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1.
Rheumatology (Oxford) ; 47(8): 1185-92, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18515867

ABSTRACT

OBJECTIVE: Systemic sclerosis (SSc) is a rare, heterogeneous disease, which affects different organs and therefore requires interdisciplinary diagnostic and therapeutic management. To improve the detection and follow-up of patients presenting with different disease manifestations, an interdisciplinary registry was founded with contributions from different subspecialties involved in the care of patients with SSc. METHODS: A questionnaire was developed to collect a core set of clinical data to determine the current disease status. Patients were grouped into five descriptive disease subsets, i.e. lcSSc, dcSSc, SSc sine scleroderma, overlap-syndrome and UCTD with scleroderma features. RESULTS: Of the 1483 patients, 45.5% of patients had lcSSc and 32.7% dcSSc. Overlap syndrome was diagnosed in 10.9% of patients, while 8.8% had an undifferentiated form. SSc sine scleroderma was present in 1.5% of patients. Organ involvement was markedly different between subsets; pulmonary fibrosis for instance was significantly more frequent in dcSSc (56.1%) than in overlap syndrome (30.6%) or lcSSc (20.8%). Pulmonary hypertension was more common in dcSSc (18.5%) compared with lcSSc (14.9%), overlap syndrome (8.2%) and undifferentiated disease (4.1%). Musculoskeletal involvement was typical for overlap syndromes (67.6%). A family history of rheumatic disease was reported in 17.2% of patients and was associated with early disease onset (P < 0.005). CONCLUSION: In this nationwide register, a descriptive classification of patients with disease manifestations characteristic of SSc in five groups allows to include a broader spectrum of patients with features of SSc.


Subject(s)
Scleroderma, Systemic/epidemiology , Adult , Age Distribution , Age of Onset , Aged , Cross-Sectional Studies , Female , Germany/epidemiology , Humans , Male , Medicine , Middle Aged , Registries , Scleroderma, Diffuse/epidemiology , Scleroderma, Diffuse/pathology , Scleroderma, Limited/epidemiology , Scleroderma, Limited/pathology , Scleroderma, Systemic/classification , Scleroderma, Systemic/pathology , Specialization
2.
IEE Proc Nanobiotechnol ; 151(4): 139-44, 2004 Aug.
Article in English | MEDLINE | ID: mdl-16475858

ABSTRACT

A new plasma-based micropatterning technique, here referred to as plasma printing, combines the well known advantages given by the nonequilibrium character of a dielectric barrier discharge (DBD) and its operation inside small gas volumes with dimension between tens and hundreds of micrometres. The discharge is run at atmospheric pressure and can be easily implemented for patterned surface treatment with applications in biotechnology and microtechnology. In this work the local modification of dielectric substrates, e.g. polymeric films, is addressed with respect to coating and chemical functionalisation, immobilisation of biomolecules and area-selective electroless plating.

3.
J Biol Chem ; 255(5): 1808-11, 1980 Mar 10.
Article in English | MEDLINE | ID: mdl-7354060

ABSTRACT

Attempts to purify the vitamin K-dependent carboxylation system from rat liver microsomes have not yet met with success. Purification procedures result in low yields of activity even after relatively mild separation methods. We have been able to demonstrate that one reason for these failures is that there are at least two components (which can be separated) necessary for the reaction. Recombination of the separated components is possible if the detergent (Triton X-100) concentration is lowered and ethylene glycol is added to the system. Under these conditions, vitamin K-dependent carboxylation of synthetic pentapeptide (Phe-Leu-Glu-Glu-Leu) can be totally reconstituted.


Subject(s)
Carbonates/metabolism , Ligases , Microsomes, Liver/metabolism , Vitamin K Deficiency/metabolism , Vitamin K/pharmacology , Animals , Glutamates , Male , Microsomes, Liver/drug effects , Oligopeptides/metabolism , Peptides/metabolism , Prothrombin , Rats
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