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Artykuły w czasopismach na temat „Hereditary effect”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Шахназаров, К. Ю. "The «fluid memory» effect in steel, cast iron and silumin." Informacionno-technologicheskij vestnik, no. 2(24) (June 17, 2020): 179–85. http://dx.doi.org/10.21499/2409-1650-2020-24-2-179-185.

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Явление структурной наследственности получило промышленное применение, несмотря на то что «механизм передачи наследственных признаков расплаву, их сохранение, зарождение в нем новых признаков и передача их твердому металлу - все это сложные, во многом неизученные вопросы» (Б.А. Баум с коллегами). На примерах стали, чугуна и алюминия предпринята попытка обоснования предположения, что одним из механизмов передачи наследственных признаков может быть эффект «памяти жидкости», который заключается в сохранении ее свойств при очень сильном разбавлении. The phenomenon of structural heredity is used by

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DURU, FERIDE, and AYTEMIZ GÜRGEY. "Effect of corticosteroids in hereditary spherocytosis." Pediatrics International 36, no. 6 (1994): 666–68. http://dx.doi.org/10.1111/j.1442-200x.1994.tb03266.x.

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Myslyakova, Yu G. "Developing a Typology of Regions Based on Their Predisposition to Scientific and Technological Development." Economics and Management 27, no. 10 (2021): 775–85. http://dx.doi.org/10.35854/1998-1627-2021-10-775-785.

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Aim. The presented study aims to describe the proposed typology of regions based on their predisposition to scientific and technological development in the context of hereditary industrial, social, and institutional determinants of economic territorial development. Tasks. The authors develop a methodological approach to forming a basic criterion for the classification of regions; develop a methodology for the classification of regions based on their predisposition to scientific and technological development with allowance for the economic impact of their hereditary core; test the authors’ deve

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Baskerville, Richard, Nykle Krijgsveld, Patrick Esser, Glen Jeffery, and Joanna Poulton. "The Effect of Photobiomodulation on the Treatment of Hereditary Mitochondrial Diseases." Journal of Lasers in Medical Sciences 14 (October 10, 2023): e41. http://dx.doi.org/10.34172/jlms.2023.41.

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Introduction: Despite a wide variety of clinical presentations in hereditary Mitochondrial Diseases, muscle fatigue is a common theme and impairs a patient’s quality of life and ability to function. Current treatments are only supportive and include nutritional supplementation and physical therapy. Photobiomodulation therapy (PBMT) using low-intensity, narrow spectrum light in the red/near infrared (NIR) range, from a low-level laser or light-emitting diode sources, enhances mitochondrial function in preclinical and clinical studies on a range of conditions. However, little research has been d

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Major, Tamás, Réka Gindele, Gábor Balogh, Péter Bárdossy, and Zsuzsanna Bereczky. "Founder Effects in Hereditary Hemorrhagic Telangiectasia." Journal of Clinical Medicine 10, no. 8 (2021): 1682. http://dx.doi.org/10.3390/jcm10081682.

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A founder effect can result from the establishment of a new population by individuals from a larger population or bottleneck events. Certain alleles may be found at much higher frequencies because of genetic drift immediately after the founder event. We provide a systematic literature review of the sporadically reported founder effects in hereditary hemorrhagic telangiectasia (HHT). All publications from the ACVRL1, ENG and SMAD4 Mutation Databases and publications searched for terms “hereditary hemorrhagic telangiectasia” and “founder” in PubMed and Scopus, respectively, were extracted. Follo

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Pootrakul, P., K. Kitcharoen, P. Yansukon, et al. "The effect of erythroid hyperplasia on iron balance." Blood 71, no. 4 (1988): 1124–29. http://dx.doi.org/10.1182/blood.v71.4.1124.1124.

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Abstract Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective erythropoiesis (beta-thalassemia/hemoglobin E), 13 subjects with ineffective erythropoiesis and hemolytic anemia (hemoglobin H), and seven subjects with hemolytic anemia (hereditary spherocytosis). A consistent relationship within each group existed between the degree of erythropoiesis and radioiron absorption. Although the effect of erythropoiesis on iron absorption was of similar magnitude in the two thalassemia groups, the effect

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Pootrakul, P., K. Kitcharoen, P. Yansukon, et al. "The effect of erythroid hyperplasia on iron balance." Blood 71, no. 4 (1988): 1124–29. http://dx.doi.org/10.1182/blood.v71.4.1124.bloodjournal7141124.

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Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective erythropoiesis (beta-thalassemia/hemoglobin E), 13 subjects with ineffective erythropoiesis and hemolytic anemia (hemoglobin H), and seven subjects with hemolytic anemia (hereditary spherocytosis). A consistent relationship within each group existed between the degree of erythropoiesis and radioiron absorption. Although the effect of erythropoiesis on iron absorption was of similar magnitude in the two thalassemia groups, the effect in heredi

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8

Can, Ferda, Tansu Büyükgül, Nuray Yılmaz Cakmak, et al. "EFFECT OF HEREDITARY THROMBOPHILIA ON ARTERIAL THROMBOSIS." Hematology, Transfusion and Cell Therapy 46 (May 2024): 3–4. http://dx.doi.org/10.1016/j.htct.2024.04.006.

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Tverdyi, Dmitrii, Evgeny Makarov, and Roman Parovik. "Hereditary Mathematical Model of the Dynamics of Radon Accumulation in the Accumulation Chamber." Mathematics 11, no. 4 (2023): 850. http://dx.doi.org/10.3390/math11040850.

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Mathematical modeling is used to study the hereditary mechanism of the accumulation of radioactive radon gas in a chamber with gas-discharge counters at several observation points in Kamchatka. Continuous monitoring of variations in radon volumetric activity in order to identify anomalies in its values is one of the effective methods for studying the stress–strain state of the geo-environment with the possibility of building strong earthquake forecasts. The model equation of radon transfer, taking into account its accumulation in the chamber and the presence of the hereditary effect (heredity

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10

Murtazina, Aysylu F., Olga A. Shchagina, Sergey S. Nikitin, Elena L. Dadali, and Alexander V. Polyakov. "Current view on phenotypic and genetic features of autosomal recessive inherited peripheral neuropathies." Annals of Clinical and Experimental Neurology 13, no. 1 (2019): 55–69. https://doi.org/10.25692/acen.2019.1.7.

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Inherited peripheral neuropathies (IPNs) are a heterogeneous group of hereditary motor and sensory neuropathies (HMSN), hereditary motor neuropathies, and hereditary sensory neuropathies. IPNs can be inherited in autosomal dominant, autosomal recessive or X-linked manner. In clinical practice, isolated cases are more common, and the absence of genealogical data significantly complicates differential diagnosis. About 45% of HMSN cases lack genetic confirmation. For a number of autosomal recessive IPNs, peculiar clinical, electrophysiological and histological features can be distinguished, howev

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Abdul, Ameer Amer AbdulAmeer, and Qasim Mohammed Asmahan. "Effect of Hemoglobinopathies Disease on Adolescent Nutritional States at Hereditary Blood Diseases Centre." INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND BIO-MEDICAL SCIENCE 04, no. 07 (2024): 608–13. https://doi.org/10.5281/zenodo.12749399.

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<strong>Background:</strong>  Understanding the impact of hemoglobinopathy on teenagers' nutritional status is critical since it affects both their physical and mental well-being. Nutritional statistics are crucial at this age, particularly for adolescents with hemoglobinopathies during adolescence.   <strong>Objective</strong>(s :( What is the extent of the effect of hemoglobinopathy on nutritional status? Low, moderate, or severe   <strong>Methodology</strong><strong>:</strong> Thirty-two adolescents with hemoglobinopathy were found at the Hematology Center, Al-Zahra

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12

Rozen, Todd D. "Can the effects of the mitochondrial DNA mutations found in Leber’s hereditary optic neuropathy be protective against the development of cluster headache in smokers?" Cephalalgia Reports 3 (January 1, 2020): 251581632093957. http://dx.doi.org/10.1177/2515816320939571.

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Is it possible that some mitochondrial DNA (mtDNA) mutations enhance the risk of developing a headache disorder while other mutations actually confer a protective effect? Mitochondrial disorders have been linked to migraine but very rarely to cluster headache (CH). The true pathogenesis of CH is unknown but a linkage to cigarette smoking is irrefutable. Leber’s hereditary optic neuropathy is a syndrome of bilateral vision loss that typically manifests in a patient’s 20s and 30s, is male predominant, and its sufferers are heavy smokers and heavy drinkers. Tobacco exposure is so linked to the co

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13

Soni-Jaiswal, A., and T. J. Woolford. "A natural obturator in hereditary haemorrhagic telangiectasia." Journal of Laryngology & Otology 123, no. 6 (2009): 695–96. http://dx.doi.org/10.1017/s0022215109004964.

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AbstractObjective:Most patients with hereditary haemorrhagic telangiectasia suffer with frequent episodes of epistaxis. The aim of this case report is to highlight the effect on epistaxis, occurring in hereditary haemorrhagic telangiectasia, when nasal airflow ceases.Case report:We present the interesting case of a patient with hereditary haemorrhagic telangiectasia who experienced cessation of her recurrent, refractory epistaxis through the development of coexisting polyp disease. The patient's enlarged, grade three nasal polyps were behaving as physiological obturators, limiting airflow thro

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14

Kühnel, Thomas S., Birgit H. Wagner, Christian P. Schurr, and Jürgen Strutz. "Clinical Strategy in Hereditary Hemorrhagic Telangiectasia." American Journal of Rhinology 19, no. 5 (2005): 508–13. http://dx.doi.org/10.1177/194589240501900515.

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Background Hereditary hemorrhagic telangiectasia (HHT) is a recurrent bleeding tendency caused by vascular malformations and preferentially involving the mucous membrane of the nose. The rhinological management of epistaxis is a challenge in which the frequency of bleeding has to be reduced without damage to the nasal mucosa, despite the fact that therapy necessarily has to be repeated. Methods The clinical course in 30 patients with HHT was monitored prospectively. Nasal mucosal efflorescences underwent Nd:YAG laser therapy at individually defined intervals, and the effect on the frequency an

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Rüfer, Axel, Gerhard Müllner, Oliver Fuchs, Wolfgang R. Sperr, and Gregor Hoermann. "Hereditary alpha-tryptasemia – a potential cause of severe anaphylactic reactions and a modifier of mast cell diseases." Swiss Medical Weekly 155, no. 4 (2025): 3679. https://doi.org/10.57187/s.3679.

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Hereditary alpha-tryptasemia (HAT) is an autosomal dominant genetic trait affecting 4% to 6% of the general population. Hereditary alpha-tryptasemia is caused by an excess of alpha tryptase encoding TPSAB1 copy numbers on one parenteral allele, most often duplications or triplications, leading to elevated levels of basal serum tryptase. There might be a gene dosage effect between the number of additional TPSAB1 copies, the level of basal serum tryptase and the severity of clinical symptoms, including atopic, cutaneous, gastrointestinal, musculoskeletal, autonomic and neuropsychiatric manifesta

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Sysák, Rastislav, Katarína Brennerová, Romana Krlín, Peter Štencl, Igor Rusňák, and Mária Vargová. "Effect of Ornithine Transcarbamylase (OTC) Deficiency on Pregnancy and Puerperium." Diagnostics 12, no. 2 (2022): 415. http://dx.doi.org/10.3390/diagnostics12020415.

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Ornithine transcarbamylase (OTC) deficiency is the most common inherited metabolic disorder in urea cycles with an incidence of 1:14,000 live births. Pregnancy, childbirth and the postpartum period are considered challenging for women with this hereditary metabolic disorder, with a risk of hyperammonemia, especially in the first week after delivery. In our article, we discuss severe hepatic failure, a pregnancy complication in an OTC deficient patient that has not previously been published. Firstly, our aim is to highlight the need for a strict adherence to the recommendation of the gradual in

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Chaucer, Benjamin, Abriella Stone, Augustus Demanes, and Shawn M. Seibert. "Nivolumab-Induced Encephalitis in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome." Case Reports in Oncological Medicine 2018 (2018): 1–3. http://dx.doi.org/10.1155/2018/4273231.

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The treatment of cancer is a rapidly evolving field. As more chemotherapeutic agents become available, reporting the side effects of these agents in clinical practice becomes increasingly important. Nivolumab is one of the chemotherapeutic agents commonly used for treatment of renal cell carcinoma, metastatic melanoma, and metastatic non-small cell lung cancer. While common side effects are known and well documented, encephalitis is documented as an extremely rare side effect. We present the case of an extremely rare side effect to a common chemotherapeutic agent.

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TAKEUCHI, Noriko, Hiroka ITO, Keiko NAMIKI, and Akira KAMEI. "Effect of Calpain on Hereditary Cataractous Rat, ICR/f." Biological & Pharmaceutical Bulletin 24, no. 11 (2001): 1246–51. http://dx.doi.org/10.1248/bpb.24.1246.

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Medejel, Nadia, Loc Garon, Corinne Guitton, Thrse Cynober, and Brigitte Bader-Meunier. "Effect of subtotal splenectomy for management of hereditary pyropoikilocytosis." British Journal of Haematology 142, no. 2 (2008): 315–17. http://dx.doi.org/10.1111/j.1365-2141.2008.07140.x.

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Gurmen, Ekim Saglam, Serkan Dogan, Eren Sert, Cesareddin Dikmetas, and Sennaz Hussein. "Effect of C1 esterase inhibitor in hereditary angioedema treatment." American Journal of Emergency Medicine 35, no. 6 (2017): 942.e5–942.e6. http://dx.doi.org/10.1016/j.ajem.2017.01.052.

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LI, Ying, Liyuan Lu, and Juan LI. "Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy." Cell Biochemistry and Biophysics 74, no. 3 (2016): 365–71. http://dx.doi.org/10.1007/s12013-016-0755-4.

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Abstract Hereditary spherocytosis is an inherited red blood cell membrane disorder resulting from mutations of genes encoding erythrocyte membrane and cytoskeletal proteins. Few equipments can observe the structural characteristics of hereditary spherocytosis directly expect for atomic force microscopy In our study, we proved atomic force microscopy is a powerful and sensitive instrument to describe the characteristics of hereditary spherocytosis. Erythrocytes from hereditary spherocytosis patients were small spheroidal, lacking a well-organized lattice on the cell membrane, with smaller cell

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Mahad, C., S. Haitami, S. Adnane, I. Chafi, and I. Benyahya. "HEREDITARY GINGIVAL FIBROMATOSIS: CLINICAL CASES AND LITERATURE REVIEW." International Journal of Advanced Research 9, no. 04 (2021): 151–57. http://dx.doi.org/10.21474/ijar01/12666.

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Gingival fibromatosis (GF) is characterized by a slow and progressive proliferation that can affect the marginal and attached gingiva, or the inter-dental papillae. This condition can be localized or generalized, with varying degrees of severity.GF may develop in susceptible individuals as a side effect of systemic medications or as idiopathic gingival fibromatosis. It may also be related to hereditary factors and occurs as a non-syndromic hereditary gingival fibromatosis or as a part of a syndrome.Our aim is to describe trought four cases of hereditary gingival fibromatosis and a literature r

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Sari, Nunik Ike Yunia, Estin Gita Maringga, and Wuri Widi Astuti. "Path Analysis of the Effect of Biological and Social Factors on the Case of Breast Cancer." JURNAL INFO KESEHATAN 17, no. 2 (2019): 88–100. http://dx.doi.org/10.31965/infokes.vol17.iss2.292.

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Breast cancer is the number one cancer as the cause of death in women in developed and developing countries. Breast cancer has the highest case in women in 161 countries. The objective of this study is to analyze the influence of biological and social factors on breast cancer cases in the Public Hospital of Kediri, East Java. The research design was analytic with a retrospective cohort approach. The research sample of 105 respondents used simple random sampling. Data collection was with medical records in January-December, 2017. Data analysis used the path analysis test. The test results obtai

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Dahlan, Randah, and Eman Bablghaith. "Hereditary thrombotic thrombocytopenic purpura (TTP) with co-occurring autosomal dominant polycystic kidney disease (ADPKD)." BMJ Case Reports 15, no. 11 (2022): e250378. http://dx.doi.org/10.1136/bcr-2022-250378.

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Hereditary thrombotic thrombocytopenic purpura (TTP) and autosomal dominant polycystic kidney disease (ADPKD) are two distinct genetic diseases that may affect the kidneys through different mechanisms. ADPKD is a common genetic disorder that leads to exponential formation and growth of cysts replacing all segments of nephrons. Hereditary TTP is a rare autosomal recessive disorder that leads to the disseminated formation of arteriolar platelet-rich thrombi, which produce manifestations of various organs dysfunction. We present a case of a pregnant female with hereditary TTP co-occurring with AD

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Samadova, J. Kh, N. A. Valizadeh, and A. Y. Amirova. "ASSESSMENT OF THE ROLE OF HEREDITARY PREDISPOSITION AND HYPEROPIA RESERVE IN THE DEVELOPMENT OF MYOPIA IN PRESCHOOL AND EARLY SCHOOL-AGE CHILDREN. MYOPIA AS THE "PLAGUE" OF THE 21ST CENTURY." Azerbaijan Journal of Ophthalmology, no. 2025/17/02/53 (June 17, 2025): 27–38. https://doi.org/10.71110/ajo791020251702532738.

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Purpose – to evaluate the impact of hereditary predisposition and hyperopic reserve on the risk of myopia development in preschool and early school-age children. Material and methods The study included 200 children with emmetropic refraction, with a mean age of 6.0±0.8 years. Observation period at least 2 years. The groups were stratified according to the level of hyperopia reserve:(+) 0.75 D (low risk) and (+) 0.75 D (high risk). Additionally, the presence of myopia in one or both parents was recorded. Descriptive statistics, the following methods were used: descriptive statistics, Pearson co

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Badalov, F. B., B. A. Khudayarov, and A. Abdukarimov. "Effect of the hereditary kernel on the solution of linear and nonlinear dynamic problems of hereditary deformable systems." Journal of Machinery Manufacture and Reliability 36, no. 4 (2007): 328–35. http://dx.doi.org/10.3103/s1052618807040048.

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Dharmawansa, K. V. Surangi, David W. Hoskin, and H. P. Vasantha Rupasinghe. "Chemopreventive Effect of Dietary Anthocyanins against Gastrointestinal Cancers: A Review of Recent Advances and Perspectives." International Journal of Molecular Sciences 21, no. 18 (2020): 6555. http://dx.doi.org/10.3390/ijms21186555.

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Anthocyanins are a group of dietary polyphenols, abundant mainly in fruits and their products. Dietary interventions of anthocyanins are being studied extensively related to the prevention of gastrointestinal (GI) cancer, among many other chronic disorders. This review summarizes the hereditary and non-hereditary characteristics of GI cancers, chemistry, and bioavailability of anthocyanins, and the most recent findings of anthocyanin in GI cancer prevention through modulating cellular signaling pathways. GI cancer-preventive attributes of anthocyanins are primarily due to their antioxidative,

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ALEKBEROV, ELMAN Z., and VAFA M. MAMEDRZAYEVA. "COMPARATIVE STUDY OF THE EFFECT OF INSULIN-DEPENDENT DIABETES MELLITUS TYPE 2, HEREDITY AND SMOKING ON THE SEVERITY OF CORONARY HEART DISEASE." Bulletin of Contemporary Clinical Medicine 14, no. 6 (2021): 7–14. http://dx.doi.org/10.20969/vskm.2021.14(6).7-14.

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Introduction. The presence of high-risk factors such as hereditary burdening, tobacco smoking, and diabetes mellitus significantly worsen the prognosis in potentially healthy individuals by increasing the incidence of coronary heart disease. Aim. To study the separate influence of insulin-dependent diabetes mellitus type 2, heredity and smoking on the severity and course of coronary heart disease. Material and methods. One hundred patients with coronary heart disease were enrolled in the study. The patients were divided according to the presence of the following high-risk factors: heredity, to

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BARTNIKOWSKA, AGNIESZKA, and JOANNA KANIA-GIERDZIEWICZ. "Effect of inbreeding on the occurrence of genetic defects in Chinese Crested dogs." Medycyna Weterynaryjna 79, no. 06 (2023): 6765–2023. http://dx.doi.org/10.21521/mw.6765.

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The aim of the study was to analyse the impact of inbreeding on the frequency of hereditary diseases and the number of genetically tested dogs. The pedigrees of 100 Chinese Crested dogs from Polish Kennel Club and information about genetic tests for hereditary eye diseases and other veterinary diagnoses were collected. Inbreeding coefficients and relatedness were estimated for all dogs examined. The relationship between the level of inbreeding and genetic testing was analysed with logistic regression. The relationship between the occurrence of eye disease carriers and sex or the level of inbre

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Alanazi, Laila Mohammed, Dalal jumah Alturaif, Miqdad Hussain Alhassan, et al. "Effect of Parental History of Periodontal Disease on Children." Saudi Journal of Oral and Dental Research 7, no. 8 (2022): 192–200. http://dx.doi.org/10.36348/sjodr.2022.v07i08.002.

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Periodontitis is a risk factor for children who practice poor oral hygiene at home. This is due to the higher frequency of association between children’s and parents’ microbiota. It is likely due to the influence of both, hereditary and environmental factors. Although it is possible for periodontal disease to be passed down across generations, the underlying mechanism behind this is still unknown. According to clinical study, genetic predisposition accounts for 50% of an individual’s sensitivity to periodontal disease. Because clear information on the issue is sparse, the purpose of this study

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Badescu, Minerva Codruta, Elena Rezus, Manuela Ciocoiu, et al. "Osteonecrosis of the Jaws in Patients with Hereditary Thrombophilia/Hypofibrinolysis—From Pathophysiology to Therapeutic Implications." International Journal of Molecular Sciences 23, no. 2 (2022): 640. http://dx.doi.org/10.3390/ijms23020640.

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Osteonecrosis of the jaws (ONJ) usually has a clear etiology. Local infection or trauma, radiotherapy and drugs that disrupt the vascular supply or bone turnover in the jaws are its major contributors. The thrombotic occlusion of the bone’s venous outflow that occurs in individuals with hereditary thrombophilia and/or hypofibrinolysis has a less known impact on jaw health and healing capability. Our research provides the most comprehensive, up-to-date and systematized information on the prevalence and significance of hereditary thrombophilia and/or hypofibrinolysis states in ONJ. We found that

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D'Ambrosi, Riccardo, Camilla Caldarini, Vincenza Ragone, and Renato Mario Facchini. "Effect of multiple hereditary exostoses on sports activity in children." Journal of Orthopaedics 15, no. 4 (2018): 927–30. http://dx.doi.org/10.1016/j.jor.2018.08.029.

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Meijer, Inge A., Nicolas Dupré, Bernard Brais, et al. "SPG4 Founder Effect in French Canadians with Hereditary Spastic Paraplegia." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 34, no. 2 (2007): 211–14. http://dx.doi.org/10.1017/s0317167100006065.

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Background:The most common cause of autosomal dominant Hereditary Spastic Paraplegia (HSP) is mutations in the SPG4 gene. We have previously identified novel SPG4 mutations in a collection of North American families including the c.G1801A mutation present in two families from Quebec. The aim of this study is to estimate the frequency of the c.G1801A mutation in the French Canadian (FC) population and to determine whether this mutation originates from a common ancestor.Methods:We collected and sequenced exon 15 in probands of 37 families. Genotypes of markers flanking the SPG4 gene were used to

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Das, Anirban, Deepak Bansal, Amita Trehan, and Reena Das. "Growth failure in hereditary spherocytosis and the effect of splenectomy." Indian Pediatrics 54, no. 7 (2017): 563–66. http://dx.doi.org/10.1007/s13312-017-1069-3.

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Eber, S. W., D. Ullrich, Ch P. Speer, R. Armbrust, and W. Schr�ter. "Glucuronyl transferase deficiency and mild hereditary spherocytosis: effect of splenectomy." European Journal of Pediatrics 147, no. 6 (1988): 639–42. http://dx.doi.org/10.1007/bf00442481.

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Казаков, Е. А. "Hereditary low-mode dynamo model." Вестник КРАУНЦ. Физико-математические науки, no. 2 (July 5, 2021): 40–47. http://dx.doi.org/10.26117/2079-6641-2021-35-2-40-47.

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В данной статье рассматривается модель динамо в виде двумерной динамической системы в интегро-дифференциальной форме. В модели реализован стабилизирующий генерацию поля механизм обратной связи в виде подавления α-эффекта функционалом сверточного типа от актуальных и предыдущих значений спиральности и энергии. Наличие этого механизма подавления вводит в модель эредитарность (память). Для модели была построена численная схема ввиде совмещение разностных схем для дифференциальной и интегральной части, двухступенчатый неявный методы Рунге-Кутты и метод трапеций соотвественно. Так же были рассмотре

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Sommers, De K., J. Moncrieff, and J. C. Avenant. "Paracetamol Conjugation: An Interethnic and Dietary Study." Human Toxicology 6, no. 5 (1987): 407–9. http://dx.doi.org/10.1177/096032718700600512.

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To test whether dietary or hereditary factors affect paracetamol metabolism, two groups of Venda and a group of Caucasian medical students were investigated. The Venda groups were selected as traditionally living villagers and those who followed a Western life-style. Salivary concentrations of paracetamol and urinary amounts of the glucuronide and sulphate metabolites eliminated over 22 h were determined by HPLC. The metabolite formation rate constants and the percentage of the dose eliminated as each metabolite were calculated. No significant differences were found between the data for total

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Conte, Carmine, Silvia Pelligra, Giuseppe Sarpietro, et al. "Hereditary Women’s Cancer: Management and Risk-Reducing Surgery." Medicina 59, no. 2 (2023): 300. http://dx.doi.org/10.3390/medicina59020300.

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Hereditary women’s syndromes due to inherited mutations result in an elevated risk of developing gynecological cancers over the lifetime of affected carriers. The BRCA 1 and 2 mutations, Lynch syndrome (LS), and mutations in rare hereditary syndromes increase this risk and require more effective management of these patients based on surveillance and prophylactic surgery. Patients need counseling regarding risk-reducing surgery (RRS) and the time required to perform it, considering the adverse effects of premenopausal surgery and the hormonal effect on quality of life, bone density, sexual acti

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Diachuk, Dmytro, Yurii Yashchenko, and Iryna Zabolotna. "PROGNOSTIC CRITERIA OF EXCESSIVE BODY WEIGHT DEVELOPMENT AMONG SCHOOLCHILDREN BY THE RESULTS OF ANAMNESTIC SURVEY." Wiadomości Lekarskie 75, no. 4 (2022): 814–17. http://dx.doi.org/10.36740/wlek202204112.

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The aim: To elaborate prognostic criteria to assess the risk of excessive body weight development among schoolchildren on the basis of hereditary and behavioral predictors. Materials and methods: 90 parents of school age children were interviewed by means of the social study method. Results: Hereditary status (1 and 2 congeniality degree to type 2 diabetes mellitus, arterial hypertension, excessive body weight, cases of myocardial infarction and/or stroke available among relatives) and behavioral characteristics (peculiarities of diet and physical activity of a child) were studied among school

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Zeigelboim, Bianca Simone, Maria Renata José, Geslaine Janaina Bueno dos Santos, et al. "Balance rehabilitation with a virtual reality protocol for patients with hereditary spastic paraplegia: Protocol for a clinical trial." PLOS ONE 16, no. 4 (2021): e0249095. http://dx.doi.org/10.1371/journal.pone.0249095.

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Background Neurodegenerative diseases are sporadic hereditary conditions characterized by progressive dysfunction of the nervous system. Among the symptoms, vestibulopathy is one of the causes of discomfort and a decrease in quality of life. Hereditary spastic paraplegia is a heterogeneous group of hereditary degenerative diseases involving the disorder of a single gene and is characterized by the progressive retrograde degeneration of fibers in the spinal cord. Objective To determine the benefits of vestibular rehabilitation involving virtual reality by comparing pre intervention and post int

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Dobryagina, Natalia. "Agricultural Entrepreneurship Motivation Policies: European Union Experience and Decision Theory Application." International Journal of Rural Management 15, no. 1 (2019): 97–115. http://dx.doi.org/10.1177/0973005219834739.

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The European Union (EU) policies devoted to entrepreneurship in agricultural motivation represent a wide spectrum of methods and approaches. However, lack of attention to the differences between different types of entrepreneurs might decrease the entrepreneurship motivation policies’ effectiveness. Applying Decision Theory (DT), one of the management sciences, the article determines that non-hereditary entrepreneurs, which include ex novo and early retirement groups, are expected to provide greater contribution to the rural areas development and have different decision-making process in contra

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Boeckhaus, Jan, and Oliver Gross. "Sodium-Glucose Cotransporter-2 Inhibitors in Patients with Hereditary Podocytopathies, Alport Syndrome, and FSGS: A Case Series to Better Plan a Large-Scale Study." Cells 10, no. 7 (2021): 1815. http://dx.doi.org/10.3390/cells10071815.

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Hereditary diseases of the glomerular filtration barrier are characterized by a more vulnerable glomerular basement membrane and dysfunctional podocytes. Recent clinical trials have demonstrated the nephroprotective effect of sodium-glucose cotransporter-2 inhibitors (SGLT2i) in chronic kidney disease (CKD). SGLT2-mediated afferent arteriole vasoconstriction is hypothesized to correct the hemodynamic overload of the glomerular filtration barrier in hereditary podocytopathies. To test this hypothesis, we report data in a case series of patients with Alport syndrome and focal segmental glomerulo

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Hitchings, Anne E., Penelope A. Lennox, Valerie J. Lund, and David J. Howard. "The Effect of Treatment for Epistaxis Secondary to Hereditary Hemorrhagic Telangiectasia." American Journal of Rhinology 19, no. 1 (2005): 75–78. http://dx.doi.org/10.1177/194589240501900113.

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FSADNI, MG, T. KLOPSTOCK, G. METZ, et al. "Persistence of treatment effect of idebenone in Leber's Hereditary Optic Neuropathy." Acta Ophthalmologica 90 (August 6, 2012): 0. http://dx.doi.org/10.1111/j.1755-3768.2012.t132.x.

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Alonso, Lillian G., and Thomas H. Maren. "Effect Of Food Restriction On Body Composition Of Hereditary Obese Mice." Nutrition Reviews 38, no. 9 (2009): 317–20. http://dx.doi.org/10.1111/j.1753-4887.1980.tb05972.x.

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Mandel, Hanna, Benjamin Brenner, Moshe Berant, et al. "Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis." New England Journal of Medicine 334, no. 12 (1996): 763–68. http://dx.doi.org/10.1056/nejm199603213341204.

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Casanova-Esteban, Paola, Nuria Guiral, Eva Andrés, et al. "Effect of phlebotomy on lipid metabolism in subjects with hereditary hemochromatosis." Metabolism 60, no. 6 (2011): 830–34. http://dx.doi.org/10.1016/j.metabol.2010.07.035.

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Alenezi, Wejdan M., Caitlin T. Fierheller, Neil Recio, and Patricia N. Tonin. "Literature Review of BARD1 as a Cancer Predisposing Gene with a Focus on Breast and Ovarian Cancers." Genes 11, no. 8 (2020): 856. http://dx.doi.org/10.3390/genes11080856.

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Soon after the discovery of BRCA1 and BRCA2 over 20 years ago, it became apparent that not all hereditary breast and/or ovarian cancer syndrome families were explained by germline variants in these cancer predisposing genes, suggesting that other such genes have yet to be discovered. BRCA1-associated ring domain (BARD1), a direct interacting partner of BRCA1, was one of the earliest candidates investigated. Sequencing analyses revealed that potentially pathogenic BARD1 variants likely conferred a low–moderate risk to hereditary breast cancer, but this association is inconsistent. Here, we revi

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Fonseca-Becerra, Martha Lizeth, Juan Sebastian Betancur-Castro, and Leidy Camila Perilla-García. "Angioedema hereditario tipo 1, limitaciones de la terapia profiláctica con lanadelumab: a propósito de un caso." Revista Alergia México 71, no. 4 (2024): 264–67. https://doi.org/10.29262/ram.v71i4.1323.

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Background: Hereditary Angioedema is an autosomal dominant disorder caused by a lack or decrease in the function of the C1 inhibitor. It is a rare disease with low prevalence. Treatment focuses on symptom relief and short- and long-term prevention of acute attacks. Case report: 53-year-old male patient, with recurrent edema in the face, feet, scrotum, associated with abdominal pain since he was 20 years old. Patient has a history of hereditary angioedema in first-degree relatives of consanguinity. Laboratory tests showed low levels of plasma protein (antigenic), functional C1-INH and C4. The p

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Broekmans, A. W., J. Conard, R. G. van Weyenberg, M. H. Horellou, C. Kluft, and R. M. Bertina. "Treatment of Hereditary Protein C Deficiency with Stanozolol." Thrombosis and Haemostasis 57, no. 01 (1987): 020–24. http://dx.doi.org/10.1055/s-0038-1651054.

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SummaryFive type I protein C deficient male patients received 5 mg stanozolol b.i.d. during 4 weeks. After four weeks of treatment plasma protein C activity increased from 0.42 to 0.74 U/ml and protein C antigen from 0.49 to 0.75 U/ml. This approximately 1.6 fold increase in plasma protein C was accompanied by an increase in factor II antigen (1.5 fold), factor V activity (1.6 fold), factor X antigen (1.1 fold), antithrombin III antigen (1.3 fold) and heparin cofactor II antigen (1.5 fold), while the concentration of factor VII, factor VIII, and factor IX activity, and of protein S antigen rem

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