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Nicola Longo
Concepts (452)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
17-alpha-Hydroxyprogesterone
1-Deoxynojirimycin
2-Aminoadipic Acid
Abnormalities, Multiple
Access to Information
Acetylcarnitine
Activities of Daily Living
Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenase, Long-Chain
Adipose Tissue, Brown
Administration, Oral
Adolescent
Adolescent Development
Adrenal Hyperplasia, Congenital
Adult
Age Factors
Age of Onset
Aged
Aging
Alcohol Oxidoreductases
Aldehyde Dehydrogenase
Aldehydes
Alleles
alpha-Galactosidase
Ambulatory Care Facilities
Amidinotransferases
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Ammonia
Androstenedione
Animals
Anti-Bacterial Agents
Antibodies
Anticonvulsants
Antineoplastic Agents
Apoptosis
Arginine
Argininosuccinate Synthase
Asymptomatic Diseases
ATP-Binding Cassette Transporters
Attention Deficit Disorder with Hyperactivity
Australia
Autism Spectrum Disorder
Base Sequence
Betaine
Binding Sites
Biological Transport
Biomarkers
Biopsy
Blood Chemical Analysis
Blotting, Western
Body Temperature
Bone Diseases, Developmental
Brain
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Canada
Capillaries
Carbon-Carbon Ligases
Cardiomyopathies
Carnitine
Carnitine Acyltransferases
Carnitine O-Palmitoyltransferase
Carrier Proteins
Case-Control Studies
Cations
Caveolins
Cell Culture Techniques
Cell Division
Cell Line
Cell Membrane
Cells, Cultured
Cerebrovascular Circulation
Child
Child Development
Child Health Services
Child Nutritional Physiological Phenomena
Child, Preschool
CHO Cells
Chromatography, High Pressure Liquid
Chromatography, Liquid
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 6
Citrates
Citric Acid
Citric Acid Cycle
Citrulline
Citrullinemia
Clinical Laboratory Techniques
Clinical Protocols
Clinical Studies as Topic
Clinical Trials, Phase III as Topic
Codon, Nonsense
Cognition
Cohort Studies
Cold Temperature
Combined Modality Therapy
Congenital Abnormalities
Consanguinity
Consensus
Consumer Behavior
Consumer Health Information
Corpus Callosum
Cough
Craniofacial Abnormalities
Creatine
Creatinine
Cricetinae
Cricetulus
Critical Care
Cross-Sectional Studies
Curcumin
Cystathionine beta-Synthase
Data Collection
Data Curation
Deficiency Diseases
Deglutition Disorders
Delayed Diagnosis
Delirium
Delphi Technique
Demography
Denmark
Developmental Disabilities
Dextrocardia
Diagnostic Errors
Diagnostic Tests, Routine
Diarrhea
Dicarboxylic Acids
Diet
Diet Therapy
Diet, Protein-Restricted
Dietary Proteins
Dietary Supplements
Disease Management
Disease Models, Animal
Disease Progression
Diseases in Twins
DNA
DNA Mutational Analysis
DNA, Complementary
DNA, Mitochondrial
Dose-Response Relationship, Drug
Double-Blind Method
Dried Blood Spot Testing
Drug Administration Schedule
Drug Compounding
Drug-Related Side Effects and Adverse Reactions
Drugs, Investigational
Early Diagnosis
Emergency Service, Hospital
Endoplasmic Reticulum
Energy Intake
Energy Metabolism
Enzyme Inhibitors
Enzyme Replacement Therapy
Epilepsy
Ergothioneine
Erythrocytes
Exons
Fabry Disease
False Positive Reactions
Fasting
Fatigue
Fatty Acid Transport Proteins
Fatty Acid-Binding Proteins
Fatty Acids
Feasibility Studies
Female
Fertility
Fever
Fibroblasts
Fingers
Fluorescent Dyes
Follow-Up Studies
Galactose
Galactosemias
Galactosephosphates
Gaucher Disease
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Frequency
Gene Knockdown Techniques
Genes, Recessive
Genetic Association Studies
Genetic Complementation Test
Genetic Diseases, Inborn
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetic Vectors
Genetics, Medical
Genomics
Genotype
Glomerular Filtration Rate
Glucosylceramidase
Glutamic Acid
Glutamine
Glutarates
Glutaryl-CoA Dehydrogenase
Glycerol
Glycine
Glycosylation
Green Fluorescent Proteins
GTP Cyclohydrolase
Guanidinoacetate N-Methyltransferase
Guidelines as Topic
Health Services Needs and Demand
Health Services Research
Healthy Volunteers
Hearing Loss, Bilateral
Hearing Loss, Sensorineural
Heart Ventricles
HeLa Cells
Hemoglobins
Hepatocyte Nuclear Factor 4
Hepatolenticular Degeneration
Heterozygote
High-Throughput Nucleotide Sequencing
Homocysteine
Homocystinuria
Homovanillic Acid
Homozygote
Hot Temperature
Humans
Hydrocortisone
Hydro-Lyases
Hyperammonemia
Hypersensitivity
Hypertrophy, Left Ventricular
Hypoglycemia
Imidazolidines
In Situ Hybridization, Fluorescence
Incidence
Indoles
Infant
Infant, Newborn
Injections, Subcutaneous
Insulin
Insulin Resistance
Intellectual Disability
Intelligence
International Cooperation
Internet
Introns
Kidney
Kinetics
Laboratories
Lactic Acid
Language Development Disorders
Leucine
Lipase
Lipid Metabolism
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Lipids
Lipolysis
Liver
Liver Failure, Acute
Liver Function Tests
Longitudinal Studies
Luminescent Proteins
Lysine
Lysosomes
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Mass Screening
Mass Spectrometry
Megalencephaly
MELAS Syndrome
Membrane Proteins
Membrane Transport Proteins
Mental Retardation, X-Linked
Merozoite Surface Protein 1
Metabolic Diseases
Metabolism, Inborn Errors
Methionine
Methylation
Methylmalonic Acid
Mice
Mice, Knockout
Microcephaly
Microscopy, Confocal
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Membrane Transport Proteins
Mitochondrial Myopathies
Mitochondrial Proteins
Mixed Function Oxygenases
Models, Biological
Models, Molecular
Molecular Sequence Data
Morbidity
Mothers
Movement Disorders
Muscle Hypotonia
Muscle Weakness
Muscle, Skeletal
Muscular Diseases
Mutagenesis, Site-Directed
Mutation
Mutation, Missense
Neonatal Screening
Nerve Tissue Proteins
Neuropsychological Tests
Neutropenia
New York
NFI Transcription Factors
Nitrogen
Nucleic Acid Denaturation
Nucleocytoplasmic Transport Proteins
Nutrition Therapy
Nutritional Status
Oligonucleotide Array Sequence Analysis
Organ Size
Organ Specificity
Organic Cation Transport Proteins
Ornithine
Ornithine Carbamoyltransferase Deficiency Disease
Ovary
Oxidation-Reduction
Oxidoreductases
Oxygen
p120 GTPase Activating Protein
Pancreas
Pediatrics
Pedigree
Phenotype
Phenylacetates
Phenylalanine
Phenylalanine Ammonia-Lyase
Phenylalanine Hydroxylase
Phenylbutyrates
Phenylketonuria, Maternal
Phenylketonurias
Phosphocreatine
Phosphorus-Oxygen Lyases
Picolinic Acids
Pilot Projects
Pipecolic Acids
Plasma Membrane Neurotransmitter Transport Proteins
Platelet Count
Point Mutation
Polyethylene Glycols
Polymerase Chain Reaction
Practice Guidelines as Topic
Practice Patterns, Physicians'
Predictive Value of Tests
Pregnancy
Primary Cell Culture
Prodrugs
Prognosis
Prolactin
Propionates
Propionic Acidemia
Prospective Studies
Protein Structure, Tertiary
Protein Transport
Psychotic Disorders
Pterins
Pyridoxine
Pyrrolidines
Quality Assurance, Health Care
Quality of Life
Quinidine
Racemases and Epimerases
Randomized Controlled Trials as Topic
Rare Diseases
Receptor, Fibroblast Growth Factor, Type 3
Receptor, Insulin
Recombinant Fusion Proteins
Recombinant Proteins
Recurrence
Reference Standards
Reference Values
Referral and Consultation
Registries
Renal Dialysis
Repressor Proteins
Research Design
Retrospective Studies
Ribs
Risk Assessment
Risk Factors
RNA Interference
RNA, Small Interfering
RNA, Transfer, Leu
Saccharopine Dehydrogenases
Saudi Arabia
Seizures
Self Report
Septo-Optic Dysplasia
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Serotonin
Severity of Illness Index
Sexual Maturation
Skin
Societies
Sodium
Sodium Benzoate
Solute Carrier Family 22 Member 5
Sotos Syndrome
Speech Disorders
Sphingolipids
Spleen
Stress, Psychological
Structure-Activity Relationship
Sturge-Weber Syndrome
Surveys and Questionnaires
Symporters
Syndrome
Tandem Mass Spectrometry
Telomere
Temperature
Thermogenesis
Thorax
Threonine
Time Factors
Toes
Transaminases
Transfection
Treatment Outcome
Triglycerides
Trihexosylceramides
Tyrosine
Ultrasonography
Uniparental Disomy
United States
Up-Regulation
Urea Cycle Disorders, Inborn
Utah
UTP-Hexose-1-Phosphate Uridylyltransferase
Valinomycin
Vascular Malformations
Verapamil
Vitamin B 12
Vitamin B Complex
Vitamin B Deficiency
Vomiting
Young Adult
Nicola's Networks
Concepts (452)
Derived automatically from this person's publications.
Phenylketonurias
Carnitine
Phenylalanine
Neonatal Screening
Organic Cation Transport Proteins
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Co-Authors (10)
People in Profiles who have published with this person.
Feigenbaum, Annette
UCSD
Gallagher, Renata
UCSF
Abdenur, Jose
UCI
Villanueva, Claudio
UCLA
Barshop, Bruce
UCSD
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_
Similar People (60)
People who share similar concepts with this person.
Giacomini, Kathy
UCSF
Abdenur, Jose
UCI
Puck, Jennifer
UCSF
Anderson, Peter
UCI
Gleeson, Joseph
UCSD
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Same Department
Benjamin, Daniel
Kruglyak, Leonid
Lange, Kenneth
Pasaniuc, Bogdan
Young, Stephen
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