Results 231 to 240 of about 35,494 (256)
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Journal of the American Academy of Nurse Practitioners, 2009
AbstractPurpose: To provide an overview of Marfan syndrome (MFS), including diagnostic criteria, genetic factors involved, emerging theories for treatment, a case study, and an overview of genetic counseling for individuals and families of those with MFS.Data Sources: Selected research, review, and clinical articles.Conclusions: MFS is a connective ...
Eric D, Shirley, Paul D, Sponseller
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AbstractPurpose: To provide an overview of Marfan syndrome (MFS), including diagnostic criteria, genetic factors involved, emerging theories for treatment, a case study, and an overview of genetic counseling for individuals and families of those with MFS.Data Sources: Selected research, review, and clinical articles.Conclusions: MFS is a connective ...
Eric D, Shirley, Paul D, Sponseller
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Nature Reviews Disease Primers, 2021
Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant condition with substantial intrafamilial and interfamilial variability. MFS is caused by pathogenetic variants in FBN1, which encodes fibrillin-1, a major structural component of the extracellular matrix that provides support to connective tissues, particularly in arteries,
Dianna M. Milewicz +8 more
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Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant condition with substantial intrafamilial and interfamilial variability. MFS is caused by pathogenetic variants in FBN1, which encodes fibrillin-1, a major structural component of the extracellular matrix that provides support to connective tissues, particularly in arteries,
Dianna M. Milewicz +8 more
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Annals of Emergency Medicine, 1980
Asfaw I, Tintinalli JE: Marfan's syndrome. Ann Emerg Med 9:105-107, February 1 980. Marfan's syndrome; syndrome, Marfan's; aortic insufficiency, Marfan's syndro me I NTRODUCTION Judith Tintinalli, MD: The case for discussion today is that of a young woman with Marfan's syndrome and chest pain.
Ingida Asfaw, Judith E. Tintinalli
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Asfaw I, Tintinalli JE: Marfan's syndrome. Ann Emerg Med 9:105-107, February 1 980. Marfan's syndrome; syndrome, Marfan's; aortic insufficiency, Marfan's syndro me I NTRODUCTION Judith Tintinalli, MD: The case for discussion today is that of a young woman with Marfan's syndrome and chest pain.
Ingida Asfaw, Judith E. Tintinalli
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American Heart Journal, 1953
Abstract A case of Marfan's syndrome exhibiting medial degeneration and aneurysmal formation with incomplete rupture of the pulmonary artery is reported with a review of the literature.
M, ANDERSON, H R, PRATT-THOMAS
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Abstract A case of Marfan's syndrome exhibiting medial degeneration and aneurysmal formation with incomplete rupture of the pulmonary artery is reported with a review of the literature.
M, ANDERSON, H R, PRATT-THOMAS
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Critical Care Nurse, 1991
Although Marfan's syndrome is not a frequent occurrence in critical care, serious cardiovascular problems can exist, requiring intensive care. This article has identified the manifestations in those coping with Marfan's syndrome. Critical care nurses need to be aware of the clinical presentation and pathophysiology of the problem to understand the ...
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Although Marfan's syndrome is not a frequent occurrence in critical care, serious cardiovascular problems can exist, requiring intensive care. This article has identified the manifestations in those coping with Marfan's syndrome. Critical care nurses need to be aware of the clinical presentation and pathophysiology of the problem to understand the ...
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American Journal of Medical Genetics, 1988
AbstractWe describe a girl with Marfan syndrome in whom the clinical expression of the disease was much more evident on the left side of the body.
BURGIO, GIUSEPPE ROBERTO +5 more
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AbstractWe describe a girl with Marfan syndrome in whom the clinical expression of the disease was much more evident on the left side of the body.
BURGIO, GIUSEPPE ROBERTO +5 more
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Cardiomyopathy in Marfan Syndrome
The Thoracic and Cardiovascular Surgeon, 2014This report aims to evaluate the existence of primary and secondary cardiomyopathy in patients with Marfan syndrome (MFS) who underwent surgical management for primary cardiovascular sequelae of this genetic disorder. Likewise, we aim to determine whether the myocardium in MFS is susceptible to ischaemia independent of myocardial protection used during
Roland, Hetzer +2 more
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Dimensions of Critical Care Nursing, 2000
Cardiac complications of Marfan syndrome can be fatal. This article reviews the assessment of a patient with this hereditary disorder, complications and their treatment, and nursing care.
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Cardiac complications of Marfan syndrome can be fatal. This article reviews the assessment of a patient with this hereditary disorder, complications and their treatment, and nursing care.
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Marfan's syndrome or the Marfan syndrome
International Journal of Cardiology, 1987The eponym of the well-characterised clinical syndrome has peculiarly been accepted both as Marfan’s syndrome and as the Marfan syndrome. Amongst the five major textbooks of internal medicine and cardiology. two have used Marfan’s syndrome (I.21 and three the Marfan syndrome [3-51. Thirty years ago McKusick wrote “Marfan’s Syndrome or better the Marfan
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