Prashant Kumar Verma

Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 12

Top Venues

BMJ case reports

Journal of the Turkish German Gynecological Association

All India Institute of Medical Sciences - Rishikesh

This page only lists publications with an associated author ORCID identifier.

Affiliation History

All India Institute of Medical Sciences - Rishikesh Jul 30 2017

India

Associate Professor :: Paediatric

Publications

Henuka Verma, Prashant Kumar Verma, Nikhil Rajvanshi, Nowneet Kumar Bhat
Loeys-Dietz syndrome and Goldenhar syndrome unveiled together. BMJ case reports 17 (3) (2024)
Henuka Verma, Prashant Kumar Verma, Nikhil Rajvanshi, Nowneet Kumar Bhat
Loeys-Dietz syndrome and Goldenhar syndrome unveiled together. BMJ case reports 17 (3) (2024)
Henuka Verma, Prashant Kumar Verma, Nikhil Rajvanshi, Nowneet Kumar Bhat
Loeys-Dietz syndrome and Goldenhar syndrome unveiled together. BMJ case reports 17 (3) (2024)
Henuka Verma, Prashant Kumar Verma, Nikhil Rajvanshi, Nowneet Kumar Bhat
Loeys-Dietz syndrome and Goldenhar syndrome unveiled together. BMJ case reports 17 (3) (2024)
Aswanth Ks, Adity Bansal, Prashant Kumar Verma, Nowneet Kumar Bhat
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variation. BMJ case reports 16 (12) (2023)
Aswanth Ks, Adity Bansal, Prashant Kumar Verma, Nowneet Kumar Bhat
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variation. BMJ case reports 16 (12) (2023)
Aswanth Ks, Adity Bansal, Prashant Kumar Verma, Nowneet Kumar Bhat
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variation. BMJ case reports 16 (12) (2023)
Aswanth Ks, Adity Bansal, Prashant Kumar Verma, Nowneet Kumar Bhat
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variation. BMJ case reports 16 (12) (2023)
Aswanth Ks, Adity Bansal, Prashant Kumar Verma, Nowneet Kumar Bhat
Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variation. BMJ case reports 16 (12) (2023)
Aarzoo Juneja, Athul Suresh Puthalath, Neeti Gupta, Prashant Kumar Verma
Isolated bilateral limbal dermoid, preauricular skin tags and ametropic amblyopia. BMJ case reports 14 (8) (2021)
Athul Suresh Puthalath, Neeti Gupta, Ramanuj Samanta, Prashant Kumar Verma
Congenital aniridia with ectopia lentis and unilateral buphthalmos: an unusual presentation. BMJ case reports 14 (8) (2021)
Latika Chawla, Aditi Jindal, Prashant Kumar Verma, Anupama Bahadur, Shashi Prateek
What is your diagnosis? Journal of the Turkish German Gynecological Association 21 (3) (2020)

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Publication Activity (10 Years)

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Prashant Kumar Verma