Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Pierre Y. Venencie"'
Publikováno v:
Journal of the American Academy of Dermatology. 32(4)
nocarcinomas and are characterized by a high metastatic potential, especially to bones, liver, and lungs.1o Dissemination occurs via three mechanisms: (1) local, (2) lymphatic, and (3) hematogenous,13 often via the vertebral venous system. The route
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::594cdbdba5be0e7f22e74e278be2f4bf
https://pubmed.ncbi.nlm.nih.gov/7896960
https://pubmed.ncbi.nlm.nih.gov/7896960
Autor:
Michele Hadchouel, Didier Armengaud, Annick Vieillefond, Christine Foldes, Pierre Y. Venencie, Laure Coulombel
Publikováno v:
Pediatric Dermatology. 5:173-177
Ichthyosis and neutral lipid storage disease (INLSD) is a nonlyso-somal. multisystemic. triglyceride storage disorder. It is characterized by non-bullous congenital ichthyosiform erythroderma (NBCIE), leukocyte vacuoles, and variable involvement of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67d4197e29ea881b0f664791f5a57c59
https://doi.org/10.1111/j.1525-1470.1988.tb01165.x
https://doi.org/10.1111/j.1525-1470.1988.tb01165.x
Autor:
Richard K. Winkelmann, Stephen J. Friedman, Robert A. Kyle, Pierre Y. Venencie, Antoine Puissant
Publikováno v:
Journal of the American Academy of Dermatology. 11:576-579
Of four patients with mycosis fungoides and monoclonal gammopathy, one died of multiple myelorna that developed 4 years after the mycosis fungoides. The other three had monoclonal gammopathy of undetermined significance. This association does not app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e87f96d2cf79523463a7cfecf2218b2
https://doi.org/10.1016/s0190-9622(84)70208-8
https://doi.org/10.1016/s0190-9622(84)70208-8
Autor:
Françoise Valensi, Marie F. D'Agay, Olivier Verola, Philippe Le Bras, Gérard Turpin, Françoise Danon, Yves Kerneis, Antoine Puissant, Pierre Y. Venencie, Christine Marchat
Publikováno v:
Cancer. 59:588-592
Necrobiotic xanthogranuloma is a newly recognized cutaneous manifestation associated with paraproteinemia. Necrobiotic xanthogranuloma is distinctive clinically by yellowish-red nodular lesions, often ulcerated, with predilection for the periorbital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9040a1aca18dd84b0d32eb6110417d7c
https://doi.org/10.1002/1097-0142(19870201)59:3<588::aid-cncr2820590339>3.0.co
https://doi.org/10.1002/1097-0142(19870201)59:3<588::aid-cncr2820590339>3.0.co
Publikováno v:
Archives of Dermatology. 120:1032-1039
• In 16 patients with anetoderma, a clinicohistologic entity related to a local dermal defect of elastic tissue, old lesions did not heal, and new lesions often continued to form for many years, despite various forms of treatment. Systemic lupus er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61ddd16a0390ac78c24980cece066540
https://doi.org/10.1001/archderm.120.8.1032
https://doi.org/10.1001/archderm.120.8.1032
Autor:
Charles H. Dicken, Pierre Y. Venencie
Publikováno v:
Journal of the American Academy of Dermatology. 10:187-192
Five patients with the yellow nail syndrome triad are described; all five had yellow nails, primary lymphedema, and respiratory tract involvement. Four of the patients noted the onset of the syndrome after an episode of pneumonia. Four patients had a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f507bacdd294faa45469638abed06db
https://doi.org/10.1016/s0190-9622(84)70021-1
https://doi.org/10.1016/s0190-9622(84)70021-1
Publikováno v:
Archives of dermatology. 120(5)
• Three patients with Sezary syndrome had monoclonal gammopathy: two had gammopathy of unknown significance and one had myeloma. The frequency of the association of Sezary syndrome and monoclonal gammopathy seems to be lower than previously suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::501bf04c8df09a676dc2cf438aa1d2d4
https://pubmed.ncbi.nlm.nih.gov/6426406
https://pubmed.ncbi.nlm.nih.gov/6426406
Autor:
Ismaïl Benkaïdali, Bernard Pillet, Jacques Frija, Pierre D. Delmas, Pierre Y. Venencie, Olivier Verola, Antoine Puissant, Georges A. Boffa
Publikováno v:
Archives of dermatology. 124(12)
• We evaluated a patient in whom pachydermoperiostosis occurred in conjunction with anemia and gastric hypertrophy. The mechanism of the anemia appears multifactorial because, besides a myelofibrosis, a serum inhibitor of the late stage of erythrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72b95b3ba5051ad09d8f790a15332130
https://pubmed.ncbi.nlm.nih.gov/3263841
https://pubmed.ncbi.nlm.nih.gov/3263841
Publikováno v:
Journal of the American Academy of Dermatology. 11(1)
A review of thirty-three cases of scleredema, with particular reference to clinical and histologic findings, revealed that the disease was often of insidious onset and the course was usually prolonged. A preceding respiratory tract infection was unco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dd58d5ffe37286a503bf4c27420622a
https://pubmed.ncbi.nlm.nih.gov/6736348
https://pubmed.ncbi.nlm.nih.gov/6736348
Autor:
Kristin M. Leiferman, Gerald J. Gleich, Heidi S. Haugen, Hugh A. Sampson, Steven J. Ackerman, Pierre Y. Venencie
Publikováno v:
The New England journal of medicine. 313(5)
Although blood eosinophilia is commonly present in atopic dermatitis, accumulation of tissue eosinophils is not prominent. To determine whether eosinophil degranulation occurs in lesions of atopic dermatitis, we analyzed tissues by immunofluorescence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08eb0d2735c1b9cea90bd48617416cea
https://pubmed.ncbi.nlm.nih.gov/3892296
https://pubmed.ncbi.nlm.nih.gov/3892296