Results 51 to 60 of about 318,063 (307)

Management of tracheobronchial obstruction in infants using metallic stents: long-term outcome [PDF]

open access: yes, 2015
© 2015, Springer-Verlag Berlin Heidelberg. Results: Twelve balloon-expandable metallic stents were placed in the trachea (n = 10) and/or bronchi (n = 2) of 5 patients with a median age of 13 months (range 5–30 months).
Chung, Patrick Ho Yu   +3 more
core   +1 more source

Pediatric intracranial dural arteriovenous fistulas: age-related differences in clinical features, angioarchitecture, and treatment outcomes. [PDF]

open access: yes, 2016
OBJECTIVE Intracranial dural arteriovenous fistulas (DAVFs) are rare in children. This study sought to better characterize DAVF presentation, angioarchitecture, and treatment outcomes.
Amans, Matthew R   +8 more
core   +1 more source

Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation

open access: yesIndian Dermatology Online Journal, 2020
Klippel–Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity.
B. Supekar   +5 more
semanticscholar   +1 more source

Lymphatic malformation of the masseter: A case report

open access: yesJournal of Oral Biology and Craniofacial Research, 2018
Intramuscular vascular malformations are rare tumours occurring in less than 1% of skeletal muscles throughout the body, about 15% arising in the head and neck.
Sanjay Kumar   +3 more
doaj   +1 more source

Cerebral venous hemodynamic abnormalities in episodic and chronic migraine [PDF]

open access: yes, 2016
Alterations of cerebral venous drainage have been demonstrated in chronic migraine (CM), suggesting that cerebral venous hemodynamic abnormalities (CVHAs) play a role in this condition.
Di Biase, A   +7 more
core   +1 more source

Imaging of adult ocular and orbital pathology - a pictorial review [PDF]

open access: yes, 2014
Orbital pathology often presents a diagnostic challenge to the reporting radiologist. The aetiology is protean, and clinical input is therefore often necessary to narrow the differential diagnosis.
Brennan, Paul   +8 more
core   +1 more source

Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly [PDF]

open access: yes, 2017
Mutations of genes within the phosphatidylinositol-3-kinase (PI3K)-AKT-MTOR pathway are well known causes of brain overgrowth (megalencephaly) as well as segmental cortical dysplasia (such as hemimegalencephaly, focal cortical dysplasia and ...
Aaron M Wenger   +68 more
core   +3 more sources

Stridor in Asian infants: assessment and treatment [PDF]

open access: yes, 2011
Stridor is the main symptomof upper airway obstruction in infants. It can be congenital or acquired, acute or chronic. Pathologies can be located from the nose down to the trachea.
Ho, WK   +4 more
core   +1 more source

A case of lymphatic malformation/lymphangioma of the scrotum

open access: yesActa Radiologica Open, 2012
Lymphatic malformation/lymphangioma of the scrotum is rare. It is caused by lymphatic abnormalities and the most common sites are the neck and axilla. The scrotum is one of the most uncommon sites.
Gensuke Akaike   +5 more
doaj   +1 more source

Microcystic lymphatic malformation localized within the diaphragm

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Localization of a microcystic lymphatic malformation within the diaphragm is an extremely rare vascular anomaly of the lymphatic system. We report the case of a 3-year-old boy who had a localized intrathoracic mass that was detected after birth.
Takatoshi Abe   +7 more
doaj   +1 more source

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