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Andreea Manole

Showing results (11-20 of 36) with videos related to

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Neurobiology of Aging|October 30, 2016
Analysis of the prion protein gene in multiple system atrophyViorica Chelban, Andreea Manole, Lasse Pihlstrøm, et al.
Neuromuscular Disorders : NMD|December 27, 2023
Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9Ros Quinlivan, Elaine Murphy, Shpresa Pula, et al.
Neurogenetics|June 9, 2016
A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermiaTiago A Mestre, Andreea Manole, Heather MacDonald, et al.
Neurogenetics|December 23, 2016
SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvementAndreea Manole, Alejandro Horga, Josep Gamez, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 18, 2022
<i>HLA-DRB1*1501</i> influences long-term disability progression and tissue damage on MRI in relapse-onset multiple sclerosisWallace J Brownlee, Carmen Tur, Andreea Manole, et al.
Biochemistry|May 12, 2015
Resonance Raman Spectra of Five-Coordinate Heme-Nitrosyl Cytochromes c': Effect of the Proximal Heme-NO EnvironmentAmy E Servid, Alison L McKay, Cherry A Davis, et al.
Free Radical Biology & Medicine|August 2, 2020
Adrenaline induces calcium signal in astrocytes and vasoconstriction via activation of monoamine oxidaseIrina N Novikova, Andreea Manole, Evgeny A Zherebtsov, et al.
NPJ Parkinson'S Disease|May 18, 2024
Upregulated ECM genes and increased synaptic activity in Parkinson's human DA neurons with PINK1/ PRKN mutationsUtkarsh Tripathi, Idan Rosh, Ran Ben Ezer, et al.
NPJ Parkinson'S Disease|February 19, 2024
Synaptic dysfunction and extracellular matrix dysregulation in dopaminergic neurons from sporadic and E326K-GBA1 Parkinson's disease patientsIdan Rosh, Utkarsh Tripathi, Yara Hussein, et al.
Neuromuscular Disorders : NMD|February 10, 2018
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)Mahalekshmi Desikan, Renata Siciliani Scalco, Andreea Manole, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Neurobiology of Aging|October 30, 2016
Analysis of the prion protein gene in multiple system atrophyViorica Chelban, Andreea Manole, Lasse Pihlstrøm, et al.
Neuromuscular Disorders : NMD|December 27, 2023
Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9Ros Quinlivan, Elaine Murphy, Shpresa Pula, et al.
Neurogenetics|June 9, 2016
A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermiaTiago A Mestre, Andreea Manole, Heather MacDonald, et al.
Neurogenetics|December 23, 2016
SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvementAndreea Manole, Alejandro Horga, Josep Gamez, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 18, 2022
<i>HLA-DRB1*1501</i> influences long-term disability progression and tissue damage on MRI in relapse-onset multiple sclerosisWallace J Brownlee, Carmen Tur, Andreea Manole, et al.
Biochemistry|May 12, 2015
Resonance Raman Spectra of Five-Coordinate Heme-Nitrosyl Cytochromes c': Effect of the Proximal Heme-NO EnvironmentAmy E Servid, Alison L McKay, Cherry A Davis, et al.
Free Radical Biology & Medicine|August 2, 2020
Adrenaline induces calcium signal in astrocytes and vasoconstriction via activation of monoamine oxidaseIrina N Novikova, Andreea Manole, Evgeny A Zherebtsov, et al.
NPJ Parkinson'S Disease|May 18, 2024
Upregulated ECM genes and increased synaptic activity in Parkinson's human DA neurons with PINK1/ PRKN mutationsUtkarsh Tripathi, Idan Rosh, Ran Ben Ezer, et al.
NPJ Parkinson'S Disease|February 19, 2024
Synaptic dysfunction and extracellular matrix dysregulation in dopaminergic neurons from sporadic and E326K-GBA1 Parkinson's disease patientsIdan Rosh, Utkarsh Tripathi, Yara Hussein, et al.
Neuromuscular Disorders : NMD|February 10, 2018
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)Mahalekshmi Desikan, Renata Siciliani Scalco, Andreea Manole, et al.
Pageof 4