Results 91 to 100 of about 12,152 (258)

Common Presentations of Mycosis Fungoides in Pakistani Population: A Clinicopathological Study

open access: yesJournal of the Dow University of Health Sciences, 2017
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]

open access: yes, 2016
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

open access: yesVestnik Dermatologii i Venerologii, 2017
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

open access: yesIndonesian Journal of Tropical and Infectious Disease, 2017
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

A novel MBTPS2 missense variant identifying keratosis follicularis spinulosa decalvans in a case of neonatal erythroderma

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Edwin Cuperus   +7 more
wiley   +1 more source

A Case of Old Age-Onset Generalized Pustular Psoriasis with a Deficiency of IL-36RN (DITRA) Treated by Granulocyte and Monocyte Apheresis

open access: yesCase Reports in Dermatology, 2015
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]

open access: yes, 2007
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]

open access: yes, 2019
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

open access: yesPrzegląd Dermatologiczny, 2011
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

open access: yesSouth African Family Practice, 2005
No abstract available.
M.H. Motswaledi
doaj   +1 more source

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