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Hematology, ISSN 1024-5332, 11/2018, Volume 23, Issue 10, pp. 817 - 822
Objective: To elucidate conditions which cause elevation of the serum ferritin, extent of the elevation in each condition, and clinical relevance of... 
hemophagocytic lymphohistiocytosis | Hyperferritinemia | ferritin | general practice | etiology | SERUM FERRITIN LEVELS | EXTREME HYPERFERRITINEMIA | HEMATOLOGY
Journal Article
Türk Patoloji Dergisi, ISSN 1018-5615, 09/2019, Volume 35, Issue 3, pp. 207 - 212
Objective: Hemophagocytic Lymphohistiocytosis (HLH) is an uncommon, life-threatening hyperinflammatory syndrome, caused by severe hypercytokinemia, due to an... 
Lymphohistiocytosis | Hyperferritinemia | Hemophagocytosis | Pancytopenia
Journal Article
Pediatric Hematology and Oncology, ISSN 0888-0018, 08/2019, Volume 36, Issue 6, pp. 390 - 393
Hyperferritinemia-cataract syndrome, characterized by high serum ferritin concentration and cataracts in early life, remains a less-known rare disease, with... 
c-160A > G (40A > G) mutation | Turkish family | hyperferritinemia-cataract syndrome | FTL gene | ONCOLOGY | PHENOTYPE | PEDIATRICS | HEREDITARY HYPERFERRITINEMIA | MUTATIONS | HEMATOLOGY | IRON OVERLOAD | c-160A > G (40A > G) mutation
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 08/2015, Volume 73, Issue 2, pp. 294 - 303
Adult-onset Still disease (AOSD) is a systemic inflammatory disorder that is clinically characterized by a heterogeneous constellation of symptoms and signs.... 
evanescent rash | persistent pruritic eruption | adult-onset Still disease | hyperferritinemia | paraneoplastic syndrome
Journal Article
BBA - General Subjects, ISSN 0304-4165, 2009, Volume 1790, Issue 7, pp. 589 - 599
Journal Article
BBA - General Subjects, ISSN 0304-4165, 2010, Volume 1800, Issue 8, pp. 783 - 792
Ferritin structure is designed to maintain large amounts of iron in a compact and bioavailable form in solution. All ferritins induce fast Fe(II) oxidation in... 
Iron homeostasis | Mitochondria | Oxidative damage | Neurodegeneration | Ferritin | HEREDITARY FERRITINOPATHY | HYPERFERRITINEMIA-CATARACT SYNDROME | FRIEDREICHS-ATAXIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | LIGHT-CHAIN GENE | CLINICAL-FEATURES | RESPONSIVE ELEMENT | HEAVY-CHAIN | BIOPHYSICS | HELA-CELLS | MESSENGER-RNA | H-FERRITIN | Index Medicus
Journal Article
Critical Care Medicine, ISSN 0090-3493, 11/2016, Volume 44, Issue 11, pp. 2119 - 2121
Journal Article
European Oncology and Haematology, ISSN 2045-5275, 2015, Volume 11, Issue 2, pp. 147 - 149
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 06/2008, Volume 50, Issue 6, pp. 1227 - 1235
Journal Article
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, ISSN 0002-9629, 08/2017, Volume 354, Issue 2, pp. 158 - 164
Background: Although high ferritin levels are associated with iron overload, it is known that ferritin is also an acute-phase reactant that may be elevated in... 
Hemophagocytic lymphohistiocytosis | MEDICINE, GENERAL & INTERNAL | Hyperferritinemia | SERUM FERRITIN LEVELS | Ferritin | HEPCIDIN | Iron
Journal Article
Nature Reviews Rheumatology, ISSN 1759-4790, 11/2018, Volume 14, Issue 11, pp. 628 - 629
A variety of comorbidities of gout exist, but most of these associations are not causally linked. Mendelian randomization analysis of genome-wide association... 
Hyperuricemia | Genome-wide association studies | Usage | Comorbidity | Development and progression | Research | Risk factors | Rheumatism | Genomes | Uric acid | Gout
Journal Article
Journal Article
La revue de médecine interne, ISSN 0248-8663, 10/2019, Volume 40, Issue 10, pp. 680 - 683
La maladie de Gaucher de type 1 est une maladie de surcharge d’origine génétique responsable de thrombopénie. Or les recommandations actuelles, devant une... 
Splenomegaly | Hyperferritinemia | Gaucher disease | Hypergammaglobulinemia | Maladie de Gaucher | Thrombopénie immunologique | Hypergammaglobulinémie | Immune thrombocytopenia | Splénomégalie | Hyperferritinémie
Journal Article
REVUE DE MEDECINE INTERNE, ISSN 0248-8663, 10/2019, Volume 40, Issue 10, pp. 680 - 683
Introduction. - Gaucher disease type 1 is a rare genetic disease. It can cause thrombocytopenia. Current guidelines do not support bone marrow examination in... 
Splenomegaly | DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | Hyperferritinemia | Gaucher disease | Hypergammaglobulinemia | Immune thrombocytopenia | EPIDEMIOLOGY
Journal Article