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Heliyon
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February 7, 2024
Improved liquid phase exfoliation technique for the fabrication of MoS<sub>2</sub>/graphene heterostructure-based photodetector
B J Akeredolu, I Ahemen, A N Amah, et al.
Journal of Chemical Neuroanatomy
|
March 3, 2018
Mapping the protein phosphorylation sites in human mitochondrial complex I (NADH: Ubiquinone oxidoreductase): A bioinformatics study with implications for brain aging and neurodegeneration
Niya Gowthami, B Sunitha, Manish Kumar, et al.
Heliyon
|
April 9, 2025
Corrigendum to "Improved liquid phase exfoliation technique for the fabrication of MoS<sub>2</sub>/graphene heterostructure-based photodetector" [Heliyon Volume 10, Issue 3, February 2024, Article e24964]
B J Akeredolu, I Ahemen, A N Amah, et al.
Neurology India
|
February 7, 2001
Centronuclear myopathy--morphological relation to developing human skeletal muscle: a clinicopathological evaluation
N Gayathri, S Das, A Vasanth, et al.
Pediatric Neurology
|
October 15, 2013
Clinical, electrophysiological, imaging, and ultrastructural description in 68 patients with neuronal ceroid lipofuscinoses and its subtypes
Rakesh H Jadav, Sanjib Sinha, T C Yasha, et al.
Chemosphere
|
September 27, 2022
A detailed review on advanced oxidation process in treatment of wastewater: Mechanism, challenges and future outlook
A Saravanan, V C Deivayanai, P Senthil Kumar, et al.
Annals of Indian Academy of Neurology
|
March 25, 2016
Tangier's disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy
Madhu Nagappa, Arun B Taly, Anita Mahadevan, et al.
Journal of Biomolecular Screening
|
April 1, 2005
Development of a microplate-based scintillation proximity assay for MraY using a modified substrate
S M Solapure, P Raphael, C N Gayathri, et al.
Neurology India
|
January 12, 2012
Glycogen storage disease type V (Mc Ardle's disease): a report on three cases
Naveen Krishnamoorthy, Vani Santosh, T C Yasha, et al.
Annals of Indian Academy of Neurology
|
March 25, 2016
Hereditary inclusion body myopathy: A myopathy with unique topography of weakness, yet frequently misdiagnosed: Case series and review of literature
Biplab Das, Manoj Kumar Goyal, Sanat Ramchandra Bhatkar, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 70) with videos related to
Sort By:
Page
of 7
Heliyon
|
February 7, 2024
Improved liquid phase exfoliation technique for the fabrication of MoS<sub>2</sub>/graphene heterostructure-based photodetector
B J Akeredolu, I Ahemen, A N Amah, et al.
Journal of Chemical Neuroanatomy
|
March 3, 2018
Mapping the protein phosphorylation sites in human mitochondrial complex I (NADH: Ubiquinone oxidoreductase): A bioinformatics study with implications for brain aging and neurodegeneration
Niya Gowthami, B Sunitha, Manish Kumar, et al.
Heliyon
|
April 9, 2025
Corrigendum to "Improved liquid phase exfoliation technique for the fabrication of MoS<sub>2</sub>/graphene heterostructure-based photodetector" [Heliyon Volume 10, Issue 3, February 2024, Article e24964]
B J Akeredolu, I Ahemen, A N Amah, et al.
Neurology India
|
February 7, 2001
Centronuclear myopathy--morphological relation to developing human skeletal muscle: a clinicopathological evaluation
N Gayathri, S Das, A Vasanth, et al.
Pediatric Neurology
|
October 15, 2013
Clinical, electrophysiological, imaging, and ultrastructural description in 68 patients with neuronal ceroid lipofuscinoses and its subtypes
Rakesh H Jadav, Sanjib Sinha, T C Yasha, et al.
Chemosphere
|
September 27, 2022
A detailed review on advanced oxidation process in treatment of wastewater: Mechanism, challenges and future outlook
A Saravanan, V C Deivayanai, P Senthil Kumar, et al.
Annals of Indian Academy of Neurology
|
March 25, 2016
Tangier's disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy
Madhu Nagappa, Arun B Taly, Anita Mahadevan, et al.
Journal of Biomolecular Screening
|
April 1, 2005
Development of a microplate-based scintillation proximity assay for MraY using a modified substrate
S M Solapure, P Raphael, C N Gayathri, et al.
Neurology India
|
January 12, 2012
Glycogen storage disease type V (Mc Ardle's disease): a report on three cases
Naveen Krishnamoorthy, Vani Santosh, T C Yasha, et al.
Annals of Indian Academy of Neurology
|
March 25, 2016
Hereditary inclusion body myopathy: A myopathy with unique topography of weakness, yet frequently misdiagnosed: Case series and review of literature
Biplab Das, Manoj Kumar Goyal, Sanat Ramchandra Bhatkar, et al.
Page
of 7