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LHF [2 records]

Filter results by subject field Alphabetical list of terms

Filter results by subject field

Alphabetical list of terms

Record 1 2022-09-28

English

Subject field(s)
  • National Bodies and Committees (Canadian)
  • Indigenous Peoples (General)
OBS

The Legacy of Hope Foundation (LHF) is a national, Indigenous-led, charitable organization that has been working to promote healing and reconciliation in Canada for more than 19 years. The LHF's goal is to educate and raise awareness about the history and existing intergenerational impacts of the Residential School System (RSS) and subsequent Sixties Scoop (SS) on Indigenous (First Nations, Inuit, and Métis) survivors, their descendants, and their communities to promote healing and reconciliation.

French

Domaine(s)
  • Organismes et comités nationaux canadiens
  • Peuples Autochtones (Généralités)
OBS

La Fondation autochtone de l'espoir (FAE) est un organisme de bienfaisance national dirigé par des Autochtones qui œuvre à la promotion de la guérison et de la réconciliation au Canada depuis plus de 19 ans. L'objectif de la FAE est d'éduquer et de sensibiliser à l'histoire et aux impacts intergénérationnels existants du Système des pensionnats indiens et de la Rafle des années 60 […] sur les survivants autochtones (Premières Nations, Inuits et métis), leurs descendants et leurs communautés pour promouvoir la guérison et la réconciliation.

Spanish

Save record 1

Record 2 2009-09-25

English

Subject field(s)
  • Human Diseases - Various
  • Blood
CONT

Primary hemophagocytic lymphohistiocytosis [HLH] ... is a heterogeneous autosomal recessive disorder found to be more prevalent with parental consanguinity. [Like secondary hemophagocytic lymphohistiocytosis, it is] characterized by the overwhelming activation of normal T lymphocytes and macrophages, invariably leading to clinical and hematologic alterations and death in the absence of treatment.

French

Domaine(s)
  • Maladies humaines diverses
  • Sang
CONT

Lymphohistiocytose hémophagocytaire familiale. Cette affection autosomique récessive touche un enfant sur 50 000. Elle se traduit par l'apparition, chez de très jeunes enfants, d'une fièvre associée à une hépatosplénomégalie, une pancytopénie, une hypertriglycéridémie, une hypofibrinogènémie et des troubles neurologiques sévères. La concentration sérique de cytokines pro-inflammatoires [...] est augmentée. Une caractéristique histologique de l'affection est l'accumulation de macrophages et de lymphocytes activés [...], avec images d'hémophagocytose dans la moelle osseuse, la rate, le foie, les ganglions et le système nerveux central.

Spanish

Save record 2

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