Jana M - Search Results

1

Nasopharyngeal teratoma, congenital diaphragmatic hernia and Dandy-Walker malformation - a yet uncharacterized syndrome.

Gupta N, Shastri S, Singh PK, Jana M, Mridha A, Verma G, Kabra M. Gupta N, et al. Among authors: jana m. Clin Genet. 2016 Nov;90(5):470-471. doi: 10.1111/cge.12830. Epub 2016 Aug 10. Clin Genet. 2016. PMID: 27506516

2

Spondylometaphyseal Dysplasia Corner Fracture (Sutcliffe) Type.

Nair N, Satapathy AK, Gupta N, Kabra M, Gupta AK, Jana M. Nair N, et al. Among authors: jana m. Indian J Pediatr. 2016 Oct;83(10):1191-4. doi: 10.1007/s12098-016-2121-3. Epub 2016 Apr 30. Indian J Pediatr. 2016. PMID: 27130511

3

Caffey's Disease: Two Cases Presenting with Unexplained Fever.

Satapathy AK, Pai G, Shruthi M, Kumar A, Jana M, Gupta N, Kabra M. Satapathy AK, et al. Among authors: jana m. Indian J Pediatr. 2016 Nov;83(12-13):1499-1500. doi: 10.1007/s12098-016-2185-0. Epub 2016 Jul 1. Indian J Pediatr. 2016. PMID: 27364822 No abstract available.

4

Unusual presentation of Erdheim-Chester disease in a child with acute lymphoblastic leukemia.

Vallonthaiel AG, Mridha AR, Gamanagatti S, Jana M, Sharma MC, Khan SA, Bakhshi S. Vallonthaiel AG, et al. Among authors: jana m. World J Radiol. 2016 Aug 28;8(8):757-63. doi: 10.4329/wjr.v8.i8.757. World J Radiol. 2016. PMID: 27648170 Free PMC article.

5

Conventional vs virtual autopsy with postmortem MRI in phenotypic characterization of stillbirths and fetal malformations.

Shruthi M, Gupta N, Jana M, Mridha AR, Kumar A, Agarwal R, Sharma R, Deka D, Gupta AK, Kabra M. Shruthi M, et al. Among authors: jana m. Ultrasound Obstet Gynecol. 2018 Feb;51(2):236-245. doi: 10.1002/uog.17468. Ultrasound Obstet Gynecol. 2018. PMID: 28295775 Free article.

6

Pelvic radiograph in skeletal dysplasias: An approach.

Jana M, Nair N, Gupta AK, Kabra M, Gupta N. Jana M, et al. Indian J Radiol Imaging. 2017 Apr-Jun;27(2):187-199. doi: 10.4103/ijri.IJRI_367_16. Indian J Radiol Imaging. 2017. PMID: 28744080 Free PMC article.

7

Asparagine Synthetase deficiency-report of a novel mutation and review of literature.

Gupta N, Tewari VV, Kumar M, Langeh N, Gupta A, Mishra P, Kaur P, Ramprasad V, Murugan S, Kumar R, Jana M, Kabra M. Gupta N, et al. Among authors: jana m. Metab Brain Dis. 2017 Dec;32(6):1889-1900. doi: 10.1007/s11011-017-0073-6. Epub 2017 Aug 3. Metab Brain Dis. 2017. PMID: 28776279 Review.

8

Erratum to: Asparagine synthetase deficiency-report of a novel mutation and review of literature.

Gupta N, Tewari VV, Kumar M, Langeh N, Gupta A, Mishra P, Kaur P, Ramprasad V, Murugan S, Kumar R, Jana M, Kabra M. Gupta N, et al. Among authors: jana m. Metab Brain Dis. 2017 Dec;32(6):1901. doi: 10.1007/s11011-017-0102-5. Metab Brain Dis. 2017. PMID: 28875262 No abstract available.

9

Growth Pattern and Clinical Profile of Indian Children with Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia on Treatment.

Meena H, Jana M, Singh V, Kabra M, Jain V. Meena H, et al. Among authors: jana m. Indian J Pediatr. 2019 Jun;86(6):496-502. doi: 10.1007/s12098-018-02848-6. Epub 2019 Jan 30. Indian J Pediatr. 2019. PMID: 30697677

10

Genetic polymorphisms associated with obesity and non-alcoholic fatty liver disease in Asian Indian adolescents.

Jain V, Kumar A, Ahmad N, Jana M, Kalaivani M, Kumar B, Shastri S, Jain O, Kabra M. Jain V, et al. Among authors: jana m. J Pediatr Endocrinol Metab. 2019 Jul 26;32(7):749-758. doi: 10.1515/jpem-2018-0543. J Pediatr Endocrinol Metab. 2019. PMID: 31216264

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