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Shivaram Shastri

Showing results (1-10 of 11) with videos related to

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Gut|June 17, 2010
Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutationsShallu Midha, Rajni Khajuria, Shivaram Shastri, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenarioManjula Maheshwari, R Vijaya, Manju Ghosh, et al.
Indian Journal of Pediatrics|June 8, 2012
Norrie disease: first mutation report and prenatal diagnosis in an Indian familyManju Ghosh, Shipra Sharma, Shivaram Shastri, et al.
Indian Pediatrics|March 2, 2019
Aquagenic Wrinkling of Skin: A Screening Test for Cystic FibrosisAnuj Singh, Rakesh Lodha, Shivaram Shastri, et al.
Indian Pediatrics|April 1, 2016
ADRB2 Polymorphism and Salbutamol Responsiveness in Northern Indian Children with Mild to Moderate Exacerbation of AsthmaPuneet Kaur Sahi, Shivaram Shastri, Rakesh Lodha, et al.
Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.
The Indian Journal of Medical Research|September 2, 2017
Identification of a novel homozygous mutation in transmembrane channel like 1 (<i>TMC1</i>) gene, one of the second-tier hearing loss genes after <i>GJB2</i> in IndiaPawan Kumar Singh, Manju Ghosh, Shipra Sharma, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 20, 2019
Genetic polymorphisms associated with obesity and non-alcoholic fatty liver disease in Asian Indian adolescentsVandana Jain, Anil Kumar, Nayeem Ahmad, et al.
Respiratory Care|October 8, 2015
Zinc Supplementation for One Year Among Children with Cystic Fibrosis Does Not Decrease Pulmonary InfectionGanesh Sharma, Rakesh Lodha, Shivaram Shastri, et al.
JIMD Reports|May 28, 2015
Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian PatientsNeerja Gupta, Pawan Kumar Singh, Manoj Kumar, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Gut|June 17, 2010
Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutationsShallu Midha, Rajni Khajuria, Shivaram Shastri, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenarioManjula Maheshwari, R Vijaya, Manju Ghosh, et al.
Indian Journal of Pediatrics|June 8, 2012
Norrie disease: first mutation report and prenatal diagnosis in an Indian familyManju Ghosh, Shipra Sharma, Shivaram Shastri, et al.
Indian Pediatrics|March 2, 2019
Aquagenic Wrinkling of Skin: A Screening Test for Cystic FibrosisAnuj Singh, Rakesh Lodha, Shivaram Shastri, et al.
Indian Pediatrics|April 1, 2016
ADRB2 Polymorphism and Salbutamol Responsiveness in Northern Indian Children with Mild to Moderate Exacerbation of AsthmaPuneet Kaur Sahi, Shivaram Shastri, Rakesh Lodha, et al.
Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.
The Indian Journal of Medical Research|September 2, 2017
Identification of a novel homozygous mutation in transmembrane channel like 1 (<i>TMC1</i>) gene, one of the second-tier hearing loss genes after <i>GJB2</i> in IndiaPawan Kumar Singh, Manju Ghosh, Shipra Sharma, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 20, 2019
Genetic polymorphisms associated with obesity and non-alcoholic fatty liver disease in Asian Indian adolescentsVandana Jain, Anil Kumar, Nayeem Ahmad, et al.
Respiratory Care|October 8, 2015
Zinc Supplementation for One Year Among Children with Cystic Fibrosis Does Not Decrease Pulmonary InfectionGanesh Sharma, Rakesh Lodha, Shivaram Shastri, et al.
JIMD Reports|May 28, 2015
Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian PatientsNeerja Gupta, Pawan Kumar Singh, Manoj Kumar, et al.
Pageof 2