Neuroimaging Features of Biotinidase Deficiency ajnr.org/content/early/…

Treatable cause of leukodystrophy: Galactosaemia iap-kpj.org/treatable-caus…

A rare case of deformity: Fibrodysplasia ossificans progressiva iap-kpj.org/a-rare-case-of…

Notes and News iap-kpj.org/notes-and-news/

rdcu.be/c7Khk

mail.google.com/mail/u/0/

Ohtahara and West Syndrome due to Pyridox(am)ine-5-Phosphate Oxidase (PNPO) Deficiency with Novel Phenotype and Goo… pubmed.ncbi.nlm.nih.gov/36922472/

My research is available on ResearchGate: researchgate.net/publication/36…

CERT1 mutations perturb human development by disrupting sphingolipid homeostasis pubmed.ncbi.nlm.nih.gov/36976648/

The 2022 Enterovirus Paradox: The AFM working group discusses data and hypotheses about the increased enterovirus circulation without acute flaccid myelitis. youtube.com/playlist?list=…

Nihaal Reddy J DASARATHA RAMAIAH Indian Academy of Pediatrics (IAP) Dr Geetha Chanda Srikanth Domala Nalinikant Panigrahy RCH PedNeuro Rural Development Trust (RDT) Prof (Dr) Vykunta Raju K N Dr. C P Ravi Kumar Fundación Vicente Ferrer Job well done J DASARATHA RAMAIAH !! Had an excellent time interacting with all delegates & catching up with Prof.Vykunta Raju K.N sir Dr. C P Ravi Kumar, meeting up with Dr Pavan. Your physical presence was missed Nihaal Reddy !!

If you have a passion to transform your research to clinical applications and excited to work in close collaboration with hospital teams, we encourage you to apply for this research position and become part of our research team. Pls retweet! Prof (Dr) Vykunta Raju K N IndiaBioscience.org

*AOCN: SIG Session on Movement Disorders in Cerebral Palsy* *11th October | 8 PM India Time* *Registration FREE but compulsory* @ _us02web.zoom.us/webinar/regist… _Register ONCE for the entire series, till December 2023_

KCTD7‐related progressive myoclonic epilepsy: Report of 42 cases and review of literature - Yoganathan - Epilepsia - Wiley Online Library onlinelibrary.wiley.com/doi/10.1111/ep…

youtu.be/8eLBbME-ufw?si…

youtu.be/_OOXrlUrOwA?si…

This genetic condition, mostly seen since birth, can weaken the muscles, leading to deformities and making simple daily activities challenging happiesthealth.com/articles/muscl…

instagram.com/p/DHEZ5Tdyw1-l…