Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Maya M Thomas"'
Autor:
Madhan Kumar, T P Murugan, Arul P Lionel, Maya M Thomas, Pavithra Mannam, Sangeetha Yoganathan
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 4, Pp 698-702 (2022)
Background: Most centers in developing countries prefer chelation therapy with D-penicillamine for the management of Wilson's disease (WD) because of its easy availability and affordability. Neurological worsening following treatment with D-penicilla
Externí odkaz:
https://doaj.org/article/4314355f68d34e12bb6989a289d6ab98
Autor:
Harsha M Dangare, Samuel P Oommen, Amisha N Sheth, Beena Koshy, Reeba Roshan, Maya M Thomas, Sumita Danda, Vivi M Srivastava
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 55, Iss 4, Pp 501-505 (2012)
The cri du chat syndrome (CdCS) is a chromosomal deletion syndrome associated with a partial deletion of the short (p) arm of chromosome 5. We describe five children who were diagnosed to have CdCS by conventional cytogenetic analysis. The deletion w
Externí odkaz:
https://doaj.org/article/66f685088ef84a6faa53dcdd04846e10
Autor:
Madhan, Kumar, T P, Murugan, Arul P, Lionel, Maya M, Thomas, Pavithra, Mannam, Sangeetha, Yoganathan
Publikováno v:
Annals of Indian Academy of Neurology. 25(4)
Most centers in developing countries prefer chelation therapy with D-penicillamine for the management of Wilson's disease (WD) because of its easy availability and affordability. Neurological worsening following treatment with D-penicillamine is not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::053066e3a3d5c90f1070f92866cd30e6
https://pubmed.ncbi.nlm.nih.gov/36211139
https://pubmed.ncbi.nlm.nih.gov/36211139
Autor:
Sardarabadi, Hamideh1 (AUTHOR), Kiani, Shirin1 (AUTHOR), Karkhanechi, Hamed1 (AUTHOR), Mousavi, Seyed Mahmoud1 (AUTHOR), Saljoughi, Ehsan1 (AUTHOR) saljoughi@um.ac.ir, Matsuyama, Hideto2 (AUTHOR)
Publikováno v:
Membranes. Dec2022, Vol. 12 Issue 12, p1232. 44p.
Autor:
Kumar, Madhan1, Murugan, T1, Lionel, Arul1, Thomas, Maya2, Mannam, Pavithra3, Yoganathan, Sangeetha2
Publikováno v:
Annals of Indian Academy of Neurology. Jul/Aug2022, Vol. 25 Issue 4, p698-702. 5p.
Biotin thiamine responsive basal ganglia disease-A potentially treatable inborn error of metabolism.
Autor:
Muthusamy, Karthik1, Ekbote, Alka V.2, Thomas, Maya M.1, Aaron, Sanjith1, Mathew, Vivek1, Patil, Anil B.1, Sivadasan, Ajith1, Prabhakar, A. T.1, Yoganathan, Sangeetha1, Alexander, Mathew1 mathewalex@cmcvellore.ac.in
Publikováno v:
Neurology India. Nov/Dec2016, Vol. 64 Issue 6, p1328-1331. 4p.
Publikováno v:
Journal of Pediatric Neurosciences; Apr-Jun2016, Vol. 11 Issue 2, p140-144, 5p