Pages that link to "Q35012638"
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The following pages link to Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era. (Q35012638):
Displaying 50 items.
- Using network analysis to study behavioural phenotypes: an example using domestic dogs. (Q28596343) (← links)
- Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension (Q28601711) (← links)
- The pathobiology of vascular malformations: insights from human and model organism genetics (Q34544980) (← links)
- Research on potential biomarkers in hereditary hemorrhagic telangiectasia. (Q35233736) (← links)
- Decreased Endoglin expression in the pulmonary vasculature of nitrofen-induced congenital diaphragmatic hernia rat model (Q36185229) (← links)
- Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1. (Q36288806) (← links)
- Transcription factor KLF6 upregulates expression of metalloprotease MMP14 and subsequent release of soluble endoglin during vascular injury (Q36761599) (← links)
- Efficacy and safety of thalidomide for the treatment of severe recurrent epistaxis in hereditary haemorrhagic telangiectasia: results of a non-randomised, single-centre, phase 2 study (Q36821724) (← links)
- Dietary supplement use and nosebleeds in hereditary haemorrhagic telangiectasia - an observational study (Q36907850) (← links)
- Alk1 controls arterial endothelial cell migration in lumenized vessels (Q37120511) (← links)
- Spinal arteriovenous fistulae in patients with hereditary hemorrhagic telangiectasia: A case report and systematic review of the literature (Q37173842) (← links)
- Defective fluid shear stress mechanotransduction mediates hereditary hemorrhagic telangiectasia (Q37285438) (← links)
- Can Iron Treatments Aggravate Epistaxis in Some Patients With Hereditary Hemorrhagic Telangiectasia? (Q37394098) (← links)
- Recent advances in understanding contextual TGFβ signaling (Q38666840) (← links)
- Bone Morphogenetic Proteins in Vascular Homeostasis and Disease (Q38872877) (← links)
- The role of genetics in pulmonary arterial hypertension (Q38988081) (← links)
- High-Output Cardiac Failure Due to Hereditary Hemorrhagic Telangiectasia: A Case of an Extra-Cardiac Left to Right Shunt (Q39342471) (← links)
- Endoglin-based biological therapy in the treatment of angiogenesis-dependent pathologies. (Q39401943) (← links)
- Diagnosis and treatment of hereditary hemorrhagic telangiectasia in a pediatric patient with chronic cyanosis (Q42327788) (← links)
- PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia (Q42357211) (← links)
- A mouse model of hereditary hemorrhagic telangiectasia generated by transmammary-delivered immunoblocking of BMP9 and BMP10. (Q42364928) (← links)
- Signs and genetics of rare cancer syndromes with gastroenterological features (Q42434480) (← links)
- Executive summary of the 11th HHT international scientific conference (Q44800182) (← links)
- Thoracic Aortic Aneurysm Development in Patients with Bicuspid Aortic Valve: What Is the Role of Endothelial Cells? (Q47156238) (← links)
- Endothelial cells respond to the direction of mechanical stimuli through SMAD signaling to regulate coronary artery size. (Q47197118) (← links)
- Non-invasive CT screening for pulmonary arteriovenous malformations in children with confirmed hereditary hemorrhagic telangiectasia: Results from two pediatric centers (Q47444178) (← links)
- Tacrolimus rescues the signaling and gene expression signature of endothelial ALK1 loss-of-function and improves HHT vascular pathology. (Q47705980) (← links)
- Characterization of pulmonary arteriovenous malformations in ACVRL1 versus ENG mutation carriers in hereditary hemorrhagic telangiectasia (Q47762430) (← links)
- ALK1 signaling in development and disease: new paradigms. (Q47856805) (← links)
- Cerebral Abscess Associated With Odontogenic Bacteremias, Hypoxemia, and Iron Loading in Immunocompetent Patients With Right-to-Left Shunting Through Pulmonary Arteriovenous Malformations (Q47913423) (← links)
- Hemoglobin Is a Vital Determinant of Arterial Oxygen Content in Hypoxemic Patients with Pulmonary Arteriovenous Malformations (Q47957323) (← links)
- Endoglin and alk1 as therapeutic targets for hereditary hemorrhagic telangiectasia (Q47968783) (← links)
- Cervical spine arteriovenous fistula associated with hereditary haemorrhagic telangiectasia (Q47979631) (← links)
- Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia. (Q48232072) (← links)
- Classifying Pulmonary Hypertension in Hereditary Hemorrhagic Telangiectasia. Hemodynamics Matter (Q48300827) (← links)
- Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia (Q49826259) (← links)
- Evaluation of Possible Proximate Mechanisms Underlying the Kinship Theory of Intragenomic Conflict in Social Insects (Q50110257) (← links)
- Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in mice. (Q55336818) (← links)
- Transcatheter occlusion of complex pulmonary arteriovenous malformations in a cyanotic child (Q57145038) (← links)
- Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia (Q58544200) (← links)
- Treatment with low-dose tacrolimus inhibits bleeding complications in a patient with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension (Q60363723) (← links)
- Significant Hematochezia and Intracranial Bleeding in Neonatal Hereditary Hemorrhagic Telangiectasia (Q61442997) (← links)
- Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia (Q61800397) (← links)
- [Diagnosis and treatment of Osler's disease] (Q64045802) (← links)
- Deregulation of Drosha in the pathogenesis of hereditary hemorrhagic telangiectasia (Q64073356) (← links)
- Gender differences in hereditary hemorrhagic telangiectasia severity (Q87183482) (← links)
- Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family (Q87183492) (← links)
- Vitamin D levels are associated with epistaxis severity and bleeding duration in hereditary hemorrhagic telangiectasia (Q88050146) (← links)
- Epigenetic signatures of attachment insecurity and childhood adversity provide evidence for role transition in the pathogenesis of perinatal depression (Q89747347) (← links)
- Severe anemia caused by hereditary hemorrhagic telangiectasia in a patient with Sjögren's syndrome and primary biliary cirrhosis (Q90017015) (← links)