Gupta N - Search Results

1

Impact of Structured Reporting of Skeletal Survey in Skeletal Dysplasia: A Single Institution Experience.

Gupta A, Gupta N, Kabra M, Kaur T, Gabra P, Khan MA, Jana M. Gupta A, et al. Among authors: gupta n. Indian J Radiol Imaging. 2023 Mar 4;33(2):144-149. doi: 10.1055/s-0043-1762935. eCollection 2023 Apr. Indian J Radiol Imaging. 2023. PMID: 37123575 Free PMC article.

2

A female with hemihypertrophy and chylous ascites - Klippel-Trenaunay syndrome or Proteus syndrome: a diagnostic dilemma.

Gupta N, Kabra M, Ramesh K, Garg G, Kaur D, Gupta A, Bal CS. Gupta N, et al. Among authors: gupta a. Clin Dysmorphol. 2006 Oct;15(4):229-231. doi: 10.1097/01.mcd.0000228420.82037.51. Clin Dysmorphol. 2006. PMID: 16957479

3

Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family.

Gupta N, Bianchi P, Fermo E, Kabra M, Warang P, Kedar P, Gupta N, Colah R. Gupta N, et al. Prenat Diagn. 2007 Feb;27(2):117-8. doi: 10.1002/pd.1616. Prenat Diagn. 2007. PMID: 17191259

4

Intravenous pamidronate therapy in osteogenesis imperfecta: response to treatment and factors influencing outcome.

Bajpai A, Kabra M, Gupta N, Sharda S, Ghosh M. Bajpai A, et al. Among authors: gupta n. J Pediatr Orthop. 2007 Mar;27(2):225-7. doi: 10.1097/bpo.0b013e3180316d06. J Pediatr Orthop. 2007. PMID: 17314651 Clinical Trial.

5

Maffucci syndrome.

Gupta N, Kabra M. Gupta N, et al. Indian Pediatr. 2007 Feb;44(2):149-50. Indian Pediatr. 2007. PMID: 17351310 Free article. No abstract available.

6

Recent advances in approach to treatment of genetic disorders: clinicians perspective.

Gupta N, Kabra M. Gupta N, et al. Indian Pediatr. 2007 May;44(5):361-9. Indian Pediatr. 2007. PMID: 17536138 Free article. Review.

7

Pyle metaphyseal dysplasia.

Gupta N, Kabra M, Das CJ, Gupta AK. Gupta N, et al. Among authors: gupta ak. Indian Pediatr. 2008 Apr;45(4):323-5. Indian Pediatr. 2008. PMID: 18451455 Free article.

8

Carbimazole embryopathy-bilateral choanal atresia and patent vitello-intestinal duct: a case report and review of literature.

Kannan L, Mishra S, Agarwal R, Kartikeyan V, Gupta N, Kabra M. Kannan L, et al. Among authors: gupta n. Birth Defects Res A Clin Mol Teratol. 2008 Sep;82(9):649-51. doi: 10.1002/bdra.20483. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18671255 Review.

9

Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases.

Halder A, Jain M, Kabra M, Gupta N. Halder A, et al. Among authors: gupta n. Mol Cytogenet. 2008 Aug 10;1:18. doi: 10.1186/1755-8166-1-18. Mol Cytogenet. 2008. PMID: 18691436 Free PMC article.

10

Larsen syndrome.

Gupta N, Kabra M. Gupta N, et al. Indian Pediatr. 2008 Sep;45(9):783-4. Indian Pediatr. 2008. PMID: 18820390 No abstract available.

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