Relevant bibliographies by topics / HBsf

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'HBsf'

Author: Grafiati
Published: 26 February 2023
Last updated: 28 July 2024

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Journal articles on the topic "HBsf"

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ATINUKE, FASOLA. "THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA." Mediterranean Journal of Hematology and Infectious Diseases 14, no. 1 (2022): e2022001. http://dx.doi.org/10.4084/mjhid.2022.001.

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Background: Sickle cell disease is a protean disease with limited data on the phenotypic and genetic variants in Nigeria. This study was conducted to provide baseline data on these variants by characterizing the existing forms of sickle cell disease and correlating these with basic hematological parameters.
 Methods: Adult and pediatric patients with SCD were recruited from a tertiary health centre in Nigeria. Patients were age and sex matched with healthy controls. Blood samples were obtained for Full Blood Count, phenotyping by High Performance Liquid Chromatography and genotyping for a
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Yu, Wan-Hui, Kuan-Lin Chen, Yeh-Tai Chou, I.-Ping Hsueh, and Ching-Lin Hsieh. "Responsiveness and Predictive Validity of the Hierarchical Balance Short Forms in People With Stroke." Physical Therapy 93, no. 6 (2013): 798–808. http://dx.doi.org/10.2522/ptj.20120259.

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BackgroundThe lack of knowledge about the responsiveness and predictive validity of a set of Hierarchical Balance Short Forms (the HBSF) in people with stroke limits the utility of the HBSF in both clinical and research settings.ObjectiveThe purpose of this study was to investigate the responsiveness and predictive validity of the HBSF in people receiving inpatient rehabilitation after stroke.DesignA prospective cohort study was conducted.MethodsSixty-six participants completed both the 6-item HBSF and the 12-item Postural Assessment Scale for Stroke (PASS) after admission to the rehabilitatio
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Wang, Cong, Xinyi Tian, Xiayin Zhang, Zhiming Zhang, Xiaoyu Zhang, and Xiaoxiong Zeng. "Physicochemical Characterizations, Digestibility, and Lipolysis Inhibitory Effects of Highland Barley Resistant Starches Prepared by Physical and Enzymatic Methods." Molecules 28, no. 3 (2023): 1065. http://dx.doi.org/10.3390/molecules28031065.

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This study aimed to investigate the differences in the physicochemical and structural characteristics, digestibility, and lipolysis inhibitory potential in vitro of highland barley resistant starches (HBRSs) prepared by autoclaving (HBSA), microwave-assisted autoclaving (HBSM), isoamylase (HBSI) and pullulanase (HBSP) debranching modifications. Results revealed that the resistant starch content of native starch was significantly elevated after modifications. HBSA and HBSM showed distinctly higher swelling power and water-binding capacities along with lower amylose amounts and solubilities than
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Colombatti, Raffaela, Soundrie Padayachee, Corrina Macmahon, et al. "Cerebral Blood Flow-Velocity Is Associated with Increased Leukocyte Count and Systolic Blood Pressure in HbSS but Not HbSC." Blood 126, no. 23 (2015): 989. http://dx.doi.org/10.1182/blood.v126.23.989.989.

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Abstract BACKGROUND Sickle Cell Disease (SCD) is the most frequent severe genetic disease worldwide. Its frequency is rising in European countries, including Italy and Ireland. In Europe Sickle SC (HbSC) is the second most common form of SCD after sickle cell anaemia (HbSS/HbSB°) and accounts for 25-30% of cases. Neurological events are among the most frequent and disabling complications in children with SCD with an important impact on quality of life, health and educational system costs (DeBaun et al., 2012). Overt and silent stroke are reported in in HbSC disease, although to a lesser extent
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Awaitey, Daniel Kpodji, Elliot Elikplim Akorsu, Emmanuel Allote Allotey, et al. "Assessment of Hemoglobin Variants in Patients Receiving Health Care at the Ho Teaching Hospital: A Three-Year Retrospective Study." Advances in Hematology 2020 (March 21, 2020): 1–6. http://dx.doi.org/10.1155/2020/7369731.

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Background. It is estimated that one out of every three Ghanaians has hemoglobin genotype mutation. This change in genetic make-up may result in genotypes such as HbAS, HbSS, and HbSC. Many children in low- and middle-income countries die even before they are diagnosed with sickle cell disease (SCD). In Africa, there are limited data on the incidence and prevalence of SCD and the Volta region of Ghana is no exception. Aim. The aim of this study was to determine the prevalence of SCD and to assess the hemoglobin variants among patients attending Ho Teaching Hospital. Methods. A retrospective st
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Gangwe, Anil B., Abhishek Singh, Swapnil M. Parchand, Deepshikha Agrawal, Chibuzo B. Ekumankama, and Raj Vardhan Azad. "Asymmetric sickle cell retinopathy in a patient with sickle cell hemoglobin D disease: A case report." Indian Journal of Ophthalmology - Case Reports 3, no. 3 (2023): 760–61. http://dx.doi.org/10.4103/ijo.ijo_981_23.

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Sickle cell disease (SCD), the most commonly inherited hemoglobinopathy, can result in vision loss due to sickle cell retinopathy (SCR), vascular occlusions, and retinal atrophy. SCR is more common in heterozygous (HbSc) than homozygous (HbSS) patients. HbD (Punjab) is a less commonly reported form of hemoglobin in SCD, seen in northwestern states of India. Patients with sickle cell hemoglobin D disease (HbSD) can clinically behave like HbSS. We report a case of asymmetric SCR and multiple branch retinal artery occlusions in a patient with sickle cell hemoglobin D disease in central India.
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Zhou, Yue, Xianchun Xia, Zhonghu He, Xing Li, Zaifeng Li, and Daqun Liu. "Fine Mapping of Leaf Rust Resistance Gene LrZH84 Using Expressed Sequence Tag and Sequence-Tagged Site Markers, and Allelism with Other Genes on Wheat Chromosome 1B." Phytopathology® 103, no. 2 (2013): 169–74. http://dx.doi.org/10.1094/phyto-08-12-0186-r.

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Zhou 8425B, possessing the leaf rust resistance gene LrZH84, is an elite wheat (Triticum aestivum) parental line in the Yellow-Huai Valley region of China. In the present study, 2,086 F2 plants derived from Zhou 8425B/Chinese Spring were used for fine mapping of LrZH84 with expressed sequence tag (EST) and sequence-tagged site (STS) markers. Seventy inter-simple sequence repeat EST and STS markers on 1BL were used to screen the two parents and resistant and susceptible bulks; those polymorphic were used to analyze the entire F2 population. Three EST markers (BF474863, BE497107, and CD373538) w
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Gil, Gislene Pereira, Galina Ananina, Mariana Maschietto, et al. "Epigenetic analysis in placentas from sickle cell disease patients reveals a hypermethylation profile." PLOS ONE 17, no. 9 (2022): e0274762. http://dx.doi.org/10.1371/journal.pone.0274762.

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Pregnancy in Sickle Cell Disease (SCD) women is associated to increased risk of clinical and obstetrical complications. Placentas from SCD pregnancies can present increased abnormal findings, which may lead to placental insufficiency, favoring adverse perinatal outcome. These placental abnormalities are well known and reported, however little is known about the molecular mechanisms, such as epigenetics. Thus, our aim was to evaluate the DNA methylation profile in placentas from women with SCD (HbSS and HbSC genotypes), compared to uncomplicated controls (HbAA). We included in this study 11 pre
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Thomas-Dewing, Rowena R., John Chambers, Nicholas Hart, and Jo Howard. "A Comparison of Echocardiogram Screening for Pulmonary Hypertension in Asymptomatic and Symptomatic Patients with Sickle Cell Disease." Blood 112, no. 11 (2008): 4801. http://dx.doi.org/10.1182/blood.v112.11.4801.4801.

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Abstract Background: Pulmonary hypertension (PHT) is an increasingly recognised complication of sickle cell disease (SCD), even in asymptomatic patients. Studies from the US have shown a prevalence of PHT of between 20–30% and this has been associated with an increased mortality. The prevalence of PHT in the UK sickle cell disease population is unknown. Method: We identified adult patients with a diagnosis of SCD (HbSS, HbSC, HbSB0thalassaemia and HbSB+ thalassaemia) who had screening for PHT using transthoracic echocardiography over a one year period. We compared the echocardiographic finding
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Telfer, Paul, Banu Kaya, Dimitris A. Tsitsikas, Filipa Barroso, and Cynthia Sangarappillai. "Hydroxyurea Therapy Does Not Impact Current Survival Estimates in the East London Sickle Cell Newborn Cohort Study." Blood 132, Supplement 1 (2018): 3655. http://dx.doi.org/10.1182/blood-2018-99-116544.

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Abstract Background: There is a lack of data to estimate current life expectancy in adults who have had continual access to best standard of care since birth. Furthermore, the effect of disease-modifying treatments on survival has not been adequately evaluated. Data from the East London Newborn Cohort Study provide information on these outcomes in the setting of the UK National Health Service. Methods: Inclusion criteria were birth in the London boroughs of Hackney and Tower Hamlets, diagnosis by newborn screening (local programme from 1983 to 2004, and national programme from 2004 onwards), r
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Dissertations / Theses on the topic "HBsf"

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MANUNZA, LAURA. "Determinanti genetici dell’espressione dell’emoglobina HbF." Doctoral thesis, Università degli Studi di Cagliari, 2016. http://hdl.handle.net/11584/266630.

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Background: Increased levels of fetal hemoglobin (HbF, α2γ2) may reduce beta thalassemia severity. We have investigated the influence of three known major loci on the HbF trait (HBG2, rs7482144; BCL11A, rs1427407; HBS1L-MYB, rs9399137), prevalent Sardinian mutations in human Kruppel-like factor 1 (KLF1) recently reported to be responsible for persistence of high levels of fetal hemoglobin (HPFH) and two new predicted polymorphisms (HBE1 rs67385638; HBG2 rs2855122) involved in the increased HbF and HbA2 levels. Methods: We selected 4 cohorts of samples with different phenotypes: 87 HPFH,
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Каплін, Микола Микитович, Николай Никитович Каплин, Mykola Mykytovych Kaplin та ін. "Динамика выявлений HBs Ag у доноров". Thesis, Издательство СумГУ, 1997. http://essuir.sumdu.edu.ua/handle/123456789/24811.

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Baier, Astrid. "Bakterielle Kontamination von HbF-Erythrozytenkonzentraten aus Plazentarestblut." Diss., lmu, 2003. http://nbn-resolving.de/urn:nbn:de:bvb:19-15274.

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Höfer, Ulrich. "Etablierung eines QCM-basierten Verfahrens zur Bestimmung von Antikörperaffinitäten und der Charakterisierung des Bindungsverhaltens mono- und polyklonaler Anti-HBs aus Patientenseren mit HBs-Antigen und ausgewählten Mutationen des HBs-Antigens /." Regensburg, 2008. http://opac.nebis.ch/cgi-bin/showAbstract.pl?sys=000253144.

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GUESNE, HERAUD CATHERINE. "Prevalence de l'antigene hbs chez les femmes enceintes suivies au chu de limoges : etude sur une periode de 4 ans." Limoges, 1988. http://www.theses.fr/1988LIMO0103.

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Tatu, Thanusak. "Genetic basis of HbF and F cell production in human adults." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393553.

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Jung, Michael. "Hochauflösende Fourier-Transform-Infrarot-Spektroskopie der dreiatomigen Moleküle HCP, DCP und HBS." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=960908080.

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Schwarz, David [Verfasser]. "Der IRF3- und IRF7-Knockout im HBs-transgenen Mausmodell / David Christian Schwarz." Gießen : Universitätsbibliothek, 2020. http://d-nb.info/1210444348/34.

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Schwarz, David Christian [Verfasser]. "Der IRF3- und IRF7-Knockout im HBs-transgenen Mausmodell / David Christian Schwarz." Gießen : Universitätsbibliothek, 2020. http://d-nb.info/1210444348/34.

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Ražanienė, Vidita. "5,7,9 klasių mokinių gebėjimų, laisvalaikio ir nelaimingų atsitikimų sąsajos Kaišiadorių ir Prienų rajone (HBSC tyrimas, 2010)." Master's thesis, Lithuanian Academic Libraries Network (LABT), 2011. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20110628_155124-34338.

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Darbo tikslas. Ištirti 5, 7, 9 klasių mokinių gebėjimų, laisvalaikio ir nelaimingų atsitikimų sąsajas Kaišiadorių ir Prienų rajone. (HBSC tyrimas, 2010). Darbo uždaviniai. Išanalizuoti paauglių fizinį aktyvumą, atsižvelgiant į aktyvią ir pasyvią veiklą; išanalizuoti tiriamosios grupės mokymosi gebėjimus paauglių požiūriu; apžvelgti tiriamosios grupės mokinių sužeidimus ir nelaimingus atsitikimus; įvertinti sąsajas tarp gebėjimų, laisvalaikio praleidimo būdo ir nelaimingų atsitikimų. Tyrimo objektas. Kaišiadorių ir Prienų rajono 5, 7, 9 klasių mokiniai. Tyrimo metodika. Atlikta Kaišiadorių i
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Books on the topic "HBsf"

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1962-, Nohria Nitin, and Khurana Rakesh 1948-, eds. Advancing leadership: An HBS centennial colloquium. Harvard Business Press, 2009.

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Kent (England). Planning Officers Group. and House-Builders Federation, eds. KPOG/HBF housing land study 1987. Kent Planning Officers' Group, 1988.

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Dabruck, Jan Philipp. Target Station Optimization for the High-Brilliance Neutron Source HBS. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-05639-1.

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Swenson, Sally. Prairie pioneers: A bibliography : Henry Bird Steinhauer (HBS), 1817-1884 ... S. Swenson, 1996.

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Harvard Business School. Student Clubs of HBS. Art Society. Global exposure project 2011: Second annual showcase of HBS photography. s.n.], 2011.

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Currie, Candace. Inequalities in young people's health: HBSC international report from the 2005/2006 Survey. World Health Organization, 2008.

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Graham-Taylor, Sue. Are you with HBF?: The private world behind the public face. University of Western Australia Press for the Hospital Benefit Fund of Western Australia in association with the Centre for Western Australian History, the University of Western Australia, 1994.

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Lobbichler, Klaus. Klinische Bedeutung der quantitativen hepatobiliären Funktionsszintigraphie (HBFS) für die Diagnostik des Galleabflusses nach Cholezystektomie. [s.n.], 1985.

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Handley, Martin James. Lithic assemblage variability at Charlie Lake Cave (HbRf-39): A stratified rockshelter in northeastern British Columbia. The author, 1994.

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United States. National Aeronautics and Space Administration., ed. Final report to NASA-Ames Research Center on characterization-curing-property studies of HBRF 55A resin formulations. Polytechnic Institute of New York, 1985.

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Book chapters on the topic "HBsf"

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Woods, Douglas W., Matthew R. Capriotti, Madison Pilato, et al. "HBSS." In Encyclopedia of Autism Spectrum Disorders. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1698-3_100659.

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Feitelson, Mark. "Anti-HBs Monoclonal Antibodies." In Molecular Components of Hepatitis B Virus. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2573-4_4.

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Lees, A. "Madopar HBS — Klinische Erfahrungen." In Möglichkeiten zur Optimierung der Parkinson-Therapie. Urban und Vogel, 1988. http://dx.doi.org/10.1007/978-3-89935-547-5_30.

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Sakr, Mahmoud F. "Hungry Bone Syndrome (HBS)." In Parathyroid Gland Disorders. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-07418-9_11.

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Woods, Douglas W., Matthew R. Capriotti, Madison Pilato, et al. "Handicaps, Behavior and Skills Schedule (HBSS)." In Encyclopedia of Autism Spectrum Disorders. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1698-3_54.

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de Jonge, Maretha. "Handicaps, Behavior and Skills Schedule (HBSS)." In Encyclopedia of Autism Spectrum Disorders. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-91280-6_54.

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Cavallo, Franco, Corrado Celata, and Veronica Velasco. "Health Behavior in School-Aged Children (HBSC)." In Encyclopedia of Quality of Life and Well-Being Research. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-0753-5_1244.

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Cavallo, Franco, Corrado Celata, and Veronica Velasco. "Health Behavior in School-Aged Children (HBSC)." In Encyclopedia of Quality of Life and Well-Being Research. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-69909-7_1244-2.

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Cavallo, Franco, Corrado Celata, and Veronica Velasco. "Health Behavior in School-Aged Children (HBSC)." In Encyclopedia of Quality of Life and Well-Being Research. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-17299-1_1244.

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Mandach, Ursula, Peter Tuchschmid, Albert Huch, and Renate Huch. "A Simple Method for HbF Analysis." In Continuous Transcutaneous Monitoring. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1927-6_36.

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Conference papers on the topic "HBsf"

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Guindo, A., Z. Cisse, I. Keita, et al. "Acceptabilité, performances diagnostiques et faisabilité du dépistage néonatal de la drépanocytose à l'aide de deux tests de diagnostic rapide: "Sicklescan" et "Hemotypesc" au Mali." In MSF Paediatric Days 2022. MSF-USA, 2022. http://dx.doi.org/10.57740/84y6-3a16.

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BACKGROUND AND AIMS La drépanocytose est une maladie potentiellement mortelle dans les populations africaines, en particulier chez les enfants de moins de 5 ans. Dans des contextes à ressources limitées, l'amélioration de leur prise en charge passe par un diagnostic précoce et fiable. Nous avons évalué l'acceptabilité maternelle et des professionnels de santé et les performances diagnostiques de deux tests de diagnostic rapide (TDR) pour le dépistage systématique de la drépanocytose chez le nouveau-né au Mali. METHODS Un dépistage systématique des Syndromes Drépanocytaires Majeurs (SDM) (HbSS,
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Ferraz, Narrimam de Oliveira, Lucas Duarte Martins, Lucas de Oliveira Barbosa, Paula Celline Duque Paiva, and Carolina Teixeira Heleno. "AVALIAÇÃO DA EFICÁCIA E DOS EFEITOS ADVERSOS DA HIDROXIUREIA NO TRATAMENTO DA DOENÇA FALCIFORME: UMA REVISÃO SISTEMÁTICA." In I Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/630.

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Introdução: A doença falciforme (DF) é um espectro de condições hematológicas caracterizado por alterações a nível molecular e estrutural da hemoglobina, implicando sua polimerização e alteração morfológica da hemácia quando há hipóxia. Isso causa obstruções no fluxo sanguíneo, implicando dor intensa e danos perfusionais. Está, portanto, associada à alta taxa de morbi-mortalidade. A hidroxiureia (HU) é o único tratamento licenciado para DF. Devido à capacidade de aumentar níveis de hemoglobina fetal (HbF), tem sido associada a melhora significativa de sintomas, principalmente dor. Objetivos: P
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Nute, Richard. "HBSE and insulation coordination." In 2015 IEEE Symposium on Product Compliance Engineering (ISPCE). IEEE, 2015. http://dx.doi.org/10.1109/ispce.2015.7138705.

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Moor, I., K. Winter, J. Markert, and M. Richter. "Die HBSC-Studie Sachsen-Anhalt." In Soziale Gesundheit neu denken: Herausforderungen für Sozialmedizin und medizinische Soziologie in der digitalen Spätmoderne – Gemeinsame Jahrestagung der DGSMP und der DGMS. Georg Thieme Verlag, 2022. http://dx.doi.org/10.1055/s-0042-1753892.

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Uygur, Ercan. "Savings and Incomes of Households and Inclusive Growth." In International Conference on Eurasian Economies. Eurasian Economists Association, 2015. http://dx.doi.org/10.36880/c06.01446.

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This paper has three aims. The first is to explore the savings behavior of different income groups of households, with an emphasis on those with low incomes. This is achieved by going through the Household Budget Surveys (HBS) in some developing and developed countries. The HBSs reveal that the majority of poor sections of the societies do not save or have negative savings. The second aim of the paper is to explain the economic and social aspects of the savings behaviour of income groups, particularly those with low incomes. The paper explains that the “no saving/dissaving” behaviour of the lo
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Queiroz, Saulo, and Edimar Bauer. "The Hidden Binary Search Tree." In III Encontro de Teoria da Computação. Sociedade Brasileira de Computação - SBC, 2018. http://dx.doi.org/10.5753/etc.2018.3160.

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In this paper we review and enhance the Hidden Binary Search Tree (HBST) presented in [Queiroz 2017]. The HBST idea builds on the assumption an n-node self-balanced tree (e.g. AVL) requires to assure O(log2 n) worst-case search, namely, comparison between keys takes constant time. Therefore the size of each key in bits is fixed to B = O(log2 n) once n is determined, otherwise the O(1)-time comparison assumption does not hold. HBST generalizes the searchtree property such that the position of a node in the tree results from comparing its key against 'ideal' reference values associated to its an
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Kager, L. "Neue Konzepte zur HbF-Induktion." In HÄMATOLOGIE HEUTE 2019. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1684061.

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Derzi, Mariane de Melo, Vivian Kelen Gonçalves de Almeida, Thamires Felix dos Santos, Júlia Gabriela Melo Carneiro da Cunha, and Doralice Conceição da Paz Neta. "USO DA ELETROFORESE NO DIAGNÓSTICO DA ANEMIA FALCIFORME: UMA REVISÃO INTEGRATIVA." In XXVII Semana de Biomedicina Inovação e Ciência. Editora IME, 2021. http://dx.doi.org/10.51161/9786588884119/10.

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Introdução: A anemia falciforme (AF) é uma doença hereditária que se caracteriza por uma mutação no cromossomo 11, onde há uma alteração no sexto códon da cadeia beta (β) substituindo Adenina por Timina (1). Dessa forma, ocorre a alteração na morfologia dando origem à hemoglobina S (HbS), que adquire a forma de foice em decorrência da baixa quantidade de oxigênio, ocasionando má circulação, dor, e lesões em órgãos como cérebro, pulmões e rins. A eletroforese é um dos principais métodos usados para diagnóstico dessa patologia, identificando as hemoglobinas HbA, HbF, HbC e HbS, servindo, portant
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Sonnet, J., and E. K. Gini. "IMPROVEMENT OF SICKLE CELL DEFORMABILITY BY PIRACETAM IN VITRO AND IN VIVO." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644214.

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Piracetam (P) (2-oxo-pyrrolidine acetamide) has Theological properties and has been used at various dosages over the past decade for the management of psychosenescent syndromes. On maintenance therapy, at the oral dosage of 160 mg/kg/day, in four divided doses, P reduces the number of vaso-occlusive crises in sickle cell homozygous patients, to about a fifth of what could be expected without drug. After oral intake at the latter dosage P's bioavailability in the blood ranges from 0.5to 1 m mol/1. Microsieving on polycarbonate filters, 5 μ m por size, of diluted suspensions (haematocrit 1%) of
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Honda, Inoue, Iwatsubo, and Sakanobe. "Protocol For Home Bus System (HBS)." In IEEE International Conference on Consumer Electronics. IEEE, 1990. http://dx.doi.org/10.1109/icce.1990.665908.

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Reports on the topic "HBsf"

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Ahmed, K., X. Bai, Y. Zhang, and B. Biner. High-Burnup-Structure (HBS): Model Development in MARMOT for HBS Formation and Stability Under Radiation and High Temperature. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1364505.

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Karthikeyan, Annamalai, Chad A. Martindale, and Steve W. Martin. A New Method to Prepare Polycrystalline Meta-Thioboric Acid, (HBS2)3. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada390409.

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Delgrande Jordan, Marina, Valentine Schmidhauser, and Nora Balsiger. Étude Health Behaviour in School-aged Children (HBSC) 2022 en Suisse. Rapport de méthodes. Addiction Suisse, 2023. http://dx.doi.org/10.58758/rech151.

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Amores, Antonio F., Henrique Basso, Johannes Simeon Bischl, et al. Inflation, fiscal policy and inequality. The distributional impact of fiscal measures to compensate for consumer inflation. Banco de España, 2024. http://dx.doi.org/10.53479/36624.

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Abstract:
This paper analyses the distributional impact of high consumer inflation in the euro area and government measures to compensate households in 2022. The study uses the tax-benefit microsimulation model for the European Union (EUROMOD) with microdata as the input – EU statistics on income and living conditions (EU-SILC) and household budget surveys (HBS) – to quantify the distributional impact of inflation, income support measures and measures aimed at containing prices. The analysis confirms that purchasing power and welfare were more severely affected by the 2022 inflation surge among lower-in
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Delgrande Jordan, Marina, and Valentine Schmidhauser. Comportements en ligne des 11 à 15 ans en Suisse – Situation en 2022 et évolution récente. Résultats de l'étude Health Behaviour in School-aged Children (HBSC). Addiction Suisse, 2023. http://dx.doi.org/10.58758/rech154.

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Delgrande Jordan, Marina, Jeanne Vorlet, Nora Balsiger, and Valentine Schmidhauser. Habitudes en matière d’alimentation et d’activité physique des 11 à 15 ans en Suisse – Situation en 2022 et évolution dans le temps. Résultats de l’étude Health Behaviour in School-aged Children (HBSC). Addiction Suisse, 2024. http://dx.doi.org/10.58758/rech163.

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Delgrande Jordan, Marina, Nora Balsiger, and Valentine Schmidhauser. La consommation de substances psychoactives des 11 à 15 ans en Suisse – Situation en 2022 et évolution dans le temps – Résultats de l’étude Health Behaviour in School-aged Children (HBSC). Rapport de recherche No 149. Addiction Suisse, 2023. http://dx.doi.org/10.58758/rech149.

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Delgrande Jordan, Marina, Valentine Schmidhauser, and Nora Balsiger. Delgrande Jordan M., Schmidhauser V. & Balsiger, N. (2023). Santé et bien-être des 11 à 15 ans en Suisse – Situation en 2022, évolution dans le temps et corrélats – Résultats de l’étude Health Behaviour in School-aged Children (HBSC) (rapport de recherche No 159). Addiction Suisse, 2023. http://dx.doi.org/10.58758/rech159.

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