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/vufind/Search/Results?lookfor=%22Rawat%2C+Amit%22&type=Person&sort=year
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PubPharm (598)
1
Heterozygous RAD50 gene variant in a family with systemic sclerosis suggests role of impaired DNA repair mechanisms in disease pathogenesis
enthalten in:
Clinical and experimental dermatology
| 2024
von
Machhua, S.
|
Sharma, S.
|
Minz, R.
| +4
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2
Wiskott-Aldrich syndrome protein expression in female WAS carriers : A flow cytometry study from North India
enthalten in:
Pediatric blood & cancer
| 2024
von
Basu, S.
|
Rikhi, R.
|
Arora, K.
| +5
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3
An Indian Family with Autosomal Dominant Hyper-IgE Syndrome Due to IL6ST Defect
enthalten in:
Journal of clinical immunology
| 2024
von
Basu, S.
|
Goel, S.
|
Rawat, A.
| +2
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4
Supplementation of High-Strength Oral Probiotics Improves Immune Regulation and Preserves Beta Cells among Children with New-Onset Type 1 Diabetes Mellitus : A Randomised, Double-Blind Placebo Control Trial
enthalten in:
Indian journal of pediatrics
| 2024
von
Lokesh, M.
|
Kumar, R.
|
Jacob, N.
| +4
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5
An Indian Family with Autosomal Dominant Hyper-IgE Syndrome Due to IL6ST Defect
enthalten in:
Journal of clinical immunology
| 2024
von
Basu, S.
|
Goel, S.
|
Rawat, A.
| +2
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6
Delay in diagnosis is the most important proximate reason for mortality in hereditary angio-oedema : our experience at Chandigarh, India
enthalten in:
Clinical and experimental dermatology
| 2024
von
Kumar Jindal, A.
|
Basu, S.
|
Tyagi, R.
| +21
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7
Transmission patterns of C1-INH deficiency hereditary angioedema favors a wild-type male offspring : Our experience at Chandigarh, India
enthalten in:
Immunobiology
| 2024
von
Machhua, S.
|
Kumar Jindal, A.
|
Basu, S.
| +13
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8
Clinical, immunological and molecular profiles of DOCK8 deficiency in six patients from a tertiary care centre in North India
enthalten in:
Clinical and experimental dermatology
| 2024
von
Kumar Jindal, A.
|
Sil, A.
|
Aggarwal, R.
| +23
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9
Markers of Endothelial Dysfunction in Kawasaki Disease : An Update
enthalten in:
Clinical reviews in allergy & immunology
| 2024
von
Kumrah, R.
|
Goyal, T.
|
Rawat, A.
| +1
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10
Early Onset Polyarthritis : An Unusual Presentation of MHC Class II Deficiency
enthalten in:
Rheumatology (Oxford, England)
| 2024
von
Sil, A.
|
Thangaraj, A.
|
Patro, D.
| +5
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598
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Journal of clinical immunology
74
Indian journal of pediatrics
34
Rheumatology international
27
Indian pediatrics
22
Clinical reviews in allergy & immunology
22
Frontiers in immunology
10
International journal of rheumatic diseases
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Genes & diseases
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International journal of pharmaceutics
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Journal of nephrology
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Indian journal of pathology & microbiology
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Indian journal of pathology and microbiology
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48
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39
Chronic granulomatous disease
34
India
25
Kawasaki disease
19
Juvenile dermatomyositis
17
Biomarkers
15
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13
Autoantibodies
13
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12
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12
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11
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10
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