Results 11 to 20 of about 37,237 (232)

ALK1 controls hepatic vessel formation, angiodiversity, and angiocrine functions in hereditary hemorrhagic telangiectasia of the liver

open access: yesHepatology, EarlyView., 2022
Hepatic endothelial Alk1 signaling protects from development of vascular malformations while maintaining organ‐specific endothelial differentiation and angiocrine portmanteau of the names Wingless and Int‐1 signaling. Abstract Background and Aims In hereditary hemorrhagic telangiectasia (HHT), severe liver vascular malformations are associated with ...
Christian David Schmid   +20 more
wiley   +1 more source

Arteriovenous malformation

open access: yesJornal Brasileiro de Pneumologia
Edson Marchiori   +2 more
doaj   +4 more sources

Uterine Arteriovenous Malformations

open access: yesJournal of Medical Ultrasound, 2023
Abstract Uterine arteriovenous malformations (AVMs) are an abnormal presence of shunts between myometrial arteries and veins within the myometrium that usually occurs after a traumatic event on the uterus and it is often diagnosed after a miscarriage.
Martina Bartolone   +7 more
openaire   +3 more sources

Pancreatic Arteriovenous Malformation [PDF]

open access: yesCase Reports in Gastroenterology, 2014
An unusual case of pancreatic arteriovenous malformation (P-AVM) combined with esophageal cancer is reported. A 59-year-old man was admitted with upper abdominal pain. Contrast-enhanced computed tomography showed numerous strongly enhanced abnormal vessels and a hypovascular lesion in the area of the pancreatic tail.
Takumi Yamabuki   +7 more
openaire   +3 more sources

Uterine arteriovenous malformation [PDF]

open access: yesBMJ Case Reports, 2013
Uterine arteriovenous malformation (AVM) is a little known condition of which, to date, very few cases have been described. It has a very diverse symptomatology, even though in most cases, it is diagnosed during a severe and acute haemorrhagic event. Its treatment can vary from expectant management to hysterectomy; however, current evidence suggests ...
Francisco, Sellers   +3 more
openaire   +5 more sources

PELVIC ARTERIOVENOUS MALFORMATIONS [PDF]

open access: yesAmerican Journal of Roentgenology, 1968
Two young men with congenital pelvic arteriovenous malformations are reported. Both had local Symptoms related to the presence of a mass. Angiographic studies were diagnostic and essential in guiding treatment.
H A, Mitty, M G, Baron, J H, Jacobson
openaire   +2 more sources

Hepatic arteriovenous malformation

open access: yesClinical Case Reports, 2022
Abstract Hepatic arteriovenous malformation occurs hyperpulsatile heart failure, hepatic encephalopathy, and ascites as clinical symptoms. Oral medication are effective, but hepatic angioembolization or heart surgery in case of its symptoms worsen.
Kento Shionoya, Makoto Kako
openaire   +3 more sources

Pulmonary arteriovenous malformations [PDF]

open access: yesQJM: An International Journal of Medicine, 2018
Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in ~ 50% individuals, it can present with the dreaded complications of stroke or ...
R Sandal   +4 more
openaire   +4 more sources

Acquired pancreatic arteriovenous malformation

open access: yesJournal of the Belgian Society of Radiology, 2015
Pancreatic arteriovenous malformation is a rare vascular anomaly which may cause abdominal pain, acute pancreatitis, gastrointestinal bleeding and portal hypertension.
A Van Holsbeeck   +4 more
doaj   +1 more source

Microcephaly and macrocephaly. A study on anthropometric and clinical data from 308 subjects [PDF]

open access: yes, 2019
Head circumference is the auxological parameter that most correlates with developmental anomalies in childhood. Head circumference (HC) two standard deviations (SD) below or above the mean defines microcephaly and macrocephaly, respectively.
Corsello G.   +7 more
core   +1 more source

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