Search results for "Mali"

showing 10 items of 3900 documents

Improving Diagnostic Performance for Thyroid Nodules Classified as Bethesda Category III or IV: How and by Whom Ultrasonography Should be Performed

2020

Background: The purpose of this prospective study is to evaluate if the association of Bethesda system and a 3-categories Ultrasonography (US) risk stratification system proposed by the American Association of Clinical Endocrinologists/American College of Endocrinology/Associazione Medici Endocrinologi improves the performance of cytology alone in III or IV categories and if further variables such as US provider (radiologist; endocrinologist, or endocrine surgeon both coming from a dedicated team) influence the accuracy of the diagnostic. Methods: 570 consecutive patients with complete clinical records, affected by Bethesda III or IV nodules, have been addressed to two public referral surgi…

AdultMaleThyroid nodulesmedicine.medical_specialtyeducationBethesda systemContext (language use)MalignancyThyroid cytologyYoung Adult03 medical and health sciences0302 clinical medicinemedicineHumansProspective StudiesThyroid NoduleProspective cohort studyThyroid ultrasoundAgedUltrasonographyAged 80 and overUnivariate analysismedicine.diagnostic_testbusiness.industryGeneral surgeryNodule (medicine)Middle Agedmedicine.diseaseSurgeon performed thyroid ultrasonographySettore MED/18 - Chirurgia GeneraleExact testLogistic Models030220 oncology & carcinogenesisFemale030211 gastroenterology & hepatologySurgerymedicine.symptombusinessJournal of Surgical Research
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High incidence of chromosomal abnormalities in large-headed and multiple-tailed spermatozoa

2006

Rodrigo Vivo, Lorena, lorovi@alumni.uv.es ; Prados Dodd, Nicolas, Nicolas.Prados@uv.es ; Gil Salom, Manuel Luis, Manuel.Gil-Salom@uv.es ; Remohi Gimenez, Jose Alejandro, J.Alejandro.Remohi@uv.es

AdultMaleUrologyEndocrinology Diabetes and Metabolismmedia_common.quotation_subjectLarge-HeadedPhysiologyBiologyEndocrinology:CIENCIAS MÉDICAS ::Medicina interna [UNESCO]Chromosomes HumanHumansIn Situ Hybridization Fluorescencemedia_commonUNESCO::CIENCIAS MÉDICAS ::Medicina internaChromosome AberrationsIncidenceChromosomal AbnormalitiesIncidence (epidemiology)Germinal cellAnatomy:CIENCIAS MÉDICAS [UNESCO]Reproductive MedicineIncidence ; Chromosomal Abnormalities ; Large-Headed ; Multiple-Tailed SpermatozoaKaryotypingSperm TailUNESCO::CIENCIAS MÉDICASSperm HeadHigh incidenceMultiple-Tailed SpermatozoaReproduction
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Maxillofacial trauma due to traffic accidents and falls: an exploratory study of associated factors

2020

Background This study aimed to determine the pattern of Maxillofacial trauma (MFT) due to traffic accidents and falls in a reference hospital in a rural region of northeastern Brazil between December 2011 and December 2018 and to identify associated factors. Material and Methods This was a cross-sectional study using 585 medical records of patients with MFT. The data were subjected to a Poisson-Tweedie multiple regression analysis to estimate the Prevalence ratio (PR), with a 95% confidence interval (95% CI) and a significance level of p<0.05. Results MFT due to traffic accidents was more prevalent among patients 21 to 40 years old (PR=2.30; 95% CI=1.20-4.41; p<0.001) diagnosed with zygomat…

AdultMaleatopyMEDLINEExploratory researchYoung AdultOral Cancer and Potentially malignant disordersStatistical significanceEnvironmental healthHumansMedicinePrevalence ratiotacrolimusGeneral DentistryUNESCO:CIENCIAS MÉDICASZygomatic Fracturesbusiness.industryResearchMedical recordAccidents TrafficRegression analysisConfidence intervalCross-Sectional StudiesOtorhinolaryngology cheilitisMaxillofacial InjuriesSurgerybusinessBrazilMedicina Oral Patología Oral y Cirugia Bucal
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Omalizumab rapidly improves angioedema-related quality of life in adult patients with chronic spontaneous urticaria: X-ACT study data

2018

Background The X-ACT study aims to examine the effect of omalizumab treatment on quality of life (QoL) in chronic spontaneous urticaria (CSU) patients with angioedema refractory to high doses of H1-antihistamines. Methods In X-ACT, a phase III, double-blind, placebo-controlled study, CSU patients (18–75 years) with ≥4 angioedema episodes during the 6 months before inclusion were randomized (1:1) to receive omalizumab 300 mg or placebo every 4 weeks for 28 weeks. Angioedema-related QoL, skin-related QoL impairment, and psychological well-being were assessed. Results Ninety-one patients were randomized and 68 (omalizumab, n=35; placebo, n=33) completed the 28-week treatment period. At baselin…

AdultMalechronic spontaneous urticariamedicine.medical_specialtyAdolescentUrticariaImmunologyOmalizumab600 Technik Medizin angewandte Wissenschaften::610 Medizin und Gesundheit::616 KrankheitenPlaceboYoung Adult030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineDouble-Blind MethodRefractoryQuality of lifeInternal medicine616Anti-Allergic AgentsmedicineHumansH1-antihistamine-refractoryImmunology and AllergyDepression (differential diagnoses)AgedAngioedemaAdult patientsbusiness.industryangioedemaDermatology Life Quality IndexMiddle AgedSurgeryquality of life030228 respiratory systemExperimental Allergy and ImmunologyomalizumabOriginal ArticleFemaleORIGINAL ARTICLESH1‐antihistamine‐refractorymedicine.symptombusinessmedicine.drugAllergy
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Two complementary recombinant chromosomes 5 in a healthy woman

2005

We report a healthy woman with two abortions who is a carrier for a rare heterozygous double recombinant of an inv(5) chromosome, karyotype 46,XX,rec(5)dup(5p) inv(5)(pl 3q22),rec(5)dup(5q)inv(5)(pl 3q22). Her father had a 46,XY,inv(5)(p13q22) karyotype; his consanguineous wife had died. Molecular investigation of 11 highly polymorphic markers spanning chromosome 5 revealed biparental inheritance for two markers (D5S406, D5S681) on 5p15.3 and 5q13.1, and an allele constellation not compatible with paternal heterodisomy for marker D5S623 on 5q11.2. Eight markers were not informative. Three mechanisms of formation are proposed: First, fertilization of a normal oocyte by a sperm carrying the t…

AdultMalecongenital hereditary and neonatal diseases and abnormalitiesAbortion HabitualDNA RecombinantBiologylaw.inventionPolymorphism (computer science)lawGeneticsHumansBase sequenceMolecular BiologyGenetics (clinical)Polymorphism GeneticBase SequenceChromosomeKaryotypebiochemical phenomena metabolism and nutritionMolecular biologyHealthKaryotypingdupChromosome InversionRecombinant DNAbacteriaChromosomes Human Pair 5Female
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MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissec…

2014

Thoracic aortic aneurysm and dissection (TAAD) is an autosomal-dominant disorder with major life-threatening complications. The disease displays great genetic heterogeneity with some forms allelic to Marfan and Loeys-Dietz syndrome, and an important number of cases still remain unexplained at the molecular level. Through whole-exome sequencing of affected members in a large TAAD-affected family, we identified the c.472CT (p.Arg158(∗)) nonsense mutation in MFAP5 encoding the extracellular matrix component MAGP-2. This protein interacts with elastin fibers and the microfibrillar network. Mutation screening of 403 additional probands identified an additional missense mutation of MFAP5 (c.62GT …

AdultMalecongenital hereditary and neonatal diseases and abnormalitiesAdolescentExtracellular matrix componentNonsense mutationHaploinsufficiencyThoracic aortic aneurysmPathogenesisContractile ProteinsReportGeneticsmedicineHumansMissense mutationGenetics(clinical)ExomeChildGenetics (clinical)AgedGlycoproteinsAged 80 and overGeneticsAortic Aneurysm ThoracicbiologyGenetic heterogeneitySequence Analysis DNAFibroblastsMiddle Agedmedicine.diseasePedigree3. Good healthAortic DissectionAmino Acid SubstitutionCodon Nonsensebiology.proteinIntercellular Signaling Peptides and ProteinsFemaleHaploinsufficiencyElastinThe American Journal of Human Genetics
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Subcortical somatosensory evoked potentials after median nerve stimulation in children.

2000

We report our normative data of subcortical somatosensory evoked potentials (SEPs) after median nerve stimulation from a group of 55 children 4–15 years of age and 18 young adults 18–29 years of age. We recorded near-field potentials from the brachial plexus, the cervical cord and the somatosensory cortex. The far-field potentials P13, P14 and N18 from the brainstem were recorded from the scalp electrodes, when a non-cephalic reference at the contralateral Erb's point or an ear reference was used. The N9 (brachial plexus), N13a (dorsal horn), P13 (caudal medulla oblongata), N18 (medulla oblongata) and N20 (somatosensory cortex) were present in all subjects. The N13b (dorsal column near the …

AdultMalecongenital hereditary and neonatal diseases and abnormalitiesAdolescentSomatosensory systemEvoked Potentials SomatosensoryMedicineHumansChildbusiness.industryMedial lemniscusGeneral MedicineAnatomyMedian nerveElectric StimulationMedian Nervebody regionsSomatosensory evoked potentialAnesthesiaChild PreschoolPediatrics Perinatology and Child HealthMedulla oblongataFemaleNeurology (clinical)BrainstemCuneate nucleusbusinessBrachial plexusBrain StemEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
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Cancer incidence rate ratios of Turkish immigrants in Hamburg, Germany: A registry based study

2009

The aim of this Study was to estimate cancer incidence rate ratios for Turkish migrants in Hamburg, Germany. We used a name-based approach and identified 1346 cases with Turkish names (as a proxy of Turkish origin) among 140,249 cases of cancer registered in the cancer registry Hamburg during 1990-2005. To estimate the size of the denominator population, we applied the name-based approach to the population of Hamburg as well. The cancer incidence of specific cancer sites was compared between Turkish and non-Turkish cases using incidence rate ratios (IRR), stratified by gender and birth cohort. Our main findings are that cancer of the respiratory organs is diagnosed less frequent among Turki…

AdultMalecongenital hereditary and neonatal diseases and abnormalitiesCancer Researchmedicine.medical_specialtyAdolescentTurkeyEpidemiologyTurkishPopulationTurkishPrevalenceEmigrants and ImmigrantsMigrantsYoung AdultBreast cancerNeoplasmsGermanymedicineHumansRegistriesChildeducationAgedAged 80 and overGynecologyeducation.field_of_studybusiness.industryIncidence (epidemiology)IncidenceInfant NewbornInfantsocial sciencesMiddle Agedmedicine.diseaselanguage.human_languageCancer registryOncologyChild PreschoolCohortlanguagepopulation characteristicsNeoplasmFemaleSkin cancerbusinessgeographic locationsDemography
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Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia

2013

Background and Objective Increased expression of fetal hemoglobin (HbF) may ameliorate the clinical course of hemoglobinopathies like sickle cell disease (SCD) and β-thalassemia. Hydroxyurea (HU) can stimulate HbF production in these diseases but the response is highly variable indicating the utility of developing an in vitro test to predict the patient's response to HU. We assessed whether the HbF response of patients with SCD and thalassemia intermedia (TI) to HU correlates with HBG (both γ-globin genes) expression in their cultured erythroid progenitors following exposure to HU. Patients and Methods We exposed primary erythroid cultures from peripheral blood mononuclear cells from 30 pat…

AdultMalecongenital hereditary and neonatal diseases and abnormalitiesCellPrimary Cell CultureGene ExpressionAnemia Sickle CellBiologyPeripheral blood mononuclear cellhydroxyurealiquid erythroid cultureYoung AdultIn vivohemic and lymphatic diseasesFetal hemoglobinmedicineHumansgamma-GlobinsRNA MessengerFetal HemoglobinAgedErythroid Precursor CellsMessenger RNAbeta-ThalassemiaBeta thalassemiaHematologyGeneral MedicineMiddle Agedmedicine.diseaseb-thalassemiaMolecular biologyReal-time polymerase chain reactionmedicine.anatomical_structureTreatment OutcomeCell cultureFemalesickle cell disease
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Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype.

2009

Recently, three reports described deletions and epimutations affecting the imprinted region at chromosome 14q32.2 in individuals with a phenotype typical for maternal uniparental disomy of chromosome 14 [upd(14)mat]. In this study, we describe another patient with upd(14)mat-like phenotype including low birth weight, neonatal feeding problems, muscular hypotonia, motor and developmental delay, small hands and feet, and truncal obesity. Conventional cytogenetic analyses, fluorescence in situ hybridization subtelomere screening, multiplex ligation-dependent probe amplification analysis of common microdeletion and microduplication syndromes, and methylation analysis of SNRPN all gave normal re…

AdultMalecongenital hereditary and neonatal diseases and abnormalitiesMolecular Sequence DataMothersBiologyMethylationPolymorphism Single NucleotideEpigenesis GeneticGenomic ImprintingIntergenic regionGeneticsmedicineHumansAbnormalities MultipleEpigeneticsChildGenetics (clinical)GeneticsChromosomes Human Pair 14Muscular hypotoniamedicine.diagnostic_testBase SequenceChromosomeUniparental DisomySubtelomerePhenotypeDifferentially methylated regionsPhenotypeMutationFemaleFluorescence in situ hybridizationClinical genetics
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