Neonatal erythroderma: differential diagnosis and management of the "red baby"
- 1 August 1998
- journal article
- review article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 79 (2) , 186-191
- https://doi.org/10.1136/adc.79.2.186
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- ErythrodermaJournal of the American Academy of Dermatology, 1996
- Severe Congenital Generalized Exfoliative Erythroderma in Newborns and Infants: A Possible Sign of Netherton SyndromePediatric Dermatology, 1996
- Inherited Ichthyoses: A Review of the Histology of the SkinPediatric Pathology & Laboratory Medicine, 1996
- Intact survival with transfusion-associated graft-versus-host disease proved by human leukocyte antigen typing of lymphocytes in skin biopsy specimensThe Journal of Pediatrics, 1995
- In utero acute graft-versus-host disease in a neonate with severe combined immunodeficiencyJournal of the American Academy of Dermatology, 1993
- Omenn's syndrome and related combined immunodeficiency syndromes: Diagnostic considerations in infants with persistent erythroderma and failure to thriveJournal of the American Academy of Dermatology, 1991
- Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).Journal of Clinical Investigation, 1991
- Photochemotherapy of Dominant, Diffuse, Cutaneous MastocytosisPediatric Dermatology, 1990
- Phenotypic variation in biotinidase deficiencyThe Journal of Pediatrics, 1983
- Congenital cutaneous candidiasisJournal of the American Academy of Dermatology, 1982