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Vascular Ehlers–Danlos syndrome

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en fr Physiopathologic aspects of the vascular Ehlers–Danlos syndrome Aspects physiopathologiques du syndrome d'Ehlers-Danlos vasculaire

... conventional vascular Doppler ultrasound apparatus, ultrafast ultrasound imaging can be easily used to determine, with a good repeatability, the carotid PWV by switching from the B mode to the ultrafast ultrasound ...

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Cervical artery dissections and type A aortic dissection in a family with a novel missense COL3A1 mutation of vascular type Ehlers-Danlos syndrome.

Cervical artery dissections and type A aortic dissection in a family with a novel missense COL3A1 mutation of vascular type Ehlers-Danlos syndrome.

... Frank, M., Albuisson, J., Ranque, B., Golmard, L., Mazzella, J.M., Bal-Theoleyre, L., Fauret, A.L., Mirault, T., Denarie, N., Mousseaux, E., Boutouyrie, P., Fiessinger, J.N., Emmerich, J., Messas, E., Jeunemaitre, X., ...

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Aspects physiopathologiques du syndrome d'Ehlers-Danlos vasculaire

Aspects physiopathologiques du syndrome d'Ehlers-Danlos vasculaire

... conventional vascular Doppler ultrasound apparatus, ultrafast ultrasound imaging can be easily used to determine, with a good repeatability, the carotid PWV by switching from the B mode to the ultrafast ultrasound ...

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Ehlers-Danlos syndrome in the University Hospital of Liege

Ehlers-Danlos syndrome in the University Hospital of Liege

... Regarding family history, 81 patients (57.0%) had at least one relative with joint hypermobility. In 20 patients (14.1%) the family history was positive for vascular problems, five patients (3.5%) had a family ...

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Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

... Periodontal Ehlers-Danlos syndrome (pEDS) is an autosomal-dominant disorder characterized by early-onset periodontitis leading to premature loss of teeth, joint hypermobility, and mild skin ...and ...

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Alport syndrome

Alport syndrome

... Alport syndrome is a multisystem disorder including progressive renal disease, senso- rineural deafness, and eye ...Alport syndrome was also described recently. The syndrome is caused by mutations in ...

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Profils langagiers dans le syndrome de l'X-fragile et le syndrome de Down

Profils langagiers dans le syndrome de l'X-fragile et le syndrome de Down

... Ferguson C.A. (1978). Learning to pronounce - the earliest stages of phonological development in the child. in Minifie F.D. & Lloyd L. 'Eds) Communicative competence and cognitive Abilities. UPP Baltimore. Gerard ...

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Le syndrome de Boerhaave

Le syndrome de Boerhaave

... Le syndrome de Boerhaave correspond à une rupture spontanée de l’œsophage; elle s’inscrit fort à propos dans le thème des douleurs paroxystiques médiastinales ...

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Le syndrome perroquet.

Le syndrome perroquet.

... Nous le répétons: les enjeux sont tout simplement de susciter une réflexion critique sur la manière dont la dimension spirituelle des arts martiaux japonais est véhiculée présentement [r] ...

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Le syndrome SAFARI

Le syndrome SAFARI

... 3 Un projet informatique préparé dans une certaine opacité administrative, une centralisation massive d’information y compris à caractère personnel, la mise en place de référentiels et d’identifiants uniques « pour plus ...

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Syndrome des antiphospholipides

Syndrome des antiphospholipides

... c.3. Syndrome Hemolysis, elevated liver enzymes, low platelet count (syndrome HELLP) Quatre à 12 % des pré-éclampsies se compliquent d’un syndrome HELLP définit par l’association d’une élévation des ...

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Syntaxe et métasyntaxe dans le syndrome de l'X-fragile et le syndrome de Down

Syntaxe et métasyntaxe dans le syndrome de l'X-fragile et le syndrome de Down

... Down's syndrome is the most frequent genetic abnormality (1/800 ...Down's syndrome than in X-fragile (see Rondal and Edwards, 1997 for a review of the literature; Comblain, 1996a; Piérart, 1997 and in ...

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Micro computed tomography for vascular exploration.

Micro computed tomography for vascular exploration.

... methods of assessment, such as histology with confocal or two-photon microscopy, laser Doppler, microangio- graphy, fluorescent microspheres, magnetic resonance angiography, positron emission tomography, are not always ...

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Therapeutic vascular growth in the heart

Therapeutic vascular growth in the heart

... and vascular bed-specific vascular endothelial angiogenesis-resistance mechanisms, as well as pharmacological options that reverse them, may be required before angiogenic therapies at last will assume their ...

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Le syndrome de Brugada

Le syndrome de Brugada

... d’un syndrome de Bru- gada, il faut proposer un dépistage auprès des parents, des frères, des sœurs et des enfants du sujet ...de syndrome de Bru- gada dans la famille ou une histoire de mort subite, on ...

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Le syndrome de Fregoli

Le syndrome de Fregoli

... Le syndrome de Fregoli apparu ? D’abord, en quoi est-ce qu’il consiste ? Il consiste en ceci que le sujet identifie toujours le même, le même persécuteur en lieu et place des autres auxquels il peut avoir affaire ...

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Building a global alliance in vascular surgery

Building a global alliance in vascular surgery

... EDITORIAL Building a global alliance in vascular surgery John V. White, MD, a Michael Conte, MD, b Andrew Bradbury, MD, c Philippe Kolh, MD, d Florian Dick, MD, e Robert Fitridge, MD, f Joseph Mills, MD, g ...

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Vascular endothelial growth factor (VEGF) in endometriosis.

Vascular endothelial growth factor (VEGF) in endometriosis.

... as vascular permeability factor, is a heparin-binding glycoprotein with potent angiogenic, endothel- ial cell-specific mitogenic and vascular permeability ...hyperstimulation syndrome (Abramov et ...

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Patterns and severity of vascular amyloid in Alzheimer’s disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer’s disease

Patterns and severity of vascular amyloid in Alzheimer’s disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer’s disease

... 15. Head E, Phelan MJ, Doran E, Kim RC, Poon WW, Schmidt FA, Lott IT (2017) Cerebrovascular pathology in Down syndrome and Alzheimer disease. Acta Neuropathol Commun 5:93 16. Hyman BT, Phelps CH, Beach TG, Bigio ...

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Le syndrome de Brown

Le syndrome de Brown

... Il peut observer cette diplopie dans ce regard spontanément s’il ne neutralise pas d’un œil.  Synoptophore Permet d’étudier la vision binoculaire. Il y a 3 mires différentes : -Mire de perception simultanée (PS) : ...

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