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Mostrando 141 - 160 Resultados de 1,452 Para Buscar '"Chester"', tiempo de consulta: 0.24s Limitar resultados
  1. 141
    “…Erdheim–Chester disease (ECD) is a rare systemic non-Langerhans cell histiocytosis. …”
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    Role of (99m)Tc-MDP bone scan in the diagnosis of Erdheim–Chester disease
  2. 142
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    Multistate Outbreak of Salmonella Chester Infections Associated with Frozen Meals — 18 States, 2010
  3. 143
    “…These clinical and radiological features were consistent with a diagnosis of Erdheim-Chester disease; however, the patient's skin biopsy was consistent with Langerhans cell histiocytosis.…”
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    A Rare Case of Erdheim-Chester Disease and Langerhans Cell Histiocytosis Overlap Syndrome
  4. 144
    “…The BRAFV600E mutation was detected, and a diagnosis of Erdheim–Chester disease was made. The extreme rarity of Erdheim–Chester disease strongly suggests the existence of potentially common element(s) that may have contributed to the pathogenesis of both disorders. …”
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    Erdheim–Chester Disease With Multiorgan Involvement, Following Polycythemia Vera: A Case Report
  5. 145
    “…BACKGROUND: Erdheim–Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis. …”
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    Long-term outcome of basilar stenosis in Erdheim–Chester disease: A case report
  6. 146
    “…BACKGROUND: Erdheim–Chester disease (ECD) is an uncommon aggressive, multisystem form of non-Langerhans’ cell histocytosis, which was firstly reported by Jakob Erdheim and William chester in 1930. …”
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    Erdheim–Chester disease (ECD): Case report, clinical and basic investigations, and review of literature
  7. 147
    “…With approximately 750 cases reported, Erdheim-Chester disease is an exceedingly rare histiocyte cell disorder. …”
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    Erdheim-Chester disease, moving away from the orphan diseases: A case report
  8. 148
    “…Between 2014 and 2015, the European Centre for Disease Prevention and Control was informed of an increase in numbers of Salmonellaenterica serotype Chester cases with travel to Morocco occurring in six European countries. …”
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    Multinational outbreak of travel-related Salmonella Chester infections in Europe, summers 2014 and 2015
  9. 149
    por Pappas, Theodore N.
    Publicado 2017
    “…Garfield died after an extended illness and Chester A. Arthur assumed the presidency on September 20, 1881. …”
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    Bright's Disease, Malaria, and Machine Politics: The Story of the Illness of President Chester A. Arthur
  10. 150
    “…We thus evaluated treatment with the IL-1 receptor antagonist anakinra in a case of extremely severe pericarditis with cardiac tamponade and heart failure secondary to Erdheim–Chester disease (ECD), a rare clonal disorder of macrophages characterized by rampant inflammation and multiorgan involvement. …”
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    Treating Heart Inflammation With Interleukin-1 Blockade in a Case of Erdheim–Chester Disease
  11. 151
    “…The juvenile (JXG) and non-juvenile xanthogranuloma (N-JXG) family of histiocytoses are N-LCH: the JXG family consisting of the JXG (cutaneous), xanthoma disseminatum (cutaneous and systemic) and Erdheim-Chester disease (ECD; systemic); and the N-JXG family consisting of the solitary reticulohistiocytoma (cutaneous), multicentric reticulohistiocytosis (cutaneous and systemic) and Rosai-Dorfman disease (RDD; systemic). …”
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    Rare diseases of bone: Erdheim-Chester and Rosai-Dorfman non-Langerhans cell histiocytoses
  12. 152
    “…BACKGROUND: Erdheim Chester disease (ECD) is a rare form of non-Langerhans histiocytosis that still presents a diagnostic and clinical dilemma. …”
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    A Rare Case of Soft Tissue Erdheim Chester Disease: Diagnostic Dilemma and Management
  13. 153
    “…Our rechallenge of cobimetinib in an Erdheim‐Chester Disease (ECD) patient for the rare adverse effect, “dropped head syndrome,” with a previously unexplored cobimetinib regimen was successful. …”
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    Cobimetinib‐induced “dropped head syndrome” and subsequent disease management in an Erdheim‐Chester patient
  14. 154
    “…BACKGROUND: Erdheim‐Chester disease (ECD) is a rare non‐Langerhans cell histiocytosis. …”
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    Real‐World Toxicity Experience with BRAF/MEK Inhibitors in Patients with Erdheim‐Chester Disease
  15. 155
    “…Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by systemic xanthogranulomatous infiltration. …”
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    Erdheim-Chester Disease With Extensive Pericardial Involvement: A Case Report and Systematic Review
  16. 156
    “…In Japan, only one outbreak of Salmonella enterica subsp. enterica serovar Chester (S. Chester) has been confirmed in 1999. We performed a single-center retrospective case review of S. …”
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    Emergence of Salmonella enterica subsp. enterica serovar Chester in a rural area of Japan
  17. 157
    “…Erdheim-Chester disease (ECD) is a rare entity throughout the world. …”
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    Erdheim Chester disease: a subtle quiddity; the first case reported from Nepal
  18. 158
    “…BACKGROUND: Erdheim-Chester Disease (ECD) is a rare type of non-Langerhans histiocytosis. …”
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    Bone mineral density and bone microarchitecture in a cohort of patients with Erdheim-Chester Disease
  19. 159
    “…The appearance of cervical adenopathies can occur in many pathologies in a non-specific manner; Erdheim–Chester disease (ECD) is characterized by xanthogranulomatous and xanthomatous infiltration of different tissues with numerous foamy histiocytes. …”
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    Cervical Lymphadenopathies as Unusual Presentations of Erdheim–Chester Disease: The Need for Knowledge for Diagnosis and Treatment
  20. 160
    “…Erdheim-Chester disease is a rare, idiopathic, multisystemic non-Langerhans cell histiocytosis. …”
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    Erdheim-Chester disease with multisystem involvement evaluated by multimodal imaging: A case report
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