Zobrazeno 1 - 10
of 22
pro vyhledávání: '"W. R. Heymann"'
Autor:
W R, Heymann
Publikováno v:
Journal of the American Academy of Dermatology. 36:611-615
Acquired angioedema (AAE) is a rare disorder that has been categorized into two forms, AAE-I and AAE-II. AAE-I is associated with other diseases, most commonly B-cell lymphoproliferative disorders. AAE-II is defined by the presence of an autoantibody
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aede647e45473265e71d2ac1155c967f
https://doi.org/10.1016/s0190-9622(97)70250-0
https://doi.org/10.1016/s0190-9622(97)70250-0
Autor:
R E, Schnur, W R, Heymann
Publikováno v:
Seminars in Cutaneous Medicine and Surgery. 16:72-80
Disorders that are characterized by a reticulate pattern of pigmentation are reviewed. Dyskeratosis congenita (DKC) is the prototype of these. In addition to reticulate hyperpigmentation, mucosal leukoplakia, bone marrow dysfunction, cytogenetic inst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da6f32bedb2afb7234fa4d755987e893
https://doi.org/10.1016/s1085-5629(97)80038-7
https://doi.org/10.1016/s1085-5629(97)80038-7
Autor:
W R, Heymann
Publikováno v:
Clinics in Dermatology. 14:279-282
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ccfd1c300be3dd7c2915503ef35d10c
https://doi.org/10.1016/0738-081x(96)00012-0
https://doi.org/10.1016/0738-081x(96)00012-0
Autor:
K W, Boucher, W R, Heymann
Publikováno v:
Archives of dermatology. 137(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e7dae72a02c43cdb3645e9d3a8544bf
https://pubmed.ncbi.nlm.nih.gov/11295934
https://pubmed.ncbi.nlm.nih.gov/11295934
Autor:
W R, Heymann
Publikováno v:
Cutis. 66(2)
A case of a diltiazem-induced morbilliform drug eruption, which spared the circumferential margin of seborrheic keratoses, is presented. Hypotheses regarding the pathogenesis of this novel exanthem are discussed. The potential mechanisms may be immun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7cdeda05bdce9cb8c18fb608f8404ff9
https://pubmed.ncbi.nlm.nih.gov/10955194
https://pubmed.ncbi.nlm.nih.gov/10955194
Autor:
W R, Heymann
Publikováno v:
Cutis. 66(1)
Black hairy tongue is characterized by an abnormal coating of the dorsal surface of the tongue. Although the cause is unknown, several precipitating factors may be implicated in the pathogenesis of this disorder. A case is presented in which black ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7999170f93be390d9009034e4191db9
https://pubmed.ncbi.nlm.nih.gov/10916687
https://pubmed.ncbi.nlm.nih.gov/10916687
Publikováno v:
Cutis. 65(4)
Dyshidrotic eczema is a chronic, enigmatic condition that usually affects the hands and feet. Modern-technique radiation therapy using megavoltage equipment for the treatment of dyshidrotic eczema has not been described in the literature before. A dr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::91d1fc4caba00b73d3c8efd55a4768eb
https://pubmed.ncbi.nlm.nih.gov/10795080
https://pubmed.ncbi.nlm.nih.gov/10795080
Autor:
R M, Levin, W R, Heymann
Publikováno v:
International journal of dermatology. 38(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::44d40963032c9297dd654fa389ab46c4
https://pubmed.ncbi.nlm.nih.gov/10192166
https://pubmed.ncbi.nlm.nih.gov/10192166
Autor:
W R, Heymann
Publikováno v:
Cutis. 61(1)
Hereditary papulotranslucent acrokeratoderma (HPA) is a rare autosomal dominant genodermatosis, characterized by persistent, asymptomatic, yellow-white translucent papules and plaques of the hands and feet. A case of HPA is presented and the literatu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f259723335e79e4d636fedc319fdf59
https://pubmed.ncbi.nlm.nih.gov/9640547
https://pubmed.ncbi.nlm.nih.gov/9640547
Publikováno v:
American journal of medical genetics. 72(1)
The "CHIME" syndrome (MIM#280000) is a rare neuroectodermal disorder comprised of Colobomas of the eye, Heart defects, Ichthyosiform dermatosis, Mental retardation, and Ear defects. We report on the sixth child with this syndrome and the first of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b6cacee2aaf9fe5234772f348fbef5e8
https://pubmed.ncbi.nlm.nih.gov/9295069
https://pubmed.ncbi.nlm.nih.gov/9295069