Agarwal S - Search Results

1

Susceptibility of glucose-6-phosphate dehydrogenase deficient red cells to primaquine enantiomers and two putative metabolites--I. Effect on reduced glutathione, methemoglobin content and release of hemoglobin.

Agarwal S, Gupta UR, Gupta RC, Anand N, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Biochem Pharmacol. 1988 Dec 15;37(24):4605-9. doi: 10.1016/0006-2952(88)90327-9. Biochem Pharmacol. 1988. PMID: 3202898

2

Susceptibility of glucose-6-phosphate dehydrogenase deficient red cells to primaquine, primaquine enantiomers, and its two putative metabolites. II. Effect on red blood cell membrane, lipid peroxidation, MC-540 staining, and scanning electron microscopic studies.

Agarwal S, Gupta UR, Daniel CS, Gupta RC, Anand N, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Biochem Pharmacol. 1991 Jan 1;41(1):17-21. doi: 10.1016/0006-2952(91)90005-p. Biochem Pharmacol. 1991. PMID: 1986741

3

Usefulness of MC-540 fluorescent dye as probe versus scanning electron microscopy for assessing membrane changes.

Agarwal S, Khardori R, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Toxicol Lett. 1990 Dec;54(2-3):169-74. doi: 10.1016/0378-4274(90)90180-t. Toxicol Lett. 1990. PMID: 2260114

4

A novel Indian beta-thalassemia mutation: Hb Lucknow [beta8(A5)Lys-->Arg]].

Agarwal S, Hattori Y, Gupta UR, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Hemoglobin. 1999 Aug;23(3):263-5. doi: 10.3109/03630269909005707. Hemoglobin. 1999. PMID: 10490139 No abstract available.

5

Characterization of beta-thalassaemia mutations in 57 beta-thalassaemia families seen at Lucknow.

Agarwal S, Naveed M, Gupta UR, Kishore P, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Indian J Med Res. 1994 Sep;100:106-10. Indian J Med Res. 1994. PMID: 7959965

6

Geographic and ethnic distribution of beta-thalassemia mutations in Uttar Pradesh, India.

Agarwal S, Pradhan M, Gupta UR, Sarwai S, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Hemoglobin. 2000 May;24(2):89-97. doi: 10.3109/03630260009003427. Hemoglobin. 2000. PMID: 10870879

7

Prenatal diagnosis in beta-thalassemia: an Indian experience.

Agarwal S, Gupta A, Gupta UR, Sarwai S, Phadke S, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Fetal Diagn Ther. 2003 Sep-Oct;18(5):328-32. doi: 10.1159/000071975. Fetal Diagn Ther. 2003. PMID: 12913343

8

Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India.

Tamhankar PM, Agarwal S, Arya V, Kumar R, Gupta UR, Agarwal SS. Tamhankar PM, et al. Among authors: agarwal s, agarwal ss. Prenat Diagn. 2009 Jan;29(1):83-8. doi: 10.1002/pd.2176. Prenat Diagn. 2009. PMID: 19090545

9

Rare beta-thalassemia mutations in Asian Indians.

Agarwal S, Hattori Y, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Am J Hematol. 2000 Dec;65(4):322-3. doi: 10.1002/1096-8652(200012)65:4<322::aid-ajh14>3.0.co;2-2. Am J Hematol. 2000. PMID: 11074564 Free article.

10

Codon 4 ACT-->ACA, codon 5 CCT-->TCT, and codon 6 GAG-->TAG mutations in cis position: a form of thalassemia trait.

Agarwal S, Wei L, Hattori Y, Agarwal SS. Agarwal S, et al. Among authors: agarwal ss. Am J Hematol. 1997 Nov;56(3):187-8. doi: 10.1002/(sici)1096-8652(199711)56:3<187::aid-ajh10>3.0.co;2-8. Am J Hematol. 1997. PMID: 9371533 Free article.

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