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1.
Clin Neurol Neurosurg ; 238: 108173, 2024 03.
Artículo en Inglés | MEDLINE | ID: mdl-38430729

RESUMEN

BACKGROUND: Cognitive evaluation was considered to be very important in the relapse period, on the basis of the presence of isolated cognitive attacks and the necessity of monitoring the patient both physically and cognitively. MATERIALS AND METHODS: People with MS (pwMS) who were hospitalized during relapse were included in the study. All MS patients were evaluated by the neurologist with Expanded Disability Status Scale (EDSS), The 9 Hole Peg Test (9HPT) and the Timed 25-Foot Walk Test (T25-FWT). Additionally, all participants were examined cognitively with the Turkish version of the Brief International Cognitive Assessment for MS (BICAMS) battery. Also, schedules were indicated as during relapse before the treatment (pre-treatment) and the first month after relapse (1-month follow-up). RESULTS: A total of 140 MS patients (mean age; 34.98±10.09, mean disease duration; 6.05±5.29 years) and 86 healthy controls (mean age; 36.94±10.83) were included to the present study. The mean EDSS scores in pre-treatment in MS patients was 2.74±1.14 and decreased significantly in the 1-month follow-up (1.74±1.24; p<0.001). The mean SDMT score was lower by 8.76 points in MS patients than in HCs) in pre-treatment and 7.66 points in 1-month follow-up (p<0.001). The mean SDMT scores of all participants increased with measurement time gradually (p<0.001). CONCLUSION: In this study, it was detected which cognitive domains were affected after relapse treatment and cognitive changes in pwMS during relapse and remission periods compared to the healthy controls. All three BICAMS test scores significantly increased in one-month follow-up than the pre-treatment period. The results showed that CVLT-II and BVMT-R scores improved more in pwMS than in HCs, and also SDMT scores of pwMS showed a trend of increase, but was not a significant improvement.


Asunto(s)
Esclerosis Múltiple , Humanos , Esclerosis Múltiple/psicología , Estudios Prospectivos , Pruebas Neuropsicológicas , Cognición , Recurrencia , Enfermedad Crónica
2.
West Indian med. j ; 69(7): 499-508, 2021. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1515713

RESUMEN

ABSTRACT Objective: To discuss cerebral sinovenous thrombosis (CSVT), an important mortality and morbidity factor, developing in the progression of ulcerative colitis (UC) in childhood age, in the light of the literature. Methods: A search of PubMed and Google Scholar database was conducted on April 2014. This study retrospectively investigates the cases diagnosed with UC with complication of CSVT below 18 years of age between years 1971 and 2014. The cases were analysed with respect to age, gender, disease duration and treatment, potential risk factors, clinical findings, location of thrombosis, thrombolytic therapeutical applications, and clinical progressions. Results: Twenty-four paediatric patients aged 5 and 18 years were included in the study. Cerebral sinovenous thrombosis had developed during active disease period in 23 (95.8%) patients. The most common complaints were headache (79.1%) and emesis (29.1%). The most frequently detected risk factors for CSVT were anaemia (58.3%) and thrombocytosis (45.8%). Inherited thrombotic disorders were encountered in 10 (41.6%) of the cases. The most common location sites for CSVT were the transverse (33.3%) and the sigmoid (33.3%) sinuses. It had been discovered that 19 (79.2%) of the cases were healed completely without a sequelae, whereas neurological sequelae remained in three (12.5%) of the cases and two (8.3%) of the cases died. Conclusion: In the presence of a prior diagnosis of UC and emergency presentation with emesis, headache, mood changes and particularly seizure, the presence of CSVT should certainly be considered.

3.
West Indian Med J ; 64(4): 444-6, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-26624604

RESUMEN

Ewing's sarcoma is one of the most aggressive primary bone tumours. Ewing's sarcoma arising from the bones of the head and neck region is extremely rare; only 4-9% of all Ewing's sarcoma originate in this region. We report a case of Ewing's sarcoma localized in the mandible because of its unusual presentation.

4.
Appl Magn Reson ; 44: 899-915, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23914071

RESUMEN

Modeling of spin Hamiltonian parameters enables correlation of crystallographic, spectroscopic, and magnetic data for transition ions in crystals. In this paper, based on the crystallographic data and utilizing the point-charge model and superposition model, the crystal field parameters (CFPs) are estimated for Ni2+(3d8) ions in the Haldane gap system Y2BaNiO5. The CFPs serve as input for the perturbation theory expressions and the crystal field analysis package for microscopic spin Hamiltonian modeling of the zero-field splitting parameters (ZFSPs) D and E. Results of an extensive literature search of the pertinent crystallographic data, experimental ZFSPs, and model parameters are briefly outlined. The modeling aims at verification of the experimental 'single ion anisotropy' parameters and explanation of the controversy concerning the maximal rhombic distortion |E/D| ≈1/3 reported for Ni2+ ions in Y2BaNiO5. The preliminary results call for reanalysis of some magnetic studies of the Haldane gap systems.

5.
Genet Couns ; 20(3): 255-60, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19852432

RESUMEN

Rubinstein-Taybi syndrome (RTS) is a rare syndrome with a frequency of approximately 1 in 125,000 affected newborns, which is characterized by mental retardation, growth retardation, a particular dysmorphology and, in a subset of cases, immunodeficiency. RTS is typically caused by CREBBP deficiency, and heterozygous mutation or deletion of the CREBBP gene has been identified in 60-70% of patients. The inheritance is autosomal dominant but reports of vertical transmission are exceedingly rare; near-all cases are caused by de novo mutations. Here we present an 8-month-old boy with varicella meningoencephalitis, RTS, and a de novo deletion of the CREBBP gene of two base pairs at position 201-202 in exon 2, c. 201 202delT. The mutation has not been described previously but it predicts a protein truncation, and truncating CREBBP mutations are typical causes of RTS.


Asunto(s)
Proteína de Unión a CREB/genética , Deleción Cromosómica , Encefalitis por Varicela Zóster/genética , Síndrome de Rubinstein-Taybi/genética , Emparejamiento Base , Mapeo Cromosómico , Análisis Mutacional de ADN , Proteína p300 Asociada a E1A/genética , Encefalitis por Varicela Zóster/diagnóstico , Exones , Tamización de Portadores Genéticos , Humanos , Hibridación Fluorescente in Situ , Lactante , Masculino , Síndrome de Rubinstein-Taybi/diagnóstico
6.
J Trop Pediatr ; 54(5): 294-9, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-18304952

RESUMEN

This study included 40 children, who were diagnosed with pneumonia and pulmonary hypertension (from the radiographic and clinical features), was performed at Yuzuncu Yil University Faculty of Medicine, Department of Pediatrics, from September 2003 to July 2005. Patients who had pneumonia and congenital heart disease or systemic hypertension or renal and liver disease together were excluded from the study. Blood gas analysis and oxygen concentration, measured with pulse oximetry, were performed in all patients. Besides chest X-ray, electrocardiography and echocardiographic search was also carried out. Echocardiographic examination was performed by using M mode, two-dimensional echocardiography and colored Doppler sonotron Vingmed CFM 725. At echocardiographic examination, pulmonary hypertension is defined as above 35 mmHg of pulmonary artery pressure. For echocardiographic examination, patients with pulmonary hypertension were divided into two groups. Captopril (2 mg/kg/day, three doses a day) and nifedipine (0.5 mg/kg/day, three doses a day) were given to the first and the second group, respectively. Echocardiography was performed daily until normal pulmonary artery pressure was achieved. At the beginning of the treatment, the patients were treated with double antibiotics and antibiotic change was carried out in needed cases at the follow up. Digoxin was administered to the cases of respiratory infection with heart failure.


Asunto(s)
Antihipertensivos/uso terapéutico , Bronconeumonía/complicaciones , Bronconeumonía/tratamiento farmacológico , Captopril/uso terapéutico , Hipertensión Pulmonar/tratamiento farmacológico , Hipertensión Pulmonar/etiología , Nifedipino/uso terapéutico , Vasodilatadores/uso terapéutico , Análisis de los Gases de la Sangre , Bronconeumonía/diagnóstico , Bronconeumonía/fisiopatología , Preescolar , Quimioterapia Combinada , Electrocardiografía , Femenino , Humanos , Hipertensión Pulmonar/diagnóstico , Hipertensión Pulmonar/fisiopatología , Lactante , Recién Nacido , Masculino , Oximetría , Estudios Retrospectivos , Resultado del Tratamiento
7.
J Microencapsul ; 13(2): 141-59, 1996.
Artículo en Inglés | MEDLINE | ID: mdl-8999120

RESUMEN

In this study microspheres of diclofenac sodium, an anti-inflammatory agent, were prepared by utilizing a natural polysaccharide, chitosan-H. The objective of this investigation was to sustain the action of diclofenac sodium and to show the effect of various conditions on release kinetics. For this reason factorial design experiments were performed. The independent variables in the 3(3) factorial design were chitosan-H concentration, tripolyphosphate concentration and stabilization time, and in the 3(2) factorial design were chitosan-H and tripolyphosphate concentrations. The dependent variables, t50% and the total drug content were investigated by the polynomial equations. The release profiles were evaluated kinetically and the best fit was obtained by the Higuchi equation.


Asunto(s)
Quitina/análogos & derivados , Diclofenaco/administración & dosificación , Química Farmacéutica , Quitosano , Diclofenaco/química , Cinética , Microesferas , Tamaño de la Partícula , Polifosfatos , Solubilidad , Propiedades de Superficie
8.
Pharmazie ; 50(4): 275-7, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7792304

RESUMEN

A biodegradable diclofenac sodium (DS) microsphere system using chitosan has been characterized and evaluated in vitro and in vivo. The particle size distribution and drug content was determined. The release rate data were investigated by using zero-order, first-order, Hixson-Crowel and Higuchi kinetics. The optimum DS-Chitosan microsphere formulation, empty chitosan microspheres, sustained release commercial product and plain drug were evaluated for pharmacological activity. The ulcerogenic index in rabbits was also determined.


Asunto(s)
Diclofenaco/administración & dosificación , Animales , Quitina/análogos & derivados , Quitosano , Preparaciones de Acción Retardada , Diclofenaco/efectos adversos , Microesferas , Tamaño de la Partícula , Conejos , Solubilidad , Úlcera Gástrica/inducido químicamente , Úlcera Gástrica/patología
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