Renjith Mani

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12 Article
1 Comment/debate

Gratification Phenomena in Infancy: A Report of Twenty-Nine Children
Koul, R., Alfutaisi, A., Mani, R., Abdelrahim, R. & Aladi, A., Jun 1 2020, In: Journal of Pediatric Neurology. 18, 3, p. 141-143 3 p.
Research output: Contribution to journal › Article › peer-review
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
Perenthaler, E., Nikoncuk, A., Yousefi, S., Berdowski, W. M., Alsagob, M., Capo, I., van der Linde, H. C., van den Berg, P., Jacobs, E. H., Putar, D., Ghazvini, M., Aronica, E., van IJcken, W. F. J., de Valk, W. G., Medici-van den Herik, E., van Slegtenhorst, M., Brick, L., Kozenko, M., Kohler, J. N., Bernstein, J. A., & 49 othersMonaghan, K. G., Begtrup, A., Torene, R., Al Futaisi, A., Al Murshedi, F., Mani, R., Al Azri, F., Kamsteeg, E. J., Mojarrad, M., Eslahi, A., Khazaei, Z., Darmiyan, F. M., Doosti, M., Karimiani, E. G., Vandrovcova, J., Zafar, F., Rana, N., Kandaswamy, K. K., Hertecant, J., Bauer, P., AlMuhaizea, M. A., Salih, M. A., Aldosary, M., Almass, R., Al-Quait, L., Qubbaj, W., Coskun, S., Alahmadi, K. O., Hamad, M. H. A., Alwadaee, S., Awartani, K., Dababo, A. M., Almohanna, F., Colak, D., Dehghani, M., Mehrjardi, M. Y. V., Gunel, M., Ercan-Sencicek, A. G., Passi, G. R., Cheema, H. A., Efthymiou, S., Houlden, H., Bertoli-Avella, A. M., Brooks, A. S., Retterer, K., Maroofian, R., Kaya, N., van Ham, T. J. & Barakat, T. S., Mar 1 2020, In: Acta Neuropathologica. 139, 3, p. 415-442 28 p.
Research output: Contribution to journal › Article › peer-review

Open Access
27 Citations (SciVal)
Rituximab treatment in myasthaenia gravis: Report of two paediatric cases
Koul, R., Al-Futaisi, A., Abdelrahim, R., Mani, R., Abdwani, R. & Al-Asmi, A., May 2018, In: Sultan Qaboos University Medical Journal. 18, 2, p. e223-e227
Research output: Contribution to journal › Article › peer-review
4 Citations (Scopus)
Blood culture contaminants in a paediatric population: Retrospective study from a tertiary hospital in Oman
El-Naggari, M. A., Al-Mulaabed, S. W., Al-Muharrmi, Z., Mani, R., Abdelrahim, R. & Abdwani, R., May 2017, In: Sultan Qaboos University Medical Journal. 17, 2, p. e202-e208
Research output: Contribution to journal › Article › peer-review
3 Citations (SciVal)
Longitudinal extensive transverse myelitis (LETM) in children: A twenty-year study from Oman
Koul, R., Alfutaisi, A. M., Mani, R., Abdel Rahim, R. A., Sankhla, D. K. & Al Azri, F. M., 2017, In: Neurosciences. 22, 2, p. 127-130 4 p.
Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus)

Renjith Mani

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Dive into details

Gratification Phenomena in Infancy: A Report of Twenty-Nine Children

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

Rituximab treatment in myasthaenia gravis: Report of two paediatric cases

Blood culture contaminants in a paediatric population: Retrospective study from a tertiary hospital in Oman

Longitudinal extensive transverse myelitis (LETM) in children: A twenty-year study from Oman

Renjith Mani

Network

Research output

Gratification Phenomena in Infancy: A Report of Twenty-Nine Children

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

Rituximab treatment in myasthaenia gravis: Report of two paediatric cases

Blood culture contaminants in a paediatric population: Retrospective study from a tertiary hospital in Oman

Longitudinal extensive transverse myelitis (LETM) in children: A twenty-year study from Oman