Hypereosinofilt syndrom

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Standard

Hypereosinofilt syndrom. / Troelsen, Lone N; Boisen, Lotte W; Andersen, Ove.

I: Ugeskrift for Laeger, Bind 167, Nr. 49, 2005, s. 4663-4.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Troelsen, LN, Boisen, LW & Andersen, O 2005, 'Hypereosinofilt syndrom', Ugeskrift for Laeger, bind 167, nr. 49, s. 4663-4.

APA

Troelsen, L. N., Boisen, L. W., & Andersen, O. (2005). Hypereosinofilt syndrom. Ugeskrift for Laeger, 167(49), 4663-4.

Vancouver

Troelsen LN, Boisen LW, Andersen O. Hypereosinofilt syndrom. Ugeskrift for Laeger. 2005;167(49):4663-4.

Author

Troelsen, Lone N ; Boisen, Lotte W ; Andersen, Ove. / Hypereosinofilt syndrom. I: Ugeskrift for Laeger. 2005 ; Bind 167, Nr. 49. s. 4663-4.

Bibtex

@article{fed7f572ba4c44d2acfad3f0f307740a,
title = "Hypereosinofilt syndrom",
abstract = "In light of a case of hypereosinophilic syndrome with no revealing underlying disease, the diagnosis and treatment of idiopathic hypereosinophilic syndrome (HES) are discussed. The recent evidence that there are two variants of HES, myeloproliferative and lymphocytic, is considered.",
author = "Troelsen, {Lone N} and Boisen, {Lotte W} and Ove Andersen",
year = "2005",
language = "Dansk",
volume = "167",
pages = "4663--4",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "49",

}

RIS

TY - JOUR

T1 - Hypereosinofilt syndrom

AU - Troelsen, Lone N

AU - Boisen, Lotte W

AU - Andersen, Ove

PY - 2005

Y1 - 2005

N2 - In light of a case of hypereosinophilic syndrome with no revealing underlying disease, the diagnosis and treatment of idiopathic hypereosinophilic syndrome (HES) are discussed. The recent evidence that there are two variants of HES, myeloproliferative and lymphocytic, is considered.

AB - In light of a case of hypereosinophilic syndrome with no revealing underlying disease, the diagnosis and treatment of idiopathic hypereosinophilic syndrome (HES) are discussed. The recent evidence that there are two variants of HES, myeloproliferative and lymphocytic, is considered.

M3 - Tidsskriftartikel

VL - 167

SP - 4663

EP - 4664

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 49

ER -

ID: 48417924