Zobrazeno 1 - 10
of 18
pro vyhledávání: '"S M, Chng"'
Autor:
S M Chng, Xavier Golay, Jeroen Hendrikse, Narayanaswamy Venketasubramanian, Esben Thade Petersen
Publikováno v:
Radiology. 254:867-875
To investigate the effect of variations in anatomic features of the circle of Willis on the perfusion territory to deep structures, including the nucleus caudatus, the nucleus lentiformis, and the thalamus.The ethics committee of the study institutio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6db8b8e88fc60511fa3b259f9b7ccd90
https://doi.org/10.1148/radiol.09090284
https://doi.org/10.1148/radiol.09090284
Autor:
Jeroen Hendrikse, S M Chng, Amandine Cheze, Xavier Golay, Esben Thade Petersen, Narayanaswamy Venketasubramanian
Publikováno v:
Stroke. 40:1617-1622
Background and Purpose— The perfusion territories of the brain-feeding arteries are difficult to assess in vivo and therefore standard cerebral perfusion territory templates are often used to determine the relation between cerebral infarcts and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a56def94813c4bf12386fdbc0fc3abef
https://doi.org/10.1161/strokeaha.108.539866
https://doi.org/10.1161/strokeaha.108.539866
Autor:
Augustin Ozanne, Georges Rodesch, S M Chng, Pierre Lasjaunias, Timo Krings, Hortensia Alvarez
Publikováno v:
Clinical Neuroradiology. 16:76-90
Hereditary hemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait with varying penetrance and expressivity. Some of the most devastating consequences of this disease result from cerebral vascular malformations that manifest them
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92ed0d9ef510ed923499a18410a742d7
https://doi.org/10.1007/s00062-006-6009-x
https://doi.org/10.1007/s00062-006-6009-x
Publikováno v:
Neuroradiology. 47:711-720
Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait with varying penetrance and expressivity. Some of the most devastating consequences of this disease result from cerebral vascular malformations that manifest the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85ebc0c206fe67cb29c41f4ff8147309
https://doi.org/10.1007/s00234-005-1390-8
https://doi.org/10.1007/s00234-005-1390-8
Publikováno v:
Interventional Neuroradiology. 10:301-307
The appearance of multiple cervical arteries may be due to a variety of anatomic situations. Arterial fenestrations and duplications have different anatomic origins, with distinct appearances on angiography. They are associated with incomplete segmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8da9dbd2ae67c4a9e80499592f81126
https://doi.org/10.1177/159101990401000403
https://doi.org/10.1177/159101990401000403
Autor:
Esben Thade Petersen, C. C. Tchoyoson Lim, Yih Yian Sitoh, Ivan Zimine, S M Chng, Xavier Golay
Publikováno v:
Stroke. 39(12)
Background and Purpose— Collateral circulation plays a vital role in patients with steno-occlusive disease, in particular for predicting stroke outcome. Digital subtraction angiography (DSA) is the gold standard for the assessment of collateral cir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::315bd38a223d98f0f27ea5cedf904491
https://pubmed.ncbi.nlm.nih.gov/18845805
https://pubmed.ncbi.nlm.nih.gov/18845805
Publikováno v:
Singapore medical journal. 49(4)
Moyamoya syndrome (MMS) is an uncommon association of neurofibromatosis type 1 (NF1). We describe a seven-year-old chinese girl with NF1 and unilateral MMS with multiple hyperintensities on T2-weighted magnetic resonance (MR) images. The ischaemic le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::547510806752c79dba8a1d7388ab5bc4
https://pubmed.ncbi.nlm.nih.gov/18418511
https://pubmed.ncbi.nlm.nih.gov/18418511
Autor:
Ricardo Garcia-Monaco, S M Chng, Pierre Lasjaunias, Hortensia Alvarez, Georges Rodesch, Marina Sachet
Publikováno v:
Scopus-Elsevier
OBJECTIVE:The vein of Galen aneurysmal malformation (VGAM) is a choroidal type of arteriovenous malformation involving the vein of Galen forerunner. This is distinct from an arteriovenous malformation with venous drainage into a dilated, but already
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82e0c5edc358e2f1dc61189d48ece6e8
https://pubmed.ncbi.nlm.nih.gov/17053602
https://pubmed.ncbi.nlm.nih.gov/17053602
Publikováno v:
Scopus-Elsevier
Hereditary haemorrhagic telangiectasia (HHT) is a heterogeneous disease that may present with different clinical phenotypes and different clinical expressions. Concerning the neurovascular expressions of this disease, the paediatric age group in part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::135373eaeeebab98e06a56539f2997a2
https://pubmed.ncbi.nlm.nih.gov/16163493
https://pubmed.ncbi.nlm.nih.gov/16163493
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 20(8-9)
Based on the study of the vascular anatomy of craniopagus twins, and particularly that of Ladan and Laleh, a theory is hypothesised regarding the embryological formation of the sagittal sinuses. The superior sagittal sinus develops in contact with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef86b1f79eb6c2952ec75039ab53b9e6
https://pubmed.ncbi.nlm.nih.gov/15309473
https://pubmed.ncbi.nlm.nih.gov/15309473