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536401 to 536500 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Psychiatric and physical morbidity effects of dementia caregiving: prevalence, correlates, and causes.
Optimism, coping, and health: assessment and implications of generalized outcome expectancies.
Hemopneumothorax, Tension Pneumothorax, Tracheal Deviation
Socioeconomic status and health. The challenge of the gradient.
The Social Readjustment Rating Scale.
The Brief Symptom Inventory: an introductory report.
Development of a rating scale for primary depressive illness.
Cinacalcet hydrochloride reduces the serum calcium concentration in inoperable parathyroid carcinoma.
Primary hyperparathyroidism and the skeleton.
Increased mortality and morbidity in mild primary hyperparathyroid patients. The Parathyroid Epidemiology and Audit Research Study (PEARS).
Calciphylaxis from nonuremic causes: a systematic review.
Surgery for asymptomatic primary hyperparathyroidism: proceedings of the third international workshop.
Intraoperative parathyroid hormone testing improves cure rates in patients undergoing minimally invasive parathyroidectomy.
Medical observation, compared with parathyroidectomy, for asymptomatic primary hyperparathyroidism: a prospective, randomized trial.
Carotid vascular abnormalities in primary hyperparathyroidism.
Cardiac structure and diastolic function in mild primary hyperparathyroidism.
Regulation of plasma fibroblast growth factor 23 by calcium in primary hyperparathyroidism.
Prospective study of surgery for primary hyperparathyroidism (HPT) in multiple endocrine neoplasia-type 1 and Zollinger-Ellison syndrome: long-term outcome of a more virulent form of HPT.
The calcium-sensing receptor: physiology, pathophysiology and CaR-based therapeutics.
Surgery or surveillance for mild asymptomatic primary hyperparathyroidism: a prospective, randomized clinical trial.
Immunohistochemical study of matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in pulmonary lymphangioleiomyomatosis (LAM).
Preserved three-dimensional cancellous bone structure in mild primary hyperparathyroidism.
Pulmonary lymphangioleiomyomatosis: a report of 46 patients including a clinicopathologic study of prognostic factors.
Presentation of asymptomatic primary hyperparathyroidism: proceedings of the third international workshop.
Estradiol and tamoxifen stimulate LAM-associated angiomyolipoma cell growth and activate both genomic and nongenomic signaling pathways.
Decline in lung function in patients with lymphangioleiomyomatosis treated with or without progesterone.
Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the third international workshop.
Comprehensive evaluation of 35 patients with lymphangioleiomyomatosis.
The natural history of primary hyperparathyroidism with or without parathyroid surgery after 15 years.
Physiology and pathophysiology of the calcium-sensing receptor in the kidney.
Prevalence and clinical characteristics of lymphangioleiomyomatosis (LAM) in patients with tuberous sclerosis complex.
Tuberous sclerosis complex: linking growth and energy signaling pathways with human disease.
Guidelines for the management of asymptomatic primary hyperparathyroidism: summary statement from the third international workshop.
Lymphangioleiomyomatosis: a clinical update.
High frequency of pulmonary lymphangioleiomyomatosis in women with tuberous sclerosis complex.
The NHLBI lymphangioleiomyomatosis registry: characteristics of 230 patients at enrollment.
Sirolimus therapy in tuberous sclerosis or sporadic lymphangioleiomyomatosis.
Molecular and genetic analysis of disseminated neoplastic cells in lymphangioleiomyomatosis.
Recurrent lymphangiomyomatosis after transplantation: genetic analyses reveal a metastatic mechanism.
Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosis.
International guidelines for the selection of lung transplant candidates: 2006 update--a consensus report from the Pulmonary Scientific Council of the International Society for Heart and Lung Transplantation.
Efficacy and safety of sirolimus in lymphangioleiomyomatosis.
Tuberin regulates p70 S6 kinase activation and ribosomal protein S6 phosphorylation. A role for the TSC2 tumor suppressor gene in pulmonary lymphangioleiomyomatosis (LAM).
Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis.
Sirolimus for angiomyolipoma in tuberous sclerosis complex or lymphangioleiomyomatosis.
Lack of cadherins Celsr2 and Celsr3 impairs ependymal ciliogenesis, leading to fatal hydrocephalus.
Microtubule reduction in Alzheimer's disease and aging is independent of tau filament formation.
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.
Infections of cerebrospinal fluid shunts: epidemiology, clinical manifestations, and therapy.
The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics.
The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus.
Bacterial Infections, Unilateral Hilar Adenopathy
Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus.
RNA-binding protein Musashi family: roles for CNS stem cells and a subpopulation of ependymal cells revealed by targeted disruption and antisense ablation.
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.
An acidic protein isolated from fibrous astrocytes.
The EPICure study: outcomes to discharge from hospital for infants born at the threshold of viability.
Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia.
SYMPTOMATIC OCCULT HYDROCEPHALUS WITH "NORMAL" CEREBROSPINAL-FLUID PRESSURE.A TREATABLE SYNDROME.
Guidelines for the management of aneurysmal subarachnoid hemorrhage: a statement for healthcare professionals from a special writing group of the Stroke Council, American Heart Association.
Molecular basis of reovirus virulence: role of the S1 gene.
p73-deficient mice have neurological, pheromonal and inflammatory defects but lack spontaneous tumours.
Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm.
Human interleukin 17-producing cells originate from a CD161+CD4+ T cell precursor.
Psoriasis vulgaris lesions contain discrete populations of Th1 and Th17 T cells.
Th22 cells represent a distinct human T cell subset involved in epidermal immunity and remodeling.
New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
Etanercept in the treatment of psoriatic arthritis and psoriasis: a randomised trial.
IL-22 regulates the expression of genes responsible for antimicrobial defense, cellular differentiation, and mobility in keratinocytes: a potential role in psoriasis.
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.
Risk of myocardial infarction in patients with psoriasis.
The validity and practicality of sun-reactive skin types I through VI.
Psoriasis is associated with increased beta-defensin genomic copy number.
Pathogenesis and therapy of psoriasis.
A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.
A peptide antibiotic from human skin.
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.
Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide.
Interleukin-22, a T(H)17 cytokine, mediates IL-23-induced dermal inflammation and acanthosis.
Development, cytokine profile and function of human interleukin 17-producing helper T cells.
Adenosine deaminase activity in the diagnosis of tuberculous peritonitis.
Abdominal tuberculosis. A 10-year review.
Tuberculous peritonitis--reports of 26 cases, detailing diagnostic and therapeutic problems.
Tuberculous enteritis and peritonitis. Report of 36 general hospital cases.
Increased Bcl-2 and reduced Bax expression in infected macrophages in slowly progressive primary murine Mycobacterium tuberculosis infection.
Diagnosis of abdominal tuberculosis: experience from 11 cases and review of the literature.
Abdominal tuberculosis in Britain.
Abdominal tuberculosis: CT evaluation.
A clinical dilemma: abdominal tuberculosis.
Intra-abdominal and gastrointestinal tuberculosis.
Systematic review: tuberculous peritonitis--presenting features, diagnostic strategies and treatment.
Starch granulomatosis of the peritoneum.
Value of adenosine deaminase (ADA) in ascitic fluid for the diagnosis of tuberculous peritonitis: a meta-analysis.
Abdominal tuberculosis--a disease revived.