 Atrophy
"Atrophy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
| Descriptor ID |
D001284
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| MeSH Number(s) |
C23.300.070
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Atrophy".
Below are MeSH descriptors whose meaning is more specific than "Atrophy".
This graph shows the total number of publications written about "Atrophy" by people in UAMS Profiles by year, and whether "Atrophy" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2024 | 1 | 0 | 1 | | 2023 | 0 | 1 | 1 | | 2022 | 0 | 2 | 2 | | 2020 | 0 | 3 | 3 | | 2019 | 1 | 1 | 2 | | 2018 | 0 | 1 | 1 | | 2015 | 0 | 2 | 2 | | 2013 | 0 | 1 | 1 | | 2011 | 0 | 3 | 3 | | 2007 | 0 | 2 | 2 | | 2005 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 | | 2002 | 1 | 0 | 1 | | 1999 | 0 | 1 | 1 | | 1997 | 0 | 1 | 1 | | 1995 | 0 | 2 | 2 |
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Below are the most recent publications written about "Atrophy" by people in Profiles over the past ten years.
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Zengin S, Guthrie J, Zoumberos N, Hamza M, Shalin SC. Sebaceous gland atrophy due to seborrheic dermatitis in a patient with alopecia: A potential pitfall. J Cutan Pathol. 2024 Jul; 51(7):513-517.
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Georgiou M, Fujinami K, Robson AG, Fujinami-Yokokawa Y, Shakarchi AF, Ji MH, Uwaydat SH, Kim A, Kolesnikova M, Arno G, Pontikos N, Mahroo OA, Tsang SH, Webster AR, Michaelides M. RBP3-Retinopathy-Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping. Am J Ophthalmol. 2024 02; 258:119-129.
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Viggars MR, Wen Y, Peterson CA, Jarvis JC. Automated cross-sectional analysis of trained, severely atrophied, and recovering rat skeletal muscles using MyoVision 2.0. J Appl Physiol (1985). 2022 03 01; 132(3):593-610.
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Sharma R, Aravindhan A, Puente C, Veerapandiyan A. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay due to Novel Mutations in the SACS Gene. J Investig Med High Impact Case Rep. 2022 Jan-Dec; 10:23247096221139670.
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Baril AA, Beiser AS, Mysliwiec V, Sanchez E, DeCarli CS, Redline S, Gottlieb DJ, Maillard P, Romero JR, Satizabal CL, Zucker JM, Seshadri S, Pase MP, Himali JJ. Slow-Wave Sleep and MRI Markers of Brain Aging in a Community-Based Sample. Neurology. 2021 03 09; 96(10):e1462-e1469.
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Steele CE, Morrell DS, Evans M. Atrophic lesion on the abdomen. Cutis. 2020 Dec; 106(6):E17-E19.
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Parolini B, Di Salvatore A, Pinackatt SJ, Baldi A, Besozzi G, Finzi A, Cardillo D, Sallam AB, Frisina R. LONG-TERM RESULTS OF AUTOLOGOUS RETINAL PIGMENT EPITHELIUM AND CHOROID TRANSPLANTATION FOR THE TREATMENT OF EXUDATIVE AND ATROPHIC MACULOPATHIES. Retina. 2020 Mar; 40(3):507-520.
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Owen AM, Patel SP, Smith JD, Balasuriya BK, Mori SF, Hawk GS, Stromberg AJ, Kuriyama N, Kaneki M, Rabchevsky AG, Butterfield TA, Esser KA, Peterson CA, Starr ME, Saito H. Chronic muscle weakness and mitochondrial dysfunction in the absence of sustained atrophy in a preclinical sepsis model. Elife. 2019 12 03; 8.
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Wang J, Rousseau J, Kim E, Ehresmann S, Cheng YT, Duraine L, Zuo Z, Park YJ, Li-Kroeger D, Bi W, Wong LJ, Rosenfeld J, Gleeson J, Faqeih E, Alkuraya FS, Wierenga KJ, Chen J, Afenjar A, Nava C, Doummar D, Keren B, Juusola J, Grompe M, Bellen HJ, Campeau PM. Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction. Am J Hum Genet. 2019 12 05; 105(6):1237-1253.
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Sullivan DR, Morrison FG, Wolf EJ, Logue MW, Fortier CB, Salat DH, Fonda JR, Stone A, Schichman S, Milberg W, McGlinchey R, Miller MW. The PPM1F gene moderates the association between PTSD and cortical thickness. J Affect Disord. 2019 12 01; 259:201-209.
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Sonderman KA, Wolf LL, Armstrong LB, Taylor K, Jiang W, Weil BR, Koehlmoos TP, Ricca RL, Weldon CB, Haider AH, Rice-Townsend SE. Testicular atrophy following inguinal hernia repair in children. Pediatr Surg Int. 2018 May; 34(5):553-560.
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Petukhova TA, Foolad N, Prakash N, Shi VY, Sharon VR, O'Brecht L, Ali IA, Feldstein S, Halls J, Wang Q, Li CS, Sivamani RK. Objective volumetric grading of postacne scarring. J Am Acad Dermatol. 2016 Jul; 75(1):229-31.
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Chepelev NL, Long AS, Williams A, Kuo B, Gagn? R, Kennedy DA, Phillips DH, Arlt VM, White PA, Yauk CL. Transcriptional Profiling of Dibenzo[def,p]chrysene-induced Spleen Atrophy Provides Mechanistic Insights into its Immunotoxicity in MutaMouse. Toxicol Sci. 2016 Jan; 149(1):251-68.
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Hasan KM, Mwangi B, Cao B, Keser Z, Tustison NJ, Kochunov P, Frye RE, Savatic M, Soares J. Entorhinal Cortex Thickness across the Human Lifespan. J Neuroimaging. 2016 05; 26(3):278-82.
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Gupta HV, Vengoechea J, Sahaya K, Virmani T. A splice site mutation in ATP6AP2 causes X-linked intellectual disability, epilepsy, and parkinsonism. Parkinsonism Relat Disord. 2015 Dec; 21(12):1473-5.
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