Found: 11
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Cost-benefit analysis of a new health insurance card and electronic prescription in Germany.
- Published in:
- Journal of Telemedicine & Telecare, 2002, v. 8, p. 54, doi. 10.1177/1357633X020080S225
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- Publication type:
- Article
Cost-benefit analysis of a new health insurance card and electronic prescription in Germany.
- Published in:
- 2002
- By:
- Publication type:
- journal article
HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-94
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- Publication type:
- Article
HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis.
- Published in:
- 2013
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- Publication type:
- journal article
Investigation of Endoglin Wild-Type and Missense Mutant Protein Heterodimerisation Using Fluorescence Microscopy Based IF, BiFC and FRET Analyses.
- Published in:
- PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0102998
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- Publication type:
- Article
Genetic and Molecular Analyses of PEG10 Reveal New Aspects of Genomic Organization, Transcription and Translation.
- Published in:
- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008686
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- Publication type:
- Article
High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients.
- Published in:
- Human Mutation, 2005, v. 25, n. 6, p. 595, doi. 10.1002/humu.9345
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- Publication type:
- Article
Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanisms.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 5, p. 745, doi. 10.1093/hmg/9.5.745
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- Publication type:
- Article
Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia.
- Published in:
- Human Mutation, 1998, v. 12, n. 2, p. 137, doi. 10.1002/(SICI)1098-1004(1998)12:2<137::AID-HUMU15>3.0.CO;2-M
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- Publication type:
- Article
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles.
- Published in:
- Human Mutation, 1998, v. 11, n. 4, p. 286, doi. 10.1002/(SICI)1098-1004(1998)11:4<286::AID-HUMU6>3.0.CO;2-B
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- Publication type:
- Article
Correlation of VEGF-expression with VEGF-serum level and microvessel density in HHT patients
- Published in:
- 2004
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- Publication type:
- Abstract