By continuing to use Symptoma®, you confirm you accept the cookies. More on
488401 to 488500 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
Somatic mutation, genomic variation, and neurological disease.
LIS1 and NudE induce a persistent dynein force-producing state.
Cooperative regulation in development by SMRT and FOXP1.
Atrial septal defect and its surgical treatment.
The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)
Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.
THE SURGICAL MANAGEMENT OF TRANSPOSITION OF THE GREAT VESSELS.
The matricellular protein CCN1 is essential for cardiac development.
Development of heart failure and congenital septal defects in mice lacking endothelial nitric oxide synthase.
High-resolution magnetic resonance histology of the embryonic and neonatal mouse: a 4D atlas and morphologic database.
Vangl2 acts via RhoA signaling to regulate polarized cell movements during development of the proximal outflow tract.
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12.
An essential role of N-terminal arginylation in cardiovascular development.
The pathology of hypertensive pulmonary vascular disease; a description of six grades of structural changes in the pulmonary arteries with special reference to congenital cardiac septal defects.
Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum.
Dysautonomia rating scales in Parkinson's disease: sialorrhea, dysphagia, and constipation--critique and recommendations by movement disorders task force on rating scales for Parkinson's disease.
Dysautonomia after severe traumatic brain injury.
Diagnosing dysautonomia after acute traumatic brain injury: evidence for overresponsiveness to afferent stimuli.
Antibody titers predict clinical features of autoimmune autonomic ganglionopathy.
Small nerve fibres, small hands and small feet: a new syndrome of pain, dysautonomia and acromesomelia in a kindred with a novel NaV1.7 mutation.
Wing Tat Chan
Purkinje cell cytoplasmic autoantibody type 1 accompaniments: the cerebellum and beyond.
Evolving concepts in neurogenic osteoporosis.
Acute-onset chronic inflammatory demyelinating polyneuropathy with cranial nerve involvement, dysautonomia, respiratory failure, and autoantibodies.
Treatment of dysautonomia associated with Parkinson's disease.
Peripherin-IgG association with neurologic and endocrine autoimmunity.
Parkinson's disease risk score: moving to a premotor diagnosis.
Olfactory dysfunction and cardiovascular dysautonomia in Parkinson's disease.
Autonomic ganglia, acetylcholine receptor antibodies, and autoimmune ganglionopathy.
Psychological adjustment and autonomic disturbances in inflammatory bowel diseases and irritable bowel syndrome.
Ganglionic acetylcholine receptor autoantibody: oncological, neurological, and serological accompaniments.
The prodromal phase of sporadic Parkinson's disease: does it exist and if so how long is it?
Dysautonomia due to reduced cholinergic neurotransmission causes cardiac remodeling and heart failure.
Cardiovascular dysautonomia in Parkinson disease: from pathophysiology to pathogenesis.
ACE2-mediated reduction of oxidative stress in the central nervous system is associated with improvement of autonomic function.
Diagnosis and the premotor phase of Parkinson disease.
Persistence of goiter despite oral iodine supplementation in goitrous children with iron deficiency anemia in Côte d'Ivoire.
Prophylaxis of endemic goitre in Mexico.
Follicular thyroid carcinoma in an iodine-replete endemic goiter region: a prospectively collected, retrospectively analyzed clinical trial.
History of thyroid diseases and subsequent thyroid cancer risk.
Fluorine-18-fluorodeoxyglucose positron emission tomography in the preoperative assessment of thyroid nodules in an endemic goiter area.
Endemic goiter in El Salvador school children.
Thyroid hormone and immunological studies in endemic goiter.
The aetiology of Himalayan endemic goitre.
Prevalence of iodine deficiency worldwide.
[Endemic goiter in Switzerland and its prevention with iodized salt].
Stable iodine metabolism in non-toxic goitre.
Recommended normative values for thyroid volume in children aged 6-15 years. World Health Organization & International Council for Control of Iodine Deficiency Disorders.
Effect of potassium iodate on endemic goitre and protein-bound iodine levels in school-children.
Increase in thyrotoxicosis in endemic goitre area after iodation of bread.
Control of thyroglobulin synthesis and secretion (second of two parts).
The disorders induced by iodine deficiency.
Current global iodine status and progress over the last decade towards the elimination of iodine deficiency.
Iodide goiter and the pharmacologic effects of excess iodide.
Neuropathic pain from an experimental neuritis of the rat sciatic nerve.
An accelerated nutrition transition in Iran.
Cytokine production and the pathogenesis of experimental autoimmune neuritis and Guillain-Barré syndrome.
T-cell antigen receptor transmembrane peptides modulate T-cell function and T cell-mediated disease.
IL-10 suppresses experimental autoimmune neuritis and down-regulates TH1-type immune responses.
Extensive peroxynitrite activity during progressive stages of central nervous system inflammation.
Experimental autoimmune autonomic neuropathy.
In vivo treatment of rats with monoclonal anti-T-cell antibodies. Immunohistochemical and functional analysis in normal rats and in experimental allergic neuritis.
Allergic neuritis: an experimental disease of rabbits induced by the injection of peripheral nervous tissue and adjuvants.
Compound A, a plant origin ligand of glucocorticoid receptors, increases regulatory T cells and M2 macrophages to attenuate experimental autoimmune neuritis with reduced side effects.
Cellular and genetic factors involved in the difference between Brown Norway and Lewis rats to develop respectively type-2 and type-1 immune-mediated diseases.
CHANGES IN NERVE CONDUCTION IN EXPERIMENTAL ALLERGIC NEURITIS.
Disruption of neurofascin and gliomedin at nodes of Ranvier precedes demyelination in experimental allergic neuritis.
A permanent rat T cell line that mediates experimental allergic neuritis in the Lewis rat in vivo.
Chemokines and chemokine receptors: multipurpose players in neuroinflammation.
Nitric oxide donors reversibly block axonal conduction: demyelinated axons are especially susceptible.
Chondroblastoma of the skull and facial bones.
Chondroblastoma of bone: long-term results and functional outcome after intralesional curettage.
Benign and malignant cartilage tumors of bone and joint: their anatomic and theoretical basis with an emphasis on radiology, pathology and clinical biology. I. The intramedullary cartilage tumors.
Metastatic chondroblastoma. Report of a fatal case with a review of the literature on atypical, aggressive, and malignant chondroblastoma.
Benign chondroblastoma. A study of 125 cases.
Long-term results of hemipelvis reconstruction with allografts.
Expression of c-met proto-oncogene product (c-MET) in benign and malignant bone tumors.
Chondroblastoma. A review of seventy cases.
Unusual benign and malignant chondroid tumors of bone. A survey of some mesenchymal cartilage tumors and malignant chondroblastic tumors, including a few multicentric ones, as well as many atypical benign chondroblastomas and chondromyxoid fibromas.
Resection-arthrodesis for malignant and potentially malignant lesions about the knee using an intramedullary rod and local bone grafts.
Chondroblastoma of bone.
Chondromyxoid fibroma of bone: a clinicopathologic review of 278 cases.
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.
Maxillary sinus infection caused by the homobasidiomycetous fungus Schizophyllum commune.
Sinonasal disease in cystic fibrosis: clinical characteristics, diagnosis, and management.
Rhino-orbito-cerebral mucormycosis. A retrospective analysis of clinical features and treatment outcomes.
Prevalence of migraine in patients with a history of self-reported or physician-diagnosed "sinus" headache.
Surgical causes of failure in endoscopic sinus surgery.
Respiratory epithelial adenomatoid hamartomas of the sinonasal tract and nasopharynx: a clinicopathologic study of 31 cases.
Chronic persistent cough. Experience in diagnosis and outcome using an anatomic diagnostic protocol.
Paranasal sinuses: CT imaging requirements for endoscopic surgery.
Analysis of symptoms and clinical signs in the maxillary sinus empyema.
Antibiotic prescribing in acute infections of the nose or sinuses: a matter of personal habit?
Patient survival factors in paranasal sinus mucormycosis.
Innate immunity of the sinonasal cavity: expression of messenger RNA for complement cascade components and toll-like receptors.
Prevalence of incidental abnormalities on computed tomographic scans of the paranasal sinuses.