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Anatomic Landmarks

Anatomic Landmarks are distinct, identifiable physical features on the body that serve as reference points for medical and surgical procedures.
These landmarks aid in locating and accessing specific structures, facilitating accurate diagnosis, treatment planning, and surgical navigation.
They are commonly used in imaging techniques, such as radiography and ultrasound, to orient the viewer and provide spatial context.
Anatomic Landmarks play a crucial role in ensuring procedural reproducibility and enhancing patient safety by helping clinicians consistently identify target sites.
This standardized terminology allows for more effective communication and collaboration among healthcare professionals, ultimatley improving the quality and reliability of patient care.

Most cited protocols related to «Anatomic Landmarks»

The method proposed so far is expected to provide a broad range of channels over the cortex and thus cover most regions that can be reached with fNIRS. However, as these channels are formed by sources and detectors placed on 10–10 international system, users interested in running EEG-fNIRS multi-modal measures would not be capable of using the toolbox, as EEG placement by standard is based on 10–20 and 10–10 international systems12 (link).
To extend the possible optodes positions to 10–5 international system positions regarding layouts available for EEG caps, we have considered as a reference a cap with 130 positions in total. With this new design, one has the possibility to use either 32 positions (Fig. 6A) or 64 positions for EEG electrodes (Fig. 6B), while the locations for fNIRS optodes do not overlap with the 10–10 system.

(A) Expansion of the method described for 10–10 international system to (B) the 10–5 system to allow for multi-modal measurements with EEG, either 32 or 64 electrodes. EEG and fNIRS positions are based on a layout accommodating 130 positions in total. EEG 1–32 electrodes positions are depicted in green, while the complimentary 33–64 are in yellow; fNIRS sources positions are in red and the detectors are in blue.

We have visually assigned sources and detectors to 10–5 system positions with the goal to maximize the number of possible channels considering adjacent optodes. This resulted on the layout illustrated in Fig. 6, which presents 28 sources positions and 28 detectors positions over the scalp. From these positions, we considered 89 possible channels in total.
Once the positions have been assigned and their coordinates have been retrieved for both head atlases (Methods section), we proceeded with the methods described in the Methods section. Therefore, we ran the photon transport simulations and computed the normalized sensitivity, ROIs specificity and channels coordinates, and obtained the anatomical landmarks results of each parcellation atlas.
The derived results were also stored in Matlab files included in the fOLD toolbox.
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Publication 2018
A-130A Anatomic Landmarks Cortex, Cerebral Head Hypersensitivity Scalp
Sixteen regions of the macaque brain spanning from early prenatal to adulthood were dissected using the same standardized protocol used for human specimens and described in the accompanying study by Li et al ((33 ); see also (32 )). The macaque brain regions and developmental timepoints matched human brain regions and timepoints analyzed in the study by Li et al ((33 )). The sampled homologous brain regions were identified using anatomical landmarks provided in the macaque brain atlas (74 ). An overview of dissected brain regions is provided in fig. S1. Translating Time model (38 (link)) was used to identify equivalent timepoints between macaque and human prenatal development. The list of macaque brains used in this study and relevant metadata are provided in tables S12. Macaque studies were carried out in accordance with a protocol approved by Yale University’s Committee on Animal Research and NIH guidelines.
We performed tissue-level RNA extraction and sequencing of all 16 regions, single-cell RNA-Seq of dorsolateral prefrontal cortex [DFC], hippocampus [HIP], amygdala [AMY], striatum [STR], mediodorsal nucleus of the thalamus [MD], and cerebellar cortex [CBC] of mid-fetal macaque, and single-nucleus RNA-Seq of DFC of adult macaque. Single cell/nucleus sample processing was done with 10X Genomics and sequencing was done with Illumina platforms.
For tissue-level analysis, we generated annotation of human-macaque orthologs using the XSAnno pipeline, and matched the developmental age of human and macaque samples based on their respective transcriptome using our algorithm TranscriptomeAge. We also developed TempShift, a method based on Gaussian process model, to reveal the inter-regional differences, inter-species divergence, and genes with heterotopic and heterochronic expression. We also queried differentially expressed genes for enrichment in transcription factor binding sites using findMotifs.pl, and analyzed inter-species differential exon usage using the R package DEXSeq.
The single cell/nucleus data was first analysed by cellranger for decoding, alignment, quality filtering, and UMI counting. After that, data was further analyzed with Seurat according to its guidelines, and cell types were clustered for classification with SpecScore.R. In order to perform direct comparisons between human and macaque at the single-cell level, we focused on the homologous genes between these species and aligned monkey and human cells together to further analyze inter-species divergence of homologous cell types (fig. S47). We used MetageneBicorPlot function to examine the correlation of neuronal and glial cell subtypes, and we employed the correlation analysis to detect the correspondence of excitatory neuron and interneuron subtypes. Finally, we did functional enrichment of disease-associated genes in both tissue-level and single-cell datasets.
Publication 2018
Adult Allogeneic Cells Amygdaloid Body Anatomic Landmarks Binding Sites Brain Cell Nucleus Cells Cortex, Cerebellar Dorsolateral Prefrontal Cortex Ectopic Tissue Exons Fetus Genes Hereditary Diseases Homo sapiens Human Development Interneurons Macaca Monkeys Neuroglia Neurons Nucleus Solitarius RNA-Seq Seahorses Single-Cell RNA-Seq Strains Striatum, Corpus Thalamic Nuclei Tissues Transcription Factor Transcriptome
All mice were housed according to IACUC guidelines and used for experiment when 8–14-weeks old. Wild-type C57BL/6.SJL mice were HSPC donors when recipients were wild type, Col2.3–GFP or WWv double mutant (backcrossed to C57BL/6 background). FVB mice were donors for wild-type or PPR littermate mice4 (link),29 (link) (gift from E. Schipani).
Mice were anaesthetized and prepared for in vivo imaging as described3 (link). Immediately before imaging 20 µl of non-targeted Qdot 800 or 655 (Invitrogen) diluted in 130 µl sterile PBS was injected retro-orbitally to allow vasculature visualization. The mouse was held in a heated tube mounted on a precision 3 axis motorized stage (Suter MP385). All mice were imaged with a custom-built confocal two-photon hybrid microscope specifically designed for live animal imaging (see Methods). At the start of each imaging session, we surveyed large areas of the skull bone surface using video rate second harmonic microscopy (see Methods) to identify the major anatomical landmarks such as sagittal and coronal sutures. We identified the locations of HSPCs within bone-marrow cavities and recorded their coordinates relative to the intersection of the sagittal and coronal sutures. SHG and GFP signals above each identified HSPC were acquired every 5 to 20 µm until the above endosteal surface was reached. After in vivo imaging, the scalp was re-closed using 3 M Vetbond veterinary glue and post-operative care was provided as described3 (link).
Images were coloured and merged using Adobe Photoshop and HSPC-microenvironment distance measures were obtained using Adobe Illustrator and Microsoft Excel. A two-tailed type 2 t-test was applied to all data. P values ≤0.05 were considered statistically significant.
Publication 2008
Anatomic Landmarks Animals Bone Marrow Cranium Dental Caries Donors Epistropheus Estrus Hybrids Institutional Animal Care and Use Committees Mice, Inbred C57BL Microscopy, Confocal Microscopy, Video Mus Postoperative Care Scalp Sterility, Reproductive Sutures

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Publication 2011
Anatomic Landmarks Cortex, Cerebral Outpatients

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Publication 2010
Anatomic Landmarks Brain Mental Recall

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Publication 2023
Anatomic Landmarks Animals Brain Females Ferrets Males Tissues Ultrasonics White Matter
During the experiment, 1 researcher was responsible for recording videos and the other was responsible for collecting plantar pressure. In order to prevent the shake of clothes from affecting the accuracy of experimental data, subjects were asked to wear black tights. At the same time, in order to ensure the accuracy of plantar pressure measurement, and the subjects completed the STS movement without wearing the shoes. To obtain kinematic data, red markers were attached to the following anatomical landmarks on the left side of the subject’s body: shoulder, waist, knee, hip, and ankle joints. The waist point is located at 60% of the line between the shoulder joint and the hip joint. Subjects were seated on the seat of an armless, backless chair, which was adjusted to 100% of each subject’s knee height. Subjects were instructed to fold their arms across the chest and to rise without bringing their arms forward. Subjects began to perform STS transfer at the word “start,” at the same time, the researchers turned on video recording and begin to measure plantar pressure. The movement ended with the subject’s self-report “stop,” at the moment, and researchers finished the data collection and checked whether there were any incorrect data. Subjects performed the STS task at natural (self-selected) speed. Four different experimental conditions of IFAs were set: Nature (N), 0°(U0), 15°(U15), 30°(U30). Data were collected for 2 trials for each subject. Subjects were given adequate rest between trials to avoid fatigue. We defined the time to complete the STS as T under each condition of IFAs.
In the process of experiment, the bias mainly came from the subject, the researcher who carried out the experiment and the measurement process, and so we paid special attention to control the possible bias factors in the experimental process to ensure the accuracy and reliability of the measurement results.
Publication 2023
Anatomic Landmarks Arm, Upper Attention Chest Fatigue Hip Joint Human Body incomplete Freund's adjuvant Joints, Ankle Knee Knee Joint Movement Pressure Shoulder Shoulder Joint Tremor
The first level comparisons of encoding (scenes) vs. delay (scrambled scenes) between high and for low WM load were output as individual subject maps in Talairach space with 2 mm isotropic resolution and thresholded using a false discovery rate of q = 0.01. They were then imported into BESA Research 7.0 as functional activation weight maps for constrained dipole source analysis (Scherg, 1990 ).
For each participant, the scalp positions of the electrodes used in the simultaneous EEG-fMRI scanning sessions were estimated initially using an approximation of locations from a standard montage template (BESA-MRI-Standard-Electrodes) and then adjusted manually based on visual inspection of the indentation-artifacts caused by electrode on the scalp, which appeared as dips on the scalp surface reconstructions. An example of electrode locations for a single subject is shown in Supplementary Figure 2. Each participant’s T1-weighted anatomical MRI was segmented manually in BESA MRI v2.0 to create a 4-layer Finite Element Model (FEM) realistic head model to be used in the source analysis. Based on individual electrode coordinates, segmentation with anatomical landmarks transformed to Talairach Space, and fMRI statistical maps imported for each condition, BESA calculated the best fitting ellipsoid of each participant (Scherg, 1992 (link)). The fMRI-informed regional EEG source estimation with anatomical constraints approach has been documented to be a better modeling than seeding dipoles based solely on anatomical locations (Phillips et al., 2002 (link); Ahlfors and Simpson, 2004 (link); Ou et al., 2010 (link)).
Seed-based dipole fitting was based on a priori hypotheses to explain ERP changes as a function of task period and WM load. For encoding, two equivalent dipoles were fitted onto bilateral parahippocampal cortex (PHC) for each participant at low and high load WM conditions. For delay, two equivalent dipoles were fitted onto bilateral thalamus. For each participant, a time window was chosen from onset to the peak of the first Global Field Potential (GFP) peak, which is a measure for spatial standard deviation as a function of time (Strik and Lehmann, 1993 (link)). An example of a single participant’s GFP waveform is shown in Supplementary Figure 3 and an example analysis window used in the source analysis is shown in Supplementary Figure 4. During seeding of dipole locations, weighting with fMRI activation maps was initially turned off to avoid potential bias in determining the initial seed location. The dipoles were then fit onto the respective sources weighted by the fMRI statistical map activation using the RAP-MUSIC algorithm as implemented in BESA source space that estimates the dipole locations using the weighted fMRI images (Grech et al., 2008 (link)). The dipole positions were constrained to stay within the target regions, but their orientations were kept free before the fit. All the dipoles fell within the appropriate brain regions (PHC and thalamus) after the fit. An example fit with fMRI weighting for thalamus is shown in Supplementary Figure 5. The dipole positions were expressed as Talairach coordinates in units of millimeters (mm) and averaged across all subjects. The source waveforms for each participant and condition were exported and then imported for group source statistical analyses in BESA Statistics v2.0.
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Publication 2023
3,5-diisopropylsalicylic acid Anatomic Landmarks Brain Cortex, Cerebral fMRI Head Mental Orientation Microtubule-Associated Proteins Reconstructive Surgical Procedures Scalp Thalamus
For each brain hemisphere in each section, all ROIs were manually drawn according to the Allen Brain Atlas and using auto fluorescence from the green channel following visible anatomical landmarks and confirming AQP4 expression visibility. Each subregion measured from 0.03 to 1.69 mm2. Therefore, a universal threshold was applied manually to all images as a preferred method for reduction of the background signal influence. Subsequently, a mean area fraction covered by AQP4 in both hemispheres/sections was measured for each ROI. In total, mean AQP4 expression was calculated for 11 ROIs (retrosplenial cortex - RSP, visual - VIS; somatosensory - SS; auditory - AUD; hippocampus - HIP; perirhinal - PERI; thalamus - TH; habenula - HAB; hypothalamus - HY; pericisternal - PCS; white matter - WM) in 4 WT mice. A nonparametric Kruskal-Wallis one-way ANOVA with Dunn’s post-hoc was employed to compare the mean AQP4 channel expressions between ROIs.
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Publication 2023
Anatomic Landmarks Auditory Perception Brain Cerebral Hemispheres Fluorescence Habenula Hypothalamus Mice, Laboratory neuro-oncological ventral antigen 2, human Retrosplenial Cortex Seahorses Thalamus White Matter
ROIs were manually outlined around each anatomical subregion according to the Allen Brain Atlas, and using visible anatomical landmarks. Due to differences in fluorescent labeling intensity, each region was thresholded individually to isolate labeled blood vessels from the background, so each region measured from 0.023 to 4.67 mm2 within each hemisphere/section. Area fraction of blood vessels above the threshold was measured for each ROI. In total, mean vascular density was calculated from multiple subregions for 17 ROI (olfactory area - OLF; cingulate cortex - CA; retrosplenial cortex - RSP; primary visual - V1; primary somatosensory - S1; primary motor area - M1; auditory - AUD; hippocampus - HIP; perirhinal - PERI; insular - INS; thalamus - TH; habenula - HAB; hypothalamus - HY; caudate putamen - CP; white matter - WM; pericisternal - PCS; ependymal around lateral ventricles - EPD) in 6 KO and 6 WT animals. Further statistical comparison was performed assuming inhomogeneous signal distribution properties between different ROI (similarly as for DWI). Hence, considering independent measurements of vascular densities among ROI analyzed and due to small group size, nonparametric Mann-Whitney U-test was employed to compare the vessel densities from KO and WT animals ROI-wise.
For ROI-wise correlation analysis, a mean value of AQP4 expressions as well as vascular densities at ROI was calculated from all respective animals strain-wise.
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Publication 2023
Anatomic Landmarks Animals Auditory Perception Blood Vessel Brain Cingulate Cortex Ependyma Habenula Hypothalamus Motor Cortex, Primary Neostriatum Retrosplenial Cortex Seahorses Sense of Smell Strains Thalamus Ventricle, Lateral White Matter

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More about "Anatomic Landmarks"

Anatomical Landmarks, Anatomic References, Fiducial Markers, Anatomical Features, Anatomical Guides, Body Landmarks, Spatial Markers, Positional Cues, Localization Aids, Orientation Guides, Imaging Landmarks, Diagnostic Markers, Surgical Targets, Treatment Guides, Clinical Topography, Spatial Coordinates, Anatomical Signifiers, Locational Identifiers, Anatomical Waypoints, Geodesic Localization, Neuromagnetic Positioning, Optical Tracking, Digital Reconstruction, Spatial Digitization.
Anatomic Landmarks are distinct, recognizable physical features on the human body that serve as reference points for various medical and surgical procedures.
These landmarks play a crucial role in locating and accessing specific structures, facilitating accurate diagnosis, treatment planning, and surgical navigation.
They are commonly used in imaging techniques, such as radiography, ultrasound, and neuroimaging (e.g., MATLAB, Visual3D, Brainsight, Geodesics EGI System, Neuromag MEG system), to orient the viewer and provide spatial context.
Anatomic Landmarks ensure procedural reproducibility and enhance patient safety by helping clinicians consistently identify target sites.
This standardized terminology allows for more effective communication and collaboration among healthcare professionals, ultimately improving the quality and reliability of patient care.
Technological advancements, such as digital reconstruction (e.g., Axio Imager Z1, Neurolucida software) and spatial digitization (e.g., Fastrak digitizer, Qualisys Track Manager), further enhance the precision and accuracy of anatomical localization, contributing to more reliable research and clinical outcomes.