Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2007 3
2008 1
2009 7
2010 1
2011 3
2012 4
2013 8
2014 6
2015 6
2016 4
2017 5
2018 9
2019 8
2020 12
2021 10
2022 10
2023 7
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

82 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Loeys-Dietz Syndrome Type 1"
Page 1
Clinical Features and Outcomes of Pregnancy-Related Acute Aortic Dissection.
Braverman AC, Mittauer E, Harris KM, Evangelista A, Pyeritz RE, Brinster D, Conklin L, Suzuki T, Fanola C, Ouzounian M, Chen E, Myrmel T, Bekeredjian R, Hutchison S, Coselli J, Gilon D, O'Gara P, Davis M, Isselbacher E, Eagle K. Braverman AC, et al. JAMA Cardiol. 2021 Jan 1;6(1):58-66. doi: 10.1001/jamacardio.2020.4876. JAMA Cardiol. 2021. PMID: 33052376 Free PMC article.
At type B aortic dissection diagnosis, the mean (SD) descending aortic diameter was 32.5 (5) mm. Twenty women (69%) had an aortopathy condition or a positive family history: 13 women (65%) with Marfan syndrome, 2 women (10%) with Loeys-Dietz syndrom …
At type B aortic dissection diagnosis, the mean (SD) descending aortic diameter was 32.5 (5) mm. Twenty women (69%) had an aortopathy …
Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease.
Regalado ES, Morris SA, Braverman AC, Hostetler EM, De Backer J, Li R, Pyeritz RE, Yetman AT, Cervi E, Shalhub S, Jeremy R, LeMaire S, Ouzounian M, Evangelista A, Boileau C, Jondeau G, Milewicz DM. Regalado ES, et al. J Am Coll Cardiol. 2022 Aug 30;80(9):857-869. doi: 10.1016/j.jacc.2022.05.054. J Am Coll Cardiol. 2022. PMID: 36007983 Free article.
METHODS: A retrospective cohort of probands and relatives with rare variants in 7 genes for HTAD (n = 1,028) was assessed for the risk of first aortic events based on the gene altered, pathogenic variant type, sex, proband status, and location of recruitment. RESULT …
METHODS: A retrospective cohort of probands and relatives with rare variants in 7 genes for HTAD (n = 1,028) was assessed for the ris …
Outcomes After Endovascular Aortic Intervention in Patients With Connective Tissue Disease.
Olsson KW, Mani K, Burdess A, Patterson S, Scali ST, Kölbel T, Panuccio G, Eleshra A, Bertoglio L, Ardita V, Melissano G, Acharya A, Bicknell C, Riga C, Gibbs R, Jenkins M, Bakthavatsalam A, Sweet MP, Kasprzak PM, Pfister K, Oikonomou K, Heloise T, Sobocinski J, Butt T, Dias N, Tang C, Cheng SWK, Vandenhaute S, Van Herzeele I, Sorber RA, Black JH 3rd, Tenorio ER, Oderich GS, Vincent Z, Khashram M, Eagleton MJ, Pedersen SF, Budtz-Lilly J, Lomazzi C, Bissacco D, Trimarchi S, Huerta A, Riambau V, Wanhainen A. Olsson KW, et al. JAMA Surg. 2023 Aug 1;158(8):832-839. doi: 10.1001/jamasurg.2023.2128. JAMA Surg. 2023. PMID: 37314760
RESULTS: In total, 171 patients were included: 142 with Marfan syndrome, 17 with Loeys-Dietz syndrome, and 12 with vascular Ehlers-Danlos syndrome (vEDS). ...Primary technical success was achieved in 168 patients (98.2%), and 30-day mortality wa …
RESULTS: In total, 171 patients were included: 142 with Marfan syndrome, 17 with Loeys-Dietz syndrome, and 12 wi …
Audiologic and Otologic Clinical Manifestations of Loeys-Dietz Syndrome: A Heritable Connective Tissue Disorder.
Jeon JW, Christensen J, Chisholm J, Zalewski C, Rasooly M, Dempsey C, Magnani A, Frischmeyer-Guerrerio P, Brewer CC, Kim HJ. Jeon JW, et al. Otolaryngol Head Neck Surg. 2022 Feb;166(2):357-362. doi: 10.1177/01945998211008899. Epub 2021 May 11. Otolaryngol Head Neck Surg. 2022. PMID: 33971761 Free PMC article.
OBJECTIVE: Loeys-Dietz syndrome (LDS) is a rare genetic connective tissue disorder resulting from TGF-ss signaling pathway defects and characterized by a wide spectrum of aortic aneurysm, arterial tortuosity, and various extravascular abnormalities. ...Postty …
OBJECTIVE: Loeys-Dietz syndrome (LDS) is a rare genetic connective tissue disorder resulting from TGF-ss signaling path …
Ocular findings in Loeys-Dietz syndrome.
Busch C, Voitl R, Goergen B, Zemojtel T, Gehle P, Salchow DJ. Busch C, et al. Br J Ophthalmol. 2018 Aug;102(8):1036-1040. doi: 10.1136/bjophthalmol-2017-311254. Epub 2017 Nov 16. Br J Ophthalmol. 2018. PMID: 29146755
BACKGROUND: Loeys-Dietz syndrome (LDS), an autosomal-dominant connective tissue disorder, is characterised by systemic manifestations including arterial aneurysm and craniofacial dysmorphologies. ...The eyes of patients with LDS tended to be more myopic (sphe …
BACKGROUND: Loeys-Dietz syndrome (LDS), an autosomal-dominant connective tissue disorder, is characterised by systemic …
Cardiovascular surgery in Loeys-Dietz syndrome types 1-4.
Krohg-Sørensen K, Lingaas PS, Lundblad R, Seem E, Paus B, Geiran OR. Krohg-Sørensen K, et al. Eur J Cardiothorac Surg. 2017 Dec 1;52(6):1125-1131. doi: 10.1093/ejcts/ezx147. Eur J Cardiothorac Surg. 2017. PMID: 28541520
OBJECTIVES: The first publication of Loeys-Dietz syndrome (LDS) described aortic rupture at young ages. ...Mean age at first surgery was 36 years, with a non-significant trend that LDS2 patients were younger. Of the 9 emergency surgeries, 7 were type A …
OBJECTIVES: The first publication of Loeys-Dietz syndrome (LDS) described aortic rupture at young ages. ...Mean age at …
Relationship between phenotypic features in Loeys-Dietz syndrome and the presence of intracranial aneurysms.
Huguenard AL, Johnson GW, Desai RR, Osbun JW, Dacey RG, Braverman AC. Huguenard AL, et al. J Neurosurg. 2022 Oct 28;138(5):1385-1392. doi: 10.3171/2022.9.JNS221373. Print 2023 May 1. J Neurosurg. 2022. PMID: 36308480
OBJECTIVE: Loeys-Dietz syndrome (LDS) is a rare autosomal dominant condition characterized by aneurysms of the aorta, aortic branches, and intracranial arteries; skeletal and cutaneous abnormalities; and craniofacial malformations. ...METHODS: This was a retr …
OBJECTIVE: Loeys-Dietz syndrome (LDS) is a rare autosomal dominant condition characterized by aneurysms of the aorta, a …
Predictors of low bone density and fracture risk in Loeys-Dietz syndrome.
Guerrerio AL, Mateja A, Rasooly M, Levin S, Magnani A, Dempsey C, MacCarrick G, Dietz HC, Brittain E, Boyce AM, Frischmeyer-Guerrerio PA. Guerrerio AL, et al. Genet Med. 2022 Feb;24(2):419-429. doi: 10.1016/j.gim.2021.10.002. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906513 Free PMC article.
PURPOSE: Loeys-Dietz syndrome (LDS) is a connective tissue disorder affecting multiple organ systems, including bone. METHODS: We defined the bone phenotype and clinical predictors of low bone density and fracture risk in 77 patients with LDS type 1 …
PURPOSE: Loeys-Dietz syndrome (LDS) is a connective tissue disorder affecting multiple organ systems, including bone. M …
Neurovascular manifestations of connective-tissue diseases: A review.
Kim ST, Brinjikji W, Lanzino G, Kallmes DF. Kim ST, et al. Interv Neuroradiol. 2016 Dec;22(6):624-637. doi: 10.1177/1591019916659262. Epub 2016 Aug 10. Interv Neuroradiol. 2016. PMID: 27511817 Free PMC article. Review.
In this report, we aim to understand the prevalence and occurrences of such neurovascular manifestations in four heritable connective tissue disorders: Marfan syndrome, Ehlers-Danlos syndrome, Neurofibromatosis Type 1, and Loeys-Dietz …
In this report, we aim to understand the prevalence and occurrences of such neurovascular manifestations in four heritable connective tissue …
The differences in surgical long-term outcomes between Marfan syndrome and Loeys-Dietz syndrome.
Seike Y, Matsuda H, Inoue Y, Sasaki H, Morisaki H, Morisaki T, Kobayashi J. Seike Y, et al. J Thorac Cardiovasc Surg. 2022 Jul;164(1):16-25.e2. doi: 10.1016/j.jtcvs.2020.07.089. Epub 2020 Aug 7. J Thorac Cardiovasc Surg. 2022. PMID: 32891455
OBJECTIVE: The aim of this study was to disclose the differences of surgical outcomes between Marfan syndrome with mutations in fibrillin-1 gene and Loeys-Dietz syndrome with mutations in transforming growth factor-beta receptor 1 and 2. …
OBJECTIVE: The aim of this study was to disclose the differences of surgical outcomes between Marfan syndrome with mutations in fibri …
82 results