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pro vyhledávání: '"Nils T, Milman"'
Autor:
Biplab K. Saha, Nils T. Milman
Publikováno v:
Prague Medical Report, Vol 123, Iss 2, Pp 65-81 (2022)
Idiopathic pulmonary hemosiderosis (IPH) is a rare cause of diffuse alveolar hemorrhage (DAH). Glucocorticosteroids (CS) represent the first line therapy for IPH. Although most patients respond to CS, steroid refractoriness is seen in an appreciable
Externí odkaz:
https://doaj.org/article/904628de702d4094aa11030552581317
Autor:
Biplab K. Saha, Nils T. Milman
Publikováno v:
Prague Medical Report, Vol 122, Iss 4, Pp 257-268 (2021)
This paper briefly reviews the safety and efficacy of liposteroid in different inflammatory and non-inflammatory diseases. Corticosteroids (CS) are the first-line therapy in many inflammatory and autoimmune disorders. Although highly efficacious, lon
Externí odkaz:
https://doaj.org/article/030ec8693014424983dbae259fb32ef9
Publikováno v:
Clinical Rheumatology. 41:977-990
Publikováno v:
Clinical Rheumatology. 41:325-336
This narrative review provides an overview of diffuse alveolar hemorrhage (DAH) associated with rheumatologic and autoimmune diseases and their differentiation from idiopathic pulmonary hemosiderosis (IPH). Relevant immunologic diseases associated wi
Publikováno v:
Cureus. 14(4)
While autoimmune antibodies or autoantibodies have been reported sporadically in adult patients with idiopathic pulmonary hemosiderosis (IPH), their true prevalence is unknown. The question as to whether any difference exists between antibody-positiv
Publikováno v:
Cureus.
Idiopathic pulmonary hemosiderosis (IPH) causes diffuse alveolar hemorrhage (DAH) by a yet unknown mechanism. The coexistence of IPH and celiac disease (CD), also known as Lane-Hamilton syndrome (LHS), has been reported in both pediatric and adult pa
Publikováno v:
Clinical rheumatology. 41(4)
Idiopathic pulmonary hemosiderosis (IPH) is a rare disease of unknown etiology. Due to the frequent findings of autoimmune antibodies - autoantibodies, immunologic causation of the diffuse alveolar hemorrhage in IPH has been proposed, to assess the p
Autor:
Nils T, Milman, Frank V, Schiødt, Anders E, Junker, Karin, Magnussen, Torben, Nathan, Thomas Damgaard, Sandahl
Publikováno v:
Ugeskrift for laeger. 180(51)
HFE-haemochromatosis is the most frequent genetic disposition for iron overload in ethnic Danes: 20,000 persons are homozygous for the C282Y mutation. The disorder has a long preclinical phase with increasing body iron overload, and 30% of males will