Results 91 to 100 of about 12,152 (258)
Common Presentations of Mycosis Fungoides in Pakistani Population: A Clinicopathological Study
Objective: To study the different clinical, pathological and immunophenotypic features in patients of Mycosis fungoides presenting to Civil Hospital Karachi.
Humaira Talat +4 more
doaj +1 more source
Calpain 12 function revealed through the study of an atypical case of autosomal recessive congenital ichthyosis [PDF]
Congenital erythroderma is a rare and often life-threatening condition, which has been shown to result from mutations in several genes encoding important components of the epidermal differentiation program.
Adase, Christopher A +28 more
core +2 more sources
Early onset of mycosis fungoides. Case from practice
Clinical and morphological heterogeneity of malignant lymphoproliferative lesions of the skin is explained by the peculiarities of their pathogenesis and organization of the lymphoid tissue in the skin.
D. V. Zaslavsky +6 more
doaj +1 more source
SEZARY SYNDROME MIMICKING GENERALIZED PSORIASIS VULGARIS
Sezary syndrome is the leukemic variant of cutaneous T cell lymphoma. This disease is characterized by some reddish patches or plaques all over the skin which extends to the whole body into erythroderma, lymphadenopathy.
Eko Rianova Lynoora, Rahmadewi Rahmadewi
doaj +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Edwin Cuperus +7 more
wiley +1 more source
A 78-year-old woman who had been suffering from psoriasis vulgaris for 31 years was admitted to hospital because of her erythroderma. A toxic eruption was suspected and she was treated with prednisolone 30 mg daily.
Chiharu Tominaga +3 more
doaj +1 more source
Hiperqueratose epidermolítica em gêmeas monozigóticas: relato de caso e revisão de literatura. [PDF]
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Sens, Mariana Mazzochi
core
Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan [PDF]
Background Autosomal recessive congenital ichthyosis (ARCI) is a genetically and phenotypically heterogeneous skin disease, associated with defects in the skin permeability barrier. Several but not all genes with underlying mutations have been identified,
Ahmad, Jamil +16 more
core +4 more sources
Erytrodermia łuszczycowa po ogólnym zastosowaniu kortykosteroidów – opis przypadku
Introduction. Erythroderma (exfoliative dermatitis) is an acute, generalizedinflammation of the skin, which affects at least 90% of its surface.It is a life threatening illness in the course of which various types anddegrees of scaling and itching are ...
Joanna Maj +3 more
doaj
Review of common cutaneous adverse drug reactions
No abstract available.
M.H. Motswaledi
doaj +1 more source

