نتایج جستجو برای: gd1

تعداد نتایج: 175  

Journal: :Journal of the Korean Institute of Electrical and Electronic Material Engineers 2012

2017
Tina M Cairns Noah T Ditto Huan Lou Benjamin D Brooks Doina Atanasiu Roselyn J Eisenberg Gary H Cohen

While HSV-2 typically causes genital lesions, HSV-1 is increasingly the cause of genital herpes. In addition, neonatal HSV infections are associated with a high rate of mortality and HSV-2 may increase the risk for HIV or Zika infections, reinforcing the need to develop an effective vaccine. In the GSK Herpevac trial, doubly sero-negative women were vaccinated with a truncated form of gD2 [gD2(...

Journal: :Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2014
L Nalysnyk A Hamed G Hurwitz J Simeone P Rotella

BACKGROUND: Gaucher disease (GD) is an inherited, rare, lysosomal storage disorder caused by a genetic deficiency of glucocerebrosidase. The result is the accumulation of the substrate, glucosylceramide, in the lysosomes of macrophage cells in the liver, spleen, bones, lungs, and other vital tissues. Three subtypes of Gaucher disease are recognized: type 1 (GD1, non-neuropathic), type 2 (GD2, a...

Journal: :Molecular genetics and metabolism 2017
Amal El-Beshlawy Anna Tylki-Szymanska Ashok Vellodi Nadia Belmatoug Gregory A Grabowski Edwin H Kolodny Julie L Batista Gerald F Cox Pramod K Mistry

In Gaucher disease (GD), deficiency of lysosomal acid β-glucosidase results in a broad phenotypic spectrum that is classified into three types based on the absence (type 1 [GD1]) or presence and severity of primary central nervous system involvement (type 2 [GD2], the fulminant neuronopathic form, and type 3 [GD3], the milder chronic neuronopathic form). Enzyme replacement therapy (ERT) with im...

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