关注
Alana C. Cecchi
Alana C. Cecchi
在 uth.tmc.edu 的电子邮件经过验证
标题
引用次数
年份
A mixed method approach to understanding the impact of COVID-19 on patients with or at risk for aortic dissection
JR Lee, C Segal, J Howitt, SO Lawrence, J Grima, K Eagle, K Woo, ...
Seminars in Vascular Surgery 35 (1), 100-109, 2022
22022
An assessment of the current medical management of thoracic aortic disease: A patient-centered scoping literature review
RCF Pena, MAH Bowman, M Ahmad, J Pham, E Kline-Rogers, MJ Case, ...
Seminars in Vascular Surgery 35 (1), 16-34, 2022
52022
An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation family
D Guo, X Duan, K Mimnagh, AC Cecchi, IC Marin, Y Yu, WV Velasco, ...
Clinical Genetics 103 (6), 704-708, 2023
32023
Aortic dissection in pregnancy and the postpartum period
M Russo, M Boehler-Tatman, C Albright, C David, AW Roberts, S Shalhub, ...
Seminars in Vascular Surgery 35 (1), 60-68, 2022
112022
Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton‐Brown‐Rahman syndrome
AC Cecchi, A Haidar, I Marin, CS Kwartler, SK Prakash, DM Milewicz
American Journal of Medical Genetics Part A 188 (2), 628-634, 2022
62022
Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy
A Pinard, MDJ Fiander, AC Cecchi, AL Rideout, M Azouz, SM Fraser, ...
Neurology 96 (13), e1783-e1791, 2021
282021
Characteristics of Moyamoya Disorder in a Racially Diverse Adult and Pediatric Cohort
H Seol, KM Chu, SM Fraser, AC Cecchi, DM Milewicz, AZ Sharrief
ANNALS OF NEUROLOGY 90, S50-S51, 2021
2021
COL3A1 Gene Mutation Predicts Arterial Involvement and Prognosis in Vascular Ehlers Danlos Syndrome
S Shalhub, N McDonnel, AC Cecchi, A Azizzadeh, KM Charlton-Ouw, ...
Journal of Vascular Surgery 57 (5), 25S-26S, 2013
2013
Correction to: Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease
A Pinard, W Ye, SM Fraser, JA Rosenfeld, P Pichurin, SE Hickey, D Guo, ...
Brain 146 (e74), e74, 2023
2023
Current state and future directions of genomic medicine in aortic dissection: a path to prevention and personalized care
AC Cecchi, M Drake, C Campos, J Howitt, J Medina, SM Damrauer, ...
Seminars in vascular surgery 35 (1), 51-59, 2022
82022
FAMILY HISTORY OF AORTIC AND ARTERIAL ANEURYSMS AND DISSECTIONS IS ASSOCIATED WITH TYPE B AORTIC DISSECTION
RL Campbell, M Bartek, M Pepin, A Cecchi, P Byers, D Milewicz, ...
JOURNAL OF INVESTIGATIVE MEDICINE 65 (1), 184-184, 2017
2017
Heterozygous Missense Mutations in PLEKHO2 Predispose to Thoracic Aortic Aneurysms and Dissections
A Pinard, XY Duang, D Guo, ES Regalado, AC Cecchi, L Gong, ...
Arteriosclerosis, Thrombosis, and Vascular Biology 39 (Suppl_1), A140-A140, 2019
2019
Histopathological Evaluation of Type A Aortic Dissection: A Comparison of Congenital versus Acquired Aortic Wall Weakness
H Sadaf, L Lelenwa, A Segura, A Cecchi, D Milewicz, HJ Safi, A Estrera, ...
LABORATORY INVESTIGATION 102 (SUPPL 1), 230-230, 2022
2022
Implementation of telemedicine in the care of patients with aortic dissection
T Nishath, K Wright, CR Burke, X Teng, N Cotter, AY Jeniann, LM Drudi, ...
Seminars in Vascular Surgery 35 (1), 43-50, 2022
72022
In-hospital outcomes and long-term survival of women of childbearing age with aortic dissection
KL Rommens, HK Sandhu, CC Miller III, AC Cecchi, SK Prakash, ...
Journal of Vascular Surgery 74 (4), 1135-1142. e1, 2021
112021
Insights From the Histopathologic Analysis of Acquired and Genetic Thoracic Aortic Aneurysms and Dissections
LM Buja, B Zhao, H Sadaf, M McDonald, AM Segura, L Li, A Cecchi, ...
Texas Heart Institute Journal 51 (1), 2024
2024
Knowledge gaps in surgical management for aortic dissection
A Tanaka, AM Hebert, A Smith-Washington, T Hoffstaetter, R Goldenberg, ...
Seminars in Vascular Surgery 35 (1), 35-42, 2022
22022
Lived experiences of people with or at risk for aortic dissection: A qualitative assessment
JR Lee, C Segal, J Howitt, M Case, N Cotter, T Soderlund, D Trotter, ...
Seminars in Vascular Surgery 35 (1), 78-87, 2022
52022
Missense mutations in FBN1 exons 41 and 42 cause Weill–Marchesani syndrome with thoracic aortic disease and Marfan syndrome
A Cecchi, N Ogawa, HR Martinez, A Carlson, Y Fan, DJ Penny, D Guo, ...
American Journal of Medical Genetics Part A 161 (9), 2305-2310, 2013
422013
Missense Pathogenic Variants in ANO1 Predispose to Moyamoya Disease
A Pinard, M He, JA Rosenfeld, W Ye, S Guey, S Hickey, AM Lewis, ...
Stroke 51 (Suppl_1), A53-A53, 2020
2020
系统目前无法执行此操作,请稍后再试。
文章 1–20