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532001 to 532100 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Damage control resuscitation: directly addressing the early coagulopathy of trauma.
An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination.
The contribution of low birth weight to infant mortality and childhood morbidity.
Deficiency of protein C in congenital thrombotic disease.
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation.
Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.
Quantitative estimation of split products of fibrinogen in human serum, relation to diagnosis and treatment.
Mechanisms of thrombus formation.
Developmental defects and p53 hyperacetylation in Sir2 homolog (SIRT1)-deficient mice.
Calibrated automated thrombin generation measurement in clotting plasma.
Systemic effects of smoking.
Acute traumatic coagulopathy.
Protein C prevents the coagulopathic and lethal effects of Escherichia coli infusion in the baboon.
Frailty and activation of the inflammation and coagulation systems with and without clinical comorbidities: results from the Cardiovascular Health Study.
The partial thromboplastin time with kaolin. A simple screening test for first stage plasma clotting factor deficiencies.
Markers of inflammation, coagulation, and renal function are elevated in adults with HIV infection.
Mutation in blood coagulation factor V associated with resistance to activated protein C.
Mediating ERK 1/2 signaling rescues congenital heart defects in a mouse model of Noonan syndrome.
Percutaneous replacement of pulmonary valve in a right-ventricle to pulmonary-artery prosthetic conduit with valve dysfunction.
Mean velocity of fiber shortening. A simplified measure of left ventricular myocardial contractility.
Intracardiac septation requires hedgehog-dependent cellular contributions from outside the heart.
Essential roles of the bHLH transcription factor Hrt2 in repression of atrial gene expression and maintenance of postnatal cardiac function.
The anatomy of common aorticopulmonary trunk (truncus arteriosus communis) and its embryologic implications. A study of 57 necropsy cases.
GATA4 is a direct transcriptional activator of cyclin D2 and Cdk4 and is required for cardiomyocyte proliferation in anterior heart field-derived myocardium.
Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study.
A comparison of the perioperative neurologic effects of hypothermic circulatory arrest versus low-flow cardiopulmonary bypass in infant heart surgery.
Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice.
Quantitative analysis of cardiac muscle cell disorganization in the ventricular septum of patients with hypertrophic cardiomyopathy.
Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique.
Frequency of 22q11 deletions in patients with conotruncal defects.
Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1.
Postoperative course and hemodynamic profile after the arterial switch operation in neonates and infants. A comparison of low-flow cardiopulmonary bypass and circulatory arrest.
Congenital heart disease in 56,109 births. Incidence and natural history.
Pattern of malformation in offspring of chronic alcoholic mothers.
Jeffrey H Worthington
Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters.
Fatty acid oxidation enzyme gene expression is downregulated in the failing heart.
Role of cardiolipin alterations in mitochondrial dysfunction and disease.
Depression in heart failure a meta-analytic review of prevalence, intervention effects, and associations with clinical outcomes.
Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine.
Results of combined chemotherapy and radiotherapy for advanced intraocular retinoblastoma.
Radiation retinopathy after external-beam irradiation: analysis of time-dose factors.
Combination intravitreal bevacizumab/panretinal photocoagulation versus panretinal photocoagulation alone in the treatment of neovascular glaucoma.
The ocular ischemic syndrome. Clinical, fluorescein angiographic and carotid angiographic features.
Systemic and ocular safety of intravitreal anti-VEGF therapies for ocular neovascular disease.
Intracameral bevacizumab for iris rubeosis.
Increased level of vascular endothelial growth factor in aqueous humor of patients with neovascular glaucoma.
Functional expression of the chemokine receptor CCR7 on fibroblast-like synoviocytes.
Regression of neovascular iris vessels by intravitreal injection of crystalline cortisone.
Evidence-based recommendations for the diagnosis and treatment of neovascular glaucoma.
Clinical variations and complications of Coats disease in 150 cases: the 2000 Sanford Gifford Memorial Lecture.
Intravitreal bevacizumab in a patient with neovascular glaucoma.
Vascular endothelial growth factor upregulation in human central retinal vein occlusion.
Intravitreal bevacizumab to treat iris neovascularization and neovascular glaucoma secondary to ischemic retinal diseases in 41 consecutive cases.
Intravitreal bevacizumab (Avastin) in the treatment of neovascular glaucoma.
Rapid improvement of rubeosis iridis from a single bevacizumab (Avastin) injection.
Upregulated expression of vascular endothelial growth factor in proliferative diabetic retinopathy.
Increased ocular levels of IGF-1 in transgenic mice lead to diabetes-like eye disease.
Vascular endothelial growth factor is sufficient to produce iris neovascularization and neovascular glaucoma in a nonhuman primate.
Anti-vascular endothelial growth factor therapy for ocular neovascular disease.
[Differential diagnosis between dysostosis enchondralis and chondrodystrophy].
Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes.
Lack of HIF-2α in limb bud mesenchyme causes a modest and transient delay of endochondral bone development.
La dysplasie spondylo-epiphysaire tardive; description clinique et radiologique.
Enchondromatosis: insights on the different subtypes.
Array-comparative genomic hybridization of central chondrosarcoma: identification of ribosomal protein S6 and cyclin-dependent kinase 4 as candidate target genes for genomic aberrations.
Absence of IHH and retention of PTHrP signalling in enchondromas and central chondrosarcomas.
Germano Forti Junior
Microvasculature and VEGF expression in cartilaginous tumors.
Anal Fissure, Chills, Oxalate Kidney Stone, Rectal Bleeding
Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.
Cartilaginous lesions of bone.
PTHrP, PTH, and the PTH/PTHrP receptor in endochondral bone development.
PTHR1 mutations associated with Ollier disease result in receptor loss of function.
A new histologic approach to the differentiation of enchondroma and chondrosarcoma of the bones. A clinicopathologic analysis of 51 cases.
The malignant potential of enchondromatosis.
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.
A mutant PTH/PTHrP type I receptor in enchondromatosis.
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
High cancer susceptibility and embryonic lethality associated with mutation of the PTEN tumor suppressor gene in mice.
Gli2, but not Gli1, is required for initial Shh signaling and ectopic activation of the Shh pathway.
Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF.
A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53.
Targeted disruption of the mouse Caspase 8 gene ablates cell death induction by the TNF receptors, Fas/Apo1, and DR3 and is lethal prenatally.
Requirement for neuregulin receptor erbB2 in neural and cardiac development.
Multiple essential functions of neuregulin in development.
Scatter factor/hepatocyte growth factor is essential for liver development.
ATR disruption leads to chromosomal fragmentation and early embryonic lethality.
Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development.
Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele.
E-cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain.
Snail, Slug, and Smad-interacting protein 1 as novel parameters of disease aggressiveness in metastatic ovarian and breast carcinoma.
Diagnostic accuracy of mammography, clinical examination, US, and MR imaging in preoperative assessment of breast cancer.
Novel markers for differentiation of lobular and ductal invasive breast carcinomas by laser microdissection and microarray analysis.
Different gene expression patterns in invasive lobular and ductal carcinomas of the breast.