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Darius Ebrahimi-Fakhari, M.D.
Concepts (332)
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Concepts are derived automatically from a person's publications.
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In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
Acetylcysteine
Acidosis, Lactic
Activating Transcription Factor 3
Adaptor Protein Complex 4
Adaptor Protein Complex beta Subunits
Adaptor Proteins, Vesicular Transport
Adolescent
Adult
Advisory Committees
Age Factors
Age of Onset
Aged
Aged, 80 and over
Alexander Disease
Alleles
alpha-Synuclein
Amino Acid Metabolism, Inborn Errors
Amyloidosis
Analysis of Variance
Animals
Animals, Genetically Modified
Antibodies, Neoplasm
Antigens, Neoplasm
Anti-Inflammatory Agents
ARNTL Transcription Factors
Ataxia
Attitude of Health Personnel
Autistic Disorder
Autophagy
Axonal Transport
Axons
Bacterial Proteins
Barbiturates
Basal Ganglia Diseases
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
Behavior, Animal
Benzamides
Benzimidazoles
Biological Assay
Blotting, Western
Brain
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Brain Neoplasms
Calpain
Carbamazepine
Carbohydrate Metabolism, Inborn Errors
Carrier Proteins
Cataract
Cell Differentiation
Cell Line
Cell Respiration
Cells, Cultured
Central Nervous System Diseases
Cerebellar Ataxia
Cerebellar Diseases
Cerebral Cortex
Cerebral Palsy
Checklist
Child
Child, Preschool
CHO Cells
Cholesterol
Chorea
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 9
Chylothorax
Circadian Clocks
Cohort Studies
Coma
Combined Modality Therapy
Computational Biology
Computer Simulation
Consanguinity
Consensus
Corpus Callosum
Corpus Striatum
Cough
Craniotomy
Cricetulus
Cross-Sectional Studies
Cryopyrin-Associated Periodic Syndromes
Curriculum
Cysteine Proteinase Inhibitors
Cytoskeletal Proteins
Cytosol
Databases, Genetic
Decontamination
Deep Brain Stimulation
Delayed Diagnosis
Dementia
Dendritic Spines
Dependovirus
Detergents
Developmental Disabilities
Diagnosis, Differential
Diagnostic Imaging
Diffusion Magnetic Resonance Imaging
Disease Management
Disease Models, Animal
Disease Progression
DNA Mutational Analysis
Dopamine
Dose-Response Relationship, Drug
Drosophila melanogaster
Drug Combinations
Dystonia
Dystonic Disorders
Early Diagnosis
Editorial Policies
Education, Medical
Electroencephalography
Endocannabinoids
Endoplasmic Reticulum
Energy Metabolism
Enzyme Inhibitors
Epilepsy
Epilepsy, Reflex
Extracellular Matrix Proteins
Facial Asymmetry
Facies
Familial Mediterranean Fever
Family
F-Box Proteins
Fellowships and Scholarships
Female
Fibroblasts
Fluorescent Antibody Technique
Folic Acid Deficiency
Follow-Up Studies
Fragile X Syndrome
Friedreich Ataxia
Gait
gamma-Aminobutyric Acid
Gangliosides
Gelsolin
Gene Expression Regulation
Gene Knockdown Techniques
Genes, X-Linked
Genetic Association Studies
Genetic Markers
Genetic Predisposition to Disease
Genetic Vectors
Genomics
Genotype
Germany
Gliosis
Glutaryl-CoA Dehydrogenase
Glutathione
Glycoproteins
Green Fluorescent Proteins
GTP Cyclohydrolase
GTP-Binding Proteins
Haploinsufficiency
Heart Failure
Hemodiafiltration
Hepatolenticular Degeneration
Hereditary Sensory and Autonomic Neuropathies
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Homeodomain Proteins
HSP90 Heat-Shock Proteins
Humans
Huntington Disease
Hydrolases
Immunohistochemistry
Indoles
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Intermediate Filaments
International Educational Exchange
Internship and Residency
Intracellular Signaling Peptides and Proteins
Iron
Iron Overload
Kidney Neoplasms
Lafora Disease
Lewy Bodies
Loss of Heterozygosity
Luminescent Proteins
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Lysosomes
Macrolides
Magnetic Resonance Imaging
Male
Membrane Glycoproteins
Membrane Potential, Mitochondrial
Membrane Proteins
Mental Disorders
Mesencephalon
Metabolic Diseases
Metabolism, Inborn Errors
Methylprednisolone
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Mutant Strains
Mice, Transgenic
MicroRNAs
Microscopy, Confocal
Microtomy
Microtubule-Associated Proteins
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Models, Biological
Models, Molecular
Molecular Chaperones
Molecular Targeted Therapy
Monoacylglycerol Lipases
Monosaccharide Transport Proteins
Motivation
Motor Neurons
Movement Disorders
Multiprotein Complexes
Muscle Hypotonia
Muscle Spasticity
Muscular Atrophy, Spinal
Mutation
Mutation, Missense
Myocardium
Myoclonus
Neostriatum
Nerve Degeneration
Nerve Tissue Proteins
Nervous System Malformations
Neural Pathways
Neuroblastoma
Neurodegenerative Diseases
Neurogenesis
Neuroimmunomodulation
Neurology
Neurons
Niemann-Pick Disease, Type C
Noonan Syndrome
Oligonucleotide Array Sequence Analysis
Opsoclonus-Myoclonus Syndrome
Paraplegia
Parents
Parkinson Disease
Parkinsonian Disorders
Pediatrics
Pedigree
Peer Review, Research
Periodicals as Topic
Peritonitis
Phagosomes
Phenotype
Phosphorylation
Plasmapheresis
Pluripotent Stem Cells
Point Mutation
Polymorphism, Single Nucleotide
Presynaptic Terminals
Prevalence
Prognosis
Prospective Studies
Proteasome Endopeptidase Complex
Protein Biosynthesis
Protein Conformation
Protein Folding
Protein Kinases
Protein Structure, Quaternary
Protein Transport
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Proteins
Proteomics
Proteostasis Deficiencies
Psychotic Disorders
Pyrimidines
Rare Diseases
Rats
Rats, Sprague-Dawley
Reactive Oxygen Species
Receptor, Platelet-Derived Growth Factor beta
Recurrence
Registries
Renal Dialysis
Retinal Degeneration
Retrospective Studies
Rett Syndrome
Rhabdomyoma
Ribonuclease III
Ribosomal Protein S6 Kinases, 90-kDa
Risk Factors
RNA, Messenger
RNA, Small Interfering
Seizures
Severity of Illness Index
Signal Transduction
Sleep
Societies, Medical
Solubility
SOXD Transcription Factors
Spasms, Infantile
Spastic Paraplegia, Hereditary
Spinocerebellar Degenerations
Status Epilepticus
Strabismus
Stress, Psychological
Stroke
Students, Medical
Subcellular Fractions
Substantia Nigra
Succinate-Semialdehyde Dehydrogenase
Survival of Motor Neuron 1 Protein
Survival of Motor Neuron 2 Protein
Synapses
Terminology as Topic
Thrombectomy
TOR Serine-Threonine Kinases
Tourette Syndrome
Transcription Factors
Transfection
trans-Golgi Network
Transients and Migrants
Treatment Outcome
Tuberous Sclerosis
Tumor Suppressor Proteins
Ubiquitin
Ubiquitin-Activating Enzymes
Ubiquitin-Protein Ligases
Vesicular Transport Proteins
Vitamin E Deficiency
Xanthomatosis, Cerebrotendinous
Young Adult
Zebrafish
Ebrahimi-Fakhari's Networks
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Concepts (332)
Derived automatically from this person's publications.
Dystonic Disorders
Spastic Paraplegia, Hereditary
Adaptor Protein Complex 4
Movement Disorders
Autophagy
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_
Co-Authors (108)
People in Profiles who have published with this person.
Sahin, Mustafa
Quiroz, Vicente
Yang, Kathryn
Alecu, Julian
Wahlster, Lara
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_
Similar People (60)
People who share similar concepts with this person.
Alkuraya, Fowzan
Sahin, Mustafa
Blackstone, Craig
Chung, Wendy
Alecu, Julian
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_
Same Department
People in same department with this person.
Gable, Dustin
Moufawad El Achkar, Christelle
Pearl, Phillip
Srivastava, Siddharth
Taherzadeh, Mahsa
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_