Literature DB >> 17296562

Therapy of adult Gaucher disease.

Joerg Schmitz, Ludger Wilhelm Poll, Stephan vom Dahl.   

Abstract

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Year:  2007        PMID： 17296562     DOI： 10.3324/haematol.11193

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  6 in total

Review 1.  New biotechnological and nanomedicine strategies for treatment of lysosomal storage disorders.

Authors:  Silvia Muro
Journal:  Wiley Interdiscip Rev Nanomed Nanobiotechnol       Date:  2010 Mar-Apr

2.  Production of active human glucocerebrosidase in seeds of Arabidopsis thaliana complex-glycan-deficient (cgl) plants.

Authors:  Xu He; Jason D Galpin; Michael B Tropak; Don Mahuran; Thomas Haselhorst; Mark von Itzstein; Daniel Kolarich; Nicolle H Packer; Yansong Miao; Liwen Jiang; Gregory A Grabowski; Lorne A Clarke; Allison R Kermode
Journal:  Glycobiology       Date:  2011-11-07       Impact factor: 4.313

3.  Membrane anchors effectively traffic recombinant human glucocerebrosidase to the protein storage vacuole of Arabidopsis seeds but do not adequately control N-glycan maturation.

Authors:  Xu He; Jason D Galpin; Yansong Miao; Liwen Jiang; Gregory A Grabowski; Allison R Kermode
Journal:  Plant Cell Rep       Date:  2014-09-04       Impact factor: 4.570

Review 4.  Hematopoietic stem cell transplantation for Gaucher disease.

Authors:  Usha R Somaraju; Krishna Tadepalli
Journal:  Cochrane Database Syst Rev       Date:  2017-10-18

5.  Splenomegaly as a primary manifestation of Gaucher disease in a young adult woman.

Authors:  Giuseppe Merra; Antonio Dal Lago; Roberta Ricci; Daniela Antuzzi; Giovanni Gasbarrini; Antonio Gasbarrini; Giovanni Ghirlanda
Journal:  Case Rep Gastroenterol       Date:  2008-11-29

Review 6.  The Importance of a Multidisciplinary Approach in the Management of a Patient with Type I Gaucher Disease.

Authors:  Miguel-Ángel Torralba-Cabeza; Susana Olivera-González; José-Luis Sierra-Monzón
Journal:  Diseases       Date:  2018-07-26
  6 in total

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