Changes for page Neurodiagnoses

Last modified by manuelmenendez on 2025/03/03 22:46

From version 27.1
edited by manuelmenendez
on 2025/01/29 18:48
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To version 4.2
edited by manuelmenendez
on 2025/01/27 22:57
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5 -= //A new tridimensional diagnostic framework for CNS diseases// =
5 += Neurodiagnoses =
6 6  
7 -This project is focused on developing a novel nosological and diagnostic framework for CNS diseases by using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies.
8 -We aim to create a structured, interpretable, and scalable diagnostic tool.
7 +This project is focused on developing a novel nosological and diagnostic framework for neurological diseases. Using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies, we aim to create a structured, interpretable, and scalable diagnostic tool.
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11 11  
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16 -= What is this about and what can I find here? =
15 += What can I find here? =
17 17  
18 -= **Overview** =
17 +* `/docs`: Documentation and contribution guidelines.
18 +* `/code`: Machine learning pipelines and scripts.
19 +* `/data`: Sample datasets for testing. - `/outputs`: Generated models, visualizations, and reports.
19 19  
20 -The //Tridimensional Diagnostic Framework// redefines CNS diseases can be classified and diagnosed by focusing on:
21 += Who has access? =
21 21  
22 -* **Axis 1**: Etiology (genetic or other causes of diseases).
23 -* **Axis 2**: Molecular Markers (biomarkers).
24 -* **Axis 3**: Neuroanatomoclinical correlations (linking clinical symptoms to structural changes in the nervous system).
25 -
26 -This methodology enables:
27 -
28 -* Greater precision in diagnosis.
29 -* Integration of incomplete datasets using AI-driven probabilistic modeling.
30 -* Stratification of patients for personalized treatment.
31 -
32 -== **The case of neurodegenerative diseases** ==
33 -
34 -There have been described these 3 diagnostic axes:
35 -
36 -[[Neurodegenerative diseases can be studied and classified in a tridimensional scheme with three axes: anatomic–clinical, molecular, and etiologic. CSF, cerebrospinal fluid; FDG, fluorodeoxyglucose; MRI, magnetic resonance imaging; PET, positron emission tomography.>>image:tridimensional.png||alt="tridimensional view of neurodegenerative diseases"]]
37 -
38 -* (((
39 -**Axis 1: Etiology**
40 -
41 -* //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers.
42 -* //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression.
43 -* //Tests//: Genetic testing, lifestyle, and cardiovascular screening.
44 -)))
45 -* (((
46 -**Axis 2: Molecular Markers**
47 -
48 -* //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression.
49 -* //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology.
50 -* //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET).
51 -)))
52 -* (((
53 -**Axis 3: Neuroanatomoclinical**
54 -
55 -* //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments.
56 -* //Examples//: Hippocampal atrophy correlating with memory deficits.
57 -* //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations.
58 -)))
59 -
60 -== **Applications** ==
61 -
62 -This system enhances:
63 -
64 -* **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials.
65 -* **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking.
66 -
67 -== Who has access? ==
68 -
69 69  We welcome contributions from the global community. Let’s build the future of neurological diagnostics together!
70 -
71 -== How to Contribute ==
72 -
73 -* Access the `/docs` folder for guidelines.
74 -* Use `/code` for the latest AI pipelines.
75 -* Share feedback and ideas in the wiki discussion pages.
76 -
77 -== Key Objectives ==
78 -
79 -* Develop interpretable AI models for diagnosis and progression tracking.
80 -* Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources.
81 -* Foster collaboration among neuroscientists, AI researchers, and clinicians.
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83 83  
84 84  
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90 90  {{box title="**Contents**"}}
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91 91  {{toc/}}
92 92  {{/box}}
93 93  
94 -== Main contents ==
95 -
96 -* `/docs`: Documentation and contribution guidelines.
97 -* `/code`: Machine learning pipelines and scripts.
98 -* `/data`: Sample datasets for testing.
99 -* `/outputs`: Generated models, visualizations, and reports.
100 -* [[Methodology>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Methodology/]]
101 -* [[Results>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Results/]]
102 -* [[to-do-list>>to-do-list]]
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