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491301 to 491400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Pathophysiology of cholestasis.
Chronic idiopathic jaundice; a review of fifty cases.
Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome.
DEFECTS IN HEPATIC TRANSPORT OF BILIRUBIN IN CONGENITAL HYPERBILIRUBINAEMIA: AN ANALYSIS OF PLASMA BILIRUBIN DISAPPEARANCE CURVES.
The apical conjugate efflux pump ABCC2 (MRP2).
Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome.
ACTIVE 'JUVENILE' CIRRHOSIS CONSIDERED AS PART OF A SYSTEMIC DISEASE AND THE EFFECT OF CORTICOSTEROID THERAPY.
Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases.
A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome.
Conjugate export pumps of the multidrug resistance protein (MRP) family: localization, substrate specificity, and MRP2-mediated drug resistance.
Correction of tibial malunion and nonunion with six-axis analysis deformity correction using the Taylor Spatial Frame.
Complications of elastic stable intramedullary nail fixation of pediatric femoral fractures, and how to avoid them.
Comparison of the efficacy of hook plate versus tension band wire in the treatment of unstable fractures of the distal clavicle.
Shaft fractures of the clavicle: current concepts.
Exchange intramedullary nailing. Its use in aseptic tibial nonunion.
Complications after tibia plateau fracture surgery.
Trigeminal neuralgia, opsoclonus-myoclonus syndrome, facial pain, nasal discharge, chronic pain, sneezing, eruptions, ulcer, pruritus, acute, acute, rash, focal, weight loss, nausea, unusual body odor, lymphadenopathy, generalized lymphadenopathy, faci...
Classification of femoral abnormalities in total hip arthroplasty.
A lack of consensus in the assessment of fracture healing among orthopaedic surgeons.
Midshaft malunions of the clavicle.
Fracture repair with ultrasound: clinical and cell-based evaluation.
Reamed intramedullary nailing of the femur: 551 cases.
Complications of internal fixation of tibial plateau fractures.
Incidence of fracture-healing complications after femoral neck fractures.
Toremifene improves lipid profiles in men receiving androgen-deprivation therapy for prostate cancer: interim analysis of a multicenter phase III study.
A prospective study of health and risk of mortality after spinal cord injury.
Bone morphogenetic protein (BMP) for fracture healing in adults.
Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.
Diagnostic test for mucopolysaccharidosis. I. Direct method for quantifying excessive urinary glycosaminoglycan excretion.
The mucopolysaccharidoses. Diagnosis, molecular genetics and treatment.
Beta-glucuronidase deficiency in a dog: a model of human mucopolysaccharidosis VII.
Prolonged expression of a lysosomal enzyme in mouse liver after Sleeping Beauty transposon-mediated gene delivery: implications for non-viral gene therapy of mucopolysaccharidoses.
Increased life span and correction of metabolic defects in murine mucopolysaccharidosis type VII after syngeneic bone marrow transplantation.
Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis.
Mechanism of glycosaminoglycan-mediated bone and joint disease: implications for the mucopolysaccharidoses and other connective tissue diseases.
The abnormalities of lysosomal enzymes in mucopolysacc- haridoses.
Differential subcellular localization of cholesterol, gangliosides, and glycosaminoglycans in murine models of mucopolysaccharide storage disorders.
Cumulative incidence rates of the mucopolysaccharidoses in Germany.
Intraventricular brain injection of adeno-associated virus type 1 (AAV1) in neonatal mice results in complementary patterns of neuronal transduction to AAV2 and total long-term correction of storage lesions in the brains of beta-glucuronidase-deficient...
Beta-glucuronidase deficiency mucopolysaccharidosis: methods for enzymatic diagnosis.
Inherited disorders of lysosomal metabolism.
Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.
The six hyaluronidase-like genes in the human and mouse genomes.
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome.
Cognitive deficits in the early stages of Parkinson's disease.
Physiology and pharmacology of striatal neurons.
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.
Positron emission tomographic analysis of central D1 and D2 dopamine receptor occupancy in patients treated with classical neuroleptics and clozapine. Relation to extrapyramidal side effects.
Cortico-striatal representation of time in animals and humans.
Effects of intravenous immunoglobulin on muscle weakness and calcium-channel autoantibodies in the Lambert-Eaton myasthenic syndrome.
Calcium channelopathies: voltage-gated calcium channels.
Autoantibodies bind solubilized calcium channel-omega-conotoxin complexes from small cell lung carcinoma: a diagnostic aid for Lambert-Eaton myasthenic syndrome.
An improved diagnostic assay for Lambert-Eaton myasthenic syndrome.
Paraneoplastic neurological syndromes.
Myasthenic syndrome in patients with amyotrophic lateral sclerosis.
The thalamostriatal system: a highly specific network of the basal ganglia circuitry.
SOX1 antibodies are markers of paraneoplastic Lambert-Eaton myasthenic syndrome.
Oscillatory nature of human basal ganglia activity: relationship to the pathophysiology of Parkinson's disease.
Striatal plasticity and basal ganglia circuit function.
Circuits and circuit disorders of the basal ganglia.
Guidelines for treatment of autoimmune neuromuscular transmission disorders.
SOX antibodies in small-cell lung cancer and Lambert-Eaton myasthenic syndrome: frequency and relation with survival.
Incidence of serum anti-P/O-type and anti-N-type calcium channel autoantibodies in the Lambert-Eaton myasthenic syndrome.
Autoimmunity to the voltage-gated calcium channel underlies the Lambert-Eaton myasthenic syndrome, a paraneoplastic disorder.
3,4-Diaminopyridine in the treatment of Lambert-Eaton myasthenic syndrome.
Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies.
Electromyography and electric stimulation of nerves in diseases of motor unit; observations on myasthenic syndrome associated with malignant tumors.
Small-cell lung cancer, paraneoplastic cerebellar degeneration and the Lambert-Eaton myasthenic syndrome.
The synaptic vesicle protein synaptotagmin associates with calcium channels and is a putative Lambert-Eaton myasthenic syndrome antigen.
Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit.
Central nervous system vasculitis.
VZV spinal cord infarction identified by diffusion-weighted MRI (DWI).
Vasculitis of the nervous system.
Primary angiitis of the central nervous system.
Absence of glutathione peroxidase-1 exacerbates cerebral ischemia-reperfusion injury by reducing post-ischemic microvascular perfusion.
The central nervous system in systemic lupus erythematosus. Part 2. Pathogenetic mechanisms of clinical syndromes: a literature investigation.
Testosterone augments endotoxin-mediated cerebrovascular inflammation in male rats.
Primary central nervous system vasculitis in children.
Inflammation and cerebral vasospasm after subarachnoid hemorrhage.
Benign angiopathy of the central nervous system: cohort of 16 patients with clinical course and long-term followup.
Association between 5-lipoxygenase expression and plaque instability in humans.
Estrogen and progestagens differentially modulate vascular proinflammatory factors.
Pediatric granulomatous arthritis: an international registry.
Age alters cerebrovascular inflammation and effects of estrogen.
Primary central nervous system vasculitis: analysis of 101 patients.
Abeta-related angiitis: primary angiitis of the central nervous system associated with cerebral amyloid angiopathy.
The value of detecting anti-VZV IgG antibody in CSF to diagnose VZV vasculopathy.
Neuropathology of multiple sclerosis-new concepts.
Spontaneous hemorrhagic stroke in a mouse model of cerebral amyloid angiopathy.
Vitamin K Deficiency Bleeding
Factors inducing retrograde degeneration of the cochlear nerve.
Auditory neuropathy/dys-synchrony and its perceptual consequences.
Metabotropic suppression of excitation in murine autaptic hippocampal neurons.
Traumatically induced axotomy adjacent to the soma does not result in acute neuronal death.
Influence of the axotomy to cell body distance in rat rubrospinal and spinal motoneurons: differential regulation of GAP-43, tubulins, and neurofilament-M.
Bone marrow chimeric rats reveal the unique distribution of resident and recruited macrophages in the contused rat spinal cord.