|A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis|
D Thyagarajan, S Shanske, M Vazquez‐Memije, D Devivo, S Dimauro
Annals of neurology 38 (3), 468-472, 1995
|A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy|
D Thyagarajan, S Bressman, C Bruno, S Przedborski, S Shanske, T Lynch, ...
Annals of neurology 48 (5), 730-736, 2000
|Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease|
DM Kirby, A Boneh, CW Chow, A Ohtake, MT Ryan, D Thyagarajan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2003
|Normal variants of human mitochondrial DNA and translation products: the building of a reference data base|
S Marzuki, AS Noer, P Lertrit, D Thyagarajan, R Kapsa, P Utthanaphol, ...
Human genetics 88 (2), 139-145, 1991
|Magnetic resonance imaging in brachial plexopathy of cancer|
D Thyagarajan, T Cascino, G Harms
Neurology 45 (3), 421-427, 1995
|The fate of human sperm-derived mtDNA in somatic cells|
G Manfredi, D Thyagarajan, LC Papadopoulou, F Pallotti, EA Schon
The American Journal of Human Genetics 61 (4), 953-960, 1997
|A tRNA (Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.|
AS Noer, H Sudoyo, P Lertrit, D Thyagarajan, P Utthanaphol, R Kapsa, ...
American journal of human genetics 49 (4), 715, 1991
|Rapid‐onset dystonia‐parkinsonism in a second family|
A Brashear, D DeLeon, SB Bressman, D Thyagarajan, MR Farlow, ...
Neurology 48 (4), 1066-1069, 1997
|A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.|
P Lertrit, AS Noer, MJ Jean-Francois, R Kapsa, X Dennett, D Thyagarajan, ...
American journal of human genetics 51 (3), 457, 1992
|Multiple Symmetrical Lipomatosis—A mitochondrial disorder of brown fat|
C Plummer, PJ Spring, R Marotta, J Chin, G Taylor, D Sharpe, ...
Mitochondrion 13 (4), 269-276, 2013
|Clinical and molecular features of adPEO due to mutations in the Twinkle gene|
S Lewis, W Hutchison, D Thyagarajan, HHM Dahl
Journal of the neurological sciences 201 (1-2), 39-44, 2002
|Platelet α-and γ-synucleins in Parkinson's disease and normal control subjects|
QX Li, BCV Campbell, CA McLean, D Thyagarajan, WP Gai, RM Kapsa, ...
Journal of Alzheimer's Disease 4 (4), 309-315, 2002
|Dominantly‐inherited adult‐onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene|
D Thyagarajan, T Chataway, R Li, WP Gai, M Brenner
Movement disorders: official journal of the Movement Disorder Society 19 (10 …, 2004
|Meningoencephalomyelitis with vasculitis due to varicella zoster virus: a case report and review of the literature|
PA McKelvie, S Collins, D Thyagarajan, N Trost, H Sheorey, E Byrne
Pathology 34 (1), 88-93, 2002
|Post-traumatic shoulder'dystonia': Persistent abnormal postures of the shoulder after minor trauma|
D Thyagarajan, K Kompoliti, B Ford
Neurology 51 (4), 1205-1207, 1998
|Abnormal vocal cord movement treated with botulinum toxin in patients with asthma resistant to optimised management|
M Baxter, N Uddin, S Raghav, P Leong, K Low, K Hamza, PW Holmes, ...
Respirology 19 (4), 531-537, 2014
|Parkinson's disease alters multisensory perception: Insights from the Rubber Hand Illusion|
C Ding, CJ Palmer, J Hohwy, GJ Youssef, B Paton, N Tsuchiya, JC Stout, ...
Neuropsychologia 97, 38-45, 2017
|Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNALeu (UUR) gene|
WM Hutchison, D Thyagarajan, J Poulton, DR Marchington, DM Kirby, ...
Archives of neurology 62 (12), 1920-1923, 2005
|Neuromyelitis optica (Devic's disease) in a patient with syphilis|
RA Wilcox, J Burrow, M Slee, J Craig, D Thyagarajan
Multiple Sclerosis Journal 14 (2), 268-271, 2008
|The mitochondrial T1095C mutation increases gentamicin-mediated apoptosis|
H Muyderman, NR Sims, M Tanaka, N Fuku, R Raghupathi, ...
Mitochondrion 12 (4), 465-471, 2012