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Journal of Pediatric Gastroenterology and Nutrition|November 1, 2024
Personalized management of hepatic glycogen storage disorders: The role of continuous glucose monitoringAmbika Gupta, Anuja Agarwala, Mani Kalaivani, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian originRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Clinical Dysmorphology|September 8, 2006
A female with hemihypertrophy and chylous ascites - Klippel-Trenaunay syndrome or Proteus syndrome: a diagnostic dilemmaNeerja Gupta, Madhulika Kabra, Konanki Ramesh, et al.
European Journal of Radiology|January 26, 2022
Post-mortem MRI in stillbirth: Normal imaging appearancesNeerja Gupta, Amit Gupta, Atin Kumar, et al.
Journal of Pediatric Genetics|September 15, 2016
Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12pPankaj Sharma, Neerja Gupta, Madhumita R Chowdhury, et al.
The Indian Journal of Radiology & Imaging|March 19, 2021
Spine radiograph in dysplasias: A pictorial essayPavan Gabra, Manisha Jana, Priyanka Naranje, et al.
Practical Neurology|July 8, 2022
Late-onset cobalamin C disease: rare but treatableAminu Aliyar, Mounika Endrakanti, Rajesh K Singh, et al.
The Indian Journal of Radiology & Imaging|May 1, 2023
Impact of Structured Reporting of Skeletal Survey in Skeletal Dysplasia: A Single Institution ExperienceAmit Gupta, Neerja Gupta, Madhulika Kabra, et al.
Indian Pediatrics|February 12, 2018
Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian GirlsMeenakshi Lallar, Archana Rai, Priyanka Srivastava, et al.
Gene|June 14, 2016
Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in IndiaPankaj Sharma, Neerja Gupta, Madhumita Roy Chowdhury, et al.
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