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Indian Academy of Pediatrics Revised (2021) Guidelines on Prevention and Treatment of Vitamin D Deficiency and Rickets.
Indian Pediatr. 2022 Feb 15;59(2):142-158. Epub 2021 Dec 29.
Indian Pediatr. 2022.
PMID: 34969941
Free article.
Glycemic Control and Long-term Complications in Pediatric Onset Type 1 Diabetes Mellitus: A Single-center Experience from Northern India.
Sudhanshu S, Nair VV, Godbole T, Reddy SVB, Bhatia E, Dabadghao P, Sharma K, Arora P, Bano S, Singh A, Bhatia V.
Sudhanshu S, et al. Among authors: godbole t.
Indian Pediatr. 2019 Mar 15;56(3):191-195.
Indian Pediatr. 2019.
PMID: 30954988
Free article.
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Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.
Gangodkar P, Khadilkar V, Raghupathy P, Kumar R, Dayal AA, Dayal D, Ayyavoo A, Godbole T, Jahagirdar R, Bhat K, Gupta N, Kamalanathan S, Jagadeesh S, Ranade S, Lohiya N, Oke RL, Ganesan K, Khatod K, Agarwal M, Phadke N, Khadilkar A.
Gangodkar P, et al. Among authors: godbole t.
Endocrine. 2021 Jan;71(1):189-198. doi: 10.1007/s12020-020-02494-z. Epub 2020 Sep 18.
Endocrine. 2021.
PMID: 32948948
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Novel mutations and spectrum of the disease of NR0B1 (DAX1)-related adrenal insufficiency in Indian children.
Gupta S, Joshi K, Zaidi G, Sarangi AN, Mandal K, Bhavani N, Pavithran PV, Pillai MG, Singh SK, Godbole T, Bhatia V, Bhatia E.
Gupta S, et al. Among authors: godbole t.
J Pediatr Endocrinol Metab. 2019 Aug 27;32(8):863-869. doi: 10.1515/jpem-2018-0440.
J Pediatr Endocrinol Metab. 2019.
PMID: 31219797
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De Sanctis-Cacchione syndrome.
Mittal H, Mehndiratta S, Kaushik JS, Godbole T.
Mittal H, et al. Among authors: godbole t.
Indian J Dermatol Venereol Leprol. 2013 Nov-Dec;79(6):849. doi: 10.4103/0378-6323.120760.
Indian J Dermatol Venereol Leprol. 2013.
PMID: 24177634
Free article.
No abstract available.
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CNS neoplasm: a missed diagnosis.
Aggarwal A, Godbole T, Mittal H, Dua R.
Aggarwal A, et al. Among authors: godbole t.
Indian J Pediatr. 2011 Jan;78(1):116-7. doi: 10.1007/s12098-010-0259-y. Epub 2010 Oct 9.
Indian J Pediatr. 2011.
PMID: 20936379
No abstract available.
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YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress.
De Franco E, Lytrivi M, Ibrahim H, Montaser H, Wakeling MN, Fantuzzi F, Patel K, Demarez C, Cai Y, Igoillo-Esteve M, Cosentino C, Lithovius V, Vihinen H, Jokitalo E, Laver TW, Johnson MB, Sawatani T, Shakeri H, Pachera N, Haliloglu B, Ozbek MN, Unal E, Yıldırım R, Godbole T, Yildiz M, Aydin B, Bilheu A, Suzuki I, Flanagan SE, Vanderhaeghen P, Senée V, Julier C, Marchetti P, Eizirik DL, Ellard S, Saarimäki-Vire J, Otonkoski T, Cnop M, Hattersley AT.
De Franco E, et al. Among authors: godbole t.
J Clin Invest. 2020 Dec 1;130(12):6338-6353. doi: 10.1172/JCI141455.
J Clin Invest. 2020.
PMID: 33164986
Free PMC article.
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