By continuing to use Symptoma®, you confirm you accept the cookies. More on
541301 to 541400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Trinucleotide repeat disorders.
The mGluR theory of fragile X mental retardation.
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
Evidence based physical activity for school-age youth.
Metabolic syndrome and altered gut microbiota in mice lacking Toll-like receptor 5.
Adiponectin and adiponectin receptors.
Variations in DNA elucidate molecular networks that cause disease.
Adiponectin and adiponectin receptors in insulin resistance, diabetes, and the metabolic syndrome.
Obesity and the metabolic syndrome in children and adolescents.
Metabolic syndrome--a new world-wide definition. A Consensus Statement from the International Diabetes Federation.
Abdominal obesity and metabolic syndrome.
Increased oxidative stress in obesity and its impact on metabolic syndrome.
Leukocyte infiltration, neuronal degeneration, and neurite outgrowth after ablation of scar-forming, reactive astrocytes in adult transgenic mice.
The metabolic syndrome and total and cardiovascular disease mortality in middle-aged men.
Mechanisms of brain injury after intracerebral haemorrhage.
The metabolic syndrome.
A controlled cortical impact model of traumatic brain injury in the rat.
The epidemiology and impact of traumatic brain injury: a brief overview.
Definition of metabolic syndrome: Report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition.
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
The parietal cortex and episodic memory: an attentional account.
Global and societal implications of the diabetes epidemic.
A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.
Characterization of the decision-making deficit of patients with ventromedial prefrontal cortex lesions.
Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.
The metabolic syndrome--a new worldwide definition.
Episodic memory: from mind to brain.
Model systems for the study of heart development and disease. Cardiac neural crest and conotruncal malformations.
The glial scar and central nervous system repair.
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
Erythropoietin crosses the blood-brain barrier to protect against experimental brain injury.
Primate anterior cingulate cortex: where motor control, drive and cognition interface.
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; Internation...
Prevalence of the metabolic syndrome among US adults: findings from the third National Health and Nutrition Examination Survey.
Principles of diffusion tensor imaging and its applications to basic neuroscience research.
The therapeutic potential of poly(ADP-ribose) polymerase inhibitors.
Astrocyte activation and reactive gliosis.
Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances.
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Mouse genetic models for prepulse inhibition: an early review.
Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development.
Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1.
The role of the thymus in immune reconstitution in aging, bone marrow transplantation, and HIV-1 infection.
Assessment of outcome after severe brain damage.
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
ATP mediates rapid microglial response to local brain injury in vivo.
Heart disease and stroke statistics--2011 update: a report from the American Heart Association.
Regeneration beyond the glial scar.
Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo.
A common molecular basis for rearrangement disorders on chromosome 22q11.
Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement.
Role of TBX1 in human del22q11.2 syndrome.
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
High rates of schizophrenia in adults with velo-cardio-facial syndrome.
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
Genome architecture, rearrangements and genomic disorders.
Large-scale transcriptional activity in chromosomes 21 and 22.
Assessing depressive symptoms in five psychiatric populations: a validation study.
Initial reliability and validity of a new retrospective measure of child abuse and neglect.
The CAGE questionnaire: validation of a new alcoholism screening instrument.
Recognition of the fetal alcohol syndrome in early infancy.
Matching Alcoholism Treatments to Client Heterogeneity: Project MATCH posttreatment drinking outcomes.
Research diagnostic criteria: rationale and reliability.
Lifetime co-occurrence of DSM-III-R alcohol abuse and dependence with other psychiatric disorders in the National Comorbidity Survey.
Towards the assessment of adolescent problem drinking.
An improved diagnostic evaluation instrument for substance abuse patients. The Addiction Severity Index.
Etiologic connections among substance dependence, antisocial behavior, and personality: modeling the externalizing spectrum.
Combined pharmacotherapies and behavioral interventions for alcohol dependence: the COMBINE study: a randomized controlled trial.
The 12-month prevalence and trends in DSM-IV alcohol abuse and dependence: United States, 1991-1992 and 2001-2002.
The Alcohol Use Disorder and Associated Disabilities Interview Schedule-IV (AUDADIS-IV): reliability of alcohol consumption, tobacco use, family history of depression and psychiatric diagnostic modules in a general population sample.
Risk and protective factors for alcohol and other drug problems in adolescence and early adulthood: implications for substance abuse prevention.
More powerful procedures for multiple significance testing.
Detecting alcoholism. The CAGE questionnaire.
A new, semi-structured psychiatric interview for use in genetic linkage studies: a report on the reliability of the SSAGA.
Comorbidity of mental disorders with alcohol and other drug abuse. Results from the Epidemiologic Catchment Area (ECA) Study.
The Fifth Edition of the Addiction Severity Index.
Development of the Alcohol Use Disorders Identification Test (AUDIT): WHO Collaborative Project on Early Detection of Persons with Harmful Alcohol Consumption--II.
Utah Growth Study: growth standards and the prevalence of growth hormone deficiency.
Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome.
Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans.
The neuroendocrinology of human puberty revisited.
The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism.
Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes.
Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group.
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.
Functional and structural alterations of the intraparietal sulcus in a developmental dyscalculia of genetic origin.
Effect of human growth hormone treatment for 1 to 7 years on growth of 100 children, with growth hormone deficiency, low birthweight, inherited smallness, Turner's syndrome, and other complaints.
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.
Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.
A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.
Global survey of escape from X inactivation by RNA-sequencing in mouse.