Works matching DE "MARFAN syndrome"
Results: 1381
Differential Oral Microbiota and Serum Cytokine Signatures in Age-Grouped Patients with Marfan Syndrome.
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- Biomedicines, 2025, v. 13, n. 2, p. 330, doi. 10.3390/biomedicines13020330
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- Article
Health-related quality of life in adults with Marfan syndrome.
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- Cardiology in the Young, 2024, v. 34, n. 12, p. 2514, doi. 10.1017/S1047951124025770
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- Article
Refractive Alterations in Marfan Syndrome: A Narrative Review.
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- Medicina (1010660X), 2025, v. 61, n. 2, p. 250, doi. 10.3390/medicina61020250
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- Article
Efficacy and outcome safety of capsular tension segment combined with capsular tension ring in children with ectopia lentis.
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- Oman Journal of Ophthalmology, 2025, v. 18, n. 1, p. 44, doi. 10.4103/ojo.ojo_15_24
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- Article
Secondary intraocular lens implantation.
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- 2025
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- Publication type:
- Editorial
Exercise for Individuals with Marfan Syndrome.
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- Cardiopulmonary Physical Therapy Journal (American Physical Therapy Association, Cardiopulmonary Section), 2006, v. 17, n. 3, p. 110, doi. 10.1097/01823246-200617030-00003
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- Article
Congenital contractural arachnodactyly (Beals-Hecht syndrome): a rare connective tissue disorder.
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- 2013
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- Publication type:
- Report
Rare aneurysm of the hepatic artery with overlap to the gastroduodenal artery in very uncommon coincidence with occurence of hepatomesenteric trunk.
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- 2013
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- Publication type:
- Report
Full-Mouth Rehabilitation With Implant-Prosthesis in Marfan Syndrome Patient: Clinical Report and Literature Review.
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- Journal of Oral Implantology, 2020, v. 46, n. 2, p. 115, doi. 10.1563/aaid-joi-D-19-00151
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- Article
Transforming Growth Factor-β and the Renin-Angiotensin System in Syndromic Thoracic Aortic Aneurysms: Implications for Treatment.
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- Cardiovascular Drugs & Therapy, 2021, v. 35, n. 6, p. 1233, doi. 10.1007/s10557-020-07116-4
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- Article
Arterial aneurysms: autosomal dominant polycystic kidney disease, Marfan syndrome or both?
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- Clinical & Experimental Nephrology, 2014, v. 18, n. 4, p. 672, doi. 10.1007/s10157-013-0876-7
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- Article
Overview of current surgical strategies for aortic disease in patients with Marfan syndrome.
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- Surgery Today, 2016, v. 46, n. 9, p. 1006, doi. 10.1007/s00595-015-1278-0
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- Article
Commentary on “Weak Ligaments and Sloping Joints: A New Hypothesis for Development of Congenital Atlantoaxial Dislocation and Basilar Invagination”.
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- Neurospine, 2020, v. 17, n. 4, p. 857, doi. 10.14245/ns.2040632.316
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- Article
From Anatomic to Genetic Understanding of Developmental Craniovertebral Junction Abnormalities.
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- Neurospine, 2020, v. 17, n. 4, p. 859, doi. 10.14245/ns.2040548.274
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- Article
Acute aortic dissection on ascending aortic aneurysm in a patient with Marfan disease: about a case.
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- E Journal of Cardiovascular Medicine, 2023, v. 11, p. 1
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- Article
Spontaneous Intracranial Hypotension Associated with Marfan Syndrome: A Case Report.
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- Clinical Practice & Cases in Emergency Medicine, 2024, v. 8, n. 3, p. 243, doi. 10.5811/cpcem.7223
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- Publication type:
- Article
Identification of Three FBN1 Mutations in Chinese Patients with Typical or Incomplete Marfan Syndrome by Whole-Exome Sequencing.
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- Cardiovascular Innovations & Applications (CVIA), 2020, v. 5, n. 1, p. 19, doi. 10.15212/CVIA.2019.0576
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- Article
Multidisciplinary team approach in management of anterior spinal dysraphism with unusual presentation: case series and surgical approach.
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- Egyptian Journal of Neurosurgery, 2024, v. 39, n. 1, p. 1, doi. 10.1186/s41984-024-00324-2
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- Article
A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis.
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- Human Genetics, 2020, v. 139, n. 4, p. 461, doi. 10.1007/s00439-019-02102-9
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- Article
Periodontal condition in growing subjects with Marfan Syndrome: a case-control study.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6606
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- Article
Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome.
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- PeerJ, 2018, p. 1, doi. 10.7717/peerj.5927
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- Publication type:
- Article
Neurological abnormalities in individuals with Marfan syndrome: results from a genetically confirmed Italian cohort.
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- Neurological Sciences, 2024, v. 45, n. 11, p. 5355, doi. 10.1007/s10072-024-07625-2
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- Article
Impact of Notch3 Activation on Aortic Aneurysm Development in Marfan Syndrome.
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- 2022
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- Publication type:
- journal article
Swallowing and quality of life in individuals with Marfan syndrome: a cross-sectional study.
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- 2022
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- Publication type:
- journal article
Homocystinuria, a Possible Solution of the Akhenaten's Mystery.
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- Collegium Antropologicum, 2010, v. 34, p. 255
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- Publication type:
- Article
Marfan's syndrome with anterior sacral pseudomeningocele.
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- Oxford Medical Case Reports, 2022, v. 2022, n. 12, p. 1, doi. 10.1093/omcr/omac139
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- Publication type:
- Article
Identification of Novel Causal FBN1 Mutations in Pedigrees of Marfan Syndrome.
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- International Journal of Genomics, 2018, p. 1, doi. 10.1155/2018/1246516
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- Publication type:
- Article
PREGNANT LADY WITH MARFAN SYNDROME PRESENTING WITH AORTIC DISSECTION.
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- Pakistan Heart Journal, 2017, v. 50, n. 3, p. 197
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- Publication type:
- Article
Dissecting aneurysms involving both anterior cerebral artery and aorta.
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- Pathology International, 2007, v. 57, n. 4, p. 224, doi. 10.1111/j.1440-1827.2007.02085.x
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- Publication type:
- Article
Mid- to long-term radiological and respiratory outcomes following surgery for older early-onset scoliosis patients with Marfan syndrome.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-75413-1
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- Publication type:
- Article
Spontaneous Intracranial Hypotension and Dural Ectasia in Marfan Syndrome: An Illustrative Case Successfully Treated with Steroid Therapy and Literature Review.
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- Brain Sciences (2076-3425), 2024, v. 14, n. 11, p. 1143, doi. 10.3390/brainsci14111143
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- Publication type:
- Article
Fibrillin-1 Regulates Arteriole Integrity in the Retina.
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- Biomolecules (2218-273X), 2022, v. 12, n. 10, p. N.PAG, doi. 10.3390/biom12101330
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- Publication type:
- Article
Pathophysiology and Therapeutics of Thoracic Aortic Aneurysm in Marfan Syndrome.
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- Biomolecules (2218-273X), 2022, v. 12, n. 1, p. 128, doi. 10.3390/biom12010128
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- Publication type:
- Article
VP16.08: Prenatal detection of infantile Marfan syndrome: a case report.
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- Ultrasound in Obstetrics & Gynecology, 2021, v. 58, p. 165, doi. 10.1002/uog.24276
- Publication type:
- Article
VP51.08: Successful maternal and fetal outcome in a patient with Marfan syndrome with aortic root dilatation of 53mm: a case report.
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- Ultrasound in Obstetrics & Gynecology, 2020, v. 56, p. 294, doi. 10.1002/uog.23215
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- Publication type:
- Article
Beals syndrome (congenital contractural arachnodactyly): prenatal ultrasound findings and molecular analysis.
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 44, n. 4, p. 486, doi. 10.1002/uog.13350
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- Publication type:
- Article
OP32.05: Prenatal diagnosis of neonatal Marfan syndrome.
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- Ultrasound in Obstetrics & Gynecology, 2011, v. 38, p. 149, doi. 10.1002/uog.9558
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- Publication type:
- Article
Marfan syndrome: insights from animal models.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1463318
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- Article
Epidural Anesthesia for Cesarean Section in a Pregnant Woman with Marfan Syndrome and Dural Ectasia.
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- Case Reports in Obstetrics & Gynecology, 2017, p. 1, doi. 10.1155/2017/2126310
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- Article
Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis.
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- 2022
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- Publication type:
- Case Study
Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review.
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- Case Reports in Genetics, 2020, p. 1, doi. 10.1155/2020/7353452
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- Publication type:
- Article
Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review.
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- Case Reports in Genetics, 2020, p. 1, doi. 10.1155/2020/7353452
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- Publication type:
- Article
Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm.
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- Case Reports in Genetics, 2018, p. 1, doi. 10.1155/2018/6780494
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- Publication type:
- Article
Psychiatric and neuropsychological issues in Marfan syndrome.
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- International Journal of Psychiatry in Medicine, 2015, v. 50, n. 4, p. 347, doi. 10.1177/0091217415612701
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- Publication type:
- Article
Underexpression of Fibrillin-1 Protects from Hypertensive and Diabetic Glomerular Disease.
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- Kidney & Blood Pressure Research, 2004, v. 27, n. 5/6, p. 346
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- Publication type:
- Article
Combined Aortic Root Replacement and Heart Transplantation in a Patient with Dilated Cardiomyopathy and Aortic Root Aneurysm.
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- International Journal of Organ Transplantation Medicine, 2018, v. 9, n. 3, p. 137
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- Publication type:
- Article
Unusual Cause of Heart Failure in a Patient with Marfan Syndrome: A Late Complication of Bioprosthetic Valved Graft Replacement.
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- Texas Heart Institute Journal, 2020, v. 47, n. 1, p. 38, doi. 10.14503/THIJ-18-6618
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- Publication type:
- Article
Giant Aortic Root Aneurysm in a Patient with D-Transposition of the Great Arteries and Marfan Syndrome.
- Published in:
- 2019
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- Publication type:
- Case Study
Echocardiographic versus Histologic Findings in Marfan Syndrome.
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- Texas Heart Institute Journal, 2015, v. 42, n. 1, p. 30, doi. 10.14503/THIJ-13-3848
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- Publication type:
- Article
Endovascular Repair as a Bridge to Surgical Repair.
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- Texas Heart Institute Journal, 2014, v. 41, n. 2, p. 198, doi. 10.14503/THIJ-12-2901
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- Publication type:
- Article