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468401 to 468500 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Role of haemophilus pleuropneumoniae lipopolysaccharide endotoxin in the pathogenesis of porcine Haemophilus pleuropneumonia.
Actinobacillus pleuropneumoniae surface polysaccharides: their role in diagnosis and immunogenicity.
Porcine Haemophilus pleuropneumonia epizootic in southwestern Ontario: clinical, microbiological, pathological and some epidemiological findings.
Pleuropneumonia of swine caused by Haemophilus parahaemolyticus. Studies on the protection obtained by vaccination.
Identification and serotyping of Haemophilus pleuropneumoniae by coagglutination test.
Isolation and biological characterization of two lipopolysaccharides and a capsular-enriched polysaccharide preparation from Haemophilus pleuropneumoniae.
[Haemophilus infection in pigs. 3. Serological studies on Haemophilus parahaemolyticus].
Serological characterization of 8 Haemophilus pleuropneumoniae strains and proposal of a new serotype: serotype 8.
Cholesterol in the growth of organisms of the pleuropneumonia group.
Comparative virulence of porcine Haemophilus bacteria.
The classification and nomenclature of organisms of the pleuropneumonia group.
Role of organisms of the pleuropneumonia group in human genital infections.
Some recommendations concerning primary isolation of Mycoplasma suipneumoniae and Mycoplasma flocculare a survey.
Cardiac arrhythmias induced by hypokalaemia and potassium loss during maintenance digoxin therapy.
Hypertension, the potassium ion and impaired carbohydrate tolerance.
Sodium and potassium intakes among US adults: NHANES 2003-2008.
POTASSIUM DEFICIENCY AND THE ROLE OF THE KIDNEY IN ITS PRODUCTION.
Normotensive salt sensitivity: effects of race and dietary potassium.
Effect of reduced endocytosis induced by hypotonic shock and potassium depletion on the infection of Hep 2 cells by picornaviruses.
ERK activation promotes neuronal degeneration predominantly through plasma membrane damage and independently of caspase-3.
The nephropathy of potassium depletion; a clinical and pathological entity.
Regulation of phosphate transport in proximal tubules.
CLINICAL CHARACTERISTICS OF PRIMARY ALDOSTERONISM FROM AN ANALYSIS OF 145 CASES.
On the mechanism of impairment of renal concentrating ability in potassium deficiency.
Metabolic and genetic analyses of apoptosis in potassium/serum-deprived rat cerebellar granule cells.
Molecules internalized by clathrin-independent endocytosis are delivered to endosomes containing transferrin receptors.
The renal lesions of electrolyte imbalance. I. The structural alterations in potassium-depleted rats.
Focal cytoplasmic degradation.
Sodium and potassium in the pathogenesis of hypertension.
Gestational Trophoblastic Disease
Fluorescence in situ hybridization in the diagnosis of soft tissue neoplasms: a review.
Dual-color, break-apart fluorescence in situ hybridization for EWS gene rearrangement distinguishes clear cell sarcoma of soft tissue from malignant melanoma.
Clear cell sarcoma of soft tissue: a clinicopathologic, immunohistochemical, and molecular analysis of 33 cases.
SMARCB1/INI1 protein expression in round cell soft tissue sarcomas associated with chromosomal translocations involving EWS: a special reference to SMARCB1/INI1 negative variant extraskeletal myxoid chondrosarcoma.
Pharmacologic suppression of MITF expression via HDAC inhibitors in the melanocyte lineage.
Detection and characterization of EWSR1/ATF1 and EWSR1/CREB1 chimeric transcripts in clear cell sarcoma (melanoma of soft parts).
Clear cell sarcoma of tendons and aponeuroses: a study of 75 patients.
Expression profiling of t(12;22) positive clear cell sarcoma of soft tissue cell lines reveals characteristic up-regulation of potential new marker genes including ERBB3.
Clear cell sarcoma of the kidney: up-regulation of neural markers with activation of the sonic hedgehog and Akt pathways.
Antigenicity of fusion proteins from sarcoma-associated chromosomal translocations.
Molecular diagnosis of clear cell sarcoma: detection of EWS-ATF1 and MITF-M transcripts and histopathological and ultrastructural analysis of 12 cases.
Clear cell sarcoma (malignant melanoma) of soft parts: A clinicopathologic study of 30 cases.
EWS-CREB1: a recurrent variant fusion in clear cell sarcoma--association with gastrointestinal location and absence of melanocytic differentiation.
Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study.
Classification of clear-cell sarcoma as a subtype of melanoma by genomic profiling.
Oncogenic MITF dysregulation in clear cell sarcoma: defining the MiT family of human cancers.
Use of an anti-interleukin-5 antibody in the hypereosinophilic syndrome with eosinophilic dermatitis.
Treatment of hypereosinophilic syndrome with imatinib mesilate.
Refining the definition of hypereosinophilic syndrome.
FIP1L1-PDGFRalpha D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRalpha T674I eosinophilic leukemia with single agent sorafenib.
ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria.
Bovine protoporphyria: the first nonhuman model of this hereditary photosensitizing disease.
Interferon-gamma stimulates the expression of galectin-9 in cultured human endothelial cells.
ERYTHROPOIETIC PROTOPORPHYRIA. A NEW TYPE OF INBORN ERROR OF METABOLISM.
Imatinib therapy for hypereosinophilic syndrome and other eosinophilic disorders.
Human eosinophils express and release IL-13 following CD28-dependent activation.
Targeted deletion of the mouse Mitoferrin1 gene: from anemia to protoporphyria.
Discovery of a fusion kinase in EOL-1 cells and idiopathic hypereosinophilic syndrome.
Increased expression of the Abcg2 transporter during erythroid maturation plays a role in decreasing cellular protoporphyrin IX levels.
Hypereosinophilic syndrome: a multicenter, retrospective analysis of clinical characteristics and response to therapy.
Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness.
Liver transplantation for erythropoietic protoporphyria liver disease.
Deficient heme synthesis as the cause of noninducibility of hemoglobin synthesis in a Friend erythroleukemia cell line.
Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria.
Approaches to the treatment of hypereosinophilic syndromes: a workshop summary report.
Anti-interleukin-5 (mepolizumab) therapy for hypereosinophilic syndromes.
Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.
Eosinophils express functional IL-13 in eosinophilic inflammatory diseases.
Lack of emo and bruising
Abnormal clones of T cells producing interleukin-5 in idiopathic eosinophilia.
The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH.
Eosinophils: changing perspectives in health and disease.
Heme-regulated eIF2alpha kinase modifies the phenotypic severity of murine models of erythropoietic protoporphyria and beta-thalassemia.
Immunostimulatory DNA sequences inhibit IL-5, eosinophilic inflammation, and airway hyperresponsiveness in mice.
The idiopathic hypereosinophilic syndrome.
Hip Pain, Night Sweats, decreased range of hip movement, hip pain, low back pain, pelvic girdle pain
Microcytic anemia, erythropoietic protoporphyria, and neurodegeneration in mice with targeted deletion of iron-regulatory protein 2.
Treatment of patients with the hypereosinophilic syndrome with mepolizumab.
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome.
Serodiagnosis of erythema migrans and acrodermatitis chronica atrophicans by the Borrelia burgdorferi flagellum enzyme-linked immunosorbent assay.
Acrodermatitis enteropathica mutations affect transport activity, localization and zinc-responsive trafficking of the mouse ZIP4 zinc transporter.
Novel proteolytic processing of the ectodomain of the zinc transporter ZIP4 (SLC39A4) during zinc deficiency is inhibited by acrodermatitis enteropathica mutations.
A novel zinc-regulated human zinc transporter, hZTL1, is localized to the enterocyte apical membrane.
Evidence for the involvement of different genospecies of Borrelia in the clinical outcome of Lyme disease in Belgium.
Impact of zinc supplementation on intestinal permeability in Bangladeshi children with acute diarrhoea and persistent diarrhoea syndrome.
Hip Pain, Night Sweats, decreased range of hip movement, hip pain, low back pain
Control of polyunsaturated acids in tissue lipids.
European Union Concerted Action on Risk Assessment in Lyme Borreliosis: clinical case definitions for Lyme borreliosis.
The mouse acrodermatitis enteropathica gene Slc39a4 (Zip4) is essential for early development and heterozygosity causes hypersensitivity to zinc deficiency.
Early and late cutaneous manifestations in Ixodes-borne borreliosis (erythema migrans borreliosis, Lyme borreliosis).
The acrodermatitis enteropathica gene ZIP4 encodes a tissue-specific, zinc-regulated zinc transporter in mice.
Identification of SLC39A4, a gene involved in acrodermatitis enteropathica.
Elective neck dissection in papillary carcinoma of the thyroid.
A novel member of a zinc transporter family is defective in acrodermatitis enteropathica.
Vocal cord paralysis following approaches to the anterior cervical spine.
A prospective study of the incidence of injury to the cranial nerves during carotid endarterectomy.
Thyroidectomy: prevention of bilateral recurrent nerve palsy. Results of identification of the nerve over 23 consecutive years (1946-69) with a description of an additional safety measure.