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Готові списки джерел за темами / Onset of diseases / Статті в журналах

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Onset of diseases.

Статті в журналах з теми "Onset of diseases"

Автор: Grafiati

Опубліковано: 7 червня 2025

Оновлено: 2 серпня 2025

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1

van Hoorn, Bastiaan T., Suzanne C. Wilkens, and David Ring. "Gradual Onset Diseases: Misperception of Disease Onset." Journal of Hand Surgery 42, no. 12 (2017): 971–77. http://dx.doi.org/10.1016/j.jhsa.2017.07.021.

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2

Pfliegler, György, Erzsébet Kovács, György Kovács, Krisztián Urbán, Valéria Nagy, and Boglárka Brúgós. "Adult-onset rare diseases." Orvosi Hetilap 155, no. 9 (2014): 334–40. http://dx.doi.org/10.1556/oh.2014.29857.

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The present paper is focusing on rare diseases manifesting in late childhood or adulthood. A part of these syndromes are not of genetic origin, such as relatively or absolutely rare infections, autoimmune diseases, tumours, or diseases due to rare environmental toxic agents. In addition, even a large proportion of genetic disorders may develop in adulthood or may have adult forms as well, affecting are almost each medical specialization. Examples are storage disorders (e.g. adult form of Tay-Sachs disease, Gaucher-disease), enzyme deficiencies (e.g. ornithin-transcarbamylase deficiency of the

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3

Asano, Koichiro, Shigeharu Ueki, Mayumi Tamari, Yoshimasa Imoto, Shigeharu Fujieda, and Masami Taniguchi. "Adult‐onset eosinophilic airway diseases." Allergy 75, no. 12 (2020): 3087–99. http://dx.doi.org/10.1111/all.14620.

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4

Mandia, Daniele, Natalia Shor, Jean-François Benoist, and Yann Nadjar. "Adolescent-Onset and Adult-Onset Vitamin-Responsive Neurogenetic Diseases." JAMA Neurology 78, no. 4 (2021): 483. http://dx.doi.org/10.1001/jamaneurol.2020.4911.

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5

Robinson, I., and S. Neilson. "Prenatal diagnosis of late onset diseases." BMJ 306, no. 6884 (1993): 1065. http://dx.doi.org/10.1136/bmj.306.6884.1065-a.

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6

JANCIN, BRUCE. "Early-, Late-Onset Psoriasis: Distinct Diseases." Rheumatology News 10, no. 8 (2011): 44. https://doi.org/10.1016/s1541-9800(11)70538-5.

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7

Fernández-Eulate, Gorka, Christophe Carreau, Jean-François Benoist, et al. "Diagnostic approach in adult-onset neurometabolic diseases." Journal of Neurology, Neurosurgery & Psychiatry 93, no. 4 (2022): 413–21. http://dx.doi.org/10.1136/jnnp-2021-328045.

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Neurometabolic diseases are a group of individually rare but numerous and heterogeneous genetic diseases best known to paediatricians. The more recently reported adult forms may present with phenotypes strikingly different from paediatric ones and may mimic other more common neurological disorders in adults. Furthermore, unlike most neurogenetic diseases, many neurometabolic diseases are treatable, with both conservative and more recent innovative therapeutics. However, the phenotypical complexity of this group of diseases and the growing number of specialised biochemical tools account for a s

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8

Shchigoleva, A. E., P. V. Shumilov, and А. Р. Shumilov. "INFLAMMATORY BOWEL DISEASES WITH VERY EARLY ONSET." Pediatria. Journal named after G.N. Speransky 97, no. 6 (2018): 141–46. http://dx.doi.org/10.24110/0031-403x-2018-97-6-141-146.

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9

Hersh, Aimee, Emily von Scheven, and Ed Yelin. "Adult outcomes of childhood-onset rheumatic diseases." Nature Reviews Rheumatology 7, no. 5 (2011): 290–95. http://dx.doi.org/10.1038/nrrheum.2011.38.

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10

Halvorsen, Matt, Slavé Petrovski, Renée Shellhaas, et al. "Mosaic mutations in early-onset genetic diseases." Genetics in Medicine 18, no. 7 (2015): 746–49. http://dx.doi.org/10.1038/gim.2015.155.

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11

Spits, C. "Preimplantation genetic diagnosis for late-onset diseases." Reproductive BioMedicine Online 16 (January 2008): s11. http://dx.doi.org/10.1016/s1472-6483(10)61326-0.

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12

Kerschbaumer, Andrea, Christina Duftner, Martin Wenger, Andrea Klauser, and Michael Schirmer. "Fibromyalgia may mask onset of autoimmune diseases." European Journal of Pain 7, no. 3 (2003): 295–96. http://dx.doi.org/10.1016/s1090-3801(02)00112-x.

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13

JANCIN, BRUCE. "Early-, Late-Onset Psoriasis Called Different Diseases." Skin & Allergy News 42, no. 8 (2011): 26. http://dx.doi.org/10.1016/s0037-6337(11)70427-2.

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14

Caga-anan, E. C. F., L. Smith, R. R. Sharp, and J. D. Lantos. "Testing Children for Adult-Onset Genetic Diseases." PEDIATRICS 129, no. 1 (2011): 163–67. http://dx.doi.org/10.1542/peds.2010-3743.

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15

Helderman-van den Enden, A. T. J. M. "Prenatal testing for late-onset neurogenetic diseases." European Journal of Human Genetics 11, no. 12 (2003): 975. http://dx.doi.org/10.1038/sj.ejhg.5201071.

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16

Lyon-Caen, O., R. Jouvent, S. Hauser, et al. "Cognitive Function in Recent-Onset Demyelinating Diseases." Archives of Neurology 43, no. 11 (1986): 1138–41. http://dx.doi.org/10.1001/archneur.1986.00520110034010.

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17

Lazarova, M., Ts. Petrova-Gotova, and R. Yaneva. "RISK FACTORS FOR SOCIALLY SIGNIFICANT DISEASES' ONSET." Sciences of Europe, no. 130 (December 11, 2023): 76–80. https://doi.org/10.5281/zenodo.10352620.

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Анотація:

Among the risk factors for the occurrence of socially significant diseases, highest attention is paid to arterial hypertonia, the consumption of tobacco products, low physical activity, unhealthy diet, low consumption of fruit and vegetables, alcohol misuse and obesity. The purpose of the present research is to study the way of life and behaviour of group of people, in order to mitigate and prevent risk factors for the occurrence of socially significant diseases. We have implemented the following methods: documentary method for surveying the accessible documentation concerning the issue, socio

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18

Vaneva, Irina. "Establishing the time of onset of epilepsy after neurological comorbidities." Bulgarian Neurology 25, no. 2 (2024): 54–57. https://doi.org/10.5281/zenodo.15359430.

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Studying the comorbidity of epilepsy with other neurological diseases provides practical information about the need to assess the appropriate antiepileptic treatment. The aim of the study is to determine the time of onset of epilepsy after the occurrence of neurological comorbidities in patients with epilepsy and comorbid neurological disease. Patients were examined at the Department for Paroxysmal Conditions of the Multiprofile Hospital for Active Treatment in Neurology and Psychiatry &bdquo;St. Naum”, Sofia, of whom 1) 71 had epilepsy and ischemic stroke, 2) 75 had epilepsy and cerebra

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19

Murodova, Saodat. "ISCHEMIC HEART DISEASES." MODERN SCIENCE AND RESEARCH 2, no. 12 (2023): 849–51. https://doi.org/10.5281/zenodo.10406133.

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<em>In this article, what is ischemic is a dangerous disease due to its sudden onset, and the treatment of coronary artery disease begins when the pain behind the sternum is noticeable even at rest.</em>

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20

Dashore, Shuken, Sushil Pande, Milind Borkar, and Abhishek Pande. "Late Onset Bradycardia." Indian Journal of Drugs in Dermatology 1, no. 1 (2015): 23–26. https://doi.org/10.4103/wkmp-0110.170754.

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Introduction: High-dose corticosteroids are used for various autoimmune and inflammatory diseases. When supra-pharmacologic doses of corticosteroids are used intravenously for the treatment of immunobullous diseases such as pemphigus, it is likely to be associated with side effects such as electrolyte disturbances, hypertension, and psychosis. Case Reports: In these case series, we report five patients receiving high-dose of dexamethasone with or without cyclophosphamide pulse, developing an unusual form of late onset bradycardia. Details of these patients developing bradycardia after dexameth

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21

Mammadbayli, A. K., S. C. Ismailova, I. B. Rahimova, S. T. Badalova, and S. E. Aliyeva. "EARLY ONSET MULTIPLE SCLEROSIS." National Journal of Neurology 1, no. 19 (2019): 81–85. http://dx.doi.org/10.61788/njn.v1i19.10.

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Анотація:

The state of health of children and teenagers of 6-12 years and their psychological characteristics depending on the nature of social adaptation is studied. At teenagers from dysfunctional families the demonstrative, getting stuck and excitable types of accentuation of character prevail. They have the deviations of physical development which are combined with advancing of biological age and high rates of sexual development more often. They revealed the deviations in the state of health connected with social factors: more frequency of infectious diseases, diseases of digestive organs, breath an

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22

Costanzi, Marco. "Predicting Psychopathological Onset: Early Signs of Neuropsychiatric Diseases." Journal of Personalized Medicine 12, no. 5 (2022): 778. http://dx.doi.org/10.3390/jpm12050778.

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Millions of people worldwide are affected by neuropsychiatric disorders, such as anxiety, major depression, bipolar disorder, schizophrenia, obsessive–compulsive disorder, autism spectrum disorders, eating disorders, addiction, and dementia [...]

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23

Lew, Alexandra R., Timot R. Kellermayer, Balint P. Sule, and Kinga Szigeti. "Copy Number Variations in Adult-onset Neuropsychiatric Diseases." Current Genomics 19, no. 6 (2018): 420–30. http://dx.doi.org/10.2174/1389202919666180330153842.

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24

Herz, Udo, and Bryon Petschow. "Perinatal Events Affecting the Onset of Allergic Diseases." Current Drug Target -Inflammation & Allergy 4, no. 5 (2005): 523–29. http://dx.doi.org/10.2174/156801005774322144.

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25

Zhang, Liyun, Leelyn Chong, Jin Cho, Pin-Chao Liao, Feichen Shen, and Yuk Fai Leung. "Drug Screening to Treat Early-Onset Eye Diseases." Asia-Pacific Journal of Ophthalmology 1, no. 6 (2012): 374–83. http://dx.doi.org/10.1097/apo.0b013e31827a9969.

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26

Bettencourt, Conceição, Davina Hensman Moss, Michael Flower, et al. "DNA REPAIR PATHWAYS MODULATE ONSET IN POLYGLUTAMINE DISEASES." Journal of Neurology, Neurosurgery & Psychiatry 87, no. 12 (2016): e1.19-e1. http://dx.doi.org/10.1136/jnnp-2016-315106.115.

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27

Lunde, Emilie R., Shannon E. Washburn, Michael C. Golding, Shameena Bake, Rajesh C. Miranda, and Jayanth Ramadoss. "Alcohol-Induced Developmental Origins of Adult-Onset Diseases." Alcoholism: Clinical and Experimental Research 40, no. 7 (2016): 1403–14. http://dx.doi.org/10.1111/acer.13114.

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28

Manfredini, Roberto, Massimo Gallerani, Francesco Portaluppi, Raffaella Salmi, and Carmelo Fersini. "Chronobiological Patterns of Onset of Acute Cerebrovascular Diseases." Thrombosis Research 88, no. 6 (1997): 451–63. http://dx.doi.org/10.1016/s0049-3848(97)00286-7.

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29

Cohen, Meryl S. "Fetal and childhood onset of adult cardiovascular diseases." Pediatric Clinics of North America 51, no. 6 (2004): 1697–719. http://dx.doi.org/10.1016/j.pcl.2004.08.001.

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30

Ansley, D. "Aging twins offer clues to late-onset diseases." Science 259, no. 5103 (1993): 1826–28. http://dx.doi.org/10.1126/science.8456309.

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31

JOHNSON, KATE. "Childhood-Onset Diseases Create Obstacles to Adult Care." Internal Medicine News 40, no. 18 (2007): 23. http://dx.doi.org/10.1016/s1097-8690(07)71118-6.

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32

Giau, Vo Van, Eva Bagyinszky, Seong Soo A. An, and SangYun Kim. "Clinical genetic strategies for early onset neurodegenerative diseases." Molecular & Cellular Toxicology 14, no. 2 (2018): 123–42. http://dx.doi.org/10.1007/s13273-018-0015-3.

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33

Mukoyama, Tokuko, and Minoru Baba. "Onset and Development of Allergic Diseases in Children." Pediatrics International 29, no. 5 (1987): 710–13. http://dx.doi.org/10.1111/j.1442-200x.1987.tb00366.x.

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34

O’Sullivan, Lee, Melissa H. Little, Alexander N. Combes, and Karen M. Moritz. "Epigenetics and developmental programming of adult onset diseases." Pediatric Nephrology 27, no. 12 (2012): 2175–82. http://dx.doi.org/10.1007/s00467-012-2108-x.

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35

Najeemuddin, R., and I. Tur-Kaspa. "Nondisclosure PGD for late onset autosomal dominant diseases." Fertility and Sterility 94, no. 4 (2010): S43. http://dx.doi.org/10.1016/j.fertnstert.2010.07.165.

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36

Topaloĝlu, R., A. Bakkaloĝlu, Ü. Saatçi, and N. Be§ba§. "Early onset of stone diseases and primary hyperoxaluria." International Urology and Nephrology 22, no. 3 (1990): 223–26. http://dx.doi.org/10.1007/bf02550396.

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37

Vera-Lastra, Olga, Gabriela Mora, Abihai Lucas-Hernández, et al. "New Onset Autoimmune Diseases after the Sputnik Vaccine." Biomedicines 11, no. 7 (2023): 1898. http://dx.doi.org/10.3390/biomedicines11071898.

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Анотація:

The vertiginous advance for identifying the genomic sequence of SARS-CoV-2 allowed the development of a vaccine including mRNA-based vaccines, inactivated viruses, protein subunits, and adenoviral vaccines such as Sputnik. This study aims to report on autoimmune disease manifestations that occurred following COVID-19 Sputnik vaccination. Patients and Methods: A retrospective study was conducted on patients with new-onset autoimmune diseases induced by a post-COVID-19 vaccine between March 2021 and December 2022, in two referral hospitals in Mexico City and Argentina. The study evaluated patien

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38

Nakao, Kumiko, Noriko Abematsu, and Taiji Sakamoto. "Systemic diseases in patients with HTLV-1-associated uveitis." British Journal of Ophthalmology 102, no. 3 (2017): 373–76. http://dx.doi.org/10.1136/bjophthalmol-2017-310658.

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BackgroundHuman T-lymphotropic virus type 1 (HTLV-1) carriers may develop severe systemic diseases, such as adult T cell leukaemia (ATL) or HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). This study aims to investigate systemic diseases of HTLV-1 carriers who had developed HTLV-1-associated uveitis (HAU).MethodsWe investigated the occurrence of systemic diseases in 200 patients with HAU by performing a retrospective investigation of their medical records and examining the results of a postal survey.ResultsThe mean age of HAU onset was 49 years, and the total person-years f

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39

Khavkin, Anatoly I., Anastasiya A. Permyakova, Mariya O. Tsepilova, et al. "Modern View on Very Early Onset and Early Onset Inflammatory Bowel Diseases in Children." Current Pediatrics 23, no. 3 (2024): 145–51. http://dx.doi.org/10.15690/vsp.v23i3.2768.

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Nowadays, an urgent problem of pediatric gastroenterology is the study of inflammatory bowel diseases with very early onset (VEO-IBD), which have unique genetic, clinical, immunological, morphological, and laboratory sings. Early VEO-IBD is usually considered as monogenic disease, especially in combination with congenital immune defects, which leads to difficulties in diagnosis and management this pathology. Despite this, systematization of information about this group of nosological forms of IBD is practically not carried out. This article presents a review of the available information on eti

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40

Hong, Ki Hoon, Jieun Park, Jihye Kim, and So Ra Kim. "Correlation and Odds Ratio between Circulatory Diseases and the Onset of Ocular Diseases." Journal of Korean Ophthalmic Optics Society 24, no. 2 (2019): 169–80. http://dx.doi.org/10.14479/jkoos.2019.24.2.169.

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41

Shadrin, O. G., R. V. Mostovenko, M. H. Horіanska, T. L. Marushko, and A. A. Kovalchuk. "Risk factors of inflammatory bowel diseases in young children." Modern pediatrics. Ukraine, no. 7(135) (November 28, 2023): 33–37. http://dx.doi.org/10.15574/sp.2023.135.33.

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Анотація:

In recent decades, there has been a rapid increase in the incidence of inflammatory bowel diseases in the children's population, especially in the age group under 6 years old. Risk factors significantly affect the reactive response of the child's organism and the probability of a pathology occurrence. Purpose - to analyze risk factors for the development of inflammatory bowel diseases with very early onset in children. Materials and methods. The anamnestic data of 78 examined patients with inflammatory bowel diseases - 17 patients with inflammatory bowel diseases with a very early onset and 61

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42

Natale, Ginny, and Sean Clouston. "CARDIOVASCULAR DISEASES PREDICT ALZHEIMER’S DISEASE ONSET IN NON-DEPRESSED ADULTS." Innovation in Aging 6, Supplement_1 (2022): 756. http://dx.doi.org/10.1093/geroni/igac059.2746.

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Abstract We examined the mediating or moderating effect of stroke on the effect of cardiovascular disease (CVD) and the onset of Alzheimer’s disease (AD) in a nationally-representative sample of older Americans with and without clinical depression. Diagnosis of CVD was adjudicated with the established Health and Retirement Study (1992–2016) methodology and included self-reported coronary heart disease, angina, heart failure, myocardial infarction, or other heart conditions. Probable-AD and probable-Stroke were identified inferentially using a validated pattern recognition algorithm. Analyses w

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43

Gracia-Ramos, Abraham Edgar, Eduardo Martin-Nares, and Gabriela Hernández-Molina. "New Onset of Autoimmune Diseases Following COVID-19 Diagnosis." Cells 10, no. 12 (2021): 3592. http://dx.doi.org/10.3390/cells10123592.

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There is growing evidence that coronavirus disease 2019 (COVID-19) can lead to a dysregulation of the immune system with the development of autoimmune phenomena. The consequence of this immune dysregulation ranges from the production of autoantibodies to the onset of rheumatic autoimmune disease. In this context, we conducted a systematic review to analyze the current data regarding the new-onset systemic and rheumatic autoimmune diseases in COVID-19 patients. A literature search in PubMed and Scopus databases from December 2019 to September 2021 identified 99 patients that fulfilled the speci

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44

Sonawale, Dr Archana, Dr Nilakshi Sabnis, and Dr Nirmal Bankar. "Study of new onset cutaneous manifestations in Rheumatic Diseases." International Journal of Medical Research and Review 6, no. 8 (2018): 510–18. http://dx.doi.org/10.17511/ijmrr.2018.i08.17.

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45

Siegmund, Kimberly D., and Alexandre A. Todorov. "Linkage Analysis for Diseases with Variable Age of Onset." Human Heredity 50, no. 3 (2000): 205–10. http://dx.doi.org/10.1159/000022916.

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46

Ariga, Hiroyoshi. "Common Mechanisms of Onset of Cancer and Neurodegenerative Diseases." Biological & Pharmaceutical Bulletin 38, no. 6 (2015): 795–808. http://dx.doi.org/10.1248/bpb.b15-00125.

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47

JOHNSON, WILLIAM G. "Late-onset neurodegenerative diseases-the role of protein insolubility." Journal of Anatomy 196, no. 4 (2000): 609–16. http://dx.doi.org/10.1046/j.1469-7580.2000.19640609.x.

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48

Matricardi, Sara, Laura Canafoglia, Anna Ardissone, et al. "Epileptic phenotypes in children with early‐onset mitochondrial diseases." Acta Neurologica Scandinavica 140, no. 3 (2019): 184–93. http://dx.doi.org/10.1111/ane.13130.

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49

Shapiro, Elsa G. "Understanding and measuring neurodegeneration in childhood onset lysosomal diseases." Molecular Genetics and Metabolism 120, no. 1-2 (2017): S122. http://dx.doi.org/10.1016/j.ymgme.2016.11.316.

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50

Ghidoni, Roberta, Giuliano Binetti, and Gabriella Marcon. "Late onset neurodegenerative diseases: A theoretical point of view." Medical Hypotheses 72, no. 1 (2009): 102. http://dx.doi.org/10.1016/j.mehy.2008.08.014.

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