Microvascular dysfunction as a systemic disease: a review of the evidence
Microvascular dysfunction describes a varied set of conditions that includes vessel
destruction, abnormal vasoreactivity, in situ thrombosis, and fibrosis, which ultimately results …
destruction, abnormal vasoreactivity, in situ thrombosis, and fibrosis, which ultimately results …
Management of Coronary Artery Disease in CADASIL Patients: Review of Current Literature
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is the most common heritable form of vascular dementia in …
leukoencephalopathy (CADASIL) is the most common heritable form of vascular dementia in …
Novel mutation of the NOTCH3 gene in a Polish family with CADASIL
J Buczek, B Błażejewska-Hyżorek, A Cudna… - … i Neurochirurgia Polska, 2016 - Elsevier
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is an inherited small blood vessels disease caused by …
leukoencephalopathy (CADASIL) is an inherited small blood vessels disease caused by …
Spontaneous coronary artery dissection in a patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy syndrome: a …
N Tsanaxidis, S Elshafie, S Munir - European Heart Journal …, 2019 - academic.oup.com
Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leucoencephalopathy (CADASIL) syndrome is a genetically inherited condition most notably …
leucoencephalopathy (CADASIL) syndrome is a genetically inherited condition most notably …
Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report
G Ranasinghe, R Sovis, S Shellvacumar… - … Heart Journal-Case …, 2023 - academic.oup.com
Background Spontaneous coronary artery dissection (SCAD) is increasingly diagnosed as
one of the infrequent causes of acute coronary syndrome. Almost no cause was identified in …
one of the infrequent causes of acute coronary syndrome. Almost no cause was identified in …
First patient with mosaic NOTCH3 gene pathogenic variant. Unrevealed mosaicisms and importance of their detection
M Moreno‐García, AR Arteche‐López… - American Journal of …, 2021 - Wiley Online Library
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is an inherited small vessel disease caused …
leukoencephalopathy (CADASIL) is an inherited small vessel disease caused …
[HTML][HTML] Autonomic Dysfunction in the Setting of CADASIL Syndrome
Autonomic Dysfunction in the Setting of CADASIL Syndrome - PMC Back to Top Skip to main
content NIH NLM Logo Access keys NCBI Homepage MyNCBI Homepage Main Content Main …
content NIH NLM Logo Access keys NCBI Homepage MyNCBI Homepage Main Content Main …
[HTML][HTML] Ricci Allen, MSc
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) syndrome is the most common monogenic inherited cause …
leukoencephalopathy (CADASIL) syndrome is the most common monogenic inherited cause …
[HTML][HTML] Alan Tseng, MD, PhD
R Allen, N Kostick - community.the-hospitalist.org
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) syndrome is the most common monogenic inherited cause …
leukoencephalopathy (CADASIL) syndrome is the most common monogenic inherited cause …
[HTML][HTML] Nathan Kostick MS
R Allen - community.the-hospitalist.org
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) syndrome is the most common monogenic inherited cause …
leukoencephalopathy (CADASIL) syndrome is the most common monogenic inherited cause …