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Jose Abdenur
Concepts (353)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
Abnormalities, Multiple
Acetylcysteine
Acidosis, Lactic
Activities of Daily Living
Acute Disease
Acyl Coenzyme A
Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenase, Long-Chain
Acyl-CoA Dehydrogenases
Acyl-CoA Oxidase
Adipose Tissue
Adolescent
Adrenal Insufficiency
Adrenoleukodystrophy
Adult
Age of Onset
Aging
Albuminuria
Alcohol Oxidoreductases
Aldehyde Dehydrogenase
Algorithms
Alleles
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acids
Amino Acids, Branched-Chain
Amyloid beta-Protein Precursor
Anemia
Anemia, Sideroblastic
Animals
Anion Transport Proteins
Anthropometry
Antiporters
Arginine
Aromatic-L-Amino-Acid Decarboxylases
Aspartate-tRNA Ligase
ATPases Associated with Diverse Cellular Activities
Autoimmune Diseases
Base Sequence
Benzoquinones
beta-Endorphin
Binding Sites
Biogenic Amines
Biological Assay
Biomarkers
Biopsy
Birth Weight
Blood Glucose
Blotting, Western
Body Composition
Body Fluids
Body Height
Body Mass Index
Brain
Brain Diseases, Metabolic, Inborn
Brain Mapping
California
Carboxy-Lyases
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiopulmonary Bypass
Carnitine
Cell Cycle Proteins
Cells, Cultured
Cerebral Palsy
Cesarean Section
Child
Child, Preschool
Chorionic Villi Sampling
Chromatography, Affinity
Circadian Rhythm
Citrates
Citric Acid
Cleavage And Polyadenylation Specificity Factor
Clinical Trials as Topic
Codon, Nonsense
Cognition
Cohort Studies
Combined Modality Therapy
Congenital Abnormalities
Congenital Disorders of Glycosylation
Consanguinity
Consensus
Costs and Cost Analysis
C-Peptide
Creatine
Creatinine
Cross Reactions
Cysteine
Deafness
Demography
Developmental Disabilities
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetic Nephropathies
Diagnosis, Differential
Diet
Diet, Protein-Restricted
Dietary Supplements
Diffuse Cerebral Sclerosis of Schilder
Disease Progression
DNA
DNA Mutational Analysis
DNA Polymerase gamma
DNA Replication
DNA, Mitochondrial
DNA-Binding Proteins
DNA-Directed DNA Polymerase
Dopamine Agents
Dried Blood Spot Testing
Dwarfism
Dystroglycans
Ear, Inner
Electron Transport Complex I
Electron Transport Complex III
Endocrine System
Endonucleases
Energy Metabolism
Enoyl-CoA Hydratase
Epigenesis, Genetic
Epilepsy
Escherichia coli
Exome
Exons
Eye Abnormalities
Facial Asymmetry
False Positive Reactions
Family
Fatal Outcome
Fatty Acid Desaturases
Fatty Acids
F-Box Proteins
Female
Fibroblasts
Follow-Up Studies
Galactosylceramidase
gamma-Aminobutyric Acid
Gas Chromatography-Mass Spectrometry
Gene Deletion
Gene Expression
Gene Expression Regulation
Gene Frequency
Genes, Lethal
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetics, Population
Genotype
Glomerular Filtration Rate
Glucagon
Glucose Tolerance Test
Glucose-6-Phosphatase
Glutarates
Glycogen Storage Disease Type I
Glycosylation
Gonadotropins, Pituitary
Graft Rejection
Graft vs Host Disease
Growth Hormone
Growth Hormone-Releasing Hormone
Guanidinoacetate N-Methyltransferase
Guanosine Diphosphate Mannose
Head Movements
Heart Defects, Congenital
HEK293 Cells
Hematopoietic Stem Cell Transplantation
Hemiterpenes
Heterozygote
Homocysteine
Homovanillic Acid
Homozygote
Hormone Replacement Therapy
Humans
Hydrocortisone
Hyperammonemia
Hyperglycemia
Hypoglycemia
Iceland
Iduronidase
Infant
Infant, Newborn
Insulin
Insulin Antibodies
Intellectual Disability
International Cooperation
Intestinal Pseudo-Obstruction
Isoleucine
Jews
Ketosis
Kinetics
Lactic Acid
Laminin
Language Development Disorders
Leigh Disease
Leucine
Leukodystrophy, Globoid Cell
Limit of Detection
Lipid Metabolism
Lipid Metabolism, Inborn Errors
Liver
Liver Diseases
Liver Failure
Lysine
Magnetic Resonance Imaging
Male
Malonates
Malonyl Coenzyme A
Mannosyltransferases
Maple Syrup Urine Disease
Mass Spectrometry
Meglutol
Membrane Proteins
Metabolic Diseases
Metabolism, Inborn Errors
Methionine
Methionine Adenosyltransferase
Methylenetetrahydrofolate Reductase (NADPH2)
Methylmalonic Acid
Methylmalonyl-CoA Mutase
Methyltransferases
Metronidazole
Mice
Mice, Inbred C57BL
Mice, Knockout
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Models, Biological
Models, Genetic
Models, Molecular
Molecular Sequence Data
Molecular Structure
Monitoring, Physiologic
Monosaccharide Transport Proteins
Mothers
Movement Disorders
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Muscle Hypotonia
Muscle, Skeletal
Muscles
Muscular Diseases
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Oculopharyngeal
Mutagenesis, Site-Directed
Mutation
Mutation, Missense
Neonatal Screening
Neural Stem Cells
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroimaging
Neuromuscular Diseases
Neuronal Ceroid-Lipofuscinoses
Neurotransmitter Agents
Nucleocytoplasmic Transport Proteins
Nucleotidyltransferases
Nutrition Disorders
Ophthalmoplegia
Organic Anion Transporters
Ornithine
Oxidation-Reduction
Oxidative Phosphorylation
Oxidative Stress
Oximes
Oxo-Acid-Lyases
Oxygen Consumption
Palliative Care
Parenteral Nutrition
Pedigree
Pentanoic Acids
Peptide Elongation Factor G
Perchlorates
Perfusion
Phenotype
Phenylalanine
Phosphotransferases (Alcohol Group Acceptor)
Plasmapheresis
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polysaccharides
Potassium Channels
Pregnancy
Pregnancy Complications
Pregnancy Outcome
Pregnancy Trimester, First
Progeria
Prognosis
Proteasome Endopeptidase Complex
Protein Conformation
Protein Folding
Protein Structure, Secondary
Puberty
Pulsatile Flow
Purpura
Pyridoxine
Rare Diseases
Rats
Recombinant Proteins
Reference Values
Remission Induction
Reproducibility of Results
Respiration, Artificial
Restriction Mapping
Retrospective Studies
Riboflavin
Riboflavin Deficiency
Ribonucleotide Reductases
RNA Splice Sites
RNA, Messenger
RNA, Transfer, Amino Acyl
Samoa
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sex Characteristics
Siblings
Skin
Software
Solute Carrier Family 22 Member 5
Structure-Activity Relationship
Succinates
Sulbactam
Sulfur
Surveys and Questionnaires
Survival Analysis
Syndrome
Tandem Mass Spectrometry
Thiolester Hydrolases
Tomography, Emission-Computed, Single-Photon
Transcription Factors
Treatment Outcome
Triglycerides
Ubiquinone
Ubiquitin
Ubiquitin-Protein Ligases
Urinary Tract Infections
Vitamin B 6
Vitamin B Complex
Vitamin B Deficiency
Vitamins
Whole Genome Sequencing
Young Adult
Zebrafish
Zellweger Syndrome
Jose's Networks
Concepts (353)
Derived automatically from this person's publications.
Neonatal Screening
Mitochondrial Diseases
Leigh Disease
Amino Acid Metabolism, Inborn Errors
Carnitine
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Co-Authors (26)
People in Profiles who have published with this person.
Wang, Raymond
UCI
Steenari, Maija-Riikka
UCI
Gallant, Natalie
UCI
Mikhael, Michel
UCI
Longo, Nicola
UCLA
Explore
_
Similar People (60)
People who share similar concepts with this person.
Longo, Nicola
UCLA
Puck, Jennifer
UCSF
Kimonis, Virginia
UCI
Gleeson, Joseph
UCSD
Lakshminrusimha, Satyanarayana
UC Davis
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Same Department
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Anderson, Peter
Nieves, Delma
Swanson, James
Tirakitsoontorn, Pornchai
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