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480701 to 480800 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Factor XIII deficiency.
A familial factor XIII subunit B deficiency.
Rheological properties of fibrin clots. Effects of fibrinogen concentration, Factor XIII deficiency, and Factor XIII inhibition.
Targeted inactivation of the mouse locus encoding coagulation factor XIII-A: hemostatic abnormalities in mutant mice and characterization of the coagulation deficit.
Factor XIII A subunit-deficient mice developed severe uterine bleeding events and subsequent spontaneous miscarriages.
Deglycosylation of fibrinogen accelerates polymerization and increases lateral aggregation of fibrin fibers.
A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency.
Human factor XIII: fibrin-stabilizing factor.
Fibrinoligase: the fibrin-stabilizing factor system of blood plasma.
Coagulation, an ancestral serine protease cascade, exerts a novel function in early immune defense.
Contribution of fibrin stabilization to clot strength. Supplementation of factor XIII-deficient plasma with the purified zymogen.
Transglutaminases in disease.
[Purpura fulminans with deficiency of Owren's Factor V and treatment with exchange transfusion].
[Intravenous corticotherapy in the treatment of purpura fulminans & severe meningococcosis].
Spectrum of purpura fulminans: report of three classical prototypes and review of management strategies.
Purpura fulminans in a newborn baby.
Orthopaedic sequelae of childhood meningococcemia: management considerations and outcome.
Meningococcal interaction to microvasculature triggers the tissular lesions of purpura fulminans.
Long-term survival of a child with homozygous protein C deficiency successfully treated with living donor liver transplantation.
In reply—Early goal-directed therapy for severe sepsis.
Early goal-directed therapy for severe sepsis.
19-year-old woman with multiorgan failure and purpura.
Purpura fulminans with afibrinogenaemia.
Protein C concentrate in preterm neonates with sepsis.
Nonbacterial purpura fulminans and severe autoimmune acquired protein S deficiency associated with human herpesvirus-6 active replication.
Purpura fulminans: recognition, diagnosis and management.
Purpura fulminans; report of two cases following scarlet fever.
Purpura fulminans treated successfully with anticoagulation; report of a case.
Protein C deficiency.
PURPURA FULMINANS. REPORT OF A CASE SUCCESSFULLY TREATED WITH HEPARIN AND HYDROCORTISONE. REVIEW OF 50 CASES FROM THE LITERATURE.
Cellular immune responses to the murine nematode parasite Trichuris muris. I. Differential cytokine production during acute or chronic infection.
Muc5ac: a critical component mediating the rejection of enteric nematodes.
The Trichuris muris system: a paradigm of resistance and susceptibility to intestinal nematode infection.
Helminth products bypass the need for TSLP in Th2 immune responses by directly modulating dendritic cell function.
Acquired immunity to Trichuris muris in the albino laboratory mouse.
Interleukin 25 regulates type 2 cytokine-dependent immunity and limits chronic inflammation in the gastrointestinal tract.
TSLP regulates intestinal immunity and inflammation in mouse models of helminth infection and colitis.
Cytokine-mediated regulation of chronic intestinal helminth infection.
RELMbeta/FIZZ2 is a goblet cell-specific immune-effector molecule in the gastrointestinal tract.
Trichuris suis therapy for active ulcerative colitis: a randomized controlled trial.
Trichuris suis therapy in Crohn's disease.
Action of agents on glucosyltransferases from Streptococcus mutans in solution and adsorbed to experimental pellicle.
The surface area of the adult human mouth and thickness of the salivary film covering the teeth and oral mucosa.
Immunochemical identification and determination of proline-rich proteins in salivary secretions, enamel pellicle, and glandular tissue specimens.
How is the development of dental biofilms influenced by the host?
Adsorption of human salivary proteins to hydroxyapatite: a comparison between whole saliva and glandular salivary secretions.
The acquired pellicle: immunofluorescent demonstration of specific proteins.
The activity of glucosyltransferase adsorbed onto saliva-coated hydroxyapatite.
Effects of apigenin and tt-farnesol on glucosyltransferase activity, biofilm viability and caries development in rats.
Role of cryptic receptors (cryptitopes) in bacterial adhesion to oral surfaces.
Streptococcus milleri (Guthof); an indigenous organism of the human oral cavity.
Saliva and dental pellicle--a review.
Human oral microbial ecology and dental caries and periodontal diseases.
Characterization of in vivo salivary-derived enamel pellicle.
Associations between periodontal disease and risk for nosocomial bacterial pneumonia and chronic obstructive pulmonary disease. A systematic review.
Human lymphoproliferative reaction to saliva and dental plaque-deposits: an in vitro correlation with periodontal disease.
Saliva-bacterium interactions in oral microbial ecology.
Adherent interactions which may affect microbial ecology in the mouth.
Dermatofibrosarcoma protuberans: recent clinical progress.
Translocation, t(17;22)(q22;q13), in dermatofibrosarcoma protuberans: a new tumor-associated chromosome rearrangement.
Overexpression of the hepatocyte growth factor (HGF) receptor (Met) and presence of a truncated and activated intracellular HGF receptor fragment in locally aggressive/malignant human musculoskeletal tumors.
Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis.
Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas.
Skin cancer in African Americans.
Dermatofibrosarcoma protuberans COL1A1-PDGFB fusion is identified in virtually all dermatofibrosarcoma protuberans cases when investigated by newly developed multiplex reverse transcription polymerase chain reaction and fluorescence in situ hybridizati...
Fibrosarcomatous ("high-grade") dermatofibrosarcoma protuberans: clinicopathologic and immunohistochemical study of a series of 41 cases with emphasis on prognostic significance.
Dermatofibrosarcoma protuberans: A clinicopathologic analysis of patients treated and followed at a single institution.
Differential sensitivity to imatinib of 2 patients with metastatic sarcoma arising from dermatofibrosarcoma protuberans.
Gene expression patterns and gene copy number changes in dermatofibrosarcoma protuberans.
Imatinib mesylate in advanced dermatofibrosarcoma protuberans: pooled analysis of two phase II clinical trials.
Platelet-derived growth factor receptor (PDGFR): a target for anticancer therapeutics.
The dermatofibrosarcoma protuberans-associated collagen type Ialpha1/platelet-derived growth factor (PDGF) B-chain fusion gene generates a transforming protein that is processed to functional PDGF-BB.
Molecular and clinical analysis of locally advanced dermatofibrosarcoma protuberans treated with imatinib: Imatinib Target Exploration Consortium Study B2225.
Spontaneous CSF Leaks.
Reversible empty sella in idiopathic intracranial hypertension: an indicator of successful therapy?
Rearrangement of chromosome 15 in the region q11.2----q12 in an individual with obesity syndrome and her normal mother.
Presence of anti-pituitary hormone antibodies in patients with empty sella syndrome and pituitary tumours.
Pituitary adenomas: early postoperative MR imaging after transsphenoidal resection.
MR imaging of pituitary morphology in idiopathic intracranial hypertension.
Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3----q21.2).
Goldmann perimetry in acromegaly: a survey of 307 cases from 1951 through 1996.
Ghrelin main action on the regulation of growth hormone release is exerted at hypothalamic level.
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy.
Empty sellae, impaired testosterone secretion, and defective hypothalamic-pituitary growth and gonadal axes in children with Bardet-Biedl syndrome.
Coexisting pituitary adenomas and partially empty sellas.
The value of pituitary magnetic resonance imaging in men with hypogonadism.
The long-term predictive accuracy of the short synacthen (corticotropin) stimulation test for assessment of the hypothalamic-pituitary-adrenal axis.
Primary empty sella.
Elevated intracranial pressures in spontaneous cerebrospinal fluid leaks.
Diagnosis, treatment, and outcome of pituitary tumors and other abnormal intrasellar masses. Retrospective analysis of 353 patients.
Antipituitary antibodies in patients with the primary empty sella syndrome.
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
CD1d-reactive T-cell activation leads to amelioration of disease caused by diabetogenic encephalomyocarditis virus.
Toll-like receptor 3 is an essential component of the innate stress response in virus-induced cardiac injury.
Therapeutic action of cannabinoids in a murine model of multiple sclerosis.
Among CXCR3 chemokines, IFN-gamma-inducible protein of 10 kDa (CXC chemokine ligand (CXCL) 10) but not monokine induced by IFN-gamma (CXCL9) imprints a pattern for the subsequent development of autoimmune disease.
The leader protein of Theiler's virus inhibits immediate-early alpha/beta interferon production.