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Refinado por: tipo de recurso: Dissertações remover
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1
Investigation of the effects of gle1 depletion in zebrafish
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Investigation of the effects of gle1 depletion in zebrafish

Seytanoglu, Adil

University of Sheffield

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2
Neuromarketing and consumer neuroscience: contributions to neurology
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Neuromarketing and consumer neuroscience: contributions to neurology

Javor, Andrija ; Koller, Monika ; Chamberlain, Laura ; Ransmayr, Gerhard ; Lee, Nick

BioMed Central Ltd

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3
Bilateral population activity in the motor cortex and its role in upper limb control
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Bilateral population activity in the motor cortex and its role in upper limb control

Dixon, Tanner Chas

eScholarship, University of California 2021

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4
A FAMILY WITH NEUROPATHIES AND AN MFN2 VARIANT
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A FAMILY WITH NEUROPATHIES AND AN MFN2 VARIANT

Miller, Leah

UVM ScholarWorks 2022

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5
Role of GFAP, IL-6 and EEG in Gut-Brain Nexus
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Role of GFAP, IL-6 and EEG in Gut-Brain Nexus

Shanker, Varnit

2023

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6
Deconstructing Sanfilippo Syndrome: On the pathophysiological basis and molecular drivers of mucopolysaccharidosis IIIA
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Deconstructing Sanfilippo Syndrome: On the pathophysiological basis and molecular drivers of mucopolysaccharidosis IIIA

ALON MOSHE DOUEK ; Victor Jan Mikael Kaslin ; Alberto Roselló-Díez

2023

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7
THETA BURST BRAIN STIMULATION IN PAINFUL DIABETIC NEUROPATHY PATIENTS: INVESTIGATING NEURAL MECHANISMS
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THETA BURST BRAIN STIMULATION IN PAINFUL DIABETIC NEUROPATHY PATIENTS: INVESTIGATING NEURAL MECHANISMS

THAKKAR, BHUSHAN

VCU Scholars Compass 2022

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8
Unraveling the role of non-coding rare variants in epilepsy and its subtypes with deep learning
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Unraveling the role of non-coding rare variants in epilepsy and its subtypes with deep learning

Girard, Alexandre

2023

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9
Genetic variants in Angelman syndrome and related disorders: relationship to phenotype and neuronal function
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Genetic variants in Angelman syndrome and related disorders: relationship to phenotype and neuronal function

Williams, Mark Geoffrey

2023

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10
Characterization of the novel “Uppsala mutation” causing a familial form of early onset Alzheimer’s disease
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Characterization of the novel “Uppsala mutation” causing a familial form of early onset Alzheimer’s disease

Pagnon de la Vega, María

Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap 2021

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