Medicine and Dentistry
1 Methyl 4 Phenylpyridinium
17%
4-Aminopyridine
17%
Adenoviridae
17%
Agyria
17%
Allergic Airway Inflammation
17%
Amphotericin
17%
Anesthesiology
17%
Antibiogram
17%
Antibiotic Resistance
66%
Arthrogryposis
17%
Asthma
26%
Asthma Exacerbation
17%
Ataxia
20%
Athelia
17%
Attention
17%
Attitude
21%
Autoinjector
17%
Autosomal Dominant Inheritance
21%
Autosomal Recessive Inheritance
57%
Autosome
26%
Bacterial Meningitis
17%
Bardet-Biedl Syndrome
17%
Benign Familial Neonatal Seizures
17%
Biocompatibility
17%
Biological Marker
45%
Biomedical Discipline
17%
Blood Cell
17%
Body Mass Index
25%
Bone Disease
17%
Bone Dysplasia
35%
Brain Malformation
17%
Bronchiolitis
20%
Camptodactyly
20%
Cardioplegia
17%
Case-Control Study
19%
Cell Respiration
49%
Choanal Atresia
17%
Cholestasis
17%
Cholinergic Receptor
17%
Chondrodysplasia
17%
Chronic Lung Disease
17%
Clavicle
17%
Codon
17%
Cohort Effect
40%
Coloboma
17%
Congenital Disorder of Glycosylation
17%
Congenital Infection
17%
Congenital Malformation
52%
Consanguinity
20%
COVID-19
52%
COVID-19 Mortality
17%
Cross Sectional Study
42%
Croup
17%
DeJerine-Sottas Disease
17%
Differential Diagnosis
26%
Dilated Cardiomyopathy
17%
Disease
46%
Disorders of Consciousness
17%
Doppler Flowmetry
17%
Dyslipidemia
17%
Dysmorphic Feature
17%
Dysplasia
52%
Echinocandin
17%
Echogenicity
17%
Edema
17%
Embryopathy
17%
Emergency Department
21%
Encephalomalacia
17%
Endothelial Dysfunction
35%
Energy-Dispersive X-Ray Spectroscopy
17%
Epileptic Seizure
21%
Exophthalmos
17%
Eye Malformation
17%
Fabry Disease
17%
Facies
35%
Family History
26%
Finger
17%
Fluconazole
17%
Foot Malformation
17%
Galactosyltransferase
17%
Gene Mutation
17%
Genetic Disorder
23%
Glibenclamide
17%
Glycon
17%
Granulomatosis
17%
Histone Deacetylase
17%
Human Genetics
20%
Hunter Syndrome
17%
Huntington's Disease
17%
Hypochromic Anemia
35%
Hyponatremia
26%
Ichthyosis
17%
Immune Complex Nephritis
17%
Immunodeficiency
17%
In Vitro
37%
Inborn Error of Metabolism
17%
Infection
31%
Influenza
20%
Influenza A
23%
Influenza B
23%
Injection Site
17%
Insulin Dependent Diabetes Mellitus
35%
Intensive Care Medicine
17%
Iron Deficiency
35%
Kidney Dysplasia
17%
Kyphosis
17%
Lactic Acidosis
17%
Larsen Syndrome
17%
Learning Disorder
17%
Leukemia Inhibitory Factor Receptor
20%
Limb
35%
Liquid Chromatography-Mass Spectrometry
17%
Loose Feces
17%
Lower Respiratory Tract Infection
21%
Lupus Nephritis
17%
Macrogyria
17%
Mammalian Target of Rapamycin Inhibitor
20%
Manganism
17%
Maternal Diabetes Mellitus
17%
Maturity Onset Diabetes of the Young
35%
McKusick Kaufman Syndrome
17%
Mean Corpuscular Volume
35%
Medicine
19%
Megalin
17%
Meta-Analysis
35%
Methylmalonic Acidemia
17%
Methyltransferase
17%
Microcytosis
35%
Micromelia
17%
Microphthalmia
17%
Monkeypox
17%
Mortality Rate
28%
Mucin 5B
17%
Multiplex Polymerase Chain Reaction
17%
Myelination
17%
Myotonia
17%
Neonatal Diabetes Mellitus
17%
Neonatal Infant
19%
Nerve Cell Differentiation
17%
Neurogenic Bladder
17%
Neurological Complication
23%
Nevo Syndrome
17%
Nucleotidase
17%
Obesity
50%
Obstructive Sleep Apnea
17%
Omipalisib
17%
Osteosclerosis
17%
Oxygen Consumption
43%
Pediatric Anesthesia
17%
Pediatric Imaging
17%
Pediatrics
52%
Peripheral T-Cell Lymphoma
17%
Pertussis
26%
Pneumococcus Vaccine
17%
Population Risk
17%
Prevalence
77%
Primary Immunodeficiency
35%
Probiotic Agent
17%
Propionic Acidemia
17%
Proteoglycan Synthesis
17%
Psychodermatology
17%
Public Health
20%
Rapamycin
52%
Recurrent Disease
26%
Recurrent Fever
17%
Renal Biopsy
24%
Renal Tubular Acidosis
17%
Retrospective Cohort Study
20%
Retrospective Study
30%
Scalp
17%
Scapula
17%
School-Aged Child
26%
Silver-Russell Syndrome
17%
Skin Appendage
17%
Smith Magenis Syndrome
17%
Speech Delay
17%
Streptococcus Vaccine
17%
Succinic Acid
17%
Systematic Review
52%
Systemic Inflammatory Response Syndrome
17%
Systemic Lupus Erythematosus
17%
Tetralogy of Fallot
17%
Thalassemia
23%
Thiamazole
17%
Toddlers
20%
Tongue
17%
Topical Corticosteroid
17%
Tracheitis
17%
Transaldolase
17%
Ubiquitin Protein Ligase E3
17%
Ulna
17%
Urinary Tract
17%
Urinary Tract Infection
35%
Urokinase Receptor
17%
Vaccine Hesitancy
35%
Vesicoureteral Reflux
19%
Vitamin D
17%
Wrist Drop
17%
Youden Index
35%
Zoledronic Acid
17%
Keyphrases
ABL1
17%
Acquisition Settings
17%
AERRPS
17%
Aflatoxin M1 (AFM1)
20%
AHI1 Gene
17%
Al Ain
23%
Altruistic Behavior
17%
Anaphylactic Shock
17%
Anesthesiology
17%
Anorectal Malformation
17%
Anterior Segment
35%
Athelia
17%
Aurès
21%
Autism Spectrum Disorder
35%
Autosomal Recessive
30%
Benign Familial Infantile Epilepsy
17%
Bifid Nose
17%
Birth Prevalence
35%
Body Dysmorphic Disorder
17%
Bone Dysplasia
26%
Bone Morphogenetic Protein Receptor
17%
Bread
17%
C57BL
20%
Candida Auris
35%
Cardiac Tissue
35%
Catecholaminergic Polymorphic Ventricular Tachycardia
17%
Cellular Bioenergetics
21%
Cellular Respiration
30%
Centriolar Satellites
17%
Centriole Duplication
17%
Centromere
17%
Cep120
17%
Children with Congenital Heart Disease
17%
Choanal Atresia
17%
Chromosome Rearrangement
17%
Chronic Lung Disease
17%
Clefting
17%
Clinical Features
35%
Communicating Hydrocephalus
17%
Community Genetics
35%
Congenital Hydrocephalus
17%
Congenital Infection
17%
Consanguineous Family
26%
Cortical Cataract
17%
COVID-19 Response
17%
Cow's Milk Protein Allergy
17%
Cranial Ultrasound
17%
Cutis Laxa
23%
Dandy-Walker Malformation
17%
Demographic Factors
21%
Dermoid
17%
Diagnostic Exome Sequencing
17%
Dried Urine Spots
17%
Dwarfism
20%
DYNC1H1
17%
DYNC1H1 Gene
17%
DYRK1A
35%
Dysequilibrium Syndrome
17%
Dysmorphic Features
17%
Dysplasia
26%
Early Infantile
17%
Early Lethality
26%
Early-life Determinants
17%
Embryopathy
17%
Erythrocyte Indices
35%
Eye Abnormalities
17%
Facial Clefting
17%
Fermented Vegetables
17%
Fibrochondrogenesis
35%
Flow Dynamics
17%
Folate Metabolism
17%
Folate Pathway
17%
Founder mutation
17%
Frameshift Variant
17%
FREM1
17%
Frizzled
17%
Fuhrmann Syndrome
17%
Gene mutant
17%
Gene mutation
19%
Genetic Gene
17%
Genetic Renal Disease
35%
German Society
17%
Germline mutation
17%
GSK2126458
17%
Haploinsufficiency
21%
Heart Inflammation
17%
Height Velocity
17%
Helicobacter Pylori Gastritis
17%
Hepatic Tissue
35%
Hepatitis A
17%
Hospitalized COVID-19 Patients
17%
Human Genetics
20%
Hypochromia
35%
Hypomyelinating Leukodystrophy
17%
In Vitro Assessment
17%
Inborn Errors of Metabolism
17%
Infant Health
17%
Inositol Phosphatase
17%
INPP5E
17%
Intellectual Disability
38%
Interpretable Machine Learning
17%
Interstitial Pulmonary Disease
17%
Intrauterine Growth
17%
Iron Deficiency
35%
Iron Deficiency Anemia
21%
KCNQ2 mutation
17%
KIF7
17%
LAMB2
17%
LAMB2 Gene
17%
Laminin-2
17%
Limb Malformation
17%
Live Birth
21%
Loose Stools
17%
Major Congenital Anomalies
35%
Malformations of Cortical Development
17%
McKusick-Kaufman Syndrome
17%
Measles-mumps-rubella
17%
Medical Faculty
35%
Methimazole
17%
Michels Syndrome
17%
Microcytosis
35%
Monkeypox
17%
Mother Health
17%
MTOR Inhibitor
35%
MUC5B
17%
Neonatal Onset
17%
Neonate
24%
Neuronal Development
17%
New Association
17%
New-onset Refractory Status Epilepticus (NORSE)
17%
Null Variants
17%
Omental Biopsy
17%
Optimal Acquisition
17%
Oral Clefts
17%
Oral Intake
17%
Overgrowth Syndrome
17%
Oxygen Measurement
17%
Pax4
17%
PDZ Domain
17%
PDZD8
17%
Pediatric Anesthesia
17%
Peripheral T-cell Lymphoma
17%
Periventricular Echogenicity
17%
Periventricular Leukomalacia
17%
Phocomelia
17%
Phosphatidylinositol Signaling
17%
Polymicrogyria
17%
Polyphenols
35%
Power Doppler
17%
Power Doppler Ultrasound
17%
Presentation Mode
19%
Prevalence at Birth
17%
Primary Nocturnal Enuresis
17%
Progeroid Features
19%
Protein Microparticles
17%
PSMD12
17%
Psychological Assessment
17%
PYCR1
19%
Quadrupedal Locomotion
17%
RaaS
17%
Radiological Features
43%
Renal Agenesis
17%
Renal Dysplasia
17%
Renal Scarring
17%
Renal Tissue
17%
Renal Tubular Acidosis
17%
Resistance to Antibiotics
17%
Rotavirus Gastroenteritis
35%
Schindler Disease
17%
Seizure
23%
Sensorineural Deafness
17%
Sensorineural Hearing Impairment
17%
Severe Asthma
17%
Severe COVID-19
17%
Shock-induced
17%
Short Limbs
35%
Short-rib Polydactyly Syndromes
17%
Single Institution
17%
Single System
20%
Sirolimus
35%
Skin Appendages
17%
Small Airways
17%
Standard Projects
17%
Subtelomeric
17%
Succinic Acid
17%
Surgery for Obesity
17%
Surveillance Cues
17%
SYNJ1
17%
Tetralogy of Fallot
17%
Thalassaemias
35%
Thin Corpus Callosum
17%
Thyroid Gland
17%
Transmission Genetics
17%
TRIP12
35%
United Arab Emirates
100%
Urinary Tract Infection
17%
Varicella Zoster
17%
Wnt7a
17%
Youden Index
21%
Zoledronic Acid
17%