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PubPharm (25)
1
Clinical and immunological analysis of a large kindred affected by autoimmune lymphoproliferative syndrome (ALPS) due to a novel TNFRSF6 mutation displaying age dependent disease activity
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2022
von
Tessarin, G.
|
Baronio, M.
|
Gazzurelli, L.
| +9
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2
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS)
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2021
von
Tessarin, G.
|
Mazza, C.
|
Baronio, M.
| +11
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3
Fatal SARS-CoV-2 infection in a male patient with Good's syndrome
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2021
von
Pozzi, M.
|
Baronio, M.
|
Janetti, M.
| +5
CommentIn: Clin Immunol. 2022 Feb;235:108789. - PMID 34197951
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4
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2020
von
Lougaris, V.
|
Malagola, M.
|
Baronio, M.
| +13
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5
Flow Cytometry Identifies Risk Factors and Dynamic Changes in Patients with COVID-19
enthalten in:
Journal of clinical immunology
| 2020
von
Moratto, D.
|
Chiarini, M.
|
Giustini, V.
| +7
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6
Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2020
von
Lougaris, V.
|
Baronio, M.
|
Castagna, A.
| +16
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7
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults
enthalten in:
European journal of immunology
| 2020
von
Moratto, D.
|
Giacomelli, M.
|
Chiarini, M.
| +11
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8
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2019
von
Lougaris, V.
|
Moratto, D.
|
Baronio, M.
| +5
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9
Multisystem autoimmune disease caused by increased STAT3 phosphorylation and dysregulated gene expression
enthalten in:
Haematologica
| 2019
von
Todaro, F.
|
Tamassia, N.
|
Pinelli, M.
| +11
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10
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency
enthalten in:
The Journal of allergy and clinical immunology
| 2019
von
Lougaris, V.
|
Chou, J.
|
Beano, A.
| +13
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Thema: Letter
Medienart
25
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25
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25
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Zeitschriftentitel
12
Clinical immunology (Orlando, Fla.)
6
The Journal of allergy and clinical immunology
2
Journal of clinical immunology
2
Pediatric allergy and immunology : official pub...
1
European journal of immunology
1
Haematologica
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Orphanet journal of rare diseases
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Letter
20
Research Support, Non-U.S. Gov't
18
Case Reports
7
B cells
4
Hypogammaglobulinemia
3
Autoimmunity
3
COVID-19
3
EC 2.7.1.137
3
Research Support, N.I.H., Extramural
3
T cells
2
ALPS
2
APDS-1
2
Bone marrow
2
CTLA-4
2
CTLA-4 Antigen
2
CTLA4 protein, human
2
Class I Phosphatidylinositol 3-Kinases
2
FAS
2
Inborn errors of immunity
2
Lymphocyte
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Erscheinungszeitraum
7
2020-
18
2010-2019
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25
Englisch
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