Mb. Gaucher type 1--behandlingsresultater ved enzymsubstitution

J Steensberg; K G Nielsen; N J Brandt

Mb. Gaucher type 1--behandlingsresultater ved enzymsubstitution

Translated title of the contribution: Gaucher disease type 1--therapeutic results of enzyme substitution

J Steensberg
, K G Nielsen
, N J Brandt

Department of Paediatrics and Adolescent Medicine

2 Citations (Scopus)

Abstract

Gaucher's disease is the most common inherited lysosomal storage disorder, displaying hepato-splenomegaly, thrombocytopenia, anaemia and bone pain as characteristic features. Substitution therapy with a modified enzyme alglucerase has revolutionized the treatment and prognosis of Gaucher's disease. The first Danish patients treated with alglucerase are reported.

Translated title of the contribution	Gaucher disease type 1--therapeutic results of enzyme substitution
Original language	Danish
Journal	Ugeskrift for Laeger
Volume	160
Issue number	26
Pages (from-to)	3929-30
Number of pages	2
ISSN	0041-5782
Publication status	Published - 22 Jun 1998

Cite this

@article{30215ef38d4d43cbb9411e7f6c356371,

title = "Mb. Gaucher type 1--behandlingsresultater ved enzymsubstitution",

abstract = "Gaucher's disease is the most common inherited lysosomal storage disorder, displaying hepato-splenomegaly, thrombocytopenia, anaemia and bone pain as characteristic features. Substitution therapy with a modified enzyme alglucerase has revolutionized the treatment and prognosis of Gaucher's disease. The first Danish patients treated with alglucerase are reported.",

keywords = "Adolescent, Adult, Female, Gaucher Disease/diagnosis, Glucosylceramidase/therapeutic use, Humans, Prognosis",

author = "J Steensberg and Nielsen, \{K G\} and Brandt, \{N J\}",

year = "1998",

month = jun,

day = "22",

language = "Dansk",

volume = "160",

pages = "3929--30",

journal = "Ugeskrift for Laeger",

issn = "0041-5782",

publisher = "Almindelige Danske L{\ae}geforening",

number = "26",

}

TY - JOUR

T1 - Mb. Gaucher type 1--behandlingsresultater ved enzymsubstitution

AU - Steensberg, J

AU - Nielsen, K G

AU - Brandt, N J

PY - 1998/6/22

Y1 - 1998/6/22

N2 - Gaucher's disease is the most common inherited lysosomal storage disorder, displaying hepato-splenomegaly, thrombocytopenia, anaemia and bone pain as characteristic features. Substitution therapy with a modified enzyme alglucerase has revolutionized the treatment and prognosis of Gaucher's disease. The first Danish patients treated with alglucerase are reported.

AB - Gaucher's disease is the most common inherited lysosomal storage disorder, displaying hepato-splenomegaly, thrombocytopenia, anaemia and bone pain as characteristic features. Substitution therapy with a modified enzyme alglucerase has revolutionized the treatment and prognosis of Gaucher's disease. The first Danish patients treated with alglucerase are reported.

KW - Adolescent

KW - Adult

KW - Female

KW - Gaucher Disease/diagnosis

KW - Glucosylceramidase/therapeutic use

KW - Humans

KW - Prognosis

M3 - Tidsskriftartikel

C2 - 9656836

SN - 0041-5782

VL - 160

SP - 3929

EP - 3930

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

IS - 26

ER -

Mb. Gaucher type 1--behandlingsresultater ved enzymsubstitution

Abstract

Fingerprint

Cite this