# Service de Santé des Armées

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/service-de-sante-des-armees/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 76 |
| Citations | 196,898 |
| City | Metz |
| Country | FR |
| Description | Service de Santé des Armées is a research organisation in Metz, FR. OpenAlex records 3,430 works and 196,898 citations for it. 1,235 researchers list it as their most recent affiliation. |
| Homepage | http://www.defense.gouv.fr/english/sante |
| OpenAlex ID | https://openalex.org/I3203470602 |
| Region | Grand Est |
| Researchers | 1,235 |
| ROR ID | https://ror.org/0103yxp25 |
| Type | government |
| Works | 3,430 |

## University papers

- [Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages](https://scholariq.org/papers/revised-classification-of-histiocytoses-and-neoplasms-of-the-macrophage/)
- [High prevalence of BRAF V600E mutations in Erdheim-Chester disease but not in other non-Langerhans cell histiocytoses](https://scholariq.org/papers/high-prevalence-of-braf-v600e-mutations-in-erdheim-chester-disease-but-not-in/)
- [Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work‐up, and treatment for patients till the age of 18 years](https://scholariq.org/papers/langerhans-cell-histiocytosis-lch-guidelines-for-diagnosis-clinical-work-up-and/)
- [The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity](https://scholariq.org/papers/the-european-society-for-immunodeficiencies-esid-registry-working-definitions/)
- [Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease](https://scholariq.org/papers/consensus-recommendations-for-the-diagnosis-and-clinical-management-of-rosai/)
- [Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies](https://scholariq.org/papers/autoimmune-and-inflammatory-manifestations-occur-frequently-in-patients-with/)
- [High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia](https://scholariq.org/papers/high-frequency-of-gata2-mutations-in-patients-with-mild-chronic-neutropenia/)
- [Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients](https://scholariq.org/papers/natural-history-of-gata2-deficiency-in-a-survey-of-79-french-and-belgian/)
- [Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study](https://scholariq.org/papers/cladribine-and-cytarabine-in-refractory-multisystem-langerhans-cell/)

## University top topics

Showing 8 of 25.

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.