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1.
Acta Chir Plast ; 66(2): 50-59, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-39174339

RESUMO

The Department of Plastic and Aesthetic Surgery, St. Anne's University Hospital in Brno, and Faculty of Medicine of Masaryk University, Brno, has a long history of surgical treatment of lymphedema and elephantiasis, which started in 1970s. There were many types of surgeries described and performed at our department - starting with prof. Barinka's radical operation of elephantiasis, then lower limb end-to-side lymphovenous anastomosis pulled through the wall to the great saphenous vein, and genital lymphedema reduction. We call this era "the first period" of surgical lymphedema treatment. "The second period" started in 2016 by using free flaps with lymph nodes or vascularized lymph nodes and using microsurgical techniques of end-to-end, end-to-side and side-to-end lymphovenous anastomoses to the subcutaneous veins of a small calibre, which then drain the lymph into the blood stream. "The third period" started 2 years ago after the visit of prof. Yang from Taiwan - we started to use the method of single stitch end-to-side anastomosis to big subcutaneous veins like the great saphenous vein or the cephalic vein.


Assuntos
Hospitais Universitários , Linfedema , Humanos , História do Século XX , Linfedema/cirurgia , História do Século XXI , Cirurgia Plástica/história , Procedimentos de Cirurgia Plástica/métodos , Itália , Anastomose Cirúrgica
2.
J Physiol Pharmacol ; 72(6)2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-35485358

RESUMO

Surgically perforated stomach (since direct injury in rats until persisting defect and huge adhesions (day 1, day 7)) fairly represent an unresolved cytoprotection issue, and thereby, we focused resolving of the immediate triad, particular vascular failure (vessels 'disappear'/empty), prolonged bleeding, debilitated defect large widening. Agents (mg/kg) or saline (controls) were given at 1 min post-injury as an abdominal bath (10 ml/rat throughout 2 min). Within 1 - 15 min post-injury period, with cytoprotective BPC 157 (0.01 µg), the rapidly restored vessels 'run' (vessels filled/reappeared) toward the perforated defect, and there is less bleeding, and defect contraction; advanced perforated lesion healing (day 1) to complete healing (day 7), and less adhesions. With pantoprazole (10 mg), early (vessels (worsening), bleeding (prolongation), defect (attenuated widening)) effect means eventual lesions and adhesions severity as in controls. Ranitidine (10 mg) early effect (vessels (improvement), bleeding (less bleeding), defect (eliminated widening, defect not changed)) means final lesions attenuation, but not complete healing, less adhesions. L-NAME (5 mg) early (vessels worsening, less bleeding, attenuated defect widening) and final (lesions aggravation, more adhesions) effect, versus L-arginine (100 mg) early (vessels improvement, more bleeding, attenuated defect widening) and final (lesions attenuation, less adhesions) effect, combined few simultaneously occurring nitric oxide (NO)-system distinct processes. Finally, in the stomach tissue surrounding defect, increased malondialdehyde (MDA)- and decreased NO-values, BPC 157 reversed to the normal healthy values, and mRNA expression studies (Cox2, VEGFa, Nos1, Nos 2, Nos3, Nkap (NF-kappa-B-activating protein gene)), done at that very early post-perforation-time, indicate a way how BPC 157 may act beneficially in the perforated stomach lesion throughout NO- and prostaglandinds-system.


Assuntos
Óxido Nítrico , Gastropatias , Animais , Arginina/farmacologia , Arginina/uso terapêutico , Citoproteção , Hemorragia , NG-Nitroarginina Metil Éster , Óxido Nítrico/metabolismo , Pantoprazol/farmacologia , Pantoprazol/uso terapêutico , Fragmentos de Peptídeos , Proteínas , Ranitidina , Ratos , Ratos Wistar
3.
Neurochem Int ; 20(3): 421-31, 1992 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-1304337

RESUMO

In this study, brain gangliosides in prenatal and postnatal human life were analyzed. Immunohistochemically, the presence of "c"-pathway of gangliosides (GQ1c) in embryonic brain was only recorded at 5 weeks of gestation. Biochemical results indicated a twofold increase in human cortex ganglioside concentration between 16 and 22 weeks of gestation. The increasing ganglioside concentration was based on an increasing GD1a ganglioside fraction in all regions analyzed except cerebellar cortex, which was characterized by increasing GT1b. In this developmental period, GD3 was found to be localized in the ventricular zone of the cortical wall. After birth, GD1b ganglioside in neuropil of granular cell layer corresponding to growing mossy fibers was expressed in cerebellar cortex. Between birth and 20/30 years of age, a cerebral neocortical difference of ganglioside composition was observed, characterized by lowest GD1a in visual cortex. Analyzing the composition of gangliosides in cortical regions during aging, they were observed to follow region-specific alterations. In frontal cortex, there was a greater decrease in GD1a and GM1 than in GT1b and GD1b, but in occipital (visual) cortex there was no change in individual gangliosides. In hippocampus, GD1a moderately decreased, whereas other fractions were stable. In cerebellar cortex, GD1b and GT1b fractions decreased with aging.


Assuntos
Envelhecimento/metabolismo , Encéfalo/metabolismo , Desenvolvimento Embrionário e Fetal , Gangliosídeos/metabolismo , Aborto Legal , Adulto , Idoso , Idoso de 80 Anos ou mais , Encéfalo/embriologia , Encéfalo/crescimento & desenvolvimento , Química Encefálica , Feminino , Lobo Frontal/química , Lobo Frontal/metabolismo , Gangliosídeos/análise , Idade Gestacional , Humanos , Lactente , Pessoa de Meia-Idade , Lobo Occipital/química , Lobo Occipital/metabolismo , Especificidade de Órgãos , Gravidez
4.
IEEE Trans Neural Netw ; 9(5): 813-21, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-18255768

RESUMO

Successful implementations of radial-basis function (RBF) networks for classification tasks must deal with architectural issues, the burden of irrelevant attributes, scaling, and some other problems. This paper addresses these issues by initializing RBF networks with decision trees that define relatively pure regions in the instance space; each of these regions then determines one basis function. The resulting network is compact, easy to induce, and has favorable classification accuracy.

5.
Biomed Tech (Berl) ; 38(4): 73-80, 1993 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8507806

RESUMO

The paper addresses the problem of automatic sleep classification. A special effort is made to find a method of extracting reasonable descriptions of the individual sleep stages from sample measurements of EGG, EMG, EOG, etc., and from a classification of these measurements provided by an expert. The method should satisfy three requirements: classification accuracy, interpretability of the results, and the ability to select the relevant and discard the irrelevant variables. The solution suggested in this paper consists of a combination of the subsymbolic algorithm LVQ with the symbolic decision tree generator ID3. Results demonstrating the feasibility and utility of our approach are also presented.


Assuntos
Polissonografia/classificação , Processamento de Sinais Assistido por Computador/instrumentação , Fases do Sono/fisiologia , Algoritmos , Sistemas Inteligentes , Feminino , Humanos , Lactente , Masculino , Polissonografia/instrumentação , Valores de Referência , Sono REM/fisiologia
6.
Lijec Vjesn ; 112(1-2): 7-12, 1990.
Artigo em Servo-Croata (Latino) | MEDLINE | ID: mdl-2366626

RESUMO

In this study, tumor and serum gangliosides were analyzed in patients bearing lung planocellular carcinoma (LPC) before and after operative therapy. Tumor tissue, pathohistologically characterized as carcinoma planocellulare corneum (Ca. epidermoide, type 8070/3, WHO, Geneva, 1981), showed an elevated concentration of gangliosides in comparison to normal tung tissue. The composition of gangliosides in LPC tissue varied from one tumor sample to another, however, two general features were observed. First, LPC contained an increased amount of GM3 and a decreased amount of GD3 gangliosides. Second, an elevated proportion of gangliosides migrating as polysialogangliosides (x3, x5, x6) characterized the majority of LPC tissues. On the other hand, serum of patients with LPC contained an elevated amount of gangliosides (15.8 +/- 0.3 mumols/L) in comparison to control serum (6.1 +/- 0.8 mumols/L) (P less than 0.01). However, analyzing the composition of serum gangliosides by thin-layer chromatography, all serum gangliosides were more or less elevated. By day 21 after the surgical removal of LPC, serum gangliosides dropped by approximately 50% approaching the normal values. It seems that elevated serum gangliosides in LPC patients were secreted from carcinoma cells, because they normalized after surgical removal of LPC. Thus, serum gangliosides might be a useful biochemical tool for diagnosis and therapy monitoring of this carcinoma.


Assuntos
Carcinoma/sangue , Gangliosídeos/sangue , Neoplasias Pulmonares/sangue , Carcinoma/cirurgia , Humanos , Neoplasias Pulmonares/cirurgia
8.
Int J Legal Med ; 120(1): 53-5, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16088410

RESUMO

Allele frequencies of 15 STR loci (D8S1179, D21S11, D7S820, CSF1PO, D3S1358, TH01, D13S317, D16S539, D2S1338, D19S433, vWA, TPOX, D18S51, D5S818, and FGA) were determined in a sample of 163 unrelated individuals from the Republic of Macedonia. AmpFISTR Identifiler Kit (Applied Biosystems) was used for PCR amplification. For all 15 loci, the combined matching chance is 6.6 x 10(18) and the power of exclusion is 99.999954%.


Assuntos
Frequência do Gene , Genética Populacional , Sequências de Repetição em Tandem , Impressões Digitais de DNA , Humanos , Reação em Cadeia da Polimerase , República da Macedônia do Norte
9.
Int J Legal Med ; 107(6): 329-30, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-7577699

RESUMO

The genotype distributions for the short tandem repeat systems (STRs) HUMVWA and HUMTH01 have been studied in 128 unrelated Caucasians fromêAustria. The allelic distributions were in accordance with Hardy-Weinberg expectations. The heterozygosities were 0.82 and 0.81, whereas the mean exclusion chance was 0.62 and 0.55, respectively. In one person, a VWA-allele consisting of 11 repeats was found.


Assuntos
Frequência do Gene/genética , Sequências Repetitivas de Ácido Nucleico/genética , População Branca/genética , Áustria , População Negra/genética , Triagem de Portadores Genéticos , Genótipo , Alemanha , Humanos , Paternidade , Fenótipo , Estados Unidos
10.
Cesk Otolaryngol ; 39(5): 281-6, 1990 Sep.
Artigo em Tcheco | MEDLINE | ID: mdl-2225165

RESUMO

In the ENT department of the Factory Institute of National Health of the uranium industry in Príbram a group of 196 men (392 ears) was examined who worked exposed to the risk of noise in different occupations, mostly as miners in the uranium mines. The noise exposure was 17.5 +/- 6.5 years, age 60.2 +/- 11.7 years, the total percentage hearing loss (calculated according to Fowler) 54.7 +/- 21.1%. The group was formed by 144 men who were examined during a preventive follow-up examination, 52 men where hypacusia was evaluated as an occupational disease. The examination of all patients was supplemented by a record of middle-ear reflexes induced by contralateral stimulation at frequencies of 0.5 kHz, 1 kHz, 2 kHz and 4 kHz and by white noise (WN). The regression equation y = 50.54-0.044X (y = percentage hearing loss per ear, x = noise exposure in years) was calculated from data of the group subjected to the preventive follow up examination and made it possible to divide the group into sub-groups, sensitive and resistant to noise. The group of occupational hypacusia comprised only sensitive subjects. The authors tested the frequency and thresholds of middle ear reflexes at different frequencies and WN, the frequency and thresholds of saturation of reflexes separately in groups sensitive and resistant to noise. It was not possible to draw conclusions from the results which would permit a forecast of the individual development of occupational hypacusia as regards early evaluation of sensitivity or resistance to noise.


Assuntos
Perda Auditiva Provocada por Ruído/fisiopatologia , Doenças Profissionais/fisiopatologia , Reflexo Acústico/fisiologia , Adulto , Idoso , Humanos , Masculino , Pessoa de Meia-Idade
11.
J Dev Physiol ; 19(1): 37-41, 1993 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-8354850

RESUMO

To make the chick embryo accessible to electrophysiological measurements in its mesonephric kidney during the period between embryonic days (e.d.) 5 and 10, a special "chick-embryo-incubation bath" was constructed. It consists of an aerated chamber covering the egg and maintaining the gas exchange across the shell, and of a warmed reservoir of the incubation medium, into which the embryo is pulled out of the egg through a window in the shell. The two compartments are separated with a rubber membrane tightly fitting to the edges of the shell-window. The incubation medium contains a modified Krebs-Henseleit-Ringer solution and anesthetic Tricaine (Sigma). Access to the mesonephric nephrons is achieved by surgical excision of the body wall on the right side performed at e.d. 5. On average only about 35 percent of the operated embryos survive till the third day after surgery but during the next two days a mortality rate recedes to zero. The tolerance of short-term survival of embryos placed in the incubation bath was tested for up to 4 1/2 h. It was very good in embryos of age 5 to 7 e.d. as assessed by a steady heart rate and the presence of arterio-venous differences. A modified differential amplifier containing circuits for frequency compensation of the two channels was used for high-fidelity registration of voltage changes in the embryonic nephron with a single double-barrel microelectrode.


Assuntos
Eletrofisiologia/métodos , Néfrons/embriologia , Néfrons/fisiologia , Animais , Embrião de Galinha , Eletrofisiologia/instrumentação , Estudos de Avaliação como Assunto , Potenciais da Membrana , Mesonefro/fisiologia , Microeletrodos
12.
Int J Legal Med ; 118(2): 119-21, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-14991368

RESUMO

The PowerPlex 16 amplification kit was used for the analysis of allele frequencies for the 15 STR loci (D3S1358, TH01, D21S11, D18S51, Penta E, D5S818, D13S317, D7S820, D16S539, CSF1PO, Penta D, VWA, D8S1179, TPOX and FGA) in unrelated, autochthonous healthy adults from Bosnia ( n=123 for TH01, Penta E, D16S539, CSF1PO, Penta D and TPOX, n=210 for D3S1358, D21S11, D18S51, D5S818, D13S317, D7S820, VWA, D8S1179 and FGA). The agreement with HWE was confirmed for all loci with the exception of Penta D (based on the chi(2)-test only). The combined power of discrimination (PD) and the combined power of exclusion (PE) for the 15 studied loci were 0.999999999999999997 and 0.999999, respectively.


Assuntos
Impressões Digitais de DNA , Genética Populacional , Repetições de Microssatélites/genética , Adulto , Bósnia e Herzegóvina/epidemiologia , Estudos de Casos e Controles , Impressões Digitais de DNA/métodos , Bases de Dados de Ácidos Nucleicos , Frequência do Gene , Genética Populacional/métodos , Humanos
13.
Int J Legal Med ; 107(4): 219-21, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-7599102

RESUMO

Population genetic studies were carried out on Caucasians from north-west Croatia (Zagreb-area) using the short tandem repeat (STR) systems HumTHO1, HumVWA and HumACTBP2. After electrophoresis in PAG, 6 alleles could be identified for HumTHO1 in a sample size of 100 unrelated individuals and 7 alleles were found for VWA. For ACTBP2, 25 alleles have been identified. No significant deviations from Hardy-Weinberg equilibrium could be observed.


Assuntos
Marcadores Genéticos/genética , Genética Populacional , Sequências Repetitivas de Ácido Nucleico/genética , Alelos , Croácia , Comparação Transcultural , Frequência do Gene/genética , Humanos , Repetições Minissatélites/genética
14.
Biol Cybern ; 70(5): 443-8, 1994.
Artigo em Inglês | MEDLINE | ID: mdl-8186305

RESUMO

The primary goal of this paper is to introduce the potential of artificial intelligence (AI) methods to researchers in sleep classification. AI provides learning procedures for the construction of a sleep classifier, prescribing how to combine the observed parameters and how to derive the corresponding decision thresholds. A case study reporting a successful application of an automatic induction of decision trees and of a learning vector quantizer to this domain is presented.


Assuntos
Inteligência Artificial , Sono , Automação , Árvores de Decisões , Humanos
15.
Cesk Otolaryngol ; 39(6): 330-4, 1990 Nov.
Artigo em Tcheco | MEDLINE | ID: mdl-2292104

RESUMO

The authors analyzed 255 cases of occupational hypacusia reported as occupational diseases in 1962-1988 in the Czechoslovak uranium industry. Up to 1975 occupational hypacusias accounted for 9-11% of the nationwide number of hypacusia notified as occupational diseases. Due to extensive social provisions, incl. preventive ones, the incidence declined since 1985 below 1% of the nationwide incidence. The group of 255 men with occupational hypacusia was examined in detail at the Health Centre of the Uranium Industry in Príbam. Their age is 49.0 +/- 8.5 years, noise exposure 14.6 +/- 5.8 years, the the ratio of miners is 82.4%, the total percentage hearing loss is 63.5 +/- 11.4%, the mean annual increment of the total percentage hearing loss is 4.8 +/- 0.6%, the greatest mean annual increment is 5.4% in the occupation of miners.


Assuntos
Perda Auditiva Provocada por Ruído , Mineração , Doenças Profissionais , Tchecoslováquia/epidemiologia , Perda Auditiva Provocada por Ruído/diagnóstico , Perda Auditiva Provocada por Ruído/epidemiologia , Humanos , Masculino , Pessoa de Meia-Idade , Doenças Profissionais/diagnóstico , Doenças Profissionais/epidemiologia , Urânio
16.
Int J Legal Med ; 110(4): 230-1, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9274951

RESUMO

Population studies were carried out on unrelated individuals of Croatian ancestry. Genomic DNA was amplified by the polymerase chain reaction (PCR) at the polymorphic microsatellite loci HUMCD4 (n = 105 individuals) and HUMF13B (n = 108 individuals). After horizontal polyacrylamide gel electrophoresis followed by silver staining 6 alleles and 12 genotypes were observed for HUMCD4 and 6 alleles and 13 genotypes could be identified for HUMF13B. Data obtained were in concordance with the prediction of Hardy-Weinberg equilibrium. The allele frequency data were compared with Austrian and Italian population samples and no significant deviations between these populations were observed.


Assuntos
Mapeamento Cromossômico , Marcadores Genéticos/genética , Genética Populacional , Polimorfismo Genético/genética , Sequências Repetitivas de Ácido Nucleico/genética , Alelos , Croácia , Frequência do Gene/genética , Triagem de Portadores Genéticos , Genótipo , Humanos , Repetições de Microssatélites/genética , Reação em Cadeia da Polimerase
17.
Int J Legal Med ; 114(1-2): 19-22, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11197622

RESUMO

This paper reports the results and methods of dental identification of 1000 human remains exhumed from mass graves in Croatia up to July 1998. Personal identification of the victims was performed at the Department of Forensic Medicine and Criminology at the School of Medicine in Zagreb. A forensic odontologist participated in the identification process by carrying out the dental identification. A total of 824 victims were positively identified, while 176 victims remained unidentified. Dental identification based on available dental antemortem data was achieved in 25% of the cases. Dental identification based on dental charts was achieved in 35%, on x-rays in 15%, on photographs of teeth in 22%, on interviews in 18%, and on confirmation by odontologists in 10% of the cases. Teeth, in combination with anthropological parameters, age, sex and height, as well as other specific characteristics such as tattoos, personal identification cards, clothes, jewellery and DNA, were helpful for identification of 64% of the victims, but the significance for the identification was not dominant. Only in 11% of the cases was identification achieved by other relevant means and teeth not used at all. Identification procedures in Croatia will continue until another 1700 people who are still missing or kept as prisoners of war since the aggression on Croatia in 1991 are found and/or identified.


Assuntos
Odontologia Legal/métodos , Guerra , Adolescente , Adulto , Determinação da Idade pelos Dentes , Idoso , Criança , Pré-Escolar , Croácia , Impressões Digitais de DNA , Polpa Dentária/patologia , Dentina/patologia , Feminino , Antropologia Forense , Direitos Humanos , Humanos , Lactente , Masculino , Pessoa de Meia-Idade
18.
J Neural Transm (Vienna) ; 111(6): 733-8, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15168220

RESUMO

Indices of disturbed serotonergic neurotransmission are the most robust biological findings in suicide. Tryptophan hydroxylase (TPH) and 5-hydroxytryptamine transporter (5HTt) are the main regulators of 5HT signaling. Owing to the assumed functionality of intronic polymorphisms of TPH (218AC) and 5HTt (VNTR-2) genes, we investigated frequencies of concurrence of the TPH and 5HTt genotypes containing "lower activity" alleles (CC and 1010, respectively), in 192 suicide victims and 377 controls. Significant differences in frequencies of 5HTt and TPH genotype combinations were found between suicide victims and control subjects (p = 0.0156), with a clear dose-effect of the suspected ("lower activity") genotypes (p = 0.0046). Concurrent presence of the two, allegedly transcriptionally less active, variants of these genes seems to be in some kind of relation to the increased susceptibility to suicide.


Assuntos
Proteínas de Transporte/genética , Predisposição Genética para Doença , Íntrons/genética , Glicoproteínas de Membrana/genética , Proteínas de Membrana Transportadoras , Proteínas do Tecido Nervoso/genética , Polimorfismo Genético , Suicídio , Triptofano Hidroxilase/genética , Croácia , Feminino , Genótipo , Humanos , Masculino , Reação em Cadeia da Polimerase , Proteínas da Membrana Plasmática de Transporte de Serotonina , Suicídio/etnologia
19.
Int J Legal Med ; 118(3): 184-6, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15108004

RESUMO

The 15 AmpF lSTR Identifiler loci (D8S1179, D21S11, D7S820, CSF1PO, D3S1358, TH01, D13S317, D16S539, D2S1338, D19S433, VWA, TPOX, D18S51, D5S818 and FGA) were analyzed in the sample of 100 unrelated, autochthonous healthy adult Serbians from Novi Sad (Vojvodina Province, Serbia and Montenegro). The agreement with HWE was confirmed for all loci with the exception of D7S820 (based on the chi2-test only). The combined power of discrimination (PD) and the combined power of exclusion (PE) for the 15 tested STR loci were 0.99999999999999995 and 0.9999990, respectively. According to the presented data, D2S1338 and D18S51 are the most informative markers. Based on allelic frequencies and statistical parameters for forensic testing, it may be suggested that the AmpF lSTR Identifiler detection system represents a powerful strategy for individual identification and parentage analysis in the Serbian population.


Assuntos
Genética Populacional , Sequências de Repetição em Tandem , Adulto , DNA/sangue , Impressões Digitais de DNA/métodos , Bases de Dados de Ácidos Nucleicos , Frequência do Gene , Genótipo , Humanos , Reação em Cadeia da Polimerase , Iugoslávia
20.
Int J Legal Med ; 115(1): 57-60, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11599771

RESUMO

Austrian and Croatian Caucasian population data were generated for eight tetrameric STR loci amplified in a single multiplex reaction. Fluorescent detection was employed using the ABI Prism 310 Genetic Analyzer, the 377 DNA Sequencer (ABI) and the 373A DNA Sequencer (ABI). The loci analyzed were HUMvWFA31 (vWA), HUMTH01, HUMTPOX, HUMCSF1PO, D5S818, D13S317, D7S820 and D16S539 as part of the GenePrint PowerPlex multiplex system.


Assuntos
Reação em Cadeia da Polimerase/métodos , Sequências de Repetição em Tandem/genética , População Branca/genética , Alelos , Áustria , Croácia , Medicina Legal , Frequência do Gene , Humanos , Espectrometria de Fluorescência
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