Results 271 to 280 of about 9,399,207 (308)
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British Journal of Dermatology, 2006
SUMMARY Electron microscopy of clinically uninvolved skin taken from a 12-month-old male child with biochemically proven angiokeratoma corporis diffusum showed characteristic lamellar lipid deposits within endothclial and perithelial cells of dermal blood vessels. Ultrastructural examination of skin may aid the early identification of males affected
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SUMMARY Electron microscopy of clinically uninvolved skin taken from a 12-month-old male child with biochemically proven angiokeratoma corporis diffusum showed characteristic lamellar lipid deposits within endothclial and perithelial cells of dermal blood vessels. Ultrastructural examination of skin may aid the early identification of males affected
openaire +2 more sources
Predictors of Clinical Evolution in Prehypertrophic Fabry Disease
Circulation Cardiovascular Imaging, 2019Background: In prehypertrophic Fabry disease, low myocardial T1 values, reflecting sphingolipid storage, are associated with early structural and ECG changes.
A. Camporeale +15 more
semanticscholar +1 more source
Radiology, 2019
Background Cardiac involvement is the leading cause of mortality in patients with Fabry disease. Identification of imaging findings that predict adverse cardiac events is needed to enable identification of high-risk patients.
Kate Hanneman +5 more
semanticscholar +1 more source
Background Cardiac involvement is the leading cause of mortality in patients with Fabry disease. Identification of imaging findings that predict adverse cardiac events is needed to enable identification of high-risk patients.
Kate Hanneman +5 more
semanticscholar +1 more source
1995
Fabry’s disease (FD) is an X-linked recessive disorder. The onset of clinical symptoms usually occurs during childhood or adolescence, but may be as late as the third or fourth decade. Early manifestations consist of episodic pain in the extremities and a teleangiectatic scaly maculopapular rash called angiokeratoma corporis diffusum.
Marjo S. van der Knaap, Jacob Valk
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Fabry’s disease (FD) is an X-linked recessive disorder. The onset of clinical symptoms usually occurs during childhood or adolescence, but may be as late as the third or fourth decade. Early manifestations consist of episodic pain in the extremities and a teleangiectatic scaly maculopapular rash called angiokeratoma corporis diffusum.
Marjo S. van der Knaap, Jacob Valk
openaire +1 more source
[Expert consensus for diagnosis and treatment of Fabry disease in China (2021)].
Zhonghua nei ke za zhi, 2021semanticscholar +1 more source
Fabry disease [Malattia di Fabry]
2006[No abstract available]
D. Innocenzi +5 more
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A tunable Fabry–Pérot quantum Hall interferometer in graphene
Nature Nanotechnology, 2021Corentin Déprez +2 more
exaly
Aharonov–Bohm effect in graphene-based Fabry–Pérot quantum Hall interferometers
Nature Nanotechnology, 2021Yuval Ronen +2 more
exaly
Video-rate hyperspectral camera based on a CMOS-compatible random array of Fabry–Pérot filters
Nature Photonics, 2023Motoki Yako, Takayuki Kiyohara
exaly