Isolated Hypoglossal Nerve Palsy due to Infected Impacted Tooth

Por Durrani, Farhan, Singh, Royana
Publicado em 2009

Intraosseous Follicular Adenomatoid Odontogenic Tumour—A Case Report

Por Durrani, Farhan, Singh, Royana
Publicado em 2009

Myeloperoxidase level around dental implants as an indicator of an inflammatory process

Por Durrani, Farhan, Singh, Royana
Publicado no Indian J Dent (2015)

Diacerein protects against iodoacetate-induced osteoarthritis in the femorotibial joints of rats

Por Jain, Achint, Singh, Royana, Singh, Saurabh, Singh, Sanjay
Publicado no J Biomed Res (2015)

Study of Dystrophinopathy in Eastern Uttar Pradesh Population of India

Por Kumari, Preeti, Joshi, Deepika, Shamal, Satya N., Singh, Royana
Publicado no J Pediatr Neurosci (2018)

Correlation of follicle-stimulating hormone receptor gene Asn 680 Ser (rs6166) polymorphism with female infertility

Por Rai, Sangeeta, Ashish, Kumari, Preeti, Singh, Anup, Singh, Royana
Publicado no J Family Med Prim Care (2019)

Effect of Tocopheryl Acetate on Maternal Cigarette Smoke Exposed Swiss Albino Mice Inbred Fetus

Por Chaudhary, Janardan, Singh, Royana, Shamal, SN, Supriya, K, Srivastava, Mona, More, RS
Publicado no J Clin Diagn Res (2016)

High incidence of neural tube defects in Northern part of India

Por Rai, Sunil Kumar, Singh, Royana, Pandey, Sharad, Singh, Kulwant, Shinde, Neeraj, Rai, Sangita, Prasad, Rajniti, Shama, Satya Narayan
Publicado no Asian J Neurosurg (2016)

The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations

Por Singh, Prajjval Pratap, Srivastava, Anshika, Sultana, Gazi Nurun Nahar, Khanam, Nargis, Pathak, Abhishek, Suravajhala, Prashanth, Singh, Royana, Shrivastava, Pankaj, van Driem, George, Thangaraj, Kumarasamy, Chaubey, Gyaneshwer
Publicado no Sci Rep (2021)

A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations

Por Iype, Thomas, Alakbarzade, Vafa, Iype, Mary, Singh, Royana, Sreekantan-Nair, Ajith, Chioza, Barry A., Mohapatra, Tribhuvan M., Baple, Emma L., Patton, Michael A., Warner, Thomas T., Proukakis, Christos, Kulkarni, Abhi, Crosby, Andrew H.
Publicado no BMC Med Genet (2015)

Copy number variation of LINGO1 in familial dystonic tremor

Por Alakbarzade, Vafa, Iype, Thomas, Chioza, Barry A., Singh, Royana, Harlalka, Gaurav V., Hardy, Holly, Sreekantan-Nair, Ajith, Proukakis, Christos, Peall, Kathryn, Clark, Lorraine N., Caswell, Richard, Lango Allen, Hana, Wakeling, Matthew, Chilton, John K., Baple, Emma L., Louis, Elan D., Warner, Thomas T., Crosby, Andrew H.
Publicado no Neurol Genet (2019)

PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment

Por Zollo, Massimo, Ahmed, Mustafa, Ferrucci, Veronica, Salpietro, Vincenzo, Asadzadeh, Fatemeh, Carotenuto, Marianeve, Maroofian, Reza, Al-Amri, Ahmed, Singh, Royana, Scognamiglio, Iolanda, Mojarrad, Majid, Musella, Luca, Duilio, Angela, Di Somma, Angela, Karaca, Ender, Rajab, Anna, Al-Khayat, Aisha, Mohan Mohapatra, Tribhuvan, Eslahi, Atieh, Ashrafzadeh, Farah, Rawlins, Lettie E., Prasad, Rajniti, Gupta, Rashmi, Kumari, Preeti, Srivastava, Mona, Cozzolino, Flora, Kumar Rai, Sunil, Monti, Maria, Harlalka, Gaurav V., Simpson, Michael A., Rich, Philip, Al-Salmi, Fatema, Patton, Michael A., Chioza, Barry A., Efthymiou, Stephanie, Granata, Francesca, Di Rosa, Gabriella, Wiethoff, Sarah, Borgione, Eugenia, Scuderi, Carmela, Mankad, Kshitij, Hanna, Michael G., Pucci, Piero, Houlden, Henry, Lupski, James R., Crosby, Andrew H., Baple, Emma L.
Publicado no Brain (2017)