- ►bmj.com [PDF] JA Sivak-Callcott, WK Lim, LL Seah, J … - British Medical Journal, 2005 - bjo.bmj.com Bevacizumab suppresses choroidal neovascularisation caused by pathological
myopia Bevacizumab (Avastin, Genentech) is a recombinant humanised, full length,
anti- VEGF monoclonal antibody that binds all isoforms of VEGF-A. It has ... Cited by 2 - Related articles - All 8 versions
SL Moschella - Journal of dermatology, 1996 - cat.inist.fr AN UPDATE OF THE BENIGN PROLIFERATIVE MONOCYTE-MACROPHAGE AND DENDRITIC
CELL DISORDERS. SL MOSCHELLA Journal of dermatology 23:1111 ... Cited by 3 - Related articles - BL Direct - All 2 versions
- ►birjournals.org AS Alexander, R Turner, L Uniate, RG Pearcy - British Journal of Radiology, 2005 - ingentaconnect.com This case report describes the neuro-opthalmologic and respiratory
manifestations of xanthoma disseminatum, a rare histiocytosis syndrome
characterized by disseminated lesions in a young male adult. Multimodality ... Cited by 4 - Related articles - All 4 versions
S Khandpur, Y Manchanda, VK Sharma, MK … - Australasian Journal of Dermatology, 2003 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 4 - Related articles - BL Direct - All 5 versions
D Früh, W Jaeger, O Käfer - Modern problems in ophthalmology, 1975 - ncbi.nlm.nih.gov 1: Mod Probl Ophthalmol. 1975;14:651-6. Orbital involvement in retroperitoneal
fibrosis (morbus Ormond). Früh D, Jaeger W, Käfer O. ... Cited by 5 - Related articles
PJ Barnes, A Foyle, KA Hache, RG Langley, S … - Breast Journal, 2005 - interscience.wiley.com Abstract: Erdheim-Chester disease (ECD) is a rare xanthomatous non-Langerhans
cell histiocytosis which involves the marrow space of the long bones.
Extraosseous sites most commonly affected include the eyes, lungs, ... Cited by 5 - Related articles - BL Direct - All 4 versions
BC Dickson, V Pethe, CTS Chung, DJC Howarth … - Virchows Archiv, 2008 - Springer Abstract Erdheim–Chester disease is a rare xanthomatosis that may present with
characteristic radiologic and histologic features. There have been conflicting
reports regarding the nature of this process, including whether it ... Cited by 6 - Related articles - BL Direct - All 2 versions
K Kovacs, JM Bilbao, VL Fornasier, E Horvath - Endocrine Pathology, 2004 - Springer Abstract Pituitary morphologic changes in patients with Erdheim–Chester
disease have not been described in detail. We report here the histologic and
immunohistochemical findings in the autopsy obtained pituitary of a ... Cited by 5 - Related articles - BL Direct - All 3 versions
A Çurgunlu, Y Karter, A Öztürk - European Journal of Internal Medicine, 2003 - Elsevier Erdheim–Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis. It
is characterized by osteosclerosis of the metaphyseal regions of long bones and
several extraskeletal manifestations. Clinically, it ranges from an ... Cited by 6 - Related articles - All 6 versions
CJ Yeo - Journal of Gastrointestinal Surgery, 2005 - Springer The role of the surgeon in the management of patients with autoimmune sclerosing
pancreatitis (ASP) is controversial and in evolution. 1–17 On the one extreme
are those who believe that surgical inter- vention or resection for this ... Cited by 6 - Related articles - All 3 versions
