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1.
Bull Entomol Res ; 104(6): 707-15, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25033090

RESUMO

The common green lacewing Chrysoperla carnea is a key biological control agent employed in integrated pest management (IPM) programs for managing various insect pests. Spinosad is used for the management of pests in ornamental plants, fruit trees, vegetable and field crops all over the world, including Pakistan. A field-collected population of C. carnea was selected with spinosad and fitness costs and realized heritability were investigated. After selection for five generations, C. carnea developed 12.65- and 73.37-fold resistance to spinosad compared to the field and UNSEL populations. The resistant population had a relative fitness of 1.47, with substantially higher emergence rate of healthy adults, fecundity and hatchability and shorter larval duration, pupal duration, and development time as compared to a susceptible laboratory population. Mean relative growth rate of larvae, intrinsic rate of natural population increase and biotic potential was higher for the spinosad-selected population compared to the susceptible laboratory population. Chrysoperla species are known to show resistance to insecticides which makes the predator compatible with most IPM systems. The realized heritability (h 2) value of spinosad resistance was 0.37 in spinosad-selected population of C. carnea.


Assuntos
Insetos/fisiologia , Resistência a Inseticidas , Inseticidas/toxicidade , Macrolídeos/toxicidade , Animais , Agentes de Controle Biológico , Combinação de Medicamentos , Aptidão Genética , Padrões de Herança , Insetos/efeitos dos fármacos , Insetos/genética , Insetos/crescimento & desenvolvimento , Resistência a Inseticidas/genética , Larva/efeitos dos fármacos , Larva/genética , Larva/fisiologia
2.
Ir J Med Sci ; 193(2): 755-760, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-37580623

RESUMO

ABSTACT: BACKGROUND: Coronavirus disease (COVID-19) currently named SARS-CoV-2 is a contagious disease caused by a coronavirus; incompatible data are present on the possible relationship among COVID-19 vaccines and hair loss. AIMS: The objective of the current study was to assess dermoscopically the prevalence of hair loss among an Egyptian population following COVID-19 vaccination. METHODS: A total of 2000 participants were enrolled in this cross-sectional study. Adult males and females who received one of recognized COVID-19 vaccine were included, irrespective of the status of previous COVID-19 infection. Those who were aged less than 18 years or above 60 years were excluded. Furthermore, subjects self-reporting hair loss were assessed by dermoscopy. RESULTS: Among the studied cases, n = 478 (23.9%) complained of hair loss following vaccination. The majority of cases noticed their hair loss during the first 2 months post-vaccination (n = 215 after the first month and n = 158 after the 2nd month respectively). CONCLUSION: We reported prevalence of post-vaccination hair fall that was confirmed by trichoscopy and which affected approximately one quarter of participants who received COVID-19 vaccines. Other factors, such as stress and infection, cannot be excluded and remain to be further investigated by larger multicenter studies.


Assuntos
Vacinas contra COVID-19 , COVID-19 , Adulto , Masculino , Feminino , Humanos , Vacinas contra COVID-19/efeitos adversos , Estudos Transversais , Dermoscopia , Egito/epidemiologia , Prevalência , SARS-CoV-2 , COVID-19/epidemiologia , COVID-19/prevenção & controle , Alopecia/epidemiologia , Alopecia/etiologia , Vacinação/efeitos adversos
3.
Nat Genet ; 14(3): 285-91, 1996 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-8896557

RESUMO

Two forms of the neurodegenerative disorder spinocerebellar ataxia are known to be caused by the expansion of a CAG (polyglutamine) trinucleotide repeat. By screening cDNA expression libraries, using an antibody specific for polyglutamine repeats, we identified six novel genes containing CAG stretches. One of them is mutated in patients with spinocerebellar ataxia linked to chromosome 12q (SCA2). This gene shows ubiquitous expression and encodes a protein of unknown function. Normal SCA2 alleles (17 to 29 CAG repeats) contain one to three CAAs in the repeat. Mutated alleles (37 to 50 repeats) appear particularly unstable, upon both paternal and maternal transmissions. The sequence of three of them revealed pure CAG stretches. The steep inverse correlation between age of onset and CAG number suggests a higher sensitivity to polyglutamine length than in the other polyglutamine expansion diseases.


Assuntos
Proteínas/genética , Sequências Repetitivas de Ácido Nucleico , Degenerações Espinocerebelares/genética , Adolescente , Adulto , Idade de Início , Alelos , Sequência de Aminoácidos , Anticorpos Monoclonais , Ataxinas , Sequência de Bases , Criança , Clonagem Molecular , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/imunologia , Feminino , Regulação da Expressão Gênica , Humanos , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Proteínas do Tecido Nervoso , Proteína de Ligação a TATA-Box , Fatores de Transcrição/genética , Fatores de Transcrição/imunologia , Repetições de Trinucleotídeos
4.
Nat Genet ; 17(1): 65-70, 1997 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9288099

RESUMO

The gene for spinocerebellar ataxia 7 (SCA7) has been mapped to chromosome 3p12-13. By positional cloning, we have identified a new gene of unknown function containing a CAG repeat that is expanded in SCA7 patients. On mutated alleles, CAG repeat size is highly variable, ranging from 38 to 130 repeats, whereas on normal alleles it ranges from 7 to 17 repeats. Gonadal instability in SCA7 is greater than that observed in any of the seven known neuro-degenerative diseases caused by translated CAG repeat expansions, and is markedly associated with paternal transmissions. SCA7 is the first such disorder in which the degenerative process also affects the retina.


Assuntos
Cromossomos Humanos Par 3 , Proteínas do Tecido Nervoso/genética , Degenerações Espinocerebelares/genética , Repetições de Trinucleotídeos , Adulto , Idade de Início , Idoso , Alelos , Sequência de Aminoácidos , Ataxina-7 , Mapeamento Cromossômico , Cromossomos Artificiais de Levedura , Clonagem Molecular , Feminino , Marcadores Genéticos , Variação Genética , Impressão Genômica , Humanos , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Proteínas do Tecido Nervoso/biossíntese , Proteínas do Tecido Nervoso/química , Retina/patologia , Degeneração Retiniana/genética , Degeneração Retiniana/fisiopatologia , Degenerações Espinocerebelares/mortalidade , Degenerações Espinocerebelares/fisiopatologia
5.
Eur Rev Med Pharmacol Sci ; 27(17): 7935-7945, 2023 09.
Artigo em Inglês | MEDLINE | ID: mdl-37750622

RESUMO

OBJECTIVE: Spinal muscular atrophy (SMA) is common among various populations because the genetic makeup is monogamous due to consanguineous marriages. Two genes, i.e., survival motor neuron (SMN1) and neuronal apoptosis inhibitory protein (NAIP) are mapped to the SMA vicinity of chromosome 5q13. The main objective of the study was to develop a solitary advanced genetic tool for the diagnosis of SMA by using SMN1 gene exon 7 and NAIP gene exon 5. PATIENTS AND METHODS: This study involved SMA patients (n=84) belonging to different clinical features and socio-economic status. The identity of the intact NAIP gene is primarily based on the amplification of exon 5 only in those SMA patients that have a deletion of SMN1 gene exon 7. Healthy controls (n=84) were also included in this study. The mutational analysis was observed through the Sanger sequencing method, where chromatograms were observed by using Chromas version 2.6.0. RESULTS: This study showed a higher prevalence of SMA in females than in males. NAIP gene is considered a phenotype modifier as most SMA patients (94.90%) have SMN1 exon 7 deletion along with a deletion in exon 5 of the NAIP gene. Single nucleotide conversion C-T in exon 7 of SMN1 gene leads to its complete deletion. Mutated proteins encoded by SMN1 and NAIP genes also result in degeneration and muscle weakness in SMA patients. CONCLUSIONS: These SMA-associated gene deletions can be used as a molecular evaluation tool for pre- and postnatal diagnosis of SMA. This will be valuable when there is a need for precise and consistent results with a strong focus on quantification.


Assuntos
Atrofia Muscular Espinal , Proteína Inibidora de Apoptose Neuronal , Proteína 1 de Sobrevivência do Neurônio Motor , Feminino , Humanos , Masculino , Proteínas Mutadas de Ataxia Telangiectasia , Éxons , Debilidade Muscular , Atrofia Muscular Espinal/diagnóstico , Atrofia Muscular Espinal/genética , Proteína Inibidora de Apoptose Neuronal/genética , Proteína 1 de Sobrevivência do Neurônio Motor/genética
6.
Eur Rev Med Pharmacol Sci ; 27(18): 8628-8638, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37782178

RESUMO

OBJECTIVE: The main objective of performing this study was the mutational analysis of Forkhead box family member (FoxP3) and Interleukin-22 (IL-22) genes and their associations with systemic lupus erythematosus (SLE). MATERIALS AND METHODS: A total of sixty blood samples were collected from SLE patients from different hospitals in Lahore. Proforma was based on American College of Rheumatology (ACR) criteria. The total time for this research was one year (2018-2019). DNA was extracted, and FoxP3 and IL-22 genes were polymerized through PCR and further sequenced through the Sanger Sequencing method. Chromas version 2.6.6 was used for the similarity index of sequences. NG_060763 and NG_007392.1 were used as Reference Sequences of IL-22 and FoxP3 genes, respectively. RESULTS: Three already identified Single Nucleotide Polymorphisms (SNPs) in the IL-22 gene i.e., rs2227491, rs2227485, and rs2227513, were confirmed in the sequencing results of SLE patients. Results showed that there were nine novel mutations (27.27%) in the case of the IL-22 gene in the studied genotyped samples. These SNPs had remarkably increased allele T frequency in rs2227485 and allele C frequency in rs2227491 and rs2227513. On the other hand, in the case of FoxP3 gene exon 2, there was an addition of T at position 10 in the intronic portion, thus not involved in the progression of the disease. CONCLUSIONS: The importance of cytokine-mediated signaling pathways, such as the IL-22 gene, is thus established. Novel variants in the IL-22 gene likely contributed significantly to the development of this autoimmune disorder. The current study found that the dysregulation of the inflammatory markers in SLE is not related to the FoxP3 gene, even though FoxP3 is implicated in the tolerance process.


Assuntos
Lúpus Eritematoso Sistêmico , Polimorfismo de Nucleotídeo Único , Humanos , Íntrons , Frequência do Gene , Mutação , Lúpus Eritematoso Sistêmico/diagnóstico , Lúpus Eritematoso Sistêmico/genética , Éxons , Fatores de Transcrição Forkhead/genética , Predisposição Genética para Doença , Estudos de Casos e Controles , Interleucina 22
7.
Pediatr Radiol ; 42(9): 1064-9, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22526282

RESUMO

BACKGROUND: Catheter rupture during CT angiography has prompted policies prohibiting the use of electronic injectors with peripherally inserted central venous catheters (PICCs) not only for CT but also for MRI. Consequently, many institutions mandate hand injection for MR angiography, limiting precision of infusion rates and durations of delivery. OBJECTIVE: To determine whether electronic injection of gadolinium-based contrast media through a range of small-caliber, single-lumen PICCs would be safe without risk of catheter rupture over the range of clinical protocols and determine whether programmed flow rates and volumes were realized when using PICCs for contrast delivery. MATERIALS AND METHODS: Experiments were performed and recorded using the Medrad Spectris Solaris EP MR Injection System. PICC sizes, contrast media and flow rates were based on common institutional protocols. RESULTS: No catheters were damaged during any experiments. Mean difference between programmed and delivered volume was 0.07 ± 0.10 mL for all experiments. Reduced flow rates and prolonged injection durations were observed when the injector's pressure-limiting algorithm was triggered, only in protocols outside the clinical range. CONCLUSION: PICCs commonly used in children can withstand in vitro power injection of gadolinium-based contrast media at protocols significantly above clinical levels.


Assuntos
Cateteres Venosos Centrais , Meios de Contraste/administração & dosagem , Análise de Falha de Equipamento , Falha de Equipamento , Meglumina/análogos & derivados , Compostos Organometálicos/administração & dosagem , Segurança de Equipamentos , Injeções Intravenosas , Meglumina/administração & dosagem
8.
Neurol Neurochir Pol ; 46(4): 351-6, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23023434

RESUMO

BACKGROUND AND PURPOSE: The aim of this study was to translate and validate the Iranian version of the Functional Assessment Measure (FAM) among patients with spinal cord injury (SCI). MATERIAL AND METHODS: Two hundred patients with SCI participated in this study. A convenience sampling approach was used for selection of the patients. The FAM was translated into Persian language and then independently translated back into English. The reliability of the FAM was assessed by test-retest methods with a 14-day interval for interrater reliability. Intraclass correlation coefficient (ICCs) was calculated and interrater reliability and intrarater reliability were assessed. RESULTS: The mean age of the patients was 35.7 years (SD, 7.2) and 86% of patients were male.The Cronbach alpha coefficient for both raters was above 0.70. Intrarater reliability of the Iranian version of the FAM ranged from good to excellent agreement. The highest level of intrarater reliability was observed for Community mobility (ICC = 0.93). There was good to excellent agreement for interrater reliability of the FAM. The FAM could differentiate between subgroups of patients based on the level of injury but not for the time elapsed from the injury. CONCLUSIONS: Based on the results of this study, the Iranian version of the FAM (FAM-Ir) was highly valid and reliable for evaluation of functional ability in patients with SCI. Therefore, we would suggest that the FAM could also be used as an assessment tool for SCI patients.


Assuntos
Avaliação da Deficiência , Índice de Gravidade de Doença , Traumatismos da Medula Espinal/reabilitação , Inquéritos e Questionários/normas , Traduções , Adulto , Comparação Transcultural , Feminino , Humanos , Irã (Geográfico) , Idioma , Masculino , Pessoa de Meia-Idade , Medição da Dor , Psicometria , Reprodutibilidade dos Testes , Traumatismos da Medula Espinal/psicologia , Adulto Jovem
9.
Int J Biol Macromol ; 217: 902-909, 2022 Sep 30.
Artigo em Inglês | MEDLINE | ID: mdl-35870631

RESUMO

Non-enzymatic sensing of chlorpyrifos (CPF) has been demonstrated over structurally functionalized the ternary bio nanocomposite comprised of cupric oxide, sodium alginate, and polyaniline-based hybrid (CuO/SA-g-PANI) based electrode using a laboratory designed portable potentiometric set up. The prepared composite and constituents were characterized for structure, morphology, and physical properties with the help of fourier transform infrared, X-ray diffraction, Scanning electron microscope, and other relevant standard methods. The obtained results revealed the formation of porous, electrical conductivity, structurally functionalized, responsiveness composite due to molecular engineering, and structural synergism for sensing applications. Further, the film of the prepared composite was explored as the electrode for nonenzymatic potentiometric sensing of residual chlorpyrifos in synthetic and natural sample i.e., tap water, soil, mango, and cabbage. The sensor exhibits a wider sensing range 1.0-120.0 µM, improved sensitivity 1.8790 mV·µM-1·cm-2, detection limit 0.375 µM, response time 120 s, recovery time 16 s with 99.80 % accuracy, and stability of 72 days at neutral 7.0 pH and ambient temperature i.e. 25 °C. Further, the sensing mechanism has been also explained on the basis of structural change in CPF and electrode materials due to their surface interaction along with formation induced electrode potential.


Assuntos
Clorpirifos , Alginatos , Compostos de Anilina , Cobre/química
10.
Br Poult Sci ; 51(3): 354-60, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20680870

RESUMO

1. Combinations of chromium and copper were added to the diet to assess their effects on broiler meat characteristics. 2. For this purpose 175 one-day-old broiler chicks were divided into 7 equal groups and were given treatment feeds containing copper sulphate, chromium chloride and nicotinic acid in different combinations. 3. The study was carried out for 5 weeks and samples were collected at the end of 15, 29 and 35 d of treatment and at 42 d after a withdrawal period of one week. 4. Cholesterol content had decreased significantly in breast meat at d 29 in all treatment groups. In thigh meat, it decreased significantly at d 29 in groups receiving two concentrations of chromium + two concentrations of copper. Cholesterol content remained lower even after withholding the treatment for one week. 5. Crude fat content decreased significantly in breast meat in all treatment groups. In thigh meat, at d 29, a significant reduction in crude fat was observed only in birds receiving low chromium and high copper. 6. Crude protein at d 29 increased significantly in breast meat of birds receiving low chromium and high copper, and low or high chromium, while it decreased significantly in treatment groups after withholding the treatment. In thigh meat, at d 29, it increased significantly in treatment groups but decreased significantly after withholding the treatment. 7. It was concluded that chromium and copper, along with nicotinic acid, have modulating effects on broiler meat under tropical conditions.


Assuntos
Galinhas/metabolismo , Cloretos/farmacologia , Compostos de Cromo/farmacologia , Sulfato de Cobre/farmacologia , Carne , Niacina/farmacologia , Ração Animal , Animais , Proteínas Aviárias/metabolismo , Distribuição da Gordura Corporal , Galinhas/crescimento & desenvolvimento , Colesterol/metabolismo , Dieta/veterinária , Valor Nutritivo , Potássio/metabolismo
11.
Sci Rep ; 10(1): 577, 2020 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-31953500

RESUMO

The present study aimed to explore a new source of montmorillonite and to develop an extraction and purification protocol for its isolation from raw clay samples acquired from the Koh-e-Suleiman mountain range in Pakistan. The process involved the collection of raw clay from the source, identification and quantification of montmorillonite. Granulometric extraction and purification protocols increased the montmorillonite content from 21.8-25.1% in the raw clay to 90.1-93.9% after small-scale extraction and 85.33-89.33% on a larger scale. A techno-economic analysis highlighted the practicality and economic benefits of large-scale extraction for industrial applications. This study highlights the existence of a substantial new source of this valuable clay which is currently used across multiple industries including construction, pottery making, pharmaceuticals, cosmetics and engineering. It is intuitively expected that the large-scale extraction of the material will improve the economic condition of the region by providing employment opportunities to locals and may be a valuable resource for export.

13.
Br J Neurosurg ; 22(2): 286-8, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18348028

RESUMO

A 52-year-old lady presented with progressive paraparesis. MRI revealed collapse of D9 vertebrae which was infiltrated by a low signal lesion both on T1 and T2. She underwent vertebrectomy and insertion of moss cage. The histology came back as amyloidoma. The presentation, investigation and management of primary amyloidoma of the spine is discussed along with a review of the literature.


Assuntos
Amiloidose/diagnóstico , Paraparesia/etiologia , Doenças da Medula Espinal/diagnóstico , Vértebras Torácicas , Amiloidose/cirurgia , Diagnóstico Diferencial , Feminino , Humanos , Pessoa de Meia-Idade , Resultado do Tratamento
15.
Pediatr Endocrinol Rev ; 6 Suppl 1: 123-6, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19337165

RESUMO

The modern radiologist is unlikely to encounter the classic radiographic features of thalassemia other than in teaching files. The main pathological change that leads to radiological skeletal changes in beta thalassemia major is extensive marrow proliferation. The severity of the skeletal responses is related to the type of thalassemia, the extent and duration of the disease, the type of treatment and the volume of blood transfusions given to the patient, as well as the side effects of transfusion-chelation therapy, and also depends on the bone involved. The radiographic features can be divided into those affecting the skeleton (axial and appendicular) and those occurring extra-medullary. Axial skeletal changes mainly include skull and facial bones, paranasal sinuses, vertebral bodies, weight-bearing bones, while appendicular skeleton manifestations are more pronounced in peripheral bones, mainly hands and feet as well as ribs. Patients on repeated blood transfusions and iron-chelation therapy may demonstrate variable range of manifestations than the scope of untreated patients.


Assuntos
Osso e Ossos/patologia , Talassemia beta/patologia , Osso e Ossos/diagnóstico por imagem , Humanos , Quelantes de Ferro/efeitos adversos , Radiografia , Reação Transfusional , Talassemia beta/diagnóstico por imagem , Talassemia beta/terapia
16.
Neotrop Entomol ; 47(5): 716, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29728982

RESUMO

Due to an unfortunate turn of events, the surname of the last author appeared incorrectly in the original publication as the name should have read Binyameen.

17.
Neotrop Entomol ; 47(5): 709-715, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29654414

RESUMO

Musca domestica Linnaeus (house fly, Diptera: Muscidae) is a major veterinary and medical important pest all over the world. These flies have ability to develop resistance to insecticides. The present trial was performed to discover the inheritance mode (autosomal, dominance, number of genes involved) and preliminary mechanism of methoxyfenozide resistance in order to provide basic information necessary to develop resistance management strategy for this pest. A strain of M. domestica (MXY-SEL) was exposed to methoxyfenozide for 44 generations which developed a 5253.90-fold level of resistance to methoxyfenozide. The overlapping fiducial limits of LC50 values of the reciprocal crosses, F1 (MXY-SEL ♂ × Susceptible ♀) and F1† (MXY-SEL ♀ × Susceptible ♂), suggest that inheritance of methoxyfenozide resistance was an autosomal and likely completely dominant trait (DLC = 0.93 and 0.94 for F1 and F1†, respectively). Backcrosses of the F1 with the parental MXY-SEL or Susceptible population predict a polygenic mode of inheritance. Piperonyl butoxide significantly altered the LC50 values, suggesting enhanced detoxification by cytochrome P450-dependent monooxygenases is a major mechanism of resistance to methoxyfenozide in the MXY-SEL strain. The estimated realized heritability was 0.07 for methoxyfenozide. These results would be helpful for the better management of M. domestica.


Assuntos
Moscas Domésticas/genética , Hidrazinas , Resistência a Inseticidas/genética , Inseticidas , Hormônios Juvenis , Animais , Cruzamentos Genéticos , Sistema Enzimático do Citocromo P-450/genética , Inibidores Enzimáticos , Genes de Insetos , Herança Multifatorial , Seleção Genética
18.
J Hazard Mater ; 353: 522-533, 2018 Jul 05.
Artigo em Inglês | MEDLINE | ID: mdl-29723813

RESUMO

The present study proposes a robust one-step hydrothermal treatment method for synthesis of high strength geopolymer-supported zeolites utilizing industrial by-products (fly ash and blast furnace slag), which can be potentially used as bulk-type solid adsorbents. The results revealed that the geopolymer-supported zeolites, possessing distinct strengths, zeolite phases (Na-P1, Na-chabazite, and analcime) and pore features depending on the mix design and synthesis conditions, can be easily synthesized employing the proposed one-step method. The geopolymer-supported zeolites exhibited the characteristics of mesoporous materials which are typically desired for commercial adsorbents. The maximum adsorption capacity for Pb2+ was found to be about 37.9 mg/g which is relatively higher than the other bulk-type adsorbents reported for Pb2+ to date. Since industrial by-products are used for synthesis of these materials, it will help in reducing the environmental hazards associated with the permanent disposal of such by-products, with an added advantage that these bulk-type solid adsorbents can be easily retrieved after use unlike granular adsorbents.

19.
Radiat Prot Dosimetry ; 123(2): 209-14, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-16973669

RESUMO

The aim of the study was to evaluate the entrance surface doses (ESDs) to patients undergoing selected diagnostic X-ray examinations in major Sudanese hospitals. ESD per examination was estimated from X-ray tube output parameters in four hospitals comprising eight X-ray units and a sample of 346 radiographs. Hospital mean ESDs estimated range from 0.17 to 0.27 mGy for chest AP, 1.04-2.26 mGy for Skull AP/PA, 0.83-1.32 mGy for Skull LAT, 1.31-1.89 mGy for Pelvis AP, 1.46-3.33 mGy for Lumbar Spine AP and 2.9-9.9 mGy for Lumbar Spine LAT. With exception of chest PA examination at two hospitals, mean ESDs were found to be within the established international reference doses. The results are useful to national and professional organisations and can be used as a baseline upon which future dose measurements may be compared.


Assuntos
Vértebras Lombares/diagnóstico por imagem , Pelve/diagnóstico por imagem , Doses de Radiação , Radiografia Torácica/normas , Radiometria/normas , Crânio/diagnóstico por imagem , Coluna Vertebral/diagnóstico por imagem , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Humanos , Pessoa de Meia-Idade , Serviço Hospitalar de Radiologia/estatística & dados numéricos , Padrões de Referência , Sudão
20.
Rev. psicol. deport ; 31(3): 240-252, Oct 16, 2022. tab, graf
Artigo em Inglês | IBECS (Espanha) | ID: ibc-214738

RESUMO

Without access to skilled coaches, sports anxiety is frequent among athletes. In Saudi Arabia, the lack of emotional intelligence and other mental problems prevent athletes from doing better with sports anxiety. This study examines the direct influence of psychological Control, coach-athlete interaction, and coach support on sports anxiety in Saudi Arabia. This study also analyzes the moderating effect of coach relationship and support on the relationship between psychological Control and athletic performance. A Likert scale questionnaire is utilized to collect cross-sectional data from Saudi Arabian college athletes. When players have a good relationship with their coach, they can have greater psychological Control over their athletic performance, as revealed by the study. This research is founded on a novel concept, and its theoretical framework contributes to our understanding of sports anxiety. In addition, the research produced exceptional practical and theoretical consequences that are crucial for combating sports anxiety practically and advancing our understanding of sports anxiety, respectively. The research findings suggest future directions based on the literature that provide researchers with new insight into investigating deeper links within the sports anxiety model.(AU)


Assuntos
Humanos , Ansiedade , Inteligência Emocional , Psicologia do Esporte , Atletas , Arábia Saudita , Inquéritos e Questionários
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