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Fabry's Disease

Archives of Ophthalmology, 1965
Introduction Our knowledge of Fabry's disease, long made up of smatterings, has recently blossomed. Just prior to the onset of the 20th century Fabry described a 13-year-old German boy with a peculiar skin eruption characterized by small, dark purple lesions, which, though heavily concentrated in the area of the thighs and genitalia, were lightly ...
G L, Spaeth, P, Frost
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Fabry disease

Neurology, 1982
Previous reports of extensive lipid accumulation within neurons of the autonomic nervous system in Fabry disease suggest an anatomicopathologic basis for the peculiar pain, diminished sweating, and gastrointestinal symptoms experienced in this disorder.
W J, Cable, E H, Kolodny, R D, Adams
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Anderson-Fabry disease*

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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Fabry's disease

The Lancet, 2011
Gomathy, Sethuraman   +3 more
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Fabry disease [Malattia di Fabry]

2006
[No abstract available]
D. Innocenzi   +5 more
openaire   +1 more source

A tunable Fabry–Pérot quantum Hall interferometer in graphene

Nature Nanotechnology, 2021
Corentin Déprez   +2 more
exaly  

Aharonov–Bohm effect in graphene-based Fabry–Pérot quantum Hall interferometers

Nature Nanotechnology, 2021
Yuval Ronen   +2 more
exaly  

Electrically driven random lasing from a modified Fabry–Pérot laser diode

Nature Photonics, 2022
Antonio Consoli   +2 more
exaly  

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