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/vufind/Search/Results?lookfor=%22Parvaneh%2C+Nima%22&type=Person&sort=year
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PubPharm (246)
1
Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency
enthalten in:
Nature immunology
| 2024
von
Oda, H.
|
Manthiram, K.
|
Chavan, P.
| +59
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2
The immunopathological landscape of human pre-TCRα deficiency : From rare to common variants
enthalten in:
Science (New York, N.Y.)
| 2024
von
Materna, M.
|
Delmonte, O.
|
Bosticardo, M.
| +96
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3
Immune reconstitution after hematopoietic stem cell transplantation with reduced intensity conditioning for inborn errors of immunity
enthalten in:
ResearchSquare.com
| 2024
von
Shahraki, Z.
|
Behfar, M.
|
Gharagozlou, S.
| +4
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4
Human inherited CCR2 deficiency underlies progressive polycystic lung disease
enthalten in:
Cell
| 2024
von
Neehus, A.
|
Carey, B.
|
Landekic, M.
| +69
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5
Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria
enthalten in:
Cell
| 2023
von
Bohlen, J.
|
Zhou, Q.
|
Philippot, Q.
| +55
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6
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
enthalten in:
Nature
| 2023
von
Le Voyer, T.
|
Parent, A.
|
Liu, X.
| +98
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7
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency : Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population
enthalten in:
Journal of clinical immunology
| 2023
von
Mousavi Khorshidi, M.
|
Seeleuthner, Y.
|
Chavoshzadeh, Z.
| +21
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8
Clinical, immunological, and genetic findings in Iranian patients with MHC-II deficiency: confirmation of c.121delG RFXANK founder mutation in the Iranian population
enthalten in:
ResearchSquare.com
| 2023
von
Khorshidi, M.
|
Seeleuthner, Y.
|
Chavoshzadeh, Z.
| +22
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9
Tumor Necrosis Factor-α (-308G>A) Gene Polymorphism and Its Association with Asthma and Atopy Status
enthalten in:
Iranian journal of allergy, asthma, and immunology
| 2023
von
Razaghian, A.
|
Parvaneh, N.
|
Amirzargar, A.
| +1
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10
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population
enthalten in:
Journal of clinical immunology
| 2023
von
Mousavi Khorshidi, M.
|
Seeleuthner, Y.
|
Chavoshzadeh, Z.
| +21
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Medienart
243
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178
E-Ressourcen
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Zeitschriftentitel
49
Journal of clinical immunology
12
European journal of pediatrics
11
Iranian journal of allergy, asthma, and immunology
6
Expert review of clinical immunology
6
International archives of allergy and immunology
6
ResearchSquare.com
5
Digestive diseases and sciences
5
Frontiers in immunology
5
Iranian journal of pediatrics
5
Orphanet journal of rare diseases
5
The Journal of experimental medicine
4
Acta diabetologica
4
British journal of haematology
4
Pediatric rheumatology
4
The journal of tropical pediatrics
3
Allergy, asthma and clinical immunology
3
Annals of clinical microbiology and antimicrobials
3
Cell
3
Human immunology
3
Journal of tropical pediatrics
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Thema
119
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40
Research Support, Non-U.S. Gov't
13
primary immunodeficiency
12
Research Support, N.I.H., Extramural
12
Review
10
Iran
9
infection
8
Epidemiology
7
Autoimmunity
7
CGD
7
EC 2.7.10.2
7
IgA deficiency
7
Letter
7
Primary immunodeficiency
7
Severe combined immunodeficiency
7
immunodeficiency
6
MSMD
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82115-62-6
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Common variable immunodeficiency
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68
2020-
117
2010-2019
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