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Volumn 12, Issue 2, 2017, Pages

Diagnostic needs for rare diseases and shared prediagnostic phenomena: Results of a German-wide expert Delphi survey

Author keywords

[No Author keywords available]

Indexed keywords

ACROMEGALY; ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; ATAXIA TELANGIECTASIA; CHRONIC GRANULOMATOUS DISEASE; CLUSTER HEADACHE; CYSTIC FIBROSIS; DELPHI STUDY; DIAGNOSTIC TEST; EHLERS DANLOS SYNDROME; FABRY DISEASE; FANCONI ANEMIA; FEMALE; FEVER; GERMANY; GLAUCOMA; GLYCOGEN STORAGE DISEASE TYPE 2; GLYCOGEN STORAGE DISEASE TYPE 5; HEALTH CARE NEED; HUMAN; HURLER SYNDROME; LEUKODYSTROPHY; MALE; MEDITERRANEAN FEVER; MENTAL DISEASE; MIDDLE AGED; MUCOPOLYSACCHARIDOSIS; MYELODYSPLASTIC SYNDROME; NIEMANN PICK DISEASE; ORNITHINE TRANSCARBAMYLASE DEFICIENCY; PSYCHOSOMATIC DISORDER; PULMONARY HYPERTENSION; RARE DISEASE; SCLERODERMA; SEVERE COMBINED IMMUNODEFICIENCY; SYSTEMIC LUPUS ERYTHEMATOSUS; SYSTEMIC SCLEROSIS; UREA CYCLE DISORDER; WILSON DISEASE; AUTOIMMUNE DISEASES; CLASSIFICATION; DELAYED DIAGNOSIS; GLYCOGEN STORAGE DISEASE TYPE II; HYPERTENSION; METABOLIC DISEASES; ORGANIZATION AND MANAGEMENT; RARE DISEASES; SCLERODERMA, SYSTEMIC; SELF HELP; SOCIAL SUPPORT;

EID: 85013953929     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0172532     Document Type: Article
Times cited : (63)

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