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Veeramani Preethish-Kumar
Veeramani Preethish-Kumar
MBBS., MRCP (UK)., SCE (Neuro)., FRCP (Lon).,PhD
在 neurofoundation.in 的电子邮件经过验证 - 首页
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引用次数
引用次数
年份
Introduction of community-based skin-to-skin care in rural Uttar Pradesh, India
GL Darmstadt, V Kumar, R Yadav, V Singh, P Singh, S Mohanty, ...
Journal of perinatology 26 (10), 597-604, 2006
1662006
Transforming growth factor alpha.
V Kumar, SA Bustin, IA McKay
Cell biology international 19 (5), 373-388, 1995
1261995
Production of Oils from Acetic Acid by the Oleaginous Yeast Cryptococcus curvatus
G Christophe, JL Deo, V Kumar, R Nouaille, P Fontanille, C Larroche
Applied biochemistry and biotechnology 167, 1270-1279, 2012
1152012
Biocontrol genes from Trichoderma species: a review
P Sharma, V Kumar, R Ramesh, K Saravanan, S Deep, M Sharma, ...
African Journal of Biotechnology 10 (86), 19898-19907, 2011
1062011
Light-induced dissociation of antenna complexes in the symbionts of scleractinian corals correlates with sensitivity to coral bleaching
R Hill, AWD Larkum, O Prášil, DM Kramer, M Szabó, V Kumar, PJ Ralph
Coral Reefs 31, 963-975, 2012
742012
Drip irrigation
RK Sivanappan, RK Sivanappan, O Padmakumari, V Kumar
Keerth Publishing House., 1987
571987
Duchenne muscular dystrophy and Becker muscular dystrophy confirmed by multiplex ligation-dependent probe amplification: genotype-phenotype correlation in a large cohort
S Vengalil, V Preethish-Kumar, K Polavarapu, M Mahadevappa, D Sekar, ...
Journal of Clinical Neurology 13 (1), 91-97, 2017
522017
Muscle MRI in Duchenne muscular dystrophy: evidence of a distinctive pattern
K Polavarapu, M Manjunath, V Preethish-Kumar, D Sekar, S Vengalil, ...
Neuromuscular Disorders 26 (11), 768-774, 2016
522016
MACF1 links Rapsyn to microtubule-and actin-binding proteins to maintain neuromuscular synapses
J Oury, Y Liu, A Töpf, S Todorovic, E Hoedt, V Preethish-Kumar, ...
Journal of Cell Biology 218 (5), 1686-1705, 2019
462019
Increasing the ROI of social media marketing
V Kumar, R Mirchandani
IEEE Engineering Management Review 41 (3), 17-23, 2013
372013
reliaR: A package for some probability distributions
V Kumar, U Ligges
352011
Chitotriosidase, a biomarker of amyotrophic lateral sclerosis, accentuates neurodegeneration in spinal motor neurons through neuroinflammation
AM Varghese, M Ghosh, SK Bhagat, K Vijayalakshmi, V Preethish-Kumar, ...
Journal of Neuroinflammation 17, 1-15, 2020
302020
Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness
D Owen, A Töpf, V Preethish‐Kumar, PJ Lorenzoni, B Vroling, RH Scola, ...
American Journal of Medical Genetics Part A 176 (7), 1594-1601, 2018
302018
Evidence for Mycobacterium leprae drug resistance in a large cohort of leprous neuropathy patients from India
NP Mahajan, M Lavania, I Singh, S Nashi, V Preethish-Kumar, S Vengalil, ...
The American Journal of Tropical Medicine and Hygiene 102 (3), 547, 2020
292020
A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study
M Manjunath, P Kiran, V Preethish-Kumar, A Nalini, RJ Singh, N Gayathri
Neurology India 63 (1), 58-62, 2015
282015
Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant
S Balaraju, A Töpf, G McMacken, VP Kumar, A Pechmann, H Roper, ...
European Journal of Human Genetics 28 (3), 373-377, 2020
262020
Brain and spinal cord lesions in leprosy: A magnetic resonance imaging–based study
K Polavarapu, V Preethish-Kumar, S Vengalil, S Nashi, M Lavania, ...
The American Journal of Tropical Medicine and Hygiene 100 (4), 921, 2019
252019
Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India
PT Thomas, MG Warrier, A Sadasivan, B Balasubramanium, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19 (7-8), 606-610, 2018
252018
Reverse split hand syndrome: dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy
RJ Singh, V Preethish-Kumar, K Polavarapu, S Vengalil, C Prasad, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18 (1-2), 10-16, 2017
252017
MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India
S Deepha, S Vengalil, V Preethish-Kumar, K Polavarapu, A Nalini, ...
BMC Medical Genetics 18, 1-10, 2017
232017
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