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510301 to 510400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Diagnosis of breast cancer using diffuse reflectance spectroscopy: Comparison of a Monte Carlo versus partial least squares analysis based feature extraction technique.
Down-regulation of caveolin-1, a candidate tumor suppressor gene, in sarcomas.
US national prevalence and correlates of low back and neck pain among adults.
Early identification of patients at risk of developing a persistent back problem: the predictive validity of the Orebro Musculoskeletal Pain Questionnaire.
Treatment of neck pain: noninvasive interventions: results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders.
Incidence and prevalence of complaints of the neck and upper extremity in general practice.
Teasing apart quality and validity in systematic reviews: an example from acupuncture trials in chronic neck and back pain.
Epidemiology of work related neck and upper limb problems: psychosocial and personal risk factors (part I) and effective interventions from a bio behavioural perspective (part II).
Patterns and perceptions of care for treatment of back and neck pain: results of a national survey.
Effect of eliminating compensation for pain and suffering on the outcome of insurance claims for whiplash injury.
Physical risk factors for neck pain.
Mental disorders among persons with chronic back or neck pain: results from the World Mental Health Surveys.
The burden and determinants of neck pain in the general population: results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders.
Efficacy of spinal manipulation and mobilization for low back pain and neck pain: a systematic review and best evidence synthesis.
Back pain prevalence and visit rates: estimates from U.S. national surveys, 2002.
The Saskatchewan Health and Back Pain Survey. The prevalence of neck pain and related disability in Saskatchewan adults.
Diarrhoea in children: an interface between developing and developed countries.
Clinical practice. Overweight children and adolescents.
Worldwide timing of growth faltering: implications for nutritional interventions.
Targeting parents exclusively in the treatment of childhood obesity: long-term results.
Community-acquired bacteremia among children admitted to a rural hospital in Mozambique.
The effects of malnutrition on child mortality in developing countries.
Child undernutrition, tropical enteropathy, toilets, and handwashing.
Relation between falciparum malaria and bacteraemia in Kenyan children: a population-based, case-control study and a longitudinal study.
Prevalence of overweight among children in Europe.
Racial and ethnic differences in secular trends for childhood BMI, weight, and height.
A review of family and social determinants of children's eating patterns and diet quality.
What is the best measure of adiposity change in growing children: BMI, BMI %, BMI z-score or BMI centile?
Preventing childhood obesity: health in the balance: executive summary.
What works? Interventions for maternal and child undernutrition and survival.
Risk factors of relative adrenocortical deficiency in intensive care patients needing mechanical ventilation.
Codon 17 polymorphism of the cytotoxic T lymphocyte antigen 4 gene in Hashimoto's thyroiditis and Addison's disease.
Premature mortality in patients with Addison's disease: a population-based study.
Immunological aspects of premature ovarian failure associated with idiopathic Addison's disease.
Adrenal antibodies in Addison's disease.
SCHMIDT'S SYNDROME (THYROID AND ADRENAL INSUFFICIENCY). A REVIEW OF THE LITERATURE AND A REPORT OF FIFTEEN NEW CASES INCLUDING TEN INSTANCES OF COEXISTENT DIABETES MELLITUS.
Adrenomyeloneuropathy: a probable variant of adrenoleukodystrophy. I. Clinical and endocrinologic aspects.
A clinical and immunological study of adrenocortical insufficiency (Addison's disease).
VARIATIONS IN PLASMA RENIN CONCENTRATION IN SEVERAL PHYSIOLOGICAL AND PATHOLOGICAL STATES.
The spectrum of diseases associated with thymoma. Coincidence or syndrome?
Clinical review 93: Autoimmune polyglandular syndrome type 1.
Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes.
Auto-antibodies in Addison's disease.
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes.
CTLA-4 in autoimmune diseases--a general susceptibility gene to autoimmunity?
Defective suppressor function of human CD4+ CD25+ regulatory T cells in autoimmune polyglandular syndrome type II.
Quality indicators for colonoscopy and the risk of interval cancer.
Cost-effectiveness of screening for colorectal cancer in the general population.
Detection of colonic dysplasia in vivo using a targeted heptapeptide and confocal microendoscopy.
Aspirin use and the risk for colorectal cancer and adenoma in male health professionals.
Risk of advanced proximal neoplasms in asymptomatic adults according to the distal colorectal findings.
Polyp miss rate determined by tandem colonoscopy: a systematic review.
Hypomethylation of DNA from benign and malignant human colon neoplasms.
Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths.
BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum.
Accuracy of CT colonography for detection of large adenomas and cancers.
Colonoscopic miss rates of adenomas determined by back-to-back colonoscopies.
Calcium plus vitamin D supplementation and the risk of colorectal cancer.
A randomized trial of aspirin to prevent colorectal adenomas in patients with previous colorectal cancer.
Screening and surveillance for the early detection of colorectal cancer and adenomatous polyps, 2008: a joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology.
Cancer risk in mutation carriers of DNA-mismatch-repair genes.
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease.
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer.
Endonucleolytic function of MutLalpha in human mismatch repair.
The crystal structure of DNA mismatch repair protein MutS binding to a G x T mismatch.
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.
Mutation of a mutL homolog in hereditary colon cancer.
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability.
Carotid Body Tumor
Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1.
Secretion of chromogranin A by peptide-producing endocrine neoplasms.
Molecular cloning and functional expression of human parathyroid calcium receptor cDNAs.
Somatic mutation of the MEN1 gene in parathyroid tumours.
Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma.
Formalin fixation for electron microscopy: a re-evaluation.
Clinical review 122: Parathyroid carcinoma.
Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.
Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2.
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.
The cyclins and cyclin-dependent kinase inhibitors in hormonal regulation of proliferation and differentiation.
Mutations in the hminK gene cause long QT syndrome and suppress IKs function.
A structural basis for drug-induced long QT syndrome.
Modelling the long QT syndrome with induced pluripotent stem cells.
KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation.
Molecular mechanism for an inherited cardiac arrhythmia.
Channelopathies linked to plasma membrane phosphoinositides.
Transcriptional upregulation of Cav3.2 mediates epileptogenesis in the pilocarpine model of epilepsy.
HCN channelopathy in external globus pallidus neurons in models of Parkinson's disease.
Mislocalization of h channel subunits underlies h channelopathy in temporal lobe epilepsy.
BK channel activation: structural and functional insights.
Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects.
NaV1.1 channels and epilepsy.