Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 15 de 15
Filter
1.
Rev. chil. endocrinol. diabetes ; 16(1): 10-16, 2023. ilus, tab
Article in Spanish | LILACS | ID: biblio-1438514

ABSTRACT

La diabetes mellitus tipo 1 (DM1) es una enfermedad autoinmune que genera dependencia exógena de insulina de forma permanente, presenta inflamación subclínica crónica lo que conlleva a una elevación de marcadores de inflamación como factor de necrosis tumoral alfa (TNF-α), proteína C reactiva (PCR) e interleuquina 6 (IL-6). OBJETIVO: determinar la relación entre el IMC sobre los marcadores de inflamación y el control metabólico en niños y jóvenes con DM1 entre 5 a 15 años de edad. METODOLOGÍA: Se realizó un estudio clínico, observacional, exploratorio. A partir de La recolección de datos de fichas clínicas y muestras de sangre en el Instituto de Investigaciones Materno Infantil (IDIMI) del Hospital San Borja Arriarán de la Universidad de Chile. Clasificación del estado nutricional utilizando datos registrados en ficha clínica. Marcadores de inflamación por medio de ELISA, hemoglobina glicosilada mediante métodos estándares. El análisis estadístico incluyó correlaciones mediante test de Spearman y diferencia de medias mediante test de Kruskal-Wallis seguido de post hoc Dunns. RESULTADOS: Un 30% de los pacientes con DM1 presentaron malnutrición por exceso. Al analizar la relación entre los niveles de marcadores inflamatorios y Hb glicosilada se observó la existencia de asociacion positiva entre usPCR y HbA1c (r= 0,30; p=0,0352) y entre IL-6 y HbA1c (r= - 0,038; p=0,0352). CONCLUSIONES: este estudio describe una posible asociación entre parámetros clásicos de inflamación con la hemoglobina glicosilada en las categorias de sobrepeso y obesidad en pacientes con DM1.


Type 1 diabetes mellitus (T1D) is an autoimmune disease that generates permanent exogenous insulin dependence, accompanied by chronic subclinical inflammation that leads to an elevation of inflammation markers such as tumor necrosis factor-alpha (TNF-α), C-reactive protein (CRP) and interleukin-6 (IL-6). OBJECTIVE: To determine the relationship between BMI on markers of inflammation and metabolic control in children and young people with T1D between 5 and 15 years of age. METHODOLOGY: A clinical, observational and exploratory study was carried out, based on the collection of data from clinical records and blood samples of children and adolescents with DM1 at the Instituto de Investigaciones Materno Infantil (IDIMI) of the Hospital San Borja Arriarán of the Universidad de Chile. Nutritional status, levels of inflammation markers and glycosylated hemoglobin were determined by standardized methods. Statistical analysis included correlations by Spearman test and mean difference by Kruskal-Wallis test followed by post hoc Dunns test. RESULTS: A total of 56 patients with T1D were analyzed, 30% of whom presented excess malnutrition. Those children or adolescents with obesity presented significantly higher usPCR levels compared to underweight patients or patients at risk of malnutrition (p=0.039). In addition, HbA1c levels were determined which were negatively associated with usPCR (r= 0.30; p=0.0352) and IL-6 (r= - 0.038; p=0.0352) levels. CONCLUSIONS: This study points out that nutritional status is associated with usPCR levels, in agreement with what is described in the literature and shows a possible association between classical parameters of inflammation with glycosylated hemoglobin in children and adolescents with nutritional diagnosis of overweight or obesity.


Subject(s)
Humans , Child , Adolescent , Glycated Hemoglobin/analysis , Biomarkers/analysis , Body Mass Index , Diabetes Mellitus, Type 1/metabolism , C-Reactive Protein/analysis , Enzyme-Linked Immunosorbent Assay , Nutritional Status , Interleukin-6/analysis , Tumor Necrosis Factor-alpha/analysis , Statistics, Nonparametric , Inflammation
2.
Rev. otorrinolaringol. cir. cabeza cuello ; 80(1): 79-84, mar. 2020. graf
Article in Spanish | LILACS | ID: biblio-1099206

ABSTRACT

La atresia congénita de coanas se caracteriza por la presencia de placas que obliteran la comunicación entre la cavidad nasal y la nasofaringe desde el nacimiento. Se considera como incompatible con la vida cuando la condición es bilateral. El siguiente es el caso de una paciente femenina, de 17 años, sin síndromes asociados, con obstrucción y descarga nasal anterior bilateral, asociado a respiración oral desde el periodo neonatal. El diagnóstico de atresia bilateral de coanas fue confirmado por medio de endoscopía nasal y tomografía computarizada (TC). La imagen confirmó la presencia de placas atrésicas de composición mixta. La paciente recibió tratamiento quirúrgicamente por vía transnasal con resección de las placas y modelado de neocoana.


Congenital choanal atresia is characterized by the presence of plates obliterating the communication between the nasal cavity and the nasopharynx from birth. If bilateral, this condition is incompatible with life. This following is the case of a 17-year-old female patient, without associated syndromes, with bilateral nasal obstruction and anterior discharge, associated to oral breathing, starting in her neonatal period. The diagnosis of bilateral choanal atresia was confirmed by nasal endoscopy and computed tomography (CT) scan, due to the presence of atretic plates of mixed composition. The patient was surgically treated with plate resection and modeling of a neochoana by means of a transnasal surgical approach.


Subject(s)
Humans , Female , Adolescent , Choanal Atresia/surgery , Choanal Atresia/diagnosis , Nasal Surgical Procedures/methods , Tomography, X-Ray Computed , Nasal Obstruction/etiology , Choanal Atresia/complications , Endoscopy
3.
Rev. otorrinolaringol. cir. cabeza cuello ; 79(2): 179-184, jun. 2019. graf
Article in Spanish | LILACS | ID: biblio-1014435

ABSTRACT

RESUMEN La tuberculosis cutánea representa menos del 2% de todos los casos de la infección por Mycobacterium tuberculosis. Su baja prevalencia, asociada a la amplia variedad en la presentación clínica de las lesiones, dificulta y retrasa el diagnóstico y, por tanto, el inicio del tratamiento. El siguiente es el caso de una paciente de 80 años, con una lesión ulcerada, crónica, en pabellón auricular izquierdo, con evolución tórpida y pobre respuesta al manejo farmacológico instaurado; con biopsia de piel que mostró reacción inflamatoria crónica y presencia de bacilos ácido-alcohol resistentes.


ABSTRACT Cutaneous tuberculosis represents less than 2% of all cases of infection with Mycobacterium tuberculosis. Its low prevalence, associated with a wide variety in clinical presentation of the lesions, hinders and delays the diagnosis and, thus, treatment initiation. The following is the case of an 80-years old, female patient with an ulcerated, chronic lesion in the left ear auricle, with a torpid evolution and poor response to established pharmacological management; with a skin biopsy that showed chronic inflammatory reaction and the presence of acid-fast bacilli.


Subject(s)
Humans , Female , Aged, 80 and over , Tuberculosis, Cutaneous/diagnosis , Tuberculosis, Cutaneous/drug therapy , Ear Auricle/pathology , Tuberculosis, Cutaneous/pathology , Ear Auricle/microbiology , Mycobacterium tuberculosis
4.
Arq. bras. med. vet. zootec. (Online) ; 71(2): 720-721, mar.-abr. 2019. tab
Article in English | LILACS, VETINDEX | ID: biblio-1038590

ABSTRACT

O objetivo desta pesquisa foi avaliar os SNPs rs471462296, rs456245081 e rs438495570 do gene DGAT1 em bovinos Nelore. Foram analisados 109 bovinos. A extração do DNA genômico foi realizada do sangue dos animais, usando-se o kit Ilustra Blood Genomic Prep Mini Spin® (GE Healthcare, UK). A concentração e o grau de pureza do DNA foram determinados por meio de espectrofotômetro (Nanodrop - Thermo Fisher Scientifc, USA). A genotipagem dos SNPs ocorreu mediante o emprego do ensaio Taqman® (Applied Biosystems, USA). Na análise genômica, não foram encontradas alterações nas frequências alélicas e genotípicas (P≥0,05) para os SNPs testados. Dessa forma, a região 5'UTR analisada apresentou-se monomórfica e a variação de SNPs não foi observada, o que limita seu uso como marcadores moleculares para o gene DGAT1 em Nelore.(AU)


Subject(s)
Animals , Cattle , Cattle/genetics , Phenotype , Genotype
5.
Rev. chil. endocrinol. diabetes ; 11(2): 62-68, abr. 2018. graf
Article in Spanish | LILACS | ID: biblio-914895

ABSTRACT

Aim: Analyze mi-146a and miR-155 expression and its correlation with the apoptosis of lymphocytes T in T1D and control patient. Patients and Methodology: 17 T1D patients (5 children between 8-14 yr and 12 adults between 19-29 yr). Activated and not activated peripheral mononuclear cells were studied were studied. Cellular activation with anti-CD3 and primary culture with interleukyne-2 by 5 days. Apoptosis assays through flow cytometry. miRNA through Taqman probes. Statistical analysis through Kruskal-Wallis and post-hoc Dunn's test. Results: Composition of virgin and memory T CD4 cells showed significant differences for stimulus response in control group (p = 0,0004). Increased memory cells count in control group activated by 7 days than basal (p = 0,0047). For early apoptosis differences were observed in days 3 and 7 with and without activation (p = 0,001). AICD apoptosis showed increases in control group after re-stimulation through TCR (p= 0,03). miR-146a expression was lower in recent-onset T1D children vs recent-onset DM1 adults (p = 0,0167). Conclusion: This study shows a differential miR-146a expression in T1D children with respect to T1D adult patients, diminished AICD mechanism in T1D and altered CD4+CD45RA-CD45R0+ memory cells generation in T1D adult patients.


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , T-Lymphocytes/immunology , Apoptosis/immunology , Diabetes Mellitus, Type 1/immunology , MicroRNAs/genetics , MicroRNAs/immunology , Diabetes Mellitus, Type 1/genetics , Immunologic Memory
6.
Biol. Res ; 51: 34, 2018. tab, graf
Article in English | LILACS | ID: biblio-983938

ABSTRACT

BACKGROUND AND AIMS: Atherosclerotic cardiovascular disease is highly prevalent and its underlying pathogenesis involves dyslipidemia including pro-atherogenic high density lipoprotein (HDL) remodeling. Vitamins C and E have been proposed as atheroprotective agents for cardiovascular disease management. However, their effects and benefits on high density lipoprotein function and remodeling are unknown. In this study, we evaluated the role of vitamin C and E on non HDL lipoproteins as well as HDL function and remodeling, along with their effects on inflammation/ oxidation biomarkers and atherosclerosis in atherogenic diet-fed SR-B1 KO/ApoER61h/h mice. METHODS AND RESULTS: Mice were pre-treated for 5 weeks before and during atherogenic diet feeding with vitamin C and E added to water and diet, respectively. Compared to a control group, combined vitamin C and E administration reduced serum total cholesterol and triglyceride levels by decreasing apo B-48-containing lipoproteins, remodeled HDL particles by reducing phospholipid as well as increasing PON1 and apo D content, and diminished PLTP activity and levels. Vitamin supplementation improved HDL antioxidant function and lowered serum TNF-α levels. Vitamin C and E combination attenuated atherogenesis and increased lifespan in atherogenic diet-fed SR-B1 KO/ApoER61h/h mice. CONCLUSIONS: Vitamin C and E administration showed significant lipid metabolism regulating effects, including HDL remodeling and decreased levels of apoB-containing lipoproteins, in mice. In addition, this vitamin supplementation generated a cardioprotective effect in a murine model of severe and lethal atherosclerotic ischemic heart disease.


Subject(s)
Animals , Male , Female , Ascorbic Acid/pharmacology , Vitamin E/pharmacology , Myocardial Ischemia/prevention & control , Apolipoprotein B-48/drug effects , Hyperlipidemias/prevention & control , Lipoproteins, HDL/drug effects , Antioxidants/pharmacology , Reference Values , Coronary Artery Disease/prevention & control , Coronary Artery Disease/blood , Enzyme-Linked Immunosorbent Assay , Cardiotonic Agents/pharmacology , Immunoblotting , Reproducibility of Results , Cytokines/blood , Treatment Outcome , Myocardial Ischemia/blood , Dietary Supplements , Phospholipid Transfer Proteins/blood , Diet, Atherogenic , Scavenger Receptors, Class B/drug effects , Scavenger Receptors, Class B/blood , Lipid Metabolism/drug effects , Apolipoprotein B-48/blood , Hyperlipidemias/blood , Lipoproteins, HDL/blood , Mice, Inbred C57BL
7.
Arq. bras. med. vet. zootec ; 68(6): 1431-1439, nov.-dez. 2016. tab, graf, ilus
Article in English | LILACS, VETINDEX | ID: biblio-827939

ABSTRACT

More than 300 species have been described in the genus Hepatozoon, occurring in different vertebrates. Among these, only Hepatozoon canis and Hepatozoon americanum are seen in dogs. Different methods may be used for laboratory diagnosis. The most common of these is direct parasitological examination of parasite stages in blood smears. The aim of this investigation was to conduct a phylogenetic study on Hepatozoon isolates from symptomatic dogs in the city of Goiânia, Goiás, Brazil. Blood samples were obtained from 40 symptomatic dogs that had been referred to the Veterinary Hospital of the Federal University of Goiás. Among these, only two samples were positive for Hepatozoon spp. using the direct parasitological method. These samples were then subjected to a DNA extraction process and amplification of a fragment of the 18S rRNA by means of PCR. Subsequently, the PCR products from each sample were purified and sequenced. The sequences obtained were then analyzed using the BLASTn algorithm, which identified both sequences of this study as Hepatozoon canis. By applying the Mega4 software, it was confirmed that these isolates of H. canis from dogs in Goiânia are similar to other reference isolates of the same species from other regions of Brazil and worldwide.(AU)


São descritas mais de 300 espécies do gênero Hepatozoon que acometem diferentes vertebrados. Entre estas, apenas Hepatozoon canis e Hepatozoon americanum são descritas em cães. Diferentes métodos podem ser utilizados para o diagnóstico laboratorial. O mais empregado é o exame parasitológico direto do parasito em esfregaços sanguíneos. O objetivo deste trabalho foi realizar um estudo filogenético em Hepatozoon isolados de cães sintomáticos de Goiânia, Goiás. As amostras de sangue foram obtidas de 40 cães sintomáticos encaminhados ao Hospital Veterinário da Universidade Federal de Goiás. Entre essas, duas únicas amostras foram positivas para Hepatozoon spp. pelo método parasitológico direto. Estas amostras foram, então, submetidas ao processo de extração de DNA e de amplificação de um fragmento de 18S rRNA por PCR. Ambas as amostras foram positivas na PCR. Posteriormente, os produtos de PCR de cada amostra foram purificados e sequenciados. As sequências obtidas foram analisadas pelo algoritmo BLASTn, sendo identificadas como Hepatozoon canis. Por meio do software Mega4 foi confirmado que estes isolados de H. canis de cães de Goiânia são semelhantes a outros isolados de referência da mesma espécie de outras regiões do Brasil e do mundo.(AU)


Subject(s)
Animals , Dogs , Eucoccidiida/isolation & purification , Parasitology , Phylogeny , Molecular Epidemiology , Polymerase Chain Reaction/veterinary
8.
Arq. bras. med. vet. zootec ; 66(4): 1171-1178, 08/2014. tab, graf
Article in Portuguese | LILACS | ID: lil-722572

ABSTRACT

A expressão de RNAm para leptina, receptor de leptina (obRb), adiponectina, receptor de adiponectina (AdipoR1) e resistina foi avaliada por meio da técnica de PCR em tempo real, em tecidos ovariano, hipofisário, adiposo do omento e da região perirrenal, em ovelhas alimentadas sem farelo de mamona ou com farelo de mamona detoxificada durante 14 meses. O tipo de dieta não afetou os níveis de RNAm para leptina, obRb, adiponectina, AdipoR1 e resistina nos diferentes tecidos avaliados (P>0,05). Nos tecidos ovariano e hipofisário, não foi verificada a expressão da adiponecina e da resistina, respectivamente. Como consequência, pode-se concluir que o farelo de mamona detoxificada pode ser utilizado como fonte proteica na dieta de ovelhas, sem afetar a expressão do gene resistina e dos genes leptina e adiponectina, bem como de seus receptores...


The expression of leptin, leptin receptor (obRb), adiponectin, adiponectin receptor (AdipoR1) and resistin was assessed by real-time PCR technique in ovarian, pituitary, and the omental adipose perirenal tissue in sheep feed without castor meal or with detoxified castor meal. The type of diet did not affect mRNA levels for leptin, obRb, adiponectin, resistin AdipoR1 evaluated in different tissues (P>0.05). However, in pituitary and ovarian tissues there was no expression of resistin and adiponectin, respectively. The detoxified castor meal can be used in sheep diets as alternative food protein without affecting the expression of leptin and adponectin as well as their receptors and resistin...


Subject(s)
Animals , Sheep/metabolism , Receptors, Adipokine/analysis , Receptors, Leptin/analysis , Reproduction/physiology , Resistin/analysis , Animal Feed , Ricinus , Polymerase Chain Reaction/veterinary
9.
Prensa méd. argent ; 95(10): 659-666, dic. 2008. ilus, graf
Article in Spanish | LILACS | ID: lil-534094

ABSTRACT

This study analyzes the temporal-spatial correlation between angio-and corticogenesis in the developing chick optic tectum (OT) by means of NADPH-diaphorase and immunolabeling methods. Qualitative and quantitative parameters were used to analyze a new vessels formation and growth of preexisting ones as a function of time and space...


Subject(s)
Chick Embryo , Cell Movement/physiology , Neovascularization, Pathologic/pathology , Cell Proliferation , Central Nervous System/embryology , Cerebral Veins/pathology , Visual Pathways/anatomy & histology , Anisotropy
10.
Rev. obstet. ginecol. Venezuela ; 68(3): 160-167, sept. 2008. ilus, tab
Article in Spanish | LILACS | ID: lil-522992

ABSTRACT

Estudiar la frecuencia, características anatomopatológicas y análisis de los factores de riesgo de embarazadas con placenta ácreta en la Maternidad “Concepción Palacios”en el lapso 1994 a 2004. Estudio retrospectivo y descriptivo, se revisaron los informes histológicos de las histerectomías obstétricas y de las historias clínicas de las embarazadas con diagnóstico de placenta ácreta, increta y percreta. Maternidad “Concepción Palacios ” de Caracas. Se encontraron 35 pacientes con placenta ácreta (85,71 por ciento) y 5 casos de placenta percreta (0,014 por ciento). Esto representa un 0,014 por ciento de los ingresos obstétricos y uno por 0,62 por ciento nacidos vivos. La mayoría de las pacientes tenían una edad entre 31 y 40 años y 3-4 partos y sin relación con las cesáreas previas. En el 57,14 por ciento no se encontró registro de control prenatal. Con respecto a edad de gestación el 54,29 por ciento tenía entre 21-36 semanas de embarazo al momento del parto y 78,57 por ciento de ellas ingresó en trabajo de parto. Se realizó cesárea segmentaria+histerectomía en 71,43 por ciento de los casos. El peso fetal y la talla fue mayor o igual que 2 501 g y 43 a 47 cm en la mayoría. Este estudio representa un aporte a esta rara complicación del embarazo. Se recomienda el empleo de los recursos tecnológicos actuales para el diagnóstico de esta patología durante el embarazo para reducir la morbilidad y mortalidad materna y perinatal.


Subject(s)
Humans , Female , Pregnancy , Middle Aged , Pregnancy, High-Risk , Placenta Accreta/pathology , Placenta/cytology , Obstetrics , Histological Techniques/methods
11.
Prensa méd. argent ; 95(5): 280-286, jul. 2008. graf
Article in Spanish | LILACS | ID: lil-521999

ABSTRACT

This report analyzes the dynamics temporo-spacial of the cellular proliferation during brain corticogenesis. It is an attempt of the authors to find operative rules of the proliferation that can explain the morpho and histogenetic effects of this activity.


Subject(s)
Chick Embryo , Nonlinear Dynamics , Cell Proliferation , Stochastic Processes
12.
Genet. mol. res. (Online) ; 6(4): 1035-1043, 2007. tab
Article in English | LILACS | ID: lil-520046

ABSTRACT

Obesity is due to the combined effects of genes, environment, lifestyle, and the interactions of these factors. The adrenergic receptor ¦Â3 (¦Â3-AR), leptin (LEP) and leptin receptor (LEPR) genes have been intensively evaluated in the search of variants that could be related to obesity and its cardiometabolic complications. The results of most of these studies have been controversial. In the present study, we investigated the relationship of the ¦Â3-AR p.W64R, LEP c.-2548G>A and LEPR p.Q223R gene variants with body mass index (BMI), in Brazilian subjects of different genetic backgrounds and ethnic origins. Two hundred obese patients (60 males, 140 females, BMI ¡Ý 30 kg/m2) were screened and compared to 150 lean healthy subjects (63 males, 87 females, BMI ¡Ü 24 kg/m2). Genomic DNA was extracted and amplified by polymerase chain reaction. Polymerase chain reaction products were digested with specific restriction enzymes and separated by electrophoresis. There was no significant difference in the genotype frequency of the ¦Â3-AR p.W64R and the LEP c.-2548G>A polymorphisms, between lean and obese subjects. However, the genotype and allele frequencies of the LEPR p.Q223R variant were significantly different between the normal weight and obese groups. Haplotype analysis has shown an association between the G/G allelic combination of c.-2548G>A LEP and c.668A>G LEPR, in obese subjects. Our results suggest that genetic variability in the leptin receptor is associated with body weight regulation, the LEPR p.Q223R variant being related to BMI increase. The haplotype combination of LEP c.-2548G>A and LEPR p.Q223R variants was related to a 58% increase in obesity risk.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Genetic Variation , Obesity/genetics , /genetics , Alleles , Body Mass Index , Brazil , Case-Control Studies , DNA , Gene Frequency , Obesity/pathology , Polymorphism, Single Nucleotide , Amino Acid Substitution/genetics
13.
Rev. bras. ecocardiogr ; 20(1): 34-42, jan.-mar. 2006. ilus, tab
Article in Portuguese | LILACS | ID: lil-451514

ABSTRACT

Objetivo: Avaliar, pelo Doppler transtorácico da artéia descendente anterior (ADA), a resposta da microcirculação coronariana ao vasodilatador. Métodos: Foram incluídos 34 pacientes com hipertrofia ventricular esqueda concêntrica(HCVE) moderada ou importante (relação volume/massa menor 0,35), média etária de 53,3 mais ou menos 10,1 anos, 26 do sexo masculino (grupo hipertrófico),sem evidências de estenose de artérias coronárias à cineangiocoronariografia, e 16 indivíduos saudáveis, média etária de 48,4 mais ou menos 9,5 anos, 11 do sexo masculino, como grupo controle.Realizou-se ecocardiograma Doppler convencional, Doppler tissular e velocidade de propagação do fluxo mitral. No segmento médio distal da ADA foi registrado a curva de velocidade do fluxo em condições basais e após a infusão de Dipiridamol em, bolus, de 0,56 mg/kg, e calculada a reserva de fluxo coronariano (RFC igual velocidade pico da vasodilatação/velocidade basal. Os dados foram comparados pelo teste, t, de Student para amostras não pareadas. Resultados: Os sintomas com HCVE tiveram relação volume/massa maior e relação E/A menor (p menor 0,05), sem diferença significante da fração de ejeção e outros parâmetros de função diastólica....


Subject(s)
Humans , Male , Female , Middle Aged , Coronary Circulation/physiology , Echocardiography/methods , Echocardiography , Hypertrophy, Left Ventricular/complications , Hypertrophy, Left Ventricular/diagnosis
14.
Genet. mol. res. (Online) ; 2(4): 360-365, Dec. 2003.
Article in English | LILACS | ID: lil-417594

ABSTRACT

Dynamic mutation involves the expansion of a tandem arrayed DNA sequence that is polymorphic in the population. This mechanism is associated with neurological/neuromuscular disorders and the pathology depends on the extension of the repeated tract, with a specific threshold for each disease. We made a PCR-based characterization of allelic polymorphism of SCA1 and SCA2 loci in a sample of 200 pairs of chromosomes in a population in Rio de Janeiro and found 23 different alleles at the SCA1 locus, varying from 10 to 39 CAG repeats (mean 27.7 +/- 3.3, mode 28) and 10 different alleles ranging from 19 to 29 CAG (mean 22.1 +/- 1.0, mode 22) at the SCA2 locus. The level of heterozygosis was 53 (SCA1) and 8 (SCA2)


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Spinocerebellar Ataxias/genetics , Gene Frequency , Brazil , DNA Mutational Analysis , Genetic Predisposition to Disease , Polymerase Chain Reaction , Nuclear Proteins/genetics , Nerve Tissue Proteins/genetics , Proteins/genetics
SELECTION OF CITATIONS
SEARCH DETAIL