Search results for "Abnormalities"

showing 8 items of 638 documents

Estudio retrospectivo de 145 dientes supernumerarios

2006

Podeu consultar la versió en anglès a http://hdl.handle.net/2445/48495

premolares supernumerarioscirugía bucalDientes supernumerariosCirurgia dentalOdontologíamesiodens:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludparamolaresDental abnormalitiesDental surgeryUNESCO::CIENCIAS MÉDICASMalformacions dentalsdistomolares
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Estudio retrospectivo de 145 dientes supernumerarios

2006

Podeu consultar la versió en castellà a http://hdl.handle.net/2445/118026

premolares supernumerarioscirugía bucalDientes supernumerariosCirurgia dentalmesiodens:CIENCIAS MÉDICAS [UNESCO]distal molarsstomatognathic diseasesstomatognathic systemparamolaresDental abnormalitiesDental surgerysupernumerary premolarsUNESCO::CIENCIAS MÉDICASMalformacions dentalsparamolarsdistomolaresSupernumerary teethoral surgery
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Sleep Disturbances in COPD are Associated with Heterogeneity of Airway Obstruction

2018

Individuals with Chronic Obstructive Pulmonary Disease (COPD) experience sleep disturbances due to the impact of respiratory symptoms on sleep quality. We explored whether sleep disturbances in COPD are linked to heterogeneity of airway constriction.The impact of breathing problems on sleep quality was measured in consecutive COPD outpatients with the COPD and Asthma Sleep Impact Scale (CASIS) questionnaire. Impulse oscillometry technique (IOS) was employed to assess heterogeneity of airway constriction. Subjects with a previous or concomitant diagnosis of asthma or obstructive sleep apnea (OSA) were excluded.Fifty COPD subjects (M/F 40/10; age: 71 +/- 8 yrs, Body Mass Index (BMI): 26.2 +/-…

sleep abnormalitieMaleSleep Wake DisordersPulmonary and Respiratory Medicinemedicine.medical_specialtyPulmonary diseaseCASISSettore MED/10 - Malattie Dell'Apparato RespiratorioPulmonary Disease Chronic Obstructive03 medical and health sciences0302 clinical medicineForced Expiratory VolumeOscillometrySurveys and QuestionnairesInternal medicinemedicineCOPDHumansSleep Wake DisorderOximetry030212 general & internal medicineRespiratory systemOxyhemoglobinAgedIOSCOPDSleep qualitybusiness.industryMiddle AgedAirway obstructionmedicine.diseaseSleep in non-human animalsSleep abnormalitiesResidual Volume030228 respiratory systemOxyhemoglobinsCardiologyFemalebusinessHumanCOPD: Journal of Chronic Obstructive Pulmonary Disease
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Oral implant rehabilitation in a patient with Moebius syndrome

2009

Introduction: Moebius syndrome is a rare congenital disorder characterized by unilateral or bilateral involvement of the sixth and seventh cranial nerves, resulting in a lack of facial expression and eye movements. These patients suffer a series of oral manifestations that may complicate their dental treatment, such as facial and tongue muscle weakness, uncontrolled salivation secondary to defi cient lip sealing, micrognathia, microstomia, bifi d uvula, gothic and fi ssured palate, fi ssured tongue, and glossoptosis. The underlying etiology remains unclear, though vascular problems during embryogenesis appear to be involved. Clinical case: We report the case of a woman with Moebius syndrome…

stomatognathic diseasesImplants dentalsDental implantsMalformacionsHuman abnormalitiesUNESCO:CIENCIAS MÉDICAS
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Race in Young Adult Speculative Fiction by Gilbert-Hickey and Gren-Barteet - books in review

2022

Race in Young Adult Speculative Fiction by Gilbert-Hickey and Gren-Barteet - books in review

stomatognathic diseasescongenital hereditary and neonatal diseases and abnormalitiesCiència-ficciónutritional and metabolic diseaseseye diseaseshumanities
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Oral manifestations of Cowden?s disease : presentation of a clinical case

2006

Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, characterized by the presence of multiple cutaneous hamartomas, oral fibromas and benign acral keratosis. It affects multiple organs (breast, thyroids, stomach, colon), with the strong possibility of malignant neoplasia developing in these organs. We present a case of this rare syndrome, highlighting the presentation of some clinical characteristics that, in suspected cases, can help to establish an early diagnosis of this disease, this being of great importance given the high frequency of tumors in people with this clinical picture.

stomatognathic diseasescongenital hereditary and neonatal diseases and abnormalitiesUNESCO::CIENCIAS MÉDICAS:CIENCIAS MÉDICAS [UNESCO]
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Multiple supernumerary teeth not associated with complex syndromes: a retrospective study

2009

Objectives: To determine the epidemiology and describe the clinical and radiographic characteristics, the type of treatment, and the possible delayed appearance of new supernumerary teeth in patients with non-syndromic multiple hyperdontia. Patients and Methods: We conducted a small retrospective observational study of 8 patients diagnosed with nonsyndromic multiple hyperdontia. Multiple hyperdontia not associated to complex syndromes was defined as apparently generally healthy patients with one or more supernumerary teeth in two or more areas. Results: The average patient age was 16.23 years; males predominated (3:1). Multiple hyperodontia with a minimum of 2 and a maximum of 9 supernumera…

stomatognathic diseasesstomatognathic systemPatologia dentalDental abnormalitiesMalformacions dentalsDental pathologyUNESCO:CIENCIAS MÉDICAS
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Interaction of the n-terminal domain of human t1r2 taste receptor with brazzein, a sweet-tasting protein

2015

Brazzein is a small (6.5 kDa) sweet-tasting protein originating from the fruit of Pentadiplandra brazzeana, a plant found in West Africa. Brazzein like all classes of sweet compounds is perceived through the activation of the T1R2/T1R3 heterodimeric sweet-taste receptor. T1R2 and T1R3 subunits are members of the small family of class C G-protein coupled receptors (GPCRs). Class C GPCRs possess a large N-terminal domain (NTD) linked to seven transmembrane domain by a cysteine rich domain (CRD). The NTD of T1R2 (T1R2-NTD) has been shown to contain the primary binding site for most of the sweet ligands. However, brazzein has been shown to require CRD of human T1R3 for receptor activation [1]. …

taste[SDV.AEN] Life Sciences [q-bio]/Food and Nutritioncongenital hereditary and neonatal diseases and abnormalities[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionreceptor[SDV.IDA]Life Sciences [q-bio]/Food engineering[ SDV.IDA ] Life Sciences [q-bio]/Food engineering[SDV.IDA] Life Sciences [q-bio]/Food engineering[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionsweet tasting protein
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