Successful Pregnancy on Enzyme Replacement Therapy with Cerezyme®

Clinical Therapeutics

Volumn 29, Issue SUPPL. C, 2007, Pages

  Mrsić, Mirando ^a   Fumić, Ksenija ^a   Vrčić, Hrvoje ^a   Potočki, Kristina ^a   Štern Padovan, Ranka ^a   Prutki, Maja ^a   Durakoviæ, Nadira ^a  

^a KBC Zagreb   (Croatia)

Author keywords

[No Author keywords available]

Indexed keywords

CHITOTRIOSIDASE; GLUCOSYLCERAMIDASE; IMIGLUCERASE;

ADULT; ANEMIA; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BLOOD CELL COUNT; CASE REPORT; CLINICAL ASSESSMENT; CLINICAL FEATURE; COST OF ILLNESS; DISEASE COURSE; DISEASE SEVERITY; DRUG COST; ENZYME DEFICIENCY; ENZYME REPLACEMENT; FEMALE; GAUCHER DISEASE; HEALTH INSURANCE; HEPATOSPLENOMEGALY; HUMAN; INFECTION RISK; LYSOSOME STORAGE DISEASE; POSTPARTUM HEMORRHAGE; PREGNANCY OUTCOME; RISK ASSESSMENT; SPONTANEOUS ABORTION; STANDARD; THROMBOCYTOPENIA; TREATMENT DURATION; TREATMENT OUTCOME; TREATMENT RESPONSE;

EID: 37049012448     PISSN: 01492918     EISSN: 1879114X     Source Type: Journal    
DOI: 10.1016/S0149-2918(07)80459-0     Document Type: Article

References (4)

1. Aporta Rodriguez R., Escobar Vedia J., Navarro Castro A., et al. Alglucerase enzyme replacement therapy used safely and effectively throughout the whole pregnancy of a Gaucher disease patient. Haematologica 83 (1998) 852-853
2. Elstein Y., Eisenberg V., Granovsky-Grisaru S., et al. Pregnancies in Gaucher disease: A 5-year study. Am J Obstet Gynecol 190 (2004) 435-441
3. Weinreb N., Charrow J., Andersson H., et al. Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: A report from the Gaucher Registry. Am J Med 113 (2002) 112-119
4. Mrsic M., Stavljenic-Rukavina A., Fumic K., et al. Management of Gaucher disease in a post-communist transitional health care system: Croatian experience. Croat Med J 44 (2003) 606-609