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Refinado por: Nome da Publicação: Journal of Vascular Surgery remover
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1
A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis
A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis
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A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis

Sherene Shalhub Peter H Byers; Kelli L Hicks; Dawn M Coleman; Frank M Davis; Giovanni De Caridi; K. Nicole Weaver; Erin M Miller; Marc L Schermerhorn; Katie Shean; Maurício Serra Ribeiro

Journal of Vascular Surgery Philadelphia v. 71, n. 1, p. 149-157, 2020

Philadelphia 2020

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3125413 Acervo Digital )(Acessar)

2
Somatic mutations in exon 17 of the TEK gene in vascular tumors and vascular malformations
Somatic mutations in exon 17 of the TEK gene in vascular tumors and vascular malformations
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Somatic mutations in exon 17 of the TEK gene in vascular tumors and vascular malformations

Ye, Caisheng, MD, PhD ; Pan, Lingxiao, MD ; Huang, Yongbo, MD ; Ye, Runyi, PhD ; Han, Anjia, MD, PhD ; Li, Songqi, MD, PhD ; Li, Xiaoxi, MD, PhD ; Wang, Shenming, MD, PhD

Journal of vascular surgery, 2011-12, Vol.54 (6), p.1760-1768.e3 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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3
Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: The Linz Peripheral Arterial Disease (LIPAD) study
Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: The Linz Peripheral Arterial Disease (LIPAD) study
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Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: The Linz Peripheral Arterial Disease (LIPAD) study

Mueller, Thomas ; Marschon, Renate ; Dieplinger, Benjamin ; Haidinger, Dieter ; Gegenhuber, Alfons ; Poelz, Werner ; Webersinke, Gerald ; Haltmayer, Meinhard

Journal of vascular surgery, 2005-05, Vol.41 (5), p.808-815 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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4
The prevalence of hyperhomocysteinemia, methylene tetrahydrofolate reductase C677T mutation, and vitamin B12 and folate deficiency in patients with chronic venous insufficiency
The prevalence of hyperhomocysteinemia, methylene tetrahydrofolate reductase C677T mutation, and vitamin B12 and folate deficiency in patients with chronic venous insufficiency
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The prevalence of hyperhomocysteinemia, methylene tetrahydrofolate reductase C677T mutation, and vitamin B12 and folate deficiency in patients with chronic venous insufficiency

Sam, Rachel C ; Burns, Paul J ; Hobbs, Simon D ; Marshall, Tim ; Wilmink, Antonius B.M ; Silverman, Stanley H ; Bradbury, Andrew W

Journal of vascular surgery, 2003-11, Vol.38 (5), p.904-908 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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5
Can screening for genetic markers improve peripheral artery bypass patency?
Can screening for genetic markers improve peripheral artery bypass patency?
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Can screening for genetic markers improve peripheral artery bypass patency?

Kibbe, Melina R. ; Hassett, Andrea L.Cortese ; McSherry, Frances ; Conner, Philip ; Bontempo, Franklin A. ; Williford, William ; Johnson, Willard ; Makaroun, Michel S.

Journal of vascular surgery, 2002-12, Vol.36 (6), p.1198-1206 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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6
Saphenous vein thrombophlebitis (SVT): A deceptively benign disease
Saphenous vein thrombophlebitis (SVT): A deceptively benign disease
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Saphenous vein thrombophlebitis (SVT): A deceptively benign disease

Hanson, Judith N. ; Ascher, Enrico ; DePippo, Patrick ; Lorensen, Elke ; Scheinman, Marcel ; Yorkovich, William ; Hingorani, Anil

Journal of vascular surgery, 1998-04, Vol.27 (4), p.677-680 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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7
Mural thrombus of the aorta in association with homozygous plasminogen activator inhibitor type 1 (PAI-1)-675(4G) and heterozygous GP Ia 807C/T genotypes
Mural thrombus of the aorta in association with homozygous plasminogen activator inhibitor type 1 (PAI-1)-675(4G) and heterozygous GP Ia 807C/T genotypes
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Mural thrombus of the aorta in association with homozygous plasminogen activator inhibitor type 1 (PAI-1)-675(4G) and heterozygous GP Ia 807C/T genotypes

Beldi, Guido ; Bissat, Andre ; Eugster, Thomas ; Gürke, Lorenz ; Stierli, Peter ; Huber, Andreas R.

Journal of vascular surgery, 2002-09, Vol.36 (3), p.632-634 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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8
Molecular biology of marfan syndrome
Molecular biology of marfan syndrome
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Molecular biology of marfan syndrome

Dietz, Harry C.

Journal of vascular surgery, 1992-05, Vol.15 (5), p.927-928 [Periódico revisado por pares]

United States: Mosby, Inc

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9
DNA sequencing as a method to identify mutations in patients with familial forms of aneurysms
DNA sequencing as a method to identify mutations in patients with familial forms of aneurysms
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DNA sequencing as a method to identify mutations in patients with familial forms of aneurysms

Tromp, Gerard ; Kuivaniemi, Helena

Journal of vascular surgery, 1992-05, Vol.15 (5), p.928-930 [Periódico revisado por pares]

United States: Mosby, Inc

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10
The role of abnormal type III collagen in the development of common aneurysms
The role of abnormal type III collagen in the development of common aneurysms
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The role of abnormal type III collagen in the development of common aneurysms

Deak, Susan B. ; Ricotta, John J. ; Mariani, Thomas J. ; Deak, Steven T. ; Zatina, Michael A. ; Mackenzie, James W. ; Boyd, Charles D.

Journal of vascular surgery, 1992-05, Vol.15 (5), p.926-927 [Periódico revisado por pares]

United States: Mosby, Inc

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