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510801 to 510900 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Spinal fractures in patients with ankylosing spinal disorders: a systematic review of the literature on treatment, neurological status and complications.
Degenerative diseases of the vertebral column.
The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure.
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.
The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins.
Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxia.
Chemistry and biology of eukaryotic iron metabolism.
The phosphotyrosine interaction domains of X11 and FE65 bind to distinct sites on the YENPTY motif of amyloid precursor protein.
Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features.
Clinical and genetic abnormalities in patients with Friedreich's ataxia.
Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia.
Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Tandem repeats finder: a program to analyze DNA sequences.
Attenuation of interstitial fibrosis and tubular apoptosis in db/db transgenic mice overexpressing catalase in renal proximal tubular cells.
A role for Wnt-4 in renal fibrosis.
Characterization of a renal tubular epithelial cell line which secretes the autologous target antigen of autoimmune experimental interstitial nephritis.
Aristolochic acid nephropathy: a worldwide problem.
HIV-associated nephropathy in transgenic mice expressing HIV-1 genes.
Renal fibrosis: novel insights into mechanisms and therapeutic targets.
Epithelial Notch signaling regulates interstitial fibrosis development in the kidneys of mice and humans.
Rapidly progressive interstitial renal fibrosis in young women: association with slimming regimen including Chinese herbs.
Loss of MicroRNA-192 promotes fibrogenesis in diabetic nephropathy.
Mechanisms of tubulointerstitial fibrosis.
Role of reactive oxygen species in TGF-beta1-induced mitogen-activated protein kinase activation and epithelial-mesenchymal transition in renal tubular epithelial cells.
Tubulointerstitial changes as a major determinant in the progression of renal damage.
Quantitative PCR on 5 genes reliably identifies CTCL patients with 5% to 99% circulating tumor cells with 90% accuracy.
Chronic hypoxia and tubulointerstitial injury: a final common pathway to end-stage renal failure.
Staphylococcus aureus: some host-parasite interactions.
Update on erythrodermic cutaneous T-cell lymphoma: report of the International Society for Cutaneous Lymphomas.
Association of erythrodermic cutaneous T-cell lymphoma, superantigen-positive Staphylococcus aureus, and oligoclonal T-cell receptor V beta gene expansion.
Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay.
Aplastic anemia, histiocytosis and erythrodermia in immunologically deficient children. Probable human runt disease.
Generalized pustular psoriasis. A clinical and epidemiological study of 104 cases.
Preferential cutaneous infiltration by neoplastic thymus-derived lymphocytes. Morphologic and functional studies.
New type of exfoliatin obtained from staphylococcal strains, belonging to phage groups other than group II, isolated from patients with impetigo and Ritter's disease.
Two serotypes of exfoliatin and their distribution in staphylococcal strains isolated from patients with scalded skin syndrome.
Stratum corneum structure and function correlates with phenotype in psoriasis.
Ichthyosiform dermatosis with systemic lipidosis.
Natural history and outcome of new AIDS-related cytomegalovirus retinitis diagnosed in the era of highly active antiretroviral therapy.
Omenn syndrome: inflammation in leaky severe combined immunodeficiency.
Staphylococcal scalded skin syndrome: the expanded clinical syndrome.
Oral ganciclovir as maintenance treatment for cytomegalovirus retinitis in patients with AIDS. Syntex Cooperative Oral Ganciclovir Study Group.
Hodgkin's disease. An immunodepleting and immunosuppressive disorder.
Occurrence of cytomegalovirus retinitis after human immunodeficiency virus immunosuppression.
Clinical failure of CMV retinitis with intravitreal cidofovir is associated with antiviral resistance.
The Sézary syndrome: a malignant proliferation of helper T cells.
Loss of cytomegalovirus-specific CD4+ T cell responses in human immunodeficiency virus type 1-infected patients with high CD4+ T cell counts and recurrent retinitis.
Treatment of cytomegalovirus retinitis with an intraocular sustained-release ganciclovir implant. A randomized controlled clinical trial.
Lack of reactivation of cytomegalovirus (CMV) retinitis after stopping CMV maintenance therapy in AIDS patients with sustained elevations in CD4 T cells in response to highly active antiretroviral therapy.
Hereditary C1q deficiency and systemic lupus erythematosus.
Characteristics of patients with cytomegalovirus retinitis in the era of highly active antiretroviral therapy.
Cytomegalovirus (CMV) viraemia detected by polymerase chain reaction identifies a group of HIV-positive patients at high risk of CMV disease.
Cytomegalovirus retinitis and viral resistance: ganciclovir resistance. CMV Retinitis and Viral Resistance Study Group.
A controlled trial of valganciclovir as induction therapy for cytomegalovirus retinitis.
Antibody-dependent cellular cytotoxicity independently predicts survival in severely immunocompromised human immunodeficiency virus-infected patients.
Intravenous cidofovir for peripheral cytomegalovirus retinitis in patients with AIDS. A randomized, controlled trial.
Longitudinal study of the ocular complications of AIDS: 1. Ocular diagnoses at enrollment.
foot muscle twitch
IL-10 in HIV infection: increasing serum IL-10 levels with disease progression--down-regulatory effect of potent anti-retroviral therapy.
Cytomegalovirus retinitis after initiation of highly active antiretroviral therapy.
Restoration of cytomegalovirus-specific CD4+ T-lymphocyte responses after ganciclovir and highly active antiretroviral therapy in individuals infected with HIV-1.
Identifying the content area for the 51-item National Eye Institute Visual Function Questionnaire: results from focus groups with visually impaired persons.
Oral ganciclovir for patients with cytomegalovirus retinitis treated with a ganciclovir implant. Roche Ganciclovir Study Group.
"Benign" monoclonal gammopathy--after 20 to 35 years of follow-up.
Obesity is associated with an increased risk of monoclonal gammopathy of undetermined significance among black and white women.
Bone marrow angiogenesis and mast cell density increase simultaneously with progression of human multiple myeloma.
Prognostic factors for malignant transformation in monoclonal gammopathy of undetermined significance and smoldering multiple myeloma.
Circulating serum free light chains as predictive markers of AIDS-related lymphoma.
Long-term follow-up of 241 patients with monoclonal gammopathy of undetermined significance: the original Mayo Clinic series 25 years later.
Possible roles for activating RAS mutations in the MGUS to MM transition and in the intramedullary to extramedullary transition in some plasma cell tumors.
Monoclonal gammopathy of undetermined significance.
Disease associations with monoclonal gammopathy of undetermined significance: a population-based study of 17,398 patients.
Aberrant global methylation patterns affect the molecular pathogenesis and prognosis of multiple myeloma.
Molecular pathogenesis of multiple myeloma and its premalignant precursor.
Increased and highly stable levels of functional soluble interleukin-6 receptor in sera of patients with monoclonal gammopathy.
Clinical and biological implications of MYC activation: a common difference between MGUS and newly diagnosed multiple myeloma.
Prevalence and risk of progression of light-chain monoclonal gammopathy of undetermined significance: a retrospective population-based cohort study.
Dysfunctional T regulatory cells in multiple myeloma.
Monoclonal gammopathy of undetermined significance (MGUS) and smoldering (asymptomatic) multiple myeloma: IMWG consensus perspectives risk factors for progression and guidelines for monitoring and management.
Serum reference intervals and diagnostic ranges for free kappa and free lambda immunoglobulin light chains: relative sensitivity for detection of monoclonal light chains.
Gene-expression signature of benign monoclonal gammopathy evident in multiple myeloma is linked to good prognosis.
MicroRNAs regulate critical genes associated with multiple myeloma pathogenesis.
Clonal populations of T cells in normal elderly humans: the T cell equivalent to "benign monoclonal gammapathy".
Pathology of human amebiasis.
Hepatic abscess: changes in clinical, bacteriologic and therapeutic aspects.
Differential detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii by a single-round PCR assay.
Changes in isoenzyme patterns of a cloned culture of nonpathogenic Entamoeba histolytica during axenization.
Antisense inhibition of expression of the light subunit (35 kDa) of the Gal/GalNac lectin complex inhibits Entamoeba histolytica virulence.
Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam.
A recombinant cysteine-rich section of the Entamoeba histolytica galactose-inhibitable lectin is efficacious as a subunit vaccine in the gerbil model of amebic liver abscess.
Diagnosis of amebic liver abscess and intestinal infection with the TechLab Entamoeba histolytica II antigen detection and antibody tests.
Monoclonal antibodies directed against the galactose-binding lectin of Entamoeba histolytica enhance adherence.
Patients treated for amebic liver abscess develop cell-mediated immune responses effective in vitro against Entamoeba histolytica.
The pathogenesis of experimentally induced amebic liver abscess in the gerbil (Meriones unguiculatus).
Association of serum antibodies to adherence lectin with invasive amebiasis and asymptomatic infection with pathogenic Entamoeba histolytica.