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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1993 1
1997 1
1999 2
2004 1
2005 1
2007 1
2008 1
2009 1
2010 5
2011 2
2012 1
2013 3
2014 6
2015 3
2016 2
2017 1
2018 1
2021 1
2024 3

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35 results

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Page 1
Johanson-blizzard syndrome.
Godbole K, Maja S, Leena H, Martin Z. Godbole K, et al. Indian Pediatr. 2013 May 8;50(5):510-2. Indian Pediatr. 2013. PMID: 23778732 Free article.
Piperacillin/tazobactam--induced petechial rash.
Abate G, Godbole K, Springston C. Abate G, et al. Among authors: godbole k. Ann Pharmacother. 2010 Jul-Aug;44(7-8):1345-6. doi: 10.1345/aph.1P247. Epub 2010 Jun 22. Ann Pharmacother. 2010. PMID: 20571103 No abstract available.
Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.
Sheth J, Nair A, Sheth F, Ajagekar M, Dhondekar T, Panigrahi I, Bavdekar A, Nampoothiri S, Datar C, Gandhi A, Muranjan M, Kaur A, Desai M, Mistri M, Patel C, Naik P, Shah M, Godbole K, Kapoor S, Gupta N, Bijarnia-Mahay S, Kadam S, Solanki D, Desai S, Iyer A, Patel K, Patel H, Shah RC, Mehta S, Shah R, Bhavsar R, Shah J, Pandya M, Patel B, Shah S, Shah H, Shah S, Bajaj S, Shah S, Thaker N, Kalane U, Kamate M, Kn VR, Tayade N, Jagadeesan S, Jain D, Chandarana M, Singh J, Mehta S, Suresh B, Sheth H. Sheth J, et al. Among authors: godbole k. Orphanet J Rare Dis. 2024 Aug 13;19(1):295. doi: 10.1186/s13023-024-03300-z. Orphanet J Rare Dis. 2024. PMID: 39138584 Free PMC article.
Fetal programming of type 2 diabetes: is sex important?
Yajnik CS, Godbole K, Otiv SR, Lubree HG. Yajnik CS, et al. Among authors: godbole k. Diabetes Care. 2007 Oct;30(10):2754-5. doi: 10.2337/dc07-1485. Diabetes Care. 2007. PMID: 17901535 No abstract available.
Bartsocas-Papas syndrome.
Godbole K, Bhide V, Godbole G. Godbole K, et al. Indian Pediatr. 2008 Sep;45(9):780-2. Indian Pediatr. 2008. PMID: 18820389
Mutations in the human UBR1 gene and the associated phenotypic spectrum.
Sukalo M, Fiedler A, Guzmán C, Spranger S, Addor MC, McHeik JN, Oltra Benavent M, Cobben JM, Gillis LA, Shealy AG, Deshpande C, Bozorgmehr B, Everman DB, Stattin EL, Liebelt J, Keller KM, Bertola DR, van Karnebeek CD, Bergmann C, Liu Z, Düker G, Rezaei N, Alkuraya FS, Oğur G, Alrajoudi A, Venegas-Vega CA, Verbeek NE, Richmond EJ, Kirbiyik O, Ranganath P, Singh A, Godbole K, Ali FA, Alves C, Mayerle J, Lerch MM, Witt H, Zenker M. Sukalo M, et al. Among authors: godbole k. Hum Mutat. 2014 May;35(5):521-31. doi: 10.1002/humu.22538. Epub 2014 Apr 9. Hum Mutat. 2014. PMID: 24599544 Review.
H syndrome--four new patients from India.
Molho-Pessach V, Varma M, Godbole K, Kamath N, Zlotogorski A. Molho-Pessach V, et al. Among authors: godbole k. Indian J Dermatol Venereol Leprol. 2014 Nov-Dec;80(6):579. doi: 10.4103/0378-6323.144229. Indian J Dermatol Venereol Leprol. 2014. PMID: 25382534 Free article. No abstract available.
Many faces of Hirschsprung's disease.
Godbole K. Godbole K. Indian Pediatr. 2004 Nov;41(11):1115-23. Indian Pediatr. 2004. PMID: 15591661 Free article. Review.
Asian paralysis syndrome.
Phadke MA, Gambhir PS, Deshpande AS, Kurlekar SU, Godbole KG. Phadke MA, et al. Among authors: godbole kg. Ann Trop Paediatr. 1999 Dec;19(4):317-20. doi: 10.1080/02724939992130. Ann Trop Paediatr. 1999. PMID: 10716023
35 results