Found: 28
Select item for more details and to access through your institution.
Helix-fixed leadless pacemaker implantation through a valve-in-valve tricuspid prosthesis via the femoral approach.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT).
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7682, doi. 10.3390/ijms25147682
- By:
- Publication type:
- Article
Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia.
- Published in:
- Child's Nervous System, 2024, v. 40, n. 7, p. 2101, doi. 10.1007/s00381-024-06366-z
- By:
- Publication type:
- Article
Reply to Eker et al. Comment on "Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12 , 2704".
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 23, p. 7462, doi. 10.3390/jcm12237462
- By:
- Publication type:
- Article
Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 7, p. 2704, doi. 10.3390/jcm12072704
- By:
- Publication type:
- Article
Choroidal melanoma with synchronous Fuchs' adenoma and novel ATRX mutation.
- Published in:
- International Journal of Retina & Vitreous, 2022, v. 8, n. 1, p. 1, doi. 10.1186/s40942-022-00374-4
- By:
- Publication type:
- Article
Late‐in‐life treadmill training rejuvenates autophagy, protein aggregate clearance, and function in mouse hearts.
- Published in:
- Aging Cell, 2021, v. 20, n. 10, p. 1, doi. 10.1111/acel.13467
- By:
- Publication type:
- Article
Cardiac-specific deletion of voltage dependent anion channel 2 leads to dilated cardiomyopathy by altering calcium homeostasis.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24869-0
- By:
- Publication type:
- Article
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Genotype–Phenotype Correlations in Children with HHT.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 9, p. 2714, doi. 10.3390/jcm9092714
- By:
- Publication type:
- Article
A novel phosphoglucomutase‐deficient mouse model reveals aberrant glycosylation and early embryonic lethality.
- Published in:
- Journal of Inherited Metabolic Disease, 2019, v. 42, n. 5, p. 998, doi. 10.1002/jimd.12110
- By:
- Publication type:
- Article
Epistaxis in children and adolescents with hereditary hemorrhagic telangiectasia.
- Published in:
- 2018
- By:
- Publication type:
- journal article
The effects of nasal closure on quality of life in patients with hereditary hemorrhagic telangiectasia.
- Published in:
- Laryngoscope Investigative Otolaryngology, 2018, v. 3, n. 3, p. 178, doi. 10.1002/lio2.157
- By:
- Publication type:
- Article
Effect of Topical Intranasal Therapy on Epistaxis Frequency in Patients With Hereditary Hemorrhagic Telangiectasia: A Randomized Clinical Trial.
- Published in:
- 2016
- By:
- Publication type:
- journal article
An evaluation of the severity and progression of epistaxis in hereditary hemorrhagic telangiectasia 1 versus hereditary hemorrhagic telangiectasia 2.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Small GTPase Rap1 Is Essential for Mouse Development and Formation of Functional Vasculature.
- Published in:
- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0145689
- By:
- Publication type:
- Article
Nrf2 deficiency prevents reductive stress-induced hypertrophic cardiomyopathy.
- Published in:
- Cardiovascular Research, 2013, v. 100, n. 1, p. 63, doi. 10.1093/cvr/cvt150
- By:
- Publication type:
- Article
Mechanistic Target of Rapamycin (Mtor) Is Essential for Murine Embryonic Heart Development and Growth.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054221
- By:
- Publication type:
- Article
Mutations in 2 distinct genetic pathways result in cerebral cavernous malformations in mice.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Reply to a Letter to Editor 'Nickel Allergy, Amplatzer Atrial Septal Occluder Device, and the Risk of Kounis Syndrome'.
- Published in:
- Clinical Cardiology, 2010, v. 33, n. 4, p. E61, doi. 10.1002/clc.20743
- By:
- Publication type:
- Article
Recent insights into cerebral cavernous malformations: animal models of CCM and the human phenotype.
- Published in:
- FEBS Journal, 2010, v. 277, n. 5, p. 1076, doi. 10.1111/j.1742-4658.2009.07536.x
- By:
- Publication type:
- Article
Unusual Presentation of Nickel Allergy Requiring Explantation of an Amplatzer Atrial Septal Occluder Device.
- Published in:
- Clinical Cardiology, 2009, v. 32, n. 8, p. E55, doi. 10.1002/clc.20427
- By:
- Publication type:
- Article
Corrigendum: The cerebral cavernous malformation signaling pathway promotes vascular integrity via Rho GTPases.
- Published in:
- 2009
- By:
- Publication type:
- Correction notice
The cerebral cavernous malformation signaling pathway promotes vascular integrity via Rho GTPases.
- Published in:
- Nature Medicine, 2009, v. 15, n. 2, p. 177, doi. 10.1038/nm.1911
- By:
- Publication type:
- Article
Intraepidermal carcinoma of the eyelid.
- Published in:
- Clinical & Experimental Ophthalmology, 2002, v. 30, n. 1, p. 23, doi. 10.1046/j.1442-9071.2002.00486.x
- By:
- Publication type:
- Article
Eccrine poroma of the eyelid.
- Published in:
- Clinical & Experimental Ophthalmology, 2001, v. 29, n. 4, p. 253, doi. 10.1046/j.1442-9071.2001.00417.x
- By:
- Publication type:
- Article
Periocular tumour of the follicular infundibulum.
- Published in:
- Clinical & Experimental Ophthalmology, 2001, v. 29, n. 2, p. 100, doi. 10.1046/j.1442-9071.2001.d01-12.x
- By:
- Publication type:
- Article
Dermatomyofibroma: A report of two cases, one occurring in a child.
- Published in:
- Australasian Journal of Dermatology, 2001, v. 42, n. 1, p. 22, doi. 10.1046/j.1440-0960.2001.00467.x
- By:
- Publication type:
- Article