| Davarian A, Mirbehbahani NB
Gaucher disease: A 10 year old girl with anemia and huge spelenomegaly (a case report). [Journal Article]
Pak J Biol Sci 2008 Apr 1; 11(7):1063-5.
Abstract | Full Citation | | Sun Y, Jia L, Williams MT, et al.
Temporal gene expression profiling reveals CEBPD as a candidate regulator of brain disease in prosaposin deficient mice. [JOURNAL ARTICLE]
BMC Neurosci 2008 Aug 1; 9(1):76.
Abstract | Full Citation | | Emre S, Gürakan F, Yüce A, et al.
Molecular analysis of Turkish Gaucher disease patients: Identification of novel mutations in glucocerebrosidase (GBA) gene. [JOURNAL ARTICLE]
Eur J Med Genet 2008 Mar 4.
Abstract | Full Citation | | Kawahara S, Kato A, Oshimi K, et al.
[Gaucher disease type I diagnosed at 63 years old presenting with thrombocytopenia] [English Abstract, Journal Article]
Rinsho Ketsueki 2008 May; 49(5):335-9.
Abstract | Full Citation | Find Related Articles | | Mehta A
Gaucher disease: unmet treatment needs. [Journal Article]
Acta Paediatr Suppl 2008 Apr; 97(457):83-7.
Abstract | Full Citation | Find Related Articles | | Sun Y, Witte DP, Ran H, et al.
Neurological deficits and glycosphingolipid accumulation in Saposin B deficient mice. [JOURNAL ARTICLE]
Hum Mol Genet 2008 May 14.
Abstract | Full Citation | Find Related Articles | | Simon G, Erdos M, Maródi L, et al.
[Gaucher disease: The importance of early diagnosis and therapy.] [English Abstract, Journal Article]
Orv Hetil 2008 Apr 20; 149(16):743-50.
Abstract | Full Citation | Find Related Articles | | Balreira A, Gaspar P, Caiola D, et al.
A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. [JOURNAL ARTICLE]
Hum Mol Genet 2008 Apr 17.
Abstract | Full Citation | Find Related Articles | | Benko WS, Hruska KS, Nagan N, et al.
Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3. [Case Reports, Journal Article]
Neurology 2008 Mar 18; 70(12):976-8.
Full Citation | Publisher Full Text | Find Related Articles | | Hruska KS, Lamarca ME, Scott CR, et al.
Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA). [JOURNAL ARTICLE]
Hum Mutat 2008 Mar 12.
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