- Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia
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Nasir H, Ali SI, Haque N, Grebe SK, Kirmani S
- KMID: 2422481
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):158-161.
- doi: 10.6065/apem.2018.23.3.158
We present a family with 2 members who received long-term steroid treatment for presumed classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, until molecular testing revealed nonclassic CAH, not... -
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- Effectiveness of Mavrilimumab in Viral Infections Including SARS-CoV-2 Infection - A Brief Review
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Bhatt K, Garimella R, Taugir R, Mehta I, Jamal M, Vijayan R, Offor R, Nwankwo K, Arif U, Waheed K, Kumari P, Lathiya M, Michel G, Pandya N, Halpern J, Nasir H, Sanchez-Gonzalez MA
- KMID: 2514848
- Infect Chemother.
- 2021 Mar;53(1):1-12.
- doi: 10.3947/ic.2020.0109
Hyperinflammation and cytokine storm has been noted as a poor prognostic factor in patients with severe pneumonia related to coronavirus disease 2019 (COVID-19). In COVID-19, pathogenic myeloid cell overactivation is... -
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