Bone events and evolution of biologic markers in Gaucher disease before and during treatment

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Bone events and evolution of biologic markers in Gaucher disease before and during treatment is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1006280180
P356DOI10.1186/AR3111
P932PMC publication ID2945057
P698PubMed publication ID20696071
P5875ResearchGate publication ID45582530

P50authorFrance MentréQ87317141
Jérôme StirnemannQ89761806
Olivier FainQ114301300
Nadia BelmatougQ117223230
P2093author name stringBruno Fantin
Corine Vincent
P2860cites workBiomarkers for lysosomal storage disorders: identification and application as exemplified by chitotriosidase in Gaucher diseaseQ33323654
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Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patientsQ33356246
Type 2 Gaucher disease: 15 new cases and review of the literatureQ33370289
Tartrate-resistant acid phosphatase staining of monocytes in Gaucher diseaseQ33459713
Molecular and cell biology of acid beta-glucosidase and prosaposinQ34070568
Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher diseaseQ34133643
Serum ferritin concentration in Gaucher's diseaseQ34992481
Recent clinical progress in Gaucher diseaseQ36191776
Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort studyQ36737076
Dose-response relationships for enzyme replacement therapy with imiglucerase/alglucerase in patients with Gaucher disease type 1.Q37221766
Timing of initiation of enzyme replacement therapy after diagnosis of type 1 Gaucher disease: effect on incidence of avascular necrosisQ37413920
Elevation of Serum Angiotensin-Converting Enzyme in Gaucher's DiseaseQ39991377
Plasma and metabolic abnormalities in Gaucher's disease.Q41719188
Neuronopathic forms of Gaucher's diseaseQ41719191
Immunochemical characterization of two activator proteins stimulating enzymic sphingomyelin degradation in vitro. Absence of one of them in a human Gaucher disease variantQ42509294
Determinants of clinical progression in antiretroviral-naive HIV-infected patients starting highly active antiretroviral therapy. Aquitaine Cohort, France, 1996-2002.Q43687450
Correlation of surrogate markers of Gaucher disease. Implications for long-term follow up of enzyme replacement therapyQ47586472
A mechanism-based disease progression model for comparison of long-term effects of pioglitazone, metformin and gliclazide on disease processes underlying Type 2 Diabetes Mellitus.Q51501369
The effect of enzyme replacement therapy on bone crisis and bone pain in patients with type 1 Gaucher disease.Q53241550
Correlation of bone marrow response with hematological, biochemical, and visceral responses to enzyme replacement therapy of nonneuronopathic (type 1) Gaucher disease in 30 adult patients.Q53968058
Evaluation of three biochemical markers in the monitoring of Gaucher diseaseQ59401760
Gaucher diseaseQ68144895
Age dependency of serum acid phosphatase in controls and Gaucher patientsQ70671847
beta-Glucosidase assays in the diagnosis of Gaucher's diseaseQ71600806
Elevation of serum acid phosphatase in Gaucher's diseaseQ73969954
Serum chitotriosidase activity in Gaucher patients on enzyme replacement therapy (ERT)Q77166181
Gaucher diseaseQ77373645
Disease system analysis: basic disease progression models in degenerative diseaseQ80390429
Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patientsQ80828454
Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher diseaseQ81123039
P433issue4
P921main subjectGaucher's diseaseQ861645
P304page(s)R156
P577publication date2010-08-09
P1433published inArthritis Research and TherapyQ15757229
P1476titleBone events and evolution of biologic markers in Gaucher disease before and during treatment
P478volume12

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cites work (P2860)
Q30235844A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments
Q89453442Accuracy of chitotriosidase activity and CCL18 concentration in assessing type I Gaucher disease severity. A systematic review with meta-analysis of individual participant data
Q38927495Assessment of Bone Health in Patients With Type 1 Gaucher Disease Using Impact Microindentation
Q64226316Gaucher Disease: New Expanded Classification Emphasizing Neurological Features
Q28067032Imiglucerase in the management of Gaucher disease type 1: an evidence-based review of its place in therapy
Q35615361Impact of imiglucerase supply constraint on the therapeutic management and course of disease in French patients with Gaucher disease type 1
Q38290826Management of bone disease in Gaucher disease type 1: clinical practice.
Q33891532Modeling changes in biomarkers in Gaucher disease patients receiving enzyme replacement therapy using a pathophysiological model
Q34485240Modelling Gaucher disease progression: long-term enzyme replacement therapy reduces the incidence of splenectomy and bone complications
Q38893633Modelling long-term evolution of chitotriosidase in non-neuronopathic Gaucher disease
Q38524847Pathogenesis of Bone Alterations in Gaucher Disease: The Role of Immune System
Q33402191Revised recommendations for the management of Gaucher disease in children
Q53128627Risk factors for fractures and avascular osteonecrosis in type 1 Gaucher disease: a study from the International Collaborative Gaucher Group (ICGG) Gaucher Registry.
Q33403714The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients
Q36727748The prognostic value of the serum ferritin in a southern Brazilian cohort of patients with Gaucher disease
Q93266143Three mutations of adult type 1 Gaucher disease found in a Chinese patient: A case report