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503701 to 503800 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Use of a decision aid to improve treatment decisions in osteoporosis: the osteoporosis choice randomized trial.
Fragility fractures of the hip and femur: incidence and patient characteristics.
Effects of intravenous zoledronic acid plus subcutaneous teriparatide [rhPTH(1-34)] in postmenopausal osteoporosis.
A systematic review of hip fracture incidence and probability of fracture worldwide.
Assessing forearm fracture risk in postmenopausal women.
Secular trends in the incidence of hip and other osteoporotic fractures.
2010 clinical practice guidelines for the diagnosis and management of osteoporosis in Canada: summary.
Physical properties of the red cell agglutinins in acquired hemolytic anemia.
C3b inactivator of man. II. Fragments produced by C3b inactivator cleavage of cell-bound or fluid phase C3b.
Autoimmune disorders and risk of non-Hodgkin lymphoma subtypes: a pooled analysis within the InterLymph Consortium.
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.
Circulating activated endothelial cells in sickle cell anemia.
Deletion of alpha4 integrins from adult hematopoietic cells reveals roles in homeostasis, regeneration, and homing.
Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects.
Role of CD47 as a marker of self on red blood cells.
Iron deficiency anemia: adverse effects on infant psychomotor development.
Iron deficiency anemia and iron therapy effects on infant developmental test performance.
Impact of anemia on mortality, cognition, and function in community-dwelling elderly.
Recombinant human erythropoietins and cancer patients: updated meta-analysis of 57 studies including 9353 patients.
An immunoradiometric assay for ferritin in the serum of normal subjects and patients with iron deficiency and iron overload.
A clinical evaluation of serum ferritin as an index of iron stores.
Treatment with iron increases weight gain and psychomotor development.
Validation of screening procedures.
Association of kidney function with anemia: the Third National Health and Nutrition Examination Survey (1988-1994).
Marylyn Martina Addo
Long-term developmental outcome of infants with iron deficiency.
Behavioral and developmental effects of preventing iron-deficiency anemia in healthy full-term infants.
Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.
Acute peripheral inflammation induces moderate glial activation and spinal IL-1beta expression that correlates with pain behavior in the rat.
The distinct roles of cyclooxygenase-1 and -2 in neuroinflammation: implications for translational research.
Neuroinflammation and regulation of glial glutamate uptake in neurological disorders.
Inflammation and Alzheimer's disease.
Chronic neuroinflammation in rats reproduces components of the neurobiology of Alzheimer's disease.
Inflammation, A beta deposition, and neurofibrillary tangle formation as correlates of Alzheimer's disease neurodegeneration.
Stimulation of neurite outgrowth using an electrically conducting polymer.
Stress and the inflammatory response: a review of neurogenic inflammation.
Role of spinal microglia in rat models of peripheral nerve injury and inflammation.
Quinolinic acid and kynurenine pathway metabolism in inflammatory and non-inflammatory neurological disease.
Primary afferent tachykinins are required to experience moderate to intense pain.
Identification of gene expression profile of dorsal root ganglion in the rat peripheral axotomy model of neuropathic pain.
Altered nociception, analgesia and aggression in mice lacking the receptor for substance P.
Pathogenesis of herpetic neuritis and ganglionitis in mice: evidence for intra-axonal transport of infection.
Inflammation as a causative factor in the aetiology of Parkinson's disease.
New advances in the diagnosis and treatment of autoimmune lymphoproliferative syndrome.
Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations.
How I treat autoimmune lymphoproliferative syndrome.
The importance of LAT in the activation, homeostasis, and regulatory function of T cells.
Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation.
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation.
Loss-of-function of the protein kinase C δ (PKCδ) causes a B-cell lymphoproliferative syndrome in humans.
Advances in the management and understanding of autoimmune lymphoproliferative syndrome (ALPS).
Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency.
Primary immunodeficiencies (PIDs) presenting with cytopenias.
Identifying autoimmune lymphoproliferative syndrome in children with Evans syndrome: a multi-institutional study.
Fas stimulation of T lymphocytes promotes rapid intercellular exchange of death signals via membrane nanotubes.
ALPS-ten lessons from an international workshop on a genetic disease of apoptosis.
Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome.
Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation.
Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome.
Distinct roles for PTEN in prevention of T cell lymphoma and autoimmunity in mice.
Whole-exome-sequencing-based discovery of human FADD deficiency.
Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop.
The Fas-FADD death domain complex structure reveals the basis of DISC assembly and disease mutations.
Mutant fibrinogen cleared from the endoplasmic reticulum via endoplasmic reticulum-associated protein degradation and autophagy: an explanation for liver disease.
Fibrinogen-independent platelet adhesion and thrombus formation on subendothelium mediated by glycoprotein IIb-IIIa complex at high shear rate.
Dimeric ristocetin flocculates proteins, binds to platelets, and mediates von Willebrand factor-dependent agglutination of platelets.
Rheology of blood.
Delayed-type hypersensitivity skin reactions in congenital afibrinogenemia lack fibrin deposition and induration.
Defibrination syndrome in pregnancy: value of various diagnostic tests.
von Willebrand factor interaction with the glycoprotein IIb/IIa complex. Its role in platelet function as demonstrated in patients with congenital afibrinogenemia.
Fibrinogen and platelets in the primary arrest of bleeding. Studies in two patients with congenital afibrinogenemia.
Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H.
Studies on the metabolism of fibrinogen in two patients with congenital afibrinogenemia.
Plasminogen deficiency leads to impaired remodeling after a toxic injury to the liver.
A total fibrinogen deficiency is compatible with the development of pulmonary fibrosis in mice.
A rapid, simple, sensitive method for measuring fibrinolytic split products in human serum.
Persistence of platelet thrombus formation in arterioles of mice lacking both von Willebrand factor and fibrinogen.
An outbreak of Legionnaires' disease associated with a contaminated air-conditioning cooling tower.
Differentiate to thrive: lessons from the Legionella pneumophila life cycle.
Current views on the relationships between amoebae, legionellae and man.
Classification of the Legionnaires' disease bacterium: Legionella pneumophila, genus novum, species nova, of the family Legionellaceae, familia nova.
Primary isolation media for Legionnaires disease bacterium.
Genetic structure of populations of Legionella pneumophila.
Detection of Legionnaires disease bacteria by direct immunofluorescent staining.
A common dominant TLR5 stop codon polymorphism abolishes flagellin signaling and is associated with susceptibility to legionnaires' disease.
Critical function for Naip5 in inflammasome activation by a conserved carboxy-terminal domain of flagellin.
Pittsburgh pneumonia agent: direct isolation from human lung tissue.
Identification of Legionella pneumophila genes required for growth within and killing of human macrophages.
The Birc1e cytosolic pattern-recognition receptor contributes to the detection and control of Legionella pneumophila infection.
Improved semiselective medium for isolation of Legionella pneumophila from contaminated clinical and environmental specimens.
Charcoal-yeast extract agar: primary isolation medium for Legionella pneumophila.
Legionella and Legionnaires' disease: 25 years of investigation.
Legionnaires' disease bacterium (Legionella pneumophila) multiples intracellularly in human monocytes.
Formation of a novel phagosome by the Legionnaires' disease bacterium (Legionella pneumophila) in human monocytes.
Mechanical and thermal allodynia in chronic central pain following spinal cord injury.
The use of behavioral assessment to prescribe and evaluate treatments for severely handicapped children.
Functional communication training to reduce challenging behavior: maintenance and application in new settings.
The Overt Aggression Scale for the objective rating of verbal and physical aggression.