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showing 10 items of 1136 documents

Systemic therapies for mucopolysaccharidosis: ocular changes following haematopoietic stem cell transplantation or enzyme replacement therapy - a rev…

2010

The management of mucopolysaccharidosis (MPS) is focused on the multi-organ, sometimes life-threatening, clinical manifestations that occur over time. In the past, the limited, symptom-based treatment options led physicians to adopt a palliative approach towards individual disease-associated complications. The availability of systemic treatments such as haematopoietic stem cell transplantation (HSCT) and enzyme replacement therapy (ERT) has created a better prognosis for MPS patients, particularly when initiated early in life. As part of an integrated management approach, these therapies could be valuable in managing the ocular features that are present in many children with MPS. HSCT has b…

congenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyVisual acuitygenetic structuresbusiness.industryMucopolysaccharidosismedicine.medical_treatmentEye diseasenutritional and metabolic diseasesEnzyme replacement therapyHematopoietic stem cell transplantationmedicine.diseaseeye diseasesSurgeryTransplantationOphthalmologymedicineOptic nervesense organsStem cellmedicine.symptomIntensive care medicinebusinessClinical & Experimental Ophthalmology
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Von Willebrand-Syndrom - Blutungsrisiko bei HNO-Eingriffen im Kindesalter

1994

Von Willebrand's disease (vWD) is the most common inherited bleeding disorder. Typical clinical features such as bleeding after surgery or trauma might suggest the disease. We present a series of 24 patients with vWD treated between 1989 and 1992. Diagnosis was confirmed by a reduction in plasma factor VIII antigen concentration, reduction of ristocetin cofactor activity and reduced factor VIII activity. Seventeen of the patients underwent surgery (7 adenoidectomies, 8 tonsillectomies, 2 paranasal sinus operations) and received preoperative stimulation of von Willebrand factor (vWF) using DDAVP. This resulted in a rapid increase in plasma vWF concentration from an average of 56% before stim…

congenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtybiologymedicine.diagnostic_testbusiness.industryPlasma factorStimulationGastroenterologySurgeryOtorhinolaryngologyVon Willebrand factorVon willebrandhemic and lymphatic diseasesInternal medicinebiology.proteinMedicineRisk factorbusinessReduced factor VIII activityComplicationcirculatory and respiratory physiologyPartial thromboplastin timeLaryngo-Rhino-Otologie
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Reproductive Dysfunction in Classical and Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

2021

Patients with congenital adrenal hyperplasia (CAH) both with severe (classical CAH) and mild (nonclassical NCAH) forms exhibit a wide spectrum of reproductive dysfunction. In this review, only CAH cases with 21-hydroxylase deficiency (21-OHd) will be discussed, as they represent almost all of the patients in reproductive clinical settings.

congenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyendocrine system diseasesbiologybusiness.industry21-Hydroxylasenutritional and metabolic diseasesClinical settingsurologic and male genital diseasesmedicine.diseasefemale genital diseases and pregnancy complicationsCongenital adrenal hyperplasia due to 21-hydroxylase deficiencyEndocrinologyInternal medicinemedicinebiology.proteinCongenital adrenal hyperplasiabusiness
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Aneurysma des Ductus arteriosus Botalli

2000

A congenital aneurysm of the ductus arteriosus Botalli was detected by chest X-ray as an intrathoracic mass in a 7-day-old infant. Following confirmation of the diagnosis by echocardiography and MRI the aneurysm was successfully resected via left lateral thoracotomy without cardiopulmonary bypass. The postoperative course was uneventful. Six years after operation the patient is asymptomatic and growing normally. An intrathoracic mass may be considered in the differential diagnosis especially in infants and children. Aneurysms of ductus arteriosus potentially are associated with serious complications. Timely diagnosis and early surgical intervention are decisive for prevention of serious com…

congenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtymedicine.diagnostic_testbusiness.industryCongenital aneurysmMagnetic resonance imagingmedicine.diseaseAsymptomaticlaw.inventionSurgeryAneurysmmedicine.anatomical_structurelawDuctus arteriosusInternal medicinecardiovascular systemmedicineCardiopulmonary bypassCardiologycardiovascular diseasesDifferential diagnosismedicine.symptomCardiology and Cardiovascular MedicinebusinessComplicationHerz
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Oromandibular dystonia: A dental approach

2010

Oromandibular dystonia consists of prolonged spasms of contraction of the muscles of the mouth and jaw. Primary idiopathic forms and secondary forms exist. Secondary dystonia develops due to environmental factors; some cases of cranial dystonia after dental procedure have been reported, but the causal relationship between these procedures and dystonia remains unclear. Traumatic situations in the mouth, such as poor aligned dentures or multiple teeth extractions may cause an impairment of proprioception of the oral cavity, leading to subsequent development of dystonia. The clinical characteristics of oromandibular dystonia are classified according to the affected muscles. The muscles involve…

congenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_treatmentDentistrystomatognathic systemTongueotorhinolaryngologic diseasesmedicineHumansGeneral DentistryDystoniaOrthodonticsProprioceptionbusiness.industryMeige SyndromeFocal dystonia:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseOromandibular dystoniaMuscles of masticationBotulinum toxinnervous system diseasesstomatognathic diseasesmedicine.anatomical_structureOtorhinolaryngologyDentistryUNESCO::CIENCIAS MÉDICASSurgeryDenturesbusinessmedicine.drugMedicina Oral Patología Oral y Cirugia Bucal
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Un modelo en Drosophila del mecanismo de patogénesis de las expansiones ctg en la distrofia miotónica.

2007

La distrofia miotónica tipo 1 (DM1) es una enfermedad neuromuscular que se debe auna expansión de repeticiones CTG inestables en la región 3' no traducida del genproteína kinasa de la DM (DMPK). La DM1 se caracteriza por la miotonía y distrofiamuscular que muestran los pacientes, los cuales también presentan cataratas,arritmias cardiacas y alteraciones neuropatológicas. A nivel bioquímico muestrandefectos en el procesado alternativo de pre-mRNAs específicos lo cual explica algunossíntomas definitorios de la DM1. El mecanismo de patogénesis se debe a la toxicidadde los RNAs con expansiones CUG para la célula. Varias proteínas de unión a RNA,como las proteínas humanas Muscleblind-like MBNL1-3…

congenital hereditary and neonatal diseases and abnormalitiesnoneFacultat de Biològiques575
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Relationship Between Glucocerebrosidase Activity and Clinical Response to Enzyme Replacement Therapy in Patients With Gaucher Disease Type I

2019

The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) has been suggested as a tool for dosage individualization, so we conducted a study to evaluate the relationship between glucocerebrosidase activity and clinical response in patients with Gaucher disease type I (GD1) to ERT. The study included patients diagnosed with GD1, who were being treated with ERT, and healthy individuals. Markers based on glucocerebrosidase activity measurement in patients' leucocytes were studied: enzyme activity at 15 min. post-infusion (Act(75)) reflects the amount of enzyme that is distributed in the body post-ERT infusion, and accumulated glucocerebrosidase activity…

congenital hereditary and neonatal diseases and abnormalitiesnutritional and metabolic diseases
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Corporate entrepreneurship and governance: Mergers and acquisitions in Europe

2022

Mergers and acquisitions (M&A) are a form of corporate entrepreneurship involving strategic decisions that require discussion and approval by the board of directors of the acquiring firm. We focus on board attributes to analyze the entrepreneurial function of the board of directors and its involvement in corporate entrepreneurship. Building on different theories (agency theory, resource dependence theory, stewardship theory, and stakeholder theory), we examine whether board composition affects the number of acquisitions, the risk involved in bids, and the creation of value for the acquirer's shareholders. For a sample of European firms over the period 2002 to 2020, we find that board size a…

corporate boardabnormal returnManagement of Technology and InnovationM&A performanceUNESCO::CIENCIAS ECONÓMICASBusiness and International Managementboard of directorsApplied Psychologymergers and acquisitions
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Evaluation of menstrual irregularities after COVID-19 vaccination: Results of the MECOVAC survey

2022

Abstract We investigated menstrual irregularities after the first and second doses of the COVID-19 vaccine. Women answered a customised online questionnaire (ClinicalTrial.gov ID: NCT05083065) aimed to assess the vaccine type, the phase of the menstrual cycle during which the vaccine was administered, the occurrence of menstrual irregularities after the first and second doses, and how long this effect lasted. We excluded women with gynaecological and non-gynaecological diseases, undergoing hormonal and non-hormonal treatments, in perimenopause or menopause, as well as those who had irregular menstrual cycles in the last 12 months before vaccine administration. According to our data analysis…

covid19mestrual irregularitymenstrual irregularitiesadverse effectvaccineabnormal uterine bleedingCOVID-19General MedicineMenstrual irregularitieabnormal uterine bleeding; adverse effect; COVID-19; menstrual irregularities; vaccine
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Darba vides riski un to samazināšana NBS 2.RNC Remonta darbnīca

2017

Kvalifikācijas darba autors Valdis Rāviņš Latvijas Universitātes, 1. līmeņa profesionālās augstākās izglītības studiju programmas “Darba aizsardzība” students. Kvalifikācijas darba tēma: “Darba vides riski un to samazināšana autotransporta servisa nozarē Nacionālie bruņoto spēku Nodrošinājuma pavēlniecības 2.Reģionālā nodrošinājuma centra Remonta darbnīca. Kvalifikācijas darba apjoms ir 68 lappuses un sastāv no piecām nodaļām un apakšnodaļām, ievada, priekšlikumiem un secinājumiem. Darbs satur 2 tabulas, 14 attēlus un 5 pielikumus. Pirmajā nodaļā tiek pētīta organizācija un tās darbība. Otrajā nodaļā LR likumi un nozares reglamentējoši dokumenti. Trešajā nodaļā atbilstība darba aizsardzības…

darba vides riski2.RNCRemonta darbnīcaDarba aizsardzība (Rīga) [RPIVA]Darba aizsardzība
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