Found: 13
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Clinical and genetic yield of familial screening after a sudden unexplained death at a young age.
- Published in:
- Polish Heart Journal / Kardiologia Polska, 2024, v. 82, n. 4, p. 382, doi. 10.33963/v.phj.99617
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- Publication type:
- Article
Cardiovascular involvement and prognosis in Loeys-Dietz syndrome.
- Published in:
- Polish Heart Journal / Kardiologia Polska, 2023, v. 81, n. 11, p. 1096, doi. 10.33963/v.kp.97390
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- Publication type:
- Article
Double chambered right ventricle in a patient with hypertrophic cardiomyopathy. A unique coexistence.
- Published in:
- Polish Heart Journal / Kardiologia Polska, 2021, v. 79, n. 7/8, p. 891, doi. 10.33963/KP.a2021.0023
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- Publication type:
- Article
Ocena kliniczna i genetyczna rodzin osób młodych zmarłych nagle. Czy sekwencjonowanie następnej generacji (NGS) może pomóc w postawieniu rozpoznania?
- Published in:
- Polish Heart Journal / Kardiologia Polska, 2020, v. 78, p. 114
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- Publication type:
- Article
Good performance of the criteria of American College of Medical Genetics and Genomics/Association for Molecular Pathology in prediction of pathogenicity of genetic variants causing thoracic aortic aneurysms and dissections.
- Published in:
- 2022
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- Publication type:
- journal article
The complete anatomy of the lingual nerve: A meta‐analysis with implications for oral and maxillofacial surgery.
- Published in:
- Clinical Anatomy, 2023, v. 36, n. 6, p. 905, doi. 10.1002/ca.24033
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- Publication type:
- Article
Troponin T Assessment Allows for Identification of Mutation Carriers among Young Relatives of Patients with LMNA -Related Dilated Cardiomyopathy.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 11, p. 3164, doi. 10.3390/jcm13113164
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- Publication type:
- Article
Titin-Related Dilated Cardiomyopathy: The Clinical Trajectory and the Role of Circulating Biomarkers in the Clinical Assessment.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 1, p. 13, doi. 10.3390/diagnostics12010013
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- Publication type:
- Article
A Novel DSP Truncating Variant in a Family with Episodic Myocardial Injury in the Course of Arrhythmogenic Cardiomyopathy—A Possible Role of a Low Penetrance NLRP3 Variant.
- Published in:
- Diagnostics (2075-4418), 2020, v. 10, n. 11, p. 955, doi. 10.3390/diagnostics10110955
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- Publication type:
- Article
A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1306333
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- Publication type:
- Article
Coexistence of Marfan syndrome and fibromuscular dysplasia.
- Published in:
- Polish Archives of Internal Medicine, 2024, v. 134, n. 9, p. 1, doi. 10.20452/pamw.16798
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- Publication type:
- Article
Intrafamilial variability of cardiovascular abnormalities associated with the p.R460H mutation of the TGFBR2 gene.
- Published in:
- Polish Archives of Internal Medicine, 2020, v. 130, n. 7/8, p. 676, doi. 10.20452/pamw.15365
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- Publication type:
- Article
A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations.
- Published in:
- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0167-0
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- Publication type:
- Article