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497401 to 497500 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Multipotential carcinogenicity of the fried food mutagen 2-amino-3-methylimidazo[4,5-f]quinoline in rats.
Autotransplantation of the lingual thyroid.
Dose-related inhibition of colon carcinogenesis by dietary piroxicam, a nonsteroidal antiinflammatory drug, during different stages of rat colon tumor development.
Exophthalmos in a woman with lingual, subhyoid and lateral-lobe thyroid glands.
Clinical characteristics of ectopic thyroid in Korea.
Shape matters: intravital microscopy reveals surprising geometrical dependence for nanoparticles in tumor models of extravasation.
The treatment of a lingual thyroid with radioactive iodine.
Therapeutic irradiation and brain injury.
Type and prevalence of BRAF mutations are closely associated with papillary thyroid carcinoma histotype and patients' age but not with tumour aggressiveness.
Increased expression of AP2 and Sp1 transcription factors in human thyroid tumors: a role in NIS expression regulation?
The risk of second primary malignancies up to three decades after the treatment of differentiated thyroid cancer.
Downregulation of Rap1GAP through epigenetic silencing and loss of heterozygosity promotes invasion and progression of thyroid tumors.
Real-time prognosis for metastatic thyroid carcinoma based on 2-[18F]fluoro-2-deoxy-D-glucose-positron emission tomography scanning.
Observer variation in the diagnosis of follicular variant of papillary thyroid carcinoma.
Changing trends in incidence and mortality of thyroid cancer in Scotland.
MicroRNA analysis as a potential diagnostic tool for papillary thyroid carcinoma.
BRAF mutations are associated with some histological types of papillary thyroid carcinoma.
Molecular profile and clinical-pathologic features of the follicular variant of papillary thyroid carcinoma. An unusually high prevalence of ras mutations.
Alterations in genomic profiles during tumor progression in a mouse model of follicular thyroid carcinoma.
The oncogene BRAF V600E is associated with a high risk of recurrence and less differentiated papillary thyroid carcinoma due to the impairment of Na+/I- targeting to the membrane.
The prevalence and prognostic value of BRAF mutation in thyroid cancer.
ras mutations are associated with aggressive tumor phenotypes and poor prognosis in thyroid cancer.
Molecular genetics and diagnosis of thyroid cancer.
Papillary and follicular thyroid carcinoma.
Mice with a mutation in the thyroid hormone receptor beta gene spontaneously develop thyroid carcinoma: a mouse model of thyroid carcinogenesis.
Mutational profile of advanced primary and metastatic radioactive iodine-refractory thyroid cancers reveals distinct pathogenetic roles for BRAF, PIK3CA, and AKT1.
Symptoms and disease associations in idiopathic intracranial hypertension (pseudotumor cerebri): a case-control study.
Cerebral blood flow and metabolism in comatose patients with acute head injury. Relationship to intracranial hypertension.
Video microscopy of cerebrocortical capillary flow: response to hypotension and intracranial hypertension.
Results of optic nerve sheath fenestration for pseudotumor cerebri. The lateral orbitotomy approach.
Idiopathic intracranial hypertension.
Factors affecting visual loss in benign intracranial hypertension.
Magnetic resonance imaging in pseudotumor cerebri.
Cerebrospinal fluid pressure in normal obese subjects and patients with pseudotumor cerebri.
The incidence of pseudotumor cerebri. Population studies in Iowa and Louisiana.
Best practice updates for pediatric/adolescent weight loss surgery.
Monitoring and interpretation of intracranial pressure.
Interstitial hypertension in head and neck tumors in patients: correlation with tumor size.
Brain swelling and ischaemia in Kenyans with cerebral malaria.
Intracranial hypertension in Africans with cerebral malaria.
Idiopathic intracranial hypertension. A prospective study of 50 patients.
Diffuse cerebral swelling following head injuries in children: the syndrome of "malignant brain edema".
Carcinomas of sweat glands: report of 60 cases.
Nucleolar organizer regions in cutaneous tumours.
LIFE HISTORY OF ORGANOID NEVI. SPECIAL REFERENCE TO NEVUS SEBACEUS OF JADASSOHN.
Immunohistochemical analysis of apocrine breast lesions. Consistent over-expression of androgen receptor accompanied by the loss of estrogen and progesterone receptors in apocrine metaplasia and apocrine carcinoma in situ.
Homologous carcinomas of the breasts, skin, and salivary glands. A histologic and immunohistochemical comparison of ductal mammary carcinoma, ductal sweat gland carcinoma, and salivary duct carcinoma.
Adnexal carcinomas of the skin. I. Eccrine carcinomas.
Overexpression of amphiregulin, a major autocrine growth factor for cultured human keratinocytes, in hyperproliferative skin diseases.
Mucin-secreting tumours of the skin with special reference to the so-called mixed-salivary tumour of the skin and its relation to hidradenoma.
Eccrine adenocarcinoma. A clinicopathologic study of 35 cases.
Chondroid syringoma. Mixed tumor of skin, salivary gland type.
The groin flap.
Quantitative PCR and HER2 testing in breast cancer: a technical and cost-effectiveness analysis.
Eccrine porocarcinoma (malignant eccrine poroma): a clinicopathologic study of 69 cases.
Gross cystic disease fluid protein-15 as a marker for breast cancer: immunohistochemical analysis of 690 human neoplasms and comparison with alpha-lactalbumin.
Diagnostic and genetical aspects of tuberous sclerosis.
Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis.
Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).
Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome.
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome.
Carcinoma of the oesophagus with keratosis palmaris et plantaris (tylosis): a study of two families.
Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma.
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.
trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation.
Intermediate filament-membrane attachments function synergistically with actin-dependent contacts to regulate intercellular adhesive strength.
Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda.
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma.
R-spondin1 is essential in sex determination, skin differentiation and malignancy.
Malignant melanoma in Uganda. (The relationship between pigmentation and malignant melanoma on the soles of the feet).
Hand-foot skin reaction increases with cumulative sorafenib dose and with combination anti-vascular endothelial growth factor therapy.
Immunopathology of experimental cutaneous leishmaniasis.
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma.
Modulatory mechanisms controlling the NLRP3 inflammasome in inflammation: recent developments.
Immunology in clinic review series; focus on autoinflammatory diseases: role of inflammasomes in autoinflammatory syndromes.
Divergence of IL-1, IL-18, and cell death in NLRP3 inflammasomopathies.
A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanism u...
Protein kinase A regulates caspase-1 via Ets-1 in bone stromal cell-derived lesions: a link between cyclic AMP and pro-inflammatory pathways in osteoblast progenitors.
Follow-up and quality of life of patients with cryopyrin-associated periodic syndromes treated with Anakinra.
Efficacy and safety of anakinra therapy in pediatric and adult patients with the autoinflammatory Muckle-Wells syndrome.
Two-year results from an open-label, multicentre, phase III study evaluating the safety and efficacy of canakinumab in patients with cryopyrin-associated periodic syndrome across different severity phenotypes.
Role of IL-1 beta in the development of human T(H)17 cells: lesson from NLPR3 mutated patients.
Current status of understanding the pathogenesis and management of patients with NOMID/CINCA.
Immunology in clinic review series; focus on autoinflammatory diseases: update on monogenic autoinflammatory diseases: the role of interleukin (IL)-1 and an emerging role for cytokines beyond IL-1.
High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study.
Mild Vertigo, fever, abdominal pain
Inflammasome and IL-1beta-mediated disorders.
Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: a cohort study to determine three- and five-year outcomes.
Autoinflammation: the prominent role of IL-1 in monogenic autoinflammatory diseases and implications for common illnesses.
Altered redox state of monocytes from cryopyrin-associated periodic syndromes causes accelerated IL-1beta secretion.
Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.
The calcium-sensing receptor regulates the NLRP3 inflammasome through Ca2+ and cAMP.
Mitochondrial reactive oxygen species promote production of proinflammatory cytokines and are elevated in TNFR1-associated periodic syndrome (TRAPS).
Mild Vertigo, fever
Natural history of impetigo. I. Site sequence of acquisition and familial patterns of spread of cutaneous streptococci.
Assessment of Streptococcus pyogenes microcolony formation in infected skin by confocal laser scanning microscopy.
Characterization of the epidemic European fusidic acid-resistant impetigo clone of Staphylococcus aureus.