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Annette Feigenbaum
Concepts (331)
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Concepts are derived automatically from a person's publications.
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Categories
Timeline
Details
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
Acidosis, Lactic
Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenase, Long-Chain
Adolescent
Adrenoleukodystrophy
Adult
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Alleles
alpha-Glucosidases
Amidohydrolases
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Ammonia
Ammonium Compounds
Anterior Eye Segment
Antineoplastic Agents
Aortic Diseases
Arginine
Argininosuccinate Synthase
Argininosuccinic Aciduria
Arteries
Ataxia
ATP-Binding Cassette Transporters
Autistic Disorder
Autoantigens
Autoimmune Diseases of the Nervous System
Base Pairing
Base Sequence
Biomarkers
Biomedical Research
Birth Weight
Blood Coagulation Disorders
Brain
Brain Chemistry
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Brain Edema
Brain Neoplasms
Brain Stem
Calcinosis
Calcium Channels
Canada
Canavan Disease
Carbohydrate Metabolism, Inborn Errors
Cardiomyopathies
Carrier Proteins
Cerebral Cortex
Cerebral Palsy
Cervical Vertebrae
Child
Child Development
Child, Preschool
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 8
Citrulline
Citrullinemia
Cleft Palate
Clinical Decision-Making
Clinical Protocols
Cochlea
Codon
Cognition
Cohort Studies
Coloboma
Congenital Disorders of Glycosylation
Consanguinity
Consciousness Disorders
Contraindications
Cooperative Behavior
Craniofacial Abnormalities
Critical Illness
Cross Reactions
Cross-Over Studies
Cross-Sectional Studies
Cystathionine
Cystathionine gamma-Lyase
Cytochromes b
Data Collection
Databases, Genetic
DEAD-box RNA Helicases
Deafness
Delivery of Health Care
Delphi Technique
Dementia
Dental Enamel Hypoplasia
Developmental Disabilities
Diagnosis, Differential
Dihydrolipoamide Dehydrogenase
Dihydrolipoyllysine-Residue Acetyltransferase
Dilatation, Pathologic
Disease Management
Disease Progression
Disease Susceptibility
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA Primers
DNA, Mitochondrial
Double-Blind Method
Down Syndrome
Dried Blood Spot Testing
Dyskinesias
Electron Transport Complex I
Electroretinography
Emergency Service, Hospital
Enzyme Replacement Therapy
Epilepsy
Evidence-Based Practice
Exercise
Exome
Eye
Eye Diseases
Face
Facies
Failure to Thrive
Family Health
Fatty Acids
Fatty Liver
Female
Fibroblasts
Follow-Up Studies
Frameshift Mutation
Fructose Intolerance
Fundus Oculi
Gastroenteritis
Gene Deletion
Gene Dosage
Gene Frequency
Genes, Dominant
Genes, Mitochondrial
Genes, Recessive
Genetic Carrier Screening
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genotype
Germ-Line Mutation
Gestational Age
Glutamine
Glutarates
Glycerol
Glycogen Storage Disease
Glycogen Storage Disease Type II
Glycogen Storage Disease Type VI
Glycosylation
Graft Rejection
Haplotypes
Health Care Costs
Health Care Surveys
Health Services Misuse
Hearing Loss, Sensorineural
Heart Diseases
Heart Transplantation
Hepatic Encephalopathy
Hepatolenticular Degeneration
Hepatomegaly
Heterozygote
Homocystinuria
Homozygote
Hospitalization
Humans
Hyperammonemia
Hyperargininemia
Hypoglycemia
Immune Tolerance
Immunohistochemistry
In Vitro Techniques
Infant
Infant Formula
Infant Mortality
Infant, Newborn
Intellectual Disability
Intelligence Tests
Intensive Care Units, Neonatal
Intercellular Signaling Peptides and Proteins
Interferon-beta
Interferon-Induced Helicase, IFIH1
Interinstitutional Relations
Isocitrate Dehydrogenase
Jews
Kaplan-Meier Estimate
Kidney Diseases
Kidney Transplantation
Kidney Tubules
Kinetics
Lactic Acid
Leigh Disease
Leukoencephalopathies
Lipid Metabolism, Inborn Errors
Liver Cirrhosis
Liver Diseases
Liver Failure
Liver Transplantation
Logistic Models
Longitudinal Studies
Lysophosphatidylcholines
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
MELAS Syndrome
Membrane Proteins
Membrane Transport Proteins
Metabolic Diseases
Metabolism, Inborn Errors
Metacarpus
Metal Metabolism, Inborn Errors
Methotrexate
Methylmalonic Acid
Microcephaly
Middle Aged
Migraine with Aura
Mitochondria
Mitochondria, Muscle
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Models, Molecular
Molecular Sequence Data
Muscle, Skeletal
Muscular Diseases
Mutation
Mutation, Missense
Myocardium
NADH Dehydrogenase
Neonatal Screening
Neoplasms
Nerve Fibers
Nervous System Malformations
Neural Cell Adhesion Molecules
Neuroimaging
Neuropsychological Tests
Nipples
Nucleotides
Odontodysplasia
Oligonucleotide Array Sequence Analysis
Ontario
Ornithine
Ornithine Carbamoyltransferase Deficiency Disease
Orotic Acid
Osteoporosis
Oxidation-Reduction
Oxidoreductases
Oxidoreductases Acting on Sulfur Group Donors
Pedigree
Phenotype
Phenylalanine
Phenylalanine Hydroxylase
Phenylbutyrates
Phenylketonurias
Phosphoglucomutase
Phosphotransferases (Alcohol Group Acceptor)
Pilot Projects
Point Mutation
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Practice Patterns, Physicians'
Precision Medicine
Predictive Value of Tests
Pregnancy
Pregnancy Complications
Prognosis
Prospective Studies
Protein Structure, Tertiary
Protein Subunits
Psoriasis
Pyruvate Dehydrogenase Complex
Pyruvate Dehydrogenase Complex Deficiency Disease
Quality of Life
Radiography
Randomized Controlled Trials as Topic
Rare Diseases
Reflex, Abnormal
Registries
Renal Insufficiency
Reproducibility of Results
Research Design
Residence Characteristics
Retina
Retinal Diseases
Retinal Dysplasia
Retrospective Studies
Rhabdomyolysis
Risk Factors
RNA, Ribosomal
Seizures
Self Report
Semicircular Canals
Sensitivity and Specificity
Sequence Analysis, DNA
Siblings
Skull
Socioeconomic Factors
Spinal Cord
Spinal Puncture
Standard of Care
Sucrose
Sulfite Oxidase
Surveys and Questionnaires
Survival Rate
Syndrome
Tandem Mass Spectrometry
Temporal Bone
Time Factors
Tomography, X-Ray Computed
Tooth Abnormalities
Tooth Loss
Transaminases
Treatment Outcome
Ubiquinone
Ultrasonography
United States
Urea Cycle Disorders, Inborn
Vascular Calcification
Vestibule, Labyrinth
Visual Acuity
Vitamin B 12
White Matter
Whole Genome Sequencing
Young Adult
Annette's Networks
Concepts (331)
Derived automatically from this person's publications.
Mitochondrial Diseases
Lipid Metabolism, Inborn Errors
Hyperammonemia
Neonatal Screening
Hyperargininemia
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Co-Authors (19)
People in Profiles who have published with this person.
Weinstein, Lawrence
UCSD
Longo, Nicola
UCLA
Barshop, Bruce
UCSD
Lamale-smith, Leah
UCSD
Wigby, Kristen
UCSD
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People who share similar concepts with this person.
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UCSD
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UCI
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