Dongerdiye R[au] - Search Results

Year	Number of Results
2018	1
2019	4
2020	2
2021	3
2022	2
2023	1

1

Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.

Sampagar A, Gosavi M, Kedar P, Patel T, Dongerdiye R, Mahantashetti N. Sampagar A, et al. Among authors: dongerdiye r. Int J Hematol. 2022 Feb;115(2):255-262. doi: 10.1007/s12185-021-03240-5. Epub 2021 Oct 27. Int J Hematol. 2022. PMID: 34704234

2

Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family.

Dongerdiye R, Jagadeesh S, Suresh B, Rajendran A, Devendra R, Warang P, Kedar PS. Dongerdiye R, et al. J Clin Pathol. 2021 Oct;74(10):620-624. doi: 10.1136/jclinpath-2020-206960. Epub 2020 Dec 25. J Clin Pathol. 2021. PMID: 33361148 Review.

3

Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian family.

Kedar P, Dongerdiye R, Chandrakala S, Bargir UA, Madkaikar M. Kedar P, et al. Among authors: dongerdiye r. Hematology. 2022 Dec;27(1):441-448. doi: 10.1080/16078454.2022.2058736. Hematology. 2022. PMID: 35413226

4

Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.

Dongerdiye R, Sampagar A, Devendra R, Warang P, Kedar P. Dongerdiye R, et al. BMC Med Genomics. 2021 Jul 28;14(1):191. doi: 10.1186/s12920-021-01038-2. BMC Med Genomics. 2021. PMID: 34321014 Free PMC article.

5

Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach.

Kedar PS, Harigae H, Ito E, Muramatsu H, Kojima S, Okuno Y, Fujiwara T, Dongerdiye R, Warang PP, Madkaikar MR. Kedar PS, et al. Among authors: dongerdiye r. Int J Hematol. 2019 Nov;110(5):618-626. doi: 10.1007/s12185-019-02716-9. Epub 2019 Aug 10. Int J Hematol. 2019. PMID: 31401766

6

Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.

More TA, Dongerdiye R, Devendra R, Warang PP, Kedar PS. More TA, et al. Among authors: dongerdiye r. Ann Hematol. 2020 Apr;99(4):715-727. doi: 10.1007/s00277-020-03955-1. Epub 2020 Feb 28. Ann Hematol. 2020. PMID: 32112123

7

Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.

More TA, Devendra R, Dongerdiye R, Warang P, Kedar P. More TA, et al. Among authors: dongerdiye r. Mol Genet Genomics. 2023 Jan 4. doi: 10.1007/s00438-022-01984-1. Online ahead of print. Mol Genet Genomics. 2023. PMID: 36598564

8

Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).

Dongerdiye R, Kamat P, Jain P, Warang P, Devendra R, Wasekar N, Sharma R, Mhaskar K, Madkaikar MR, Manglani MV, Kedar PS. Dongerdiye R, et al. J Clin Pathol. 2019 Jun;72(6):393-398. doi: 10.1136/jclinpath-2019-205718. Epub 2019 Mar 27. J Clin Pathol. 2019. PMID: 30918013

9

Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.

Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S, Madkaikar M. Kedar PS, et al. Among authors: dongerdiye r. Indian J Pediatr. 2019 Aug;86(8):692-699. doi: 10.1007/s12098-019-02928-1. Epub 2019 Apr 27. Indian J Pediatr. 2019. PMID: 31030358

10

Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients.

Kedar PS, Gupta V, Dongerdiye R, Chiddarwar A, Warang P, Madkaikar MR. Kedar PS, et al. Among authors: dongerdiye r. J Clin Pathol. 2019 Jan;72(1):81-85. doi: 10.1136/jclinpath-2018-205420. Epub 2018 Oct 18. J Clin Pathol. 2019. PMID: 30337328

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results