Giri N - Search Results

1

Fanconi anaemia: A syndrome with distinct subgroups.

Alter BP, Giri N, McReynolds LJ, Altintas B. Alter BP, et al. Among authors: giri n. Br J Haematol. 2022 May;197(4):467-474. doi: 10.1111/bjh.18091. Epub 2022 Feb 22. Br J Haematol. 2022. PMID: 35191533

2

Clinical and laboratory evidence for a trilineage haematopoietic defect in patients with refractory Diamond-Blackfan anaemia.

Giri N, Kang E, Tisdale JF, Follman D, Rivera M, Schwartz GN, Kim S, Young NS, Rick ME, Dunbar CE. Giri N, et al. Br J Haematol. 2000 Jan;108(1):167-75. doi: 10.1046/j.1365-2141.2000.01796.x. Br J Haematol. 2000. PMID: 10651740 Free article.

3

Thrombocytopenia, multiple mucosal squamous cell carcinomas, and dyspigmentation.

Braun M, Giri N, Alter BP, Cowen EW. Braun M, et al. Among authors: giri n. J Am Acad Dermatol. 2006 Jun;54(6):1056-9. doi: 10.1016/j.jaad.2006.02.065. J Am Acad Dermatol. 2006. PMID: 16713462 No abstract available.

4

Intensive immunosuppression therapy for aplastic anemia associated with dyskeratosis congenita.

Al-Rahawan MM, Giri N, Alter BP. Al-Rahawan MM, et al. Among authors: giri n. Int J Hematol. 2006 Apr;83(3):275-6. doi: 10.1532/IJH97.06030. Int J Hematol. 2006. PMID: 16720563 No abstract available.

5

Endocrine abnormalities in patients with Fanconi anemia.

Giri N, Batista DL, Alter BP, Stratakis CA. Giri N, et al. J Clin Endocrinol Metab. 2007 Jul;92(7):2624-31. doi: 10.1210/jc.2007-0135. Epub 2007 Apr 10. J Clin Endocrinol Metab. 2007. PMID: 17426088

6

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.

Alter BP, Baerlocher GM, Savage SA, Chanock SJ, Weksler BB, Willner JP, Peters JA, Giri N, Lansdorp PM. Alter BP, et al. Among authors: giri n. Blood. 2007 Sep 1;110(5):1439-47. doi: 10.1182/blood-2007-02-075598. Epub 2007 Apr 27. Blood. 2007. PMID: 17468339 Free PMC article. Clinical Trial.

7

Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor.

Giri N, Pitel PA, Green D, Alter BP. Giri N, et al. Br J Haematol. 2007 Sep;138(6):815-7. doi: 10.1111/j.1365-2141.2007.06718.x. Br J Haematol. 2007. PMID: 17760812 Free article. No abstract available.

8

TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.

Savage SA, Giri N, Baerlocher GM, Orr N, Lansdorp PM, Alter BP. Savage SA, et al. Among authors: giri n. Am J Hum Genet. 2008 Feb;82(2):501-9. doi: 10.1016/j.ajhg.2007.10.004. Epub 2008 Jan 31. Am J Hum Genet. 2008. PMID: 18252230 Free PMC article.

9

All in the family: disclosure of "unwanted" information to an adolescent to benefit a relative.

Denny CC, Wilfond BS, Peters JA, Giri N, Alter BP. Denny CC, et al. Among authors: giri n. Am J Med Genet A. 2008 Nov 1;146A(21):2719-24. doi: 10.1002/ajmg.a.32362. Am J Med Genet A. 2008. PMID: 18831063 Free PMC article.

10

Oral and dental phenotype of dyskeratosis congenita.

Atkinson JC, Harvey KE, Domingo DL, Trujillo MI, Guadagnini JP, Gollins S, Giri N, Hart TC, Alter BP. Atkinson JC, et al. Among authors: giri n. Oral Dis. 2008 Jul;14(5):419-27. doi: 10.1111/j.1601-0825.2007.01394.x. Oral Dis. 2008. PMID: 18938267 Free PMC article.

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