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Prashant Kumar Verma

Showing results (1-10 of 25) with videos related to

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Contemporary Clinical Dentistry|January 24, 2022
Oro-Facial-Digital Syndrome: Unspecified Type with the Spontaneous Fusion of Cleft PalatePrashant Kumar Verma, Nowneet Kumar Bhat
Frontiers in Pediatrics|February 27, 2015
Review of literature: genes related to postaxial polydactylyPrashant Kumar Verma, Ashraf A El-Harouni
EJIFCC|November 30, 2022
Systemic Pseudohypoaldosteronism Type 1 Due to a Novel Mutation in SCNN1B Gene: A Case ReportKamal Joshi, Prashant Kumar Verma, Manidipa Barman
The Indian Journal of Tuberculosis|October 20, 2020
Gross hematuria: A rare presentation of disseminated tuberculosisNikhil Rajvanshi, Vinod Paul, Prashant Kumar Verma, et al.
Journal of Orthopaedic Case Reports|June 18, 2021
Genetic Association and Role of Surgery for the Treatment of Lower Limb Deformities in Diastrophic Dysplasia: A Case ReportAnchal Kumar Tripathi, Sunny Choudhary, Vivek Singh, et al.
BMJ Case Reports|September 9, 2020
A rare case of coexisting tuberculosis with hydatid disease from North India with review of literaturePrashant Kumar Verma, Ranjana Rohilla, Vivekanand Natarajan, et al.
Journal of Pediatric Genetics|August 1, 2024
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies in a Young Infant: First Case Entity of Casamassima-Morton-Nance Syndrome from AsiaRadhapyari Lourembam, Manish Kumar Gupta, Poonam Sherwani, et al.
BMJ Case Reports|December 30, 2023
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variationAswanth Ks, Adity Bansal, Prashant Kumar Verma, et al.
BMJ Case Reports|March 12, 2024
Loeys-Dietz syndrome and Goldenhar syndrome unveiled togetherHenuka Verma, Prashant Kumar Verma, Nikhil Rajvanshi, et al.
BMJ Case Reports|August 18, 2021
Congenital aniridia with ectopia lentis and unilateral buphthalmos: an unusual presentationAthul Suresh Puthalath, Neeti Gupta, Ramanuj Samanta, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Contemporary Clinical Dentistry|January 24, 2022
Oro-Facial-Digital Syndrome: Unspecified Type with the Spontaneous Fusion of Cleft PalatePrashant Kumar Verma, Nowneet Kumar Bhat
Frontiers in Pediatrics|February 27, 2015
Review of literature: genes related to postaxial polydactylyPrashant Kumar Verma, Ashraf A El-Harouni
EJIFCC|November 30, 2022
Systemic Pseudohypoaldosteronism Type 1 Due to a Novel Mutation in SCNN1B Gene: A Case ReportKamal Joshi, Prashant Kumar Verma, Manidipa Barman
The Indian Journal of Tuberculosis|October 20, 2020
Gross hematuria: A rare presentation of disseminated tuberculosisNikhil Rajvanshi, Vinod Paul, Prashant Kumar Verma, et al.
Journal of Orthopaedic Case Reports|June 18, 2021
Genetic Association and Role of Surgery for the Treatment of Lower Limb Deformities in Diastrophic Dysplasia: A Case ReportAnchal Kumar Tripathi, Sunny Choudhary, Vivek Singh, et al.
BMJ Case Reports|September 9, 2020
A rare case of coexisting tuberculosis with hydatid disease from North India with review of literaturePrashant Kumar Verma, Ranjana Rohilla, Vivekanand Natarajan, et al.
Journal of Pediatric Genetics|August 1, 2024
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies in a Young Infant: First Case Entity of Casamassima-Morton-Nance Syndrome from AsiaRadhapyari Lourembam, Manish Kumar Gupta, Poonam Sherwani, et al.
BMJ Case Reports|December 30, 2023
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variationAswanth Ks, Adity Bansal, Prashant Kumar Verma, et al.
BMJ Case Reports|March 12, 2024
Loeys-Dietz syndrome and Goldenhar syndrome unveiled togetherHenuka Verma, Prashant Kumar Verma, Nikhil Rajvanshi, et al.
BMJ Case Reports|August 18, 2021
Congenital aniridia with ectopia lentis and unilateral buphthalmos: an unusual presentationAthul Suresh Puthalath, Neeti Gupta, Ramanuj Samanta, et al.
Pageof 3