منابع مشابه
, Didier RENARD
One of the main challenges of geostatistics in reservoir characterization is to populate a portion of 3-D earth model with its petrophysical properties. This operation must be carried out while still honoring the information available along well logs: in our jargon, we say that it must be conditional. No restriction is required on this conditioning information, either in number or in its geomet...
متن کاملDidier Astruc.
Didier Astruc’s group in Bordeaux is working on the interplay between metallodendrimers and t r a n s i t i o n m e t a l nanopar t ic les . The starting point is hard-core transition-metal inorganic and organometallic chemistry, electron-transfer processes and molecular electronics. Applications of this basic research range, in his group, from molecular nanobatteries and catalysis inside nanor...
متن کاملDidier Fassin & Richard Rechtman :
Didier Fassin & Richard Rechtman: The Empire of Trauma is published by Princeton University Press and copyrighted, © 2009, by Princeton University Press. All rights reserved. No part of this book may be reproduced in any form by any electronic or mechanical means (including photocopying, recording, or information storage and retrieval) without permission in writing from the publisher, except fo...
متن کامل[Weill-Marchesani's syndrome: familial involvement].
CASE REPORT We report the case of a child short in stature with brachydactyly and brachymorphy who was referred to our office complaining of poor vision. This was a case of Weill-Marchesani's syndrome described in a family, in which four of the eight children were affected by spherophakia, brachymorphy and brachydactyly. DISCUSSION There are few familial cases of Weill-Marchesani's syndrome r...
متن کامل[Weill-Marchesani syndrome].
Weill-Marchesani syndrome is a rare systemic connective tissue disease characterized by short stature, brachydactyly, ectopia lentis and spherophakia. This was first reported by Weill in 1932 and subsequently well characterized by Marchesani in 1939(1). Genetically this syndrome often shows autosomal recessive inheritance. Frequent consanguinity between parents support this model. There have be...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Trivium: Estudos Interdisciplinares
سال: 2019
ISSN: 2176-4891
DOI: 10.18379/2176-4891.2019v1p.3