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464101 to 464200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Pathogenic potential of novel Chlamydiae and diagnostic approaches to infections due to these obligate intracellular bacteria.
Chlamydia trachomatis and invasive cervical cancer: a pooled analysis of the IARC multicentric case-control study.
Molecular evolution of the Chlamydiaceae.
Emended description of the order Chlamydiales, proposal of Parachlamydiaceae fam. nov. and Simkaniaceae fam. nov., each containing one monotypic genus, revised taxonomy of the family Chlamydiaceae, including a new genus and five new species, and standa...
Pneumonia of Calves, Enzootic
Uterine Cervical Erosion
Geographic clustering of leishmaniasis in northeastern Brazil.
Cytotoxic T cells mediate pathology and metastasis in cutaneous leishmaniasis.
Cutaneous leishmaniasis: clinical features and diagnosis.
Expression of inducible nitric oxide synthase in skin lesions of patients with american cutaneous leishmaniasis.
Diffuse cutaneous leishmaniasis responds to miltefosine but then relapses.
Serum levels of tumor necrosis factor in patients with American cutaneous leishmaniasis.
Genetic variability within the species Leishmania aethiopica does not correlate with clinical variations of cutaneous leishmaniasis.
Resistance of Leishmania (Leishmania) amazonensis and Leishmania (Viannia) braziliensis to nitric oxide correlates with disease severity in Tegumentary Leishmaniasis.
Pathogenic role of B cells and antibodies in murine Leishmania amazonensis infection.
Cutaneous leishmaniasis: clinical aspect.
CD8 cells of patients with diffuse cutaneous leishmaniasis display functional exhaustion: the latter is reversed, in vitro, by TLR2 agonists.
Clinical and immunopathological aspects of disseminated cutaneous leishmaniasis.
Neutrophils and macrophages cooperate in host resistance against Leishmania braziliensis infection.
The clinical and immunological spectrum of American cutaneous leishmaniasis.
Mucosal leishmaniasis patients display an activated inflammatory T-cell phenotype associated with a nonbalanced monocyte population.
Disseminated leishmaniasis: a new and emerging form of leishmaniasis observed in northeastern Brazil.
Differential expression of chemokines in patients with localized and diffuse cutaneous American leishmaniasis.
Impaired expression of inflammatory cytokines and chemokines at early stages of infection with Leishmania amazonensis.
no pain, firm mass, sessile , x-ray abnormal
no pain, firm mass, sessile
no pain, firm mass
temporary, paralysis, Loss of Vision, Vertigo
temporary paralysis , Loss of Vision, Vertigo
Long QT Syndrome 1
Caused by Mutation in the SNCA gene
Hypernatremia, Hypomagnesemia, Polyuria
Cough, Dyspnea, rigor chills
Jervell and Lange-Nielsen Syndrome 1
Long QT Syndrome 2
Long QT Syndrome 3
Long QT Syndrome 5
Dysarthria, Homonymous Hemianopsia
Anorchia, Down Syndrome
Non-Small Cell Lung Carcinoma
Nidal M F H Abu Laban
Burning Micturition, X-Ray Abnormal
Burning Micturition, Flank Pain, X-Ray Abnormal
Gary R Pickrell
Abdominal Pain, Hemoglobin Decreased, Jaundice, Weight Loss
Autoantibodies (Antinuclear, Anti-dsDNA, Anti Cardiolipin)
lymphocytosis, c-reactive protein increased, fever
lymphocytosis, c-reactive protein increased
Iliotibial Band Syndrome
Roberta M Ray
Anxiety Neurosis, Early Satiety, intermittent
Hereditary fructose intolerance and celiac disease: a novel genetic association.
Fructosuria: report of a case.
Comparative frequency and severity of hypoglycemia in selected organic acidemias, branched chain amino acidemia, and disorders of fructose metabolism.
Biochemical and clinical observations in four patients with fructose-1,6-diphosphatase deficiency.
Isolated fructose malabsorption.
Inherited disorders of carbohydrate metabolism in children studied by 13C-labelled precursors, NMR and GC-MS.
Colonic bacterial activity determines the symptoms in people with fructose-malabsorption.
An independent diagnosis.
[Adults with hereditary fructose intolerance: risks of fructose infusion].
Mutation of aldolase B genes in hereditary fructose intolerance.
Inborn errors of carbohydrate metabolism.
Hereditary fructose intolerance.
Changes of liver metabolite concentrations in adults with disorders of fructose metabolism after intravenous fructose by 31P magnetic resonance spectroscopy.
Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene.
Partial aldolase B gene deletions in hereditary fructose intolerance.
Molecular evidence for compound heterozygosity in hereditary fructose intolerance.
Molecular analysis of aldolase B genes in the diagnosis of hereditary fructose intolerance in the United Kingdom.
[The enzymatic defect of benign fructosuria].
Properties of normal and mutant recombinant human ketohexokinases and implications for the pathogenesis of essential fructosuria.
[Gene mutation analysis in four Chinese patients with multiple carboxylase deficiency].
[Diagnosis, treatment and gene mutation analysis in children with holocarboxylase synthetas deficiency].
[Delayed onset holocarboxylase synthetase deficiency with normal pyruvate carboxylase activity].
[A clinical and genetic analysis of a pedigree with two 46,XY patients suffering from 17alpha-hydroxylase deficiency].
Severe holocarboxylase synthetase deficiency with incomplete biotin responsiveness resulting in antenatal insult in samoan neonates.
Reduced half-life of holocarboxylase synthetase from patients with severe multiple carboxylase deficiency.
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects.
A case of holocarboxylase synthetase deficiency with insufficient response to prenatal biotin therapy.