Zobrazeno 1 - 10
of 53
pro vyhledávání: '"G J, Anhalt"'
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 91:2833-2838
Autoimmune polyglandular syndrome type I (APS I) is characterized by multiple endocrine gland failures, with other manifestations such as gastrointestinal (GI) symptoms.The objective of the study was to study the histopathological and immunological f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::427b218d9b9bd7a441ec70436971761e
https://doi.org/10.1210/jc.2005-2506
https://doi.org/10.1210/jc.2005-2506
Publikováno v:
British Journal of Dermatology. 144:610-613
Paraneoplastic pemphigus (PNP) is an autoimmune mucocutaneous blistering disease characterized by IgG autoantibodies that bind to various epithelia and immunoprecipitate a complex of 250, 230, 210, 190 and 170 kDa proteins. A recent study has suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee93b17c52a65a214eb2b1c375fd16cb
https://doi.org/10.1046/j.1365-2133.2001.04095.x
https://doi.org/10.1046/j.1365-2133.2001.04095.x
Autor:
C D Stone, A M Gillinov, Victor A. McKusick, K J Fleischer, Diane Alejo, Duke E. Cameron, H C Dietz, G J Anhalt, Peter S. Greene, Reed E. Pyeritz, Vincent L. Gott, John C. Laschinger
Publikováno v:
European Journal of Cardio-Thoracic Surgery. 10:149-158
The authors present the current status of surgery for the cardiovascular manifestations of the Marfan syndrome. In addition, a brief review of current Marfan genetic research is presented. Data on all Marfan patients undergoing aortic root replacemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42c27d04f2fca9c8dc28255bf10a6049
https://doi.org/10.1016/s1010-7940(96)80289-2
https://doi.org/10.1016/s1010-7940(96)80289-2
Publikováno v:
Dermatology. 190:245-250
A patient with Castleman's tumor is reported in whom painful mucosal erosions and a maculopapular eruption developed. Complete remission occurred 1 year after surgical tumor resection. The clinical, histological and immunological features were consis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793fdb5f496521173fb35454d6a224e2
https://doi.org/10.1159/000246701
https://doi.org/10.1159/000246701
Publikováno v:
The Journal of Immunology. 151:5742-5750
Bullous pemphigoid (BP) and herpes gestationis (HG) are skin diseases characterized by subepidermal blisters and autoantibodies against two hemidesmosomal Ag, i.e., BP230 and BP180. Based on sequence analysis the BP180 Ag was predicted to be a transm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4c6bd1b711ad7fe96c32fa7034f7aa1
https://doi.org/10.4049/jimmunol.151.10.5742
https://doi.org/10.4049/jimmunol.151.10.5742
Publikováno v:
Cutis. 67(3)
Pemphigus foliaceus is a cutaneous autoimmune blistering disease that is characterized by lower morbidity and mortality than those observed in pemphigus vulgaris or paraneoplastic pemphigus. However, erythrodermic forms of the endemic variant of pemp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::deab9ec7763fe02770e5a9d207cfb151
https://pubmed.ncbi.nlm.nih.gov/11270302
https://pubmed.ncbi.nlm.nih.gov/11270302
Autor:
G J, Anhalt, L A, Diaz
Publikováno v:
JAMA. 285(5)
Pemphigus is an autoimmune disorder, known to be caused by autoantibodies directed against critical adhesion molecules of squamous epithelial cells, the desmogleins. These autoantibodies induce blistering of skin and mucosal surfaces and lead to seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc4af72162a407f7570031286b9944f7
https://pubmed.ncbi.nlm.nih.gov/11176877
https://pubmed.ncbi.nlm.nih.gov/11176877
Autor:
A. Shibaki, P. Di Meglio, C. Hundhausen, S. Turner, R. Moriuchi, B. Büchele, S. Kase, C. Smith, R. Kastelein, T. Yayoi, V. Kalia, T. Simmet, S. Pflanz, H. Shimizu, J. Mumm, Y. Tateishi, M. Akiyama, S. Shibata, O. Lunov, D. Hoshina, S. Beissert, H. Ujiie, P. Bourne, N. Yoshioka, T. McClanahan, K. Masahiro, K. Scharffetter-Kochanek, T. Syrovets, F. O. Nestle, U. Laggner, M. Kubo, K. Masaru, N. Yu, H. Nakamura, A. Yoshimura, Y. Fujita, D. Mimouni, D. Cua, D. Sawamura, K. Hiromichi, Q. Li, T. Kunihiko, S. Hidehisa, W. Nishie, M. Tomomitsu, N. Kiyoko, G. J. Anhalt, G. Perera, N. Kitaichi, G. Wang, N. Solomons, R. Abe, E. Murphy, S. Suzuki, A. C. Hayday, H. Qiao, W. Shinichi, S. Shinichi, A. Rankin, H. Wang, M. Ozaki, A. J. Kanwar, A. Uto-Konomi, R. Pierce, K. Naoko
Publikováno v:
International Immunology. 22:iii67-iii68
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a6e98abcd8c839cc12d0eba2935883
https://doi.org/10.1093/intimm/dxq403
https://doi.org/10.1093/intimm/dxq403
Publikováno v:
The British journal of dermatology. 138(4)
We describe a 19-year-old female patient who developed recurrent ulcerations limited to the orogenital mucosa for the last 3 years. She also developed dyspnoea 5 months after the onset of the orogenital lesions. Castleman's tumour of the retroperiton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb7ae83df10ad70698be136c66d0b809
https://pubmed.ncbi.nlm.nih.gov/9640377
https://pubmed.ncbi.nlm.nih.gov/9640377
Publikováno v:
The British journal of dermatology. 137(6)
Cicatricial pemphigoid is an autoimmune disease predominantly of elderly patients. Recently, a subtype of cicatricial pemphigoid with antibodies to epiligrin (laminin 5) was described. We report a patient in whom anti-epiligrin cicatricial pemphigoid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0123a311157e94d3e0dcaf784f7314e
https://pubmed.ncbi.nlm.nih.gov/9470922
https://pubmed.ncbi.nlm.nih.gov/9470922