 37454339
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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.
Maccari ME, Wolkewitz M, Schwab C, Lorenzini T, Leiding JW, Aladjdi N, Abolhassani H, Abou-Chahla W, Aiuti A, Azarnoush S, Baris S, Barlogis V, Barzaghi F, Baumann U, Bloomfield M, Bohynikova N, Bodet D, Boutboul D, Bucciol G, [...] European Society for Immunodeficiencies Registry Working Party
J Allergy Clin Immunol, 152(4):984-996.e10, 28 Jun 2023
Cited by: 9 articles | PMID: 37390899
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Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia.
García-García A, Pérez de Diego R, Flores C, Rinchai D, Solé-Violán J, Deyà-Martínez À, García-Solis B, Lorenzo-Salazar JM, Hernández-Brito E, Lanz AL, Moens L, Bucciol G, Almuqamam M, Domachowske JB, Colino E, Santos-Perez JL, Marco FM, Pignata C, Bousfiha A, [...] Rodríguez-Gallego C
J Exp Med, 220(5):e20220170, 03 Mar 2023
Cited by: 13 articles | PMID: 36880831 | PMCID: PMC9998661
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Human inherited complete STAT2 deficiency underlies inflammatory viral diseases.
Bucciol G, Moens L, Ogishi M, Rinchai D, Matuozzo D, Momenilandi M, Kerrouche N, Cale CM, Treffeisen ER, Al Salamah M, Al-Saud BK, Lachaux A, Duclaux-Loras R, Meignien M, Bousfiha A, Benhsaien I, Shcherbina A, Roppelt A, COVID Human Genetic Effort, [...] Meyts I
J Clin Invest, 133(12):e168321, 15 Jun 2023
Cited by: 10 articles | PMID: 36976641 | PMCID: PMC10266780
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A narrative review of the neurological manifestations of human adenosine deaminase 2 deficiency
Mariia D, Ehlers L, Wouters M, Jansen K, Schrijvers R, De Somer L, Vanderschueren S, Baggio M, Moens L, Verhaaren B, Lories R, Bucciol G, Meyts I
Research Square, 30 May 2023
Cited by: 0 articles | PPR: PPR678341
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Homozygous DBF4 mutation as a cause of severe congenital neutropenia.
Willemsen M, Barber JS, Nieuwenhove EV, Staels F, Gerbaux M, Neumann J, Prezzemolo T, Pasciuto E, Lagou V, Boeckx N, Filtjens J, De Visscher A, Matthys P, Schrijvers R, Tousseyn T, O'Driscoll M, Bucciol G, Schlenner S, Meyts I, [...] Liston A
J Allergy Clin Immunol, 152(1):266-277, 24 Feb 2023
Cited by: 3 articles | PMID: 36841265
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Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children.
Bucciol G, COVID Human Genetic Effort, Meyts I
J Allergy Clin Immunol, 151(4):832-840, 24 Feb 2023
Cited by: 6 articles | PMID: 36841740 | PMCID: PMC9951110
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Clinical, immunologic, and genetic characteristics of children with ALPS: A single-center experience.
Vanhye L, Bossuyt X, Meyts I, Bucciol G
Pediatr Allergy Immunol, 34(2):e13924, 01 Feb 2023
Cited by: 0 articles | PMID: 36825743
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Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children.
Lee D, Le Pen J, Yatim A, Dong B, Aquino Y, Ogishi M, Pescarmona R, Talouarn E, Rinchai D, Zhang P, Perret M, Liu Z, Jordan I, Elmas Bozdemir S, Bayhan GI, Beaufils C, Bizien L, Bisiaux A, Lei W, [...] Casanova JL
Science, 379(6632):eabo3627, 10 Feb 2023
Cited by: 58 articles | PMID: 36538032 | PMCID: PMC10451000
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Correction: Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
Campbell TM, Liu Z, Zhang Q, Moncada-Velez M, Covill LE, Zhang P, Darazam IA, Bastard P, Bizien L, Bucciol G, Enoksson SL, Jouanguy E, Karabela ŞN, Khan T, Kendir-Demirkol Y, Arias AA, Mansouri D, Marits P, Marr N, [...] Bryceson YT
J Exp Med, 219(12):e2022020210282022c, 07 Nov 2022
Cited by: 1 article | PMID: 36342405 | PMCID: PMC9811997
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ADA2 Deficiency Mimicking Acute Disseminated Encephalomyelitis.
Ehlers L, Bucciol G, KU Leuven - UZA DADA2 team, Beysen D, Meyts I
J Clin Immunol, 43(3):536-539, 06 Dec 2022
Cited by: 1 article | PMID: 36472692 | PMCID: PMC9957855
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Aichivirus: an Emerging Pathogen in Patients with Primary and Secondary B-Cell Deficiency.
Meyts I, Bucciol G, Jansen K, Wollants E, Breuer J
J Clin Immunol, 43(3):532-535, 30 Nov 2022
Cited by: 2 articles | PMID: 36449139
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Correction to: Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients.
Hashem H, Bucciol G, Ozen S, Unal S, Bozkaya IO, Akarsu N, Taskinen M, Koskenvuo M, Saarela J, Dimitrova D, Hickstein DD, Hsu AP, Holland SM, Krance R, Sasa G, Kumar AR, Müller I, de Sousa MA, Delafontaine S, [...] Meyts I
J Clin Immunol, 42(7):1580-1581, 01 Oct 2022
Cited by: 1 article | PMID: 35499644 | PMCID: PMC9674743
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Child Neurology: Familial Hemophagocytic Lymphohistiocytosis Underlying Isolated CNS Inflammation.
Bucciol G, Willemyns N, Verhaaren B, Bossuyt X, Lagrou K, Corveleyn A, Moshous D, Jansen K, De Waele L, Meyts I
Neurology, 99(15):660-664, 10 Aug 2022
Cited by: 2 articles | PMID: 36216522
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