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501901 to 502000 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Functional circuitry underlying visual neglect.
Unconscious vision: new insights into the neuronal correlate of blindsight using diffusion tractography.
Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons.
Magnetically induced phosphenes in sighted, blind and blindsighted observers.
Computer-based training for the treatment of partial blindness.
Differential extrageniculostriate and amygdala responses to presentation of emotional faces in a cortically blind field.
Purine and pyrimidine synthesis by the avian malaria parasite, Plasmodium lophurae.
Global phylogeographic limits of Hawaii's avian malaria.
A molecular clock for malaria parasites.
Transfection of the malaria parasite and expression of firefly luciferase.
Within-population variation in prevalence and lineage distribution of avian malaria in blue tits, Cyanistes caeruleus.
Chitinases of the avian malaria parasite Plasmodium gallinaceum, a class of enzymes necessary for parasite invasion of the mosquito midgut.
Cross-species infection of blood parasites between resident and migratory songbirds in Africa.
Diversification and host switching in avian malaria parasites.
Sex determination in malaria parasites.
Comparison of circumsporozoite proteins from avian and mammalian malarias: biological and phylogenetic implications.
High prevalence of dysfibrinogenemia among patients with chronic thromboembolic pulmonary hypertension.
Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII.
A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO.
Inflammatory bowel disease and cerebrovascular arterial and venous thromboembolic events in 4 pediatric patients: a case series and review of the literature.
Guidelines for the laboratory investigation of heritable disorders of platelet function.
Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders. A United Kingdom Haemophilia Center Doctors' Organisation (UKHCDO) guideline approved by the British Committee for Standards in Hae...
Inherited platelet disorders.
Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency.
Recessively inherited coagulation disorders.
Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.
An electron microscopic study of the vascular sinuses of the bone marrow of the rabbit.
Diagnosis and management of aortoenteric fistulas.
Coronary artery fistulas: how to manage them.
Congenital anomalies of the coronary arteries.
The long-term prognosis of congenital portosystemic venous shunt.
Primary aortoenteric fistula.
Cardiac kallikrein-kinin system is upregulated in chronic volume overload and mediates an inflammatory induced collagen loss.
Ureteroiliac artery fistula: diagnosis and treatment algorithm.
Sinus of Valsalva aneurysms--47 years of a single center experience and systematic overview of published reports.
Echocardiography in infective endocarditis.
Prognostic significance of clinically silent coronary artery fistulas.
Use of laboratory tests and clinical symptoms for identification of primary HIV infection.
Telaprevir for previously treated chronic HCV infection.
Radiotherapy plus cetuximab for locoregionally advanced head and neck cancer: 5-year survival data from a phase 3 randomised trial, and relation between cetuximab-induced rash and survival.
Screening for epidermal growth factor receptor mutations in lung cancer.
Pathogenesis of lentivirus infections.
Mechanisms of cancer cachexia.
Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wasting during systemic diseases.
NF-kappaB-induced loss of MyoD messenger RNA: possible role in muscle decay and cachexia.
Cytokine stimulation of energy expenditure through p38 MAP kinase activation of PPARgamma coactivator-1.
Cachectin and tumour necrosis factor as two sides of the same biological coin.
Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences.
Elevated plasma ghrelin levels in Prader Willi syndrome.
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C.
The Drosophila tuberous sclerosis complex gene homologs restrict cell growth and cell proliferation.
The TSC-mTOR signaling pathway regulates the innate inflammatory response.
Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis.
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
Identification and characterization of the tuberous sclerosis gene on chromosome 16.
Rheb is a direct target of the tuberous sclerosis tumour suppressor proteins.
Tuberous sclerosis complex gene products, Tuberin and Hamartin, control mTOR signaling by acting as a GTPase-activating protein complex toward Rheb.
The tuberous sclerosis complex.
Identification of the tuberous sclerosis complex-2 tumor suppressor gene product tuberin as a target of the phosphoinositide 3-kinase/akt pathway.
Bacterial translocation and gram-negative bacteremia in patients with hematological malignancies.
Empiric therapy with carbenicillin and gentamicin for febrile patients with cancer and granulocytopenia.
Fungal infections complicating acute leukemia.
Chronic silastic central venous catheterization for induction, maintenance and support of persistent granulocytopenia in rabbits.
Reduction of the extent of ischemic myocardial injury by neutrophil depletion in the dog.
ADAMTS-13 cysteine-rich/spacer domains are functionally essential for von Willebrand factor cleavage.
The United States National Prospective Hemolytic Uremic Syndrome Study: microbiologic, serologic, clinical, and epidemiologic findings.
ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients.
Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice.
Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura.
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura.
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.
ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions.
Abnormal Abdominal CT Scan, Electrolyte Imbalance, Polyuria, loss of appetite, abdominal mass, pain, acute pain, fever, headache, chills, acute headache, unilateral, throbbing headache, bone pain, pallor, pain, leukocytosis, thrombocytosis, blood in st...
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.
Mite-related bacterial antigens stimulate inflammatory cells in rosacea.
Eradication programs for the arthropod parasites of livestock.
A single dose of topical moxidectin as an effective treatment for murine acariasis due to Myocoptes musculinus.
Synergistic parasite-pathogen interactions mediated by host immunity can drive the collapse of honeybee colonies.
[The first report of the rickettsial infections of spotted fever group in Japan: three clinical cases].
Varroa jacobsoni (Acari: Varroidae) is more than one species.
Differential gene expression of the honey bee Apis mellifera associated with Varroa destructor infection.
Deformed wing virus.
Deformed wing virus: replication and viral load in mites (Varroa destructor).
Biology and control of Varroa destructor.
Quantitative real-time reverse transcription-PCR analysis of deformed wing virus infection in the honeybee (Apis mellifera L.).
Cell-mediated immunity to Theileria-transformed cell lines.
DNA probes detect genomic diversity in Theileria parva stocks.
Cytotoxic T-cells elicited in cattle challenged with Theileria parva (Muguga): evidence for restriction by class I MHC determinants and parasite strain specificity.
Characterisation of stocks of Theileria parva by monoclonal antibody profiles.
Adoptive transfer of immunity to Theileria parva in the CD8+ fraction of responding efferent lymph.
Bovine T cells, B cells, and null cells are transformed by the protozoan parasite Theileria parva.
Novel anti-malarial hydroxynaphthoquinones with potent broad spectrum anti-protozoal activity.
Bovine cytotoxic T-cell clones specific for cells infected with the protozoan parasite Theileria parva: parasite strain specificity and class I major histocompatibility complex restriction.
Letter: Infection and transformation of bovine lymphoid cells in vitro by infective particles of Theileria parva.
Simultaneous detection of bovine Theileria and Babesia species by reverse line blot hybridization.
Abnormal Abdominal CT Scan, Electrolyte Imbalance, Polyuria, loss of appetite, abdominal mass, pain, acute pain, fever, headache, chills, acute headache, unilateral, throbbing headache, bone pain, pallor, pain, leukocytosis, thrombocytosis, blood in stool
Pangloss revisited: a critique of the dilution effect and the biodiversity-buffers-disease paradigm.