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PubPharm (74)
1
Novel CARMIL2 (RLTPR) Mutation Presenting with Hyper-IgE and Eosinophilia : A Case Report
enthalten in:
Endocrine, metabolic & immune disorders drug targets
| 2023
von
Zamani, R.
|
Zoghi, S.
|
Shahkarami, S.
| +4
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2
Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis
enthalten in:
Blood
| 2023
von
Kostel Bal, S.
|
Giuliani, S.
|
Block, J.
| +32
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3
Systemic Inflammation and Normocytic Anemia in DOCK11 Deficiency
enthalten in:
The New England journal of medicine
| 2023
von
Block, J.
|
Rashkova, C.
|
Castanon, I.
| +56
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4
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease : a case report of twin brothers
enthalten in:
Journal of medical case reports
| 2023
von
Rayzan, E.
|
Sadeghalvad, M.
|
Shahkarami, S.
| +5
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5
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers
enthalten in:
Journal of medical case reports
| 2023
von
Rayzan, E.
|
Sadeghalvad, M.
|
Shahkarami, S.
| +5
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6
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers
enthalten in:
Journal of medical case reports
| 2023
von
Rayzan, E.
|
Sadeghalvad, M.
|
Shahkarami, S.
| +5
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7
Severe congenital neutropenia due to G6PC3 deficiency : early and delayed phenotype of a patient
enthalten in:
Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology
| 2023
von
Moradian, N.
|
Zoghi, S.
|
Rayzan, E.
| +4
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8
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype of a patient
enthalten in:
Allergy, asthma and clinical immunology
| 2023
von
Moradian, N.
|
Zoghi, S.
|
Rayzan, E.
| +4
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9
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype of a patient
enthalten in:
Allergy, asthma and clinical immunology
| 2023
von
Moradian, N.
|
Zoghi, S.
|
Rayzan, E.
| +4
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10
Novel DNMT3B Mutation in a Patient with Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome and a Bronchopulmonary Collateral Artery
enthalten in:
Endocrine, metabolic & immune disorders drug targets
| 2023
von
Aminorroaya, A.
|
Rayzan, E.
|
Shahkarami, S.
| +8
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Erscheinungszeitraum
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2020-
48
2010-2019
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