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514901 to 515000 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Morvan syndrome: clinical and serological observations in 29 cases.
Elucidating the pathophysiology of syringomyelia.
Pathophysiology of syringomyelia associated with Chiari I malformation of the cerebellar tonsils. Implications for diagnosis and treatment.
Asymptomatic Chiari Type I malformations identified on magnetic resonance imaging.
Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations.
Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.
Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia.
Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations.
Interaction between alk1 and blood flow in the development of arteriovenous malformations.
Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia.
Loss of distinct arterial and venous boundaries in mice lacking endoglin, a vascular-specific TGFbeta coreceptor.
Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.
RASA1: variable phenotype with capillary and arteriovenous malformations.
Pathogenesis of arteriovenous malformations in the absence of endoglin.
The anatomical basis of symptomatic hemidystonia.
Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia.
The transcription factor MEF2C-null mouse exhibits complex vascular malformations and reduced cardiac expression of angiopoietin 1 and VEGF.
Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations.
Conformity index: a review.
ALK1 signaling inhibits angiogenesis by cooperating with the Notch pathway.
Endothelial expression of constitutively active Notch4 elicits reversible arteriovenous malformations in adult mice.
Klf2 is an essential regulator of vascular hemodynamic forces in vivo.
The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development.
Arteriovenous malformations in mice lacking activin receptor-like kinase-1.
Comparison of duodenal stent placement with surgical gastrojejunostomy for palliation in patients with duodenal obstructions caused by pancreaticobiliary malignancies.
Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.
Malignant obstruction of gastric outlet and duodenum: palliation with flexible covered metallic stents.
Impact of the discovery of human zinc deficiency on health.
Duodenal Crohn's disease: an analysis of 89 cases.
Nutritional modulation of malaria morbidity and mortality.
Metallic stent placement in the palliative treatment of malignant gastroduodenal obstructions: prospective evaluation of results and factors influencing outcome in 213 patients.
Factors affecting the healing rate of duodenal and pyloric ulcers with low-dose antacid treatment.
Conservation of pancreatic tissue by combined gastric, biliary, and pancreatic duct drainage for pain from chronic pancreatitis.
Surgical treatment of acute necrotizing pancreatitis.
Cushing's Disease, Hypophosphatemia, Striae Distensae
High risk of HIV-related mortality is associated with selenium deficiency.
Primary carcinoma of the duodenum.
Nutrients and foods for the primary prevention of asthma and allergy: systematic review and meta-analysis.
Long-term outcome of biliary and duodenal stents in palliative treatment of patients with unresectable adenocarcinoma of the head of pancreas.
Chronic and recurrent volvulus of the stomach with late results of "colonic displacement".
Low circulating folate and vitamin B6 concentrations: risk factors for stroke, peripheral vascular disease, and coronary artery disease. European COMAC Group.
Intestinal atresia and stenosis: a 25-year experience with 277 cases.
Impaired immunity in vitamin A-deficient mice.
Nutrition, immunity, and infection: present knowledge and future directions.
Anomalies in Down syndrome individuals in a large population-based registry.
Malnutrition in surgical patients. An unrecognised problem.
Malignant gastroduodenal obstructions: treatment by means of a covered expandable metallic stent-initial experience.
Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.
Clinical and epidemiologic studies of cleft lip and palate in the Philippines.
Surgical experience with pancreatic and periampullary cancer.
Contribution of selected vitamins and trace elements to immune function.
Vitamins for chronic disease prevention in adults: scientific review.
Prospective controlled trial of transhepatic biliary endoprosthesis versus bypass surgery for incurable carcinoma of head of pancreas.
Experimental nutritional folate deficiency in man.
The minimum vitamin requirements of the L and HeLa cells in tissue culture, the production of specific vitamin deficiencies, and their cure.
The role of the microsomal triglygeride transfer protein in abetalipoproteinemia.
Vitamin dificiencies and neural tube defects.
Up-regulation of the extracellular matrix remodeling genes, biglycan, neutrophil gelatinase-associated lipocalin, and matrix metalloproteinase-9 in familial amyloid polyneuropathy.
Ten years of international experience with liver transplantation for familial amyloidotic polyneuropathy: results from the Familial Amyloidotic Polyneuropathy World Transplant Registry.
Only amyloidogenic intermediates of transthyretin induce apoptosis.
Endoplasmic reticulum stress associated with extracellular aggregates. Evidence from transthyretin deposition in familial amyloid polyneuropathy.
Control of granule exocytosis in neutrophils.
Energetic characteristics of the new transthyretin variant A25T may explain its atypical central nervous system pathology.
Evidence for early cytotoxic aggregates in transgenic mice for human transthyretin Leu55Pro.
Transthyretin fibrillogenesis entails the assembly of monomers: a molecular model for in vitro assembled transthyretin amyloid-like fibrils.
Transthyretin-related familial amyloidotic polyneuropathy.
Transthyretin and familial amyloidotic polyneuropathy. Recent progress in understanding the molecular mechanism of neurodegeneration.
Reducing cerebral microvascular amyloid-beta protein deposition diminishes regional neuroinflammation in vasculotropic mutant amyloid precursor protein transgenic mice.
Familial amyloid polyneuropathy.
Safety and efficacy of RNAi therapy for transthyretin amyloidosis.
Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis.
D18G transthyretin is monomeric, aggregation prone, and not detectable in plasma and cerebrospinal fluid: a prescription for central nervous system amyloidosis?
Molecular imaging of amyloid beta peptides in mouse brain sections using mass spectrometry.
Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial.
Therapeutic strategies for human amyloid diseases.
Evidence for novel beta-sheet structures in Iowa mutant beta-amyloid fibrils.
Deposition of transthyretin in early stages of familial amyloidotic polyneuropathy: evidence for toxicity of nonfibrillar aggregates.
Mutations in apoptosis-related gene, PDCD10, cause cerebral cavernous malformation 3.
Cerebral cavernous malformation: new molecular and clinical insights.
Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.
Recent insights into cerebral cavernous malformations: a complex jigsaw puzzle under construction.
Impact of signal-to-noise on functional MRI.
Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion.
Tissue-specific conditional CCM2 knockout mice establish the essential role of endothelial CCM2 in angiogenesis: implications for human cerebral cavernous malformations.
CCM3 signaling through sterile 20-like kinases plays an essential role during zebrafish cardiovascular development and cerebral cavernous malformations.
PDCD10 interacts with Ste20-related kinase MST4 to promote cell growth and transformation via modulation of the ERK pathway.
Mutations within the MGC4607 gene cause cerebral cavernous malformations.
Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis.
A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells.
CCM1 regulates vascular-lumen organization by inducing endothelial polarity.
Proteomic identification of the cerebral cavernous malformation signaling complex.
Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation.
CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations.
Cerebral cavernous malformations proteins inhibit Rho kinase to stabilize vascular integrity.
Regulation of cardiovascular development and integrity by the heart of glass-cerebral cavernous malformation protein pathway.
Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations.