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Pancreatic Arteriovenous Malformation
Journal of Gastrointestinal Surgery, 2013Pancreatic arteriovenous malformation is very rare, but may cause significant clinical symptoms such as catastrophic bleeding. Herein, we discuss the clinical presentation and management of patients pancreatic arteriovenous malformations.The data pool for the analysis was collected from pancreatic arteriovenous malformation cases encountered by our ...
Shu-Cheng Chou +2 more
exaly +3 more sources
Uterine Arteriovenous Malformation: A Pictorial Review of Diagnosis and Management
Journal of Endovascular Therapy, 2021Uterine arteriovenous malformation (UAVM) is a rare condition and is classified as either congenital or acquired UAVM. Patients with UAVMs usually experience miscarriages or recurrent menorrhagia.
Van Trung Hoang +2 more
exaly +2 more sources
Pediatric dermatology, 2022
Capillary malformation‐arteriovenous malformation (CM‐AVM) syndrome is an autosomal dominant condition characterized by multifocal, noncontiguous pink patches on the skin that often have a surrounding pale halo.
C. Nicholson +7 more
semanticscholar +1 more source
Capillary malformation‐arteriovenous malformation (CM‐AVM) syndrome is an autosomal dominant condition characterized by multifocal, noncontiguous pink patches on the skin that often have a surrounding pale halo.
C. Nicholson +7 more
semanticscholar +1 more source
Capillary malformation−arteriovenous malformation syndrome: a multicentre study
Clincal and Experimental Dermatology, 2020Capillary malformation–arteriovenous malformation (CM‐AVM) syndrome is a rare syndrome with characteristic skin lesions that are associated with fast‐flow vascular malformations (FFVMs) in one‐third of patients.
M. Valdivielso-Ramos +19 more
semanticscholar +1 more source
Human Mutation, 2013 Capillary malformation–arteriovenous malformation (CM–AVM) is an autosomal‐dominant disorder, caused by heterozygous RASA1 mutations, and manifesting multifocal CMs and high risk for fast‐flow lesions.
Nicole Revencu +2 more
exaly +2 more sources
Dermatologic Clinics, 2022
Arteriovenous malformations (AVMs) are a group of high-flow congenital vascular malformations. They are characterized by abnormal shunting of the blood supply from fast-flow feeding arteries to low-resistance draining veins via a cluster of aberrant blood vessels termed a central nidus. They are often sporadic but can be associated with syndromes. AVMs
openaire +2 more sources
Arteriovenous malformations (AVMs) are a group of high-flow congenital vascular malformations. They are characterized by abnormal shunting of the blood supply from fast-flow feeding arteries to low-resistance draining veins via a cluster of aberrant blood vessels termed a central nidus. They are often sporadic but can be associated with syndromes. AVMs
openaire +2 more sources
The Lancet, 2002
Arteriovenous malformations of the brain are congenital vascular lesions that affect 0.01-0.50% of the population, and are generally present in patients aged 20-40 years. The usual clinical presentations are haemorrhage, seizures, progressive neurological deficit, or headache. Results of natural history studies have shown a yearly haemorrhage rate of 1-
Ian G, Fleetwood, Gary K, Steinberg
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Arteriovenous malformations of the brain are congenital vascular lesions that affect 0.01-0.50% of the population, and are generally present in patients aged 20-40 years. The usual clinical presentations are haemorrhage, seizures, progressive neurological deficit, or headache. Results of natural history studies have shown a yearly haemorrhage rate of 1-
Ian G, Fleetwood, Gary K, Steinberg
openaire +2 more sources
Journal of Neurosurgery, 2007
Object. Important central nervous system (CNS) manifestations in patients with hereditary hemorrhagic telangiectasia (HHT) include arteriovenous malformations (AVMs) and dural arteriovenous fistulas (DAVFs). Hereditary hemorrhagic telangiectasia is caused by germline mutations of two genes: ENG (HHT Type 1) and ACVRL1 (HHT Type 2).
William L, Young +6 more
openaire +2 more sources
Object. Important central nervous system (CNS) manifestations in patients with hereditary hemorrhagic telangiectasia (HHT) include arteriovenous malformations (AVMs) and dural arteriovenous fistulas (DAVFs). Hereditary hemorrhagic telangiectasia is caused by germline mutations of two genes: ENG (HHT Type 1) and ACVRL1 (HHT Type 2).
William L, Young +6 more
openaire +2 more sources