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1980 1
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Page 1
Infectious eczematoid dermatitis: a comprehensive review.
Yamany T, Schwartz RA. Yamany T, et al. J Eur Acad Dermatol Venereol. 2015 Feb;29(2):203-208. doi: 10.1111/jdv.12715. Epub 2014 Sep 11. J Eur Acad Dermatol Venereol. 2015. PMID: 25209074 Review.
Other eczematous rashes, including autoeczemitization and contact dermatitis, should be on the differential diagnosis list. The treatment centres on topical antibiotics and soaks. Prognosis has improved since the advent of antibiotics. However, cases with multiple relapses …
Other eczematous rashes, including autoeczemitization and contact dermatitis, should be on the differential diagnosis list. The treatment ce …
Risk factors in wheezing infants.
Karaman O, Uguz A, Uzuner N. Karaman O, et al. Pediatr Int. 1999 Apr;41(2):147-50. doi: 10.1046/j.1442-200x.1999.4121046.x. Pediatr Int. 1999. PMID: 10221017
Effect of "aminopterin" on epithelial tissues.
Gubner R. Gubner R. Arch Dermatol. 1983 Jun;119(6):513-24. Arch Dermatol. 1983. PMID: 6859892
Treatment was interrupted in most patients after an initial course of 14 to 28 mg. because of the regular occurrence of shallow ulceration of the buccal mucosa and frequent development of abdominal cramps. Remissions persisted for periods ranging from two weeks to several …
Treatment was interrupted in most patients after an initial course of 14 to 28 mg. because of the regular occurrence of shallow ulcer …
Hematopoietic stem cell transplantation from a donor with Klinefelter syndrome for Wiskott-Aldrich syndrome.
Balci YI, Turul T, Daar G, Anak S, Devecioglu O, Tezcan I, Cetinkaya DU. Balci YI, et al. Pediatr Transplant. 2008 Aug;12(5):597-9. doi: 10.1111/j.1399-3046.2008.00908.x. Epub 2008 Mar 10. Pediatr Transplant. 2008. PMID: 18331539
WAS is a rare X-linked recessive disorder characterized by primary progressive T cell immunodeficiency, impaired antipolysaccharide antibody response, thrombocytopenia with small platelet, and eczematoid dermatitis. Untreated patients with typical WAS have poor prognosis w …
WAS is a rare X-linked recessive disorder characterized by primary progressive T cell immunodeficiency, impaired antipolysaccharide antibody …