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HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis

Published:2013 Issue:1 Volume:8 Page:94
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Lux Andreas,Müller Ralf,Tulk Mark,Olivieri Carla,Zarrabeita Roberto,Salonikios Theresia,Wirnitzer Bernhard

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Reference22 articles.

1. Hereditary haemorrhagic telangiectasia: a clinical and scientific review

2. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia

3. Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

4. Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

5. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)

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1. Exploring the Steps of Infrared (IR) Spectral Analysis: Pre-Processing, (Classical) Data Modelling, and Deep Learning;Molecules;2023-09-30

2. Improving tuberculosis treatment using mid-infrared spectroscopy for bedside therapeutic drug monitoring;Silicon Photonics XVIII;2023-03-13

3. Up-conversion detection of mid-infrared light carrying orbital angular momentum;Chinese Physics B;2022-09-01

4. Post-mortem evaluation of the pathological degree of myocardial infarction by Fourier transform infrared microspectroscopy;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2022-03

5. Translational medicine in hereditary hemorrhagic telangiectasia;European Journal of Internal Medicine;2022-01

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