Mandal K - Search Results

1

Genetic Variation in SOD1 Gene Promoter Ins/Del and Its Influence on Oxidative Stress in Beta Thalassemia Major Patients.

Tripathi P, Agarwal S, Sarangi AN, Tewari S, Mandal K. Tripathi P, et al. Among authors: mandal k. Int J Hematol Oncol Stem Cell Res. 2020 Apr 1;14(2):110-117. Int J Hematol Oncol Stem Cell Res. 2020. PMID: 32461794 Free PMC article.

2

Novel mutations and spectrum of the disease of NR0B1 (DAX1)-related adrenal insufficiency in Indian children.

Gupta S, Joshi K, Zaidi G, Sarangi AN, Mandal K, Bhavani N, Pavithran PV, Pillai MG, Singh SK, Godbole T, Bhatia V, Bhatia E. Gupta S, et al. Among authors: mandal k. J Pediatr Endocrinol Metab. 2019 Aug 27;32(8):863-869. doi: 10.1515/jpem-2018-0440. J Pediatr Endocrinol Metab. 2019. PMID: 31219797

3

Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia.

Tripathi P, Agarwal S, Gupta A, Mandal K. Tripathi P, et al. Among authors: mandal k. Ann Hematol. 2020 Nov;99(11):2719-2722. doi: 10.1007/s00277-020-04017-2. Epub 2020 Apr 15. Ann Hematol. 2020. PMID: 32296912 No abstract available.

4

Molecular spectrum, family screening and genetic counselling of Spinocerebellar Ataxia (SCA) cases in an Indian scenario.

Vishwakarma P, Agarwal S, Dean DD, Muthuswamy S, Mandal K. Vishwakarma P, et al. Among authors: mandal k. J Neurogenet. 2021 Sep-Dec;35(4):370-380. doi: 10.1080/01677063.2021.1940172. Epub 2021 Jun 23. J Neurogenet. 2021. PMID: 34159894

5

Status of Catalase, Glutathione Peroxidase, Glutathione S-Transferase, and Myeloperoxidase Gene Polymorphisms in Beta-Thalassemia Major Patients to Assess Oxidative Injury and Its Association with Enzyme Activities.

Tripathi P, Agarwal S, Tewari S, Mandal K. Tripathi P, et al. Among authors: mandal k. J Pediatr Genet. 2021 Apr 12;11(3):198-212. doi: 10.1055/s-0041-1723961. eCollection 2022 Sep. J Pediatr Genet. 2021. PMID: 35990028 Free PMC article.

6

High Frequency of Recessive WFS1 Mutations Among Indian Children With Islet Antibody-negative Type 1 Diabetes.

Menon JC, Singh P, Archana A, Singh P, Mittal M, Kanga U, Mandal K, Seth A, Bhatia V, Dabadghao P, Sudhanshu S, Garg A, Vishwakarma R, Sarangi AN, Verma S, Singh SK, Bhatia E. Menon JC, et al. Among authors: mandal k. J Clin Endocrinol Metab. 2024 Feb 20;109(3):e1072-e1082. doi: 10.1210/clinem/dgad644. J Clin Endocrinol Metab. 2024. PMID: 37931151

7

Molecular analysis of severe hemophilia B in Indian families: Identification of mutational hotspot and novel variants.

Agrawal N, Kumar R, Masih S, Srivastava P, Singh P, Jaiswal SK, Moirangthem A, Saxena D, Phadke SR, Mandal K. Agrawal N, et al. Among authors: mandal k. Int J Lab Hematol. 2022 Feb;44(1):186-192. doi: 10.1111/ijlh.13715. Epub 2021 Sep 29. Int J Lab Hematol. 2022. PMID: 34590426

8

Study of the association of forkhead box P3 (FOXP3) gene polymorphisms with unexplained recurrent spontaneous abortions in Indian population.

Mishra S, Srivastava A, Mandal K, Phadke SR. Mishra S, et al. Among authors: mandal k. J Genet. 2018 Jun;97(2):405-410. J Genet. 2018. PMID: 29932060 Free article.

9

Red cell alloimmunization and associated risk factors in multiply transfused thalassemia patients: A prospective cohort study conducted at a tertiary care center in Northern India.

Yadav BK, Chaudhary RK, Elhence P, Phadke SR, Mandal K, Saxena D, Moirangthem A. Yadav BK, et al. Among authors: mandal k. Asian J Transfus Sci. 2023 Jul-Dec;17(2):145-150. doi: 10.4103/ajts.ajts_2_23. Epub 2023 May 11. Asian J Transfus Sci. 2023. PMID: 38274964 Free PMC article.

10

Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL).

Mishra S, Pandey H, Srivastava P, Mandal K, Phadke SR. Mishra S, et al. Among authors: mandal k. Indian J Pediatr. 2018 Dec;85(12):1061-1066. doi: 10.1007/s12098-018-2654-8. Epub 2018 Mar 15. Indian J Pediatr. 2018. PMID: 29542069 Review.

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