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496501 to 496600 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Synovial sarcoma: a clinicopathologic, staging, and prognostic assessment.
A phase II study of imatinib mesylate in children with refractory or relapsed solid tumors: a Children's Oncology Group study.
Analysis of transforming activity of human synovial sarcoma-associated chimeric protein SYT-SSX1 bound to chromatin remodeling factor hBRM/hSNF2 alpha.
Synovial sarcoma: a multivariate analysis of prognostic factors in 112 patients with primary localized tumors of the extremity.
Fusions of the SYT and SSX genes in synovial sarcoma.
CLEAR-CELL SARCOMA OF TENDONS AND APONEUROSES. AN ANALYSIS OF 21 CASES.
Synovial sarcoma: a retrospective analysis of 271 patients of all ages treated at a single institution.
Histologic grade, but not SYT-SSX fusion type, is an important prognostic factor in patients with synovial sarcoma: a multicenter, retrospective analysis.
The human primary immune response to keyhole limpet haemocyanin: interrelationships of delayed hypersensitivity, antibody response and in vitro blast transformation.
A novel fusion gene, SYT-SSX4, in synovial sarcoma.
The SSX-2 gene, which is involved in the t(X;18) translocation of synovial sarcomas, codes for the human tumor antigen HOM-MEL-40.
Expression profiling of synovial sarcoma by cDNA microarrays: association of ERBB2, IGFBP2, and ELF3 with epithelial differentiation.
Impact of SYT-SSX fusion type on the clinical behavior of synovial sarcoma: a multi-institutional retrospective study of 243 patients.
Fusion of SYT to two genes, SSX1 and SSX2, encoding proteins with homology to the Kruppel-associated box in human synovial sarcoma.
A conditional mouse model of synovial sarcoma: insights into a myogenic origin.
SYT-SSX gene fusion as a determinant of morphology and prognosis in synovial sarcoma.
Identification of novel genes, SYT and SSX, involved in the t(X;18)(p11.2;q11.2) translocation found in human synovial sarcoma.
Tumor regression in patients with metastatic synovial cell sarcoma and melanoma using genetically engineered lymphocytes reactive with NY-ESO-1.
Gastrinoma (duodenal and pancreatic).
A prospective study of intraoperative methods to diagnose and resect duodenal gastrinomas.
Prospective study of surgical resection of duodenal and pancreatic gastrinomas in multiple endocrine neoplasia type 1.
Population-based study of islet cell carcinoma.
Surgery in Zollinger-Ellison syndrome alters the natural history of gastrinoma.
Duminda N Wijeysundera
Serum gastrin in Zollinger-Ellison syndrome: I. Prospective study of fasting serum gastrin in 309 patients from the National Institutes of Health and comparison with 2229 cases from the literature.
Small-bowel diverticulosis: perceptions and reality.
IL-18 regulates intestinal mastocytosis and Th2 cytokine production independently of IFN-gamma during Trichinella spiralis infection.
Expression of the two isoforms of the vesicular monoamine transporter (VMAT1 and VMAT2) in the endocrine pancreas and pancreatic endocrine tumors.
Effect of proinflammatory interleukins on jejunal nutrient transport.
Does the use of routine duodenotomy (DUODX) affect rate of cure, development of liver metastases, or survival in patients with Zollinger-Ellison syndrome?
Mucosal intra-epithelial lymphocytes in enteropathy-associated T-cell lymphoma, ulcerative jejunitis, and refractory celiac disease constitute a neoplastic population.
Value of somatostatin receptor scintigraphy: a prospective study in gastrinoma of its effect on clinical management.
Superselective microcoil embolization for the treatment of lower gastrointestinal hemorrhage.
Expression of vascular endothelial growth factor in digestive neuroendocrine tumours.
Morbidity and mortality of aggressive resection in patients with advanced neuroendocrine tumors.
Reversible expression of tryptases and chymases in the jejunal mast cells of mice infected with Trichinella spiralis.
Enteroscopic diagnosis of small bowel ulceration in patients receiving non-steroidal anti-inflammatory drugs.
Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome.
Hepatic inflammation in rats with experimental small intestinal bacterial overgrowth.
Early experience with laparoscopic resections of islet cell tumors.
Multiple endocrine neoplasia type 1 and Zollinger-Ellison syndrome: a prospective study of 107 cases and comparison with 1009 cases from the literature.
Primary peptic ulcerations of the jejunum associated with islet cell tumors. Twenty-five-year appraisal.
The diagnosis of small bowel bacterial overgrowth. Reliability of jejunal culture and inadequacy of breath hydrogen testing.
Ultrastructural and biochemical changes in human jejunal mucosa associated with enteropathogenic Escherichia coli (0111) infection.
MicroRNAs control intestinal epithelial differentiation, architecture, and barrier function.
Antibodies to IFN-gamma prevent immunologically mediated intestinal damage in murine graft-versus-host reaction.
Lack of cortical contrast gain control in human photosensitive epilepsy.
Increased persistent Na+ current contributes to seizure in the slamdance bang-sensitive Drosophila mutant.
Evidence supporting a role of serotonin in modulation of sudden death induced by seizures in DBA/2 mice.
Comparative fos immunoreactivity in the brain after forebrain, brainstem, or combined seizures induced by electroshock, pentylenetetrazol, focally induced and audiogenic seizures in rats.
Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome.
Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.
Vlgr1 knockout mice show audiogenic seizure susceptibility.
Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome.
Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice.
Anticonvulsant and antiepileptic actions of 2-deoxy-D-glucose in epilepsy models.
A null mutation for Fmr1 in female mice: effects on regional cerebral metabolic rate for glucose and relationship to behavior.
Lacosamide, a novel anti-convulsant drug, shows efficacy with a wide safety margin in rodent models for epilepsy.
Acetoacetate, acetone, and dibenzylamine (a contaminant in l-(+)-beta-hydroxybutyrate) exhibit direct anticonvulsant actions in vivo.
A novel gene causing a mendelian audiogenic mouse epilepsy.
A moderate and transient deficiency of maternal thyroid function at the beginning of fetal neocorticogenesis alters neuronal migration.
Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.
Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.
Cholesterol involvement in the pathogenesis of neurodegenerative diseases.
The adult form of Niemann-Pick disease type C.
Recommendations for the diagnosis and management of Niemann-Pick disease type C: an update.
A sensitive and specific LC-MS/MS method for rapid diagnosis of Niemann-Pick C1 disease from human plasma.
Weekly cyclodextrin administration normalizes cholesterol metabolism in nearly every organ of the Niemann-Pick type C1 mouse and markedly prolongs life.
The effect of indomethacin on eggshell quality.
Sterol regulators of cholesterol homeostasis and beyond: the oxysterol hypothesis revisited and revised.
Recommendations on the diagnosis and management of Niemann-Pick disease type C.
Structural basis of sterol binding by NPC2, a lysosomal protein deficient in Niemann-Pick type C2 disease.
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C.
Mutation and polymorphism spectrum of the GALNS gene in mucopolysaccharidosis IVA (Morquio A).
Lipids on trial: the search for the offending metabolite in Niemann-Pick type C disease.
Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase.
Cyclodextrin overcomes deficient lysosome-to-endoplasmic reticulum transport of cholesterol in Niemann-Pick type C cells.
Cardiac Arrhythmia, Mural Thrombus
[Pseudo-achondroplastic forms of spondylo-epiphyseal dysplasias].
Niemann-Pick type C disease: molecular mechanisms and potential therapeutic approaches.
Acid mucopolysaccharides in cultured human fibroblasts.
Vitreoretinal degeneration as a sign of generalized connective tissue diseases.
Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acid.
Mucopolysaccharidosis type IVA (Morquio syndrome): a clinical review.
Molecular basis of GM1 gangliosidosis and Morquio disease, type B. Structure-function studies of lysosomal beta-galactosidase and the non-lysosomal beta-galactosidase-like protein.
Endocytosis of beta-cyclodextrins is responsible for cholesterol reduction in Niemann-Pick type C mutant cells.
Enhancement of drug delivery: enzyme-replacement therapy for murine Morquio A syndrome.
Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome.
A unique rough surfaced endoplasmic reticulum inclusion in pseudoachondroplasia.
Cholesterol oxidation products are sensitive and specific blood-based biomarkers for Niemann-Pick C1 disease.
Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment.
Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7-RILP-p150 Glued and late endosome positioning.
Mannose 6-phosphate receptor-mediated transport of sulfamidase across the blood-brain barrier in the newborn mouse.
Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study.
Niemann-Pick disease type C.
Enzyme replacement therapy in a murine model of Morquio A syndrome.
Chronic cyclodextrin treatment of murine Niemann-Pick C disease ameliorates neuronal cholesterol and glycosphingolipid storage and disease progression.
Morquio disease: isolation, characterization and expression of full-length cDNA for human N-acetylgalactosamine-6-sulfate sulfatase.