Results 161 to 170 of about 7,879 (209)

A Storm of Polyserositis: Unravelling Multisystem Effusions in Hypereosinophilic Syndrome. [PDF]

Cureus
Fadel A, Ahmed Y.
europepmc   +1 more source

Hypereosinophilic syndrome: Case report

The Turkish Journal of Gastroenterology, 2002
Özlem YÖRÜK, Nilüfer BULUT, Rana ÇERİKÇİ, İ. Safa YILDIRIM   +3 more
doaj  

Expansion of multiple CD4⁺ T-cell lineages in lymphocytic variant hypereosinophilic syndrome. [PDF]

J Allergy Clin Immunol
Anderson CF, Makiya M, Xiong K, Penrod L, Wetzler L, Ware J, Constantine GM, Khoury P, Klion AD.   +8 more
europepmc   +1 more source

Steroid-sparing benefits of biologic use in hypereosinophilic syndrome and substantial disease burden across subtypes. [PDF]

Front Allergy
Hwee J, Huynh L, da Costa W, Rothenberg ME, Duh MS, Alfonso-Cristancho R.   +5 more
europepmc   +1 more source

Hypereosinophilic syndrome in children

Leukemia Research, 2012
Recently, according to the Hypereosinophilic Diseases Working Group of the International Eosinophil Society, six variants of hypereosinophilic syndrome have been proposed, i.e. (1) myeloproliferative, (2) lymphoproliferative, (3) idiopathic/undefined, (4) overlapping, (5) associated and (6) familial variant.
M De Hoog, R R De Krijger, H B Beverloo   +2 more
exaly   +4 more sources

The Hypereosinophilic Syndrome Revisited

Annual Review of Medicine, 2003
Clinical and biological features of patients with the idiopathic hypereosinophilic syndrome (HES) are heterogeneous. Recent evidence suggests at least two distinct underlying hematological disorders involving myeloid and lymphoid cells, respectively. We therefore suggest that the term idiopathic should be abandoned in the classification of HES.
Roufosse, Florence, Cogan, Elie, Goldman, Michel   +2 more
openaire   +4 more sources

Polyneuropathy in hypereosinophilic syndrome

Neurology, 1988
We investigated two patients with the idiopathic hypereosinophilic syndrome and peripheral neuropathy. Clinical, EMG, and pathological findings were consistent with axonal polyneuropathy. Morphologic changes of the nerve biopsies suggested axonal damage secondary to increased endoneurial pressure from leakage of capillaries.
Monaco S., Lucci B., Laperchia N., Tezzon F., Curro-Dossi B., Nardelli E., Giannini C., Rizzuto N.   +7 more
openaire   +3 more sources

Management of Hypereosinophilic Syndromes

Immunology and Allergy Clinics of North America, 2015
The symptomatic hypereosinophilic patient must be approached in a stepwise manner, with thorough assessment to determine whether the hypereosinophilia itself is contributing to damage and disease manifestations (thereby defining a hypereosinophilic syndrome), and to identify an eventual cause of hypereosinophilia, followed by initiation of treatment ...
Roufosse, Florence
openaire   +4 more sources

Treatment of Patients with the Hypereosinophilic Syndrome with Mepolizumab

New England Journal of Medicine, 2008
BACKGROUND: The hypereosinophilic syndrome is a group of diseases characterized by persistent blood eosinophilia, defined as more than 1500 cells per microliter with end-organ involvement and no recognized secondary cause.
Marc E Rothenberg, Amy D Klion, Jean-Emmanuel Kahn   +2 more
exaly   +4 more sources

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Hypereosinophilic syndrome

Allergy and Asthma Proceedings, 2017
Hypereosinophilic syndrome (HES) is a myeloproliferative disorder characterized by persistent eosinophilia associated with multiple organ damage.To increase awareness of the rare but potentially life-threatening disease and to provide a brief overview of the clinical presentation, diagnosis, and management of HES.Pertinent data from the patient's ...
Heung R, Noh, Gil G, Magpantay
openaire   +2 more sources