Search PubMed⌕ Search

Biomedical subjects

C Garcia

Publications and source records attributed to C Garcia.

At least 235 records · Page 13Linked to original sources
PubMed1990

Effect of sodium and potassium ingestion on renal growth in rats.

To determine whether differences in dietary Na and K intake influence renal growth and compensatory renal growth following unilateral nephrectomy (uni), rats were given 2 diets for 2 weeks which differed only in Na-K concentrations. Diet 1 (High Na, Low K) contained 1.0% Na, 0.36% K and diet 2 (Low Na, High K) contained 0.05% Na, 2.0% K. Half of the rats consuming diets 1 and 2 for 1 week received uni and the other half of sham operation (sham). The rats were followed for another week while consuming the experimental diets. Uni and sham rats on diet 1 showed significant increase in blood pressure (BP) (136 +/- 4 v 126 +/- 3 mm Hg, P less than .05). Uni itself did not alter blood pressure. Body weight and heart rate were unchanged by diet or operation. Kidney weight, renal RNA, protein, RNA/DNA, and protein/DNA increased significantly after uni but the differences were not affected by diet. Serum blood urea nitrogen (BUN) and creatinine were not markedly different among any group of rats suggesting no major renal damage. We conclude that dietary changes of Na-K which cause no obvious renal damage even though BP is elevated moderately do not influence renal growth or compensatory renal growth. Based on RNA, DNA and protein metabolism, the form of growth (hypertrophy or hyperplasia) is also not influenced by renal electrolyte handling.

Analysis of Variance↗
PubMed1990

Serological diagnosis of neurobrucellosis.

The presence of antibodies was determined in the serum and cerebrospinal fluid in six patients with neurobrucellosis using the Rose Bengal test, the microdilution agglutination test, and the Coombs' test. Four of the patients were followed up for more than three months. The Rose Bengal test and the microagglutination test were positive in cerebrospinal fluid in five of the six cases at some stage. The Coombs' test was positive in cerebrospinal fluid in every patient and in one was the only positive serological test. Cerebrospinal fluid positivity is not excluded by low titres or negative results of antibodies in the serum for any of the three methods. A Coombs' test or some equivalent must always be made on the cerebrospinal fluid to diagnose neurobrucellosis.

Adolescent↗
PubMed1990

Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.

We report the isolation of a new marker (S6.1) from band p11.2 of human chromosome 17 by differential Alu-polymerase chain reaction (Alu-PCR) of both a monochromosomal hybrid retaining a single human chromosome 17 and a hybrid retaining a del(17)(p11.2p11.2) in addition to other human chromosomes. The method is based on the preferential PCR amplification of human DNA in rodent/human hybrids when primers specific to the human Alu repeat element are used. MspI and SstI RFLPs associated with S6.1 were identified and used in linkage analysis of both a previously reported and a newly identified French-Acadian kindred segregating autosomal dominant Charcot-Marie-Tooth disease (CMT). A cumulative peak lod score of 3.41 at a peak recombination fraction of .12 indicates that this marker is linked to the CMT 1A locus but is at a distance from the disease gene. Thus, the marker S6.1 will be useful in further delineating the candidate region for the CMT gene when its location with respect to pA10-41 and 1516, two other markers from 17p11.2 which have previously demonstrated close linkage to the CMT locus, has been determined.

Animals↗
PubMed1990

Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.

We have performed linkage analysis in a large French-Acadian kindred segregating one form of autosomal dominant Charcot-Marie-Tooth disease (CMTD) (type IA) using 17 polymorphic DNA markers spanning human chromosome 17 and demonstrate linkage to several markers in the pericentromeric region, including DNA probes pA10-41, EW301, S12-30, pTH17.19, c11-2B, and p11-2c11.5. Linkage of markers pA10-41 and EW301 to CMTD type IA has been reported elsewhere. Four new markers, 1516, 1517, 1541, and LL101, which map to chromosome 17 have been identified. The marker 1516 appears to be closely linked to the CMTD locus on chromosome 17 as demonstrated by a maximum lod score of 3.42 at theta (recombination fraction) = 0. This marker has been mapped to 17p11.2 using a somatic cell hybrid constructed from a patient with Smith-Magenis syndrome [46,XY, del(17)(p11.2p11.2)]. A lod score of 6.16 has been obtained by multipoint linkage analysis with 1516 and two markers from 17q11.2, pTH17.19, and c11-2B. The markers 1517 and 1541 have been mapped to 17p12-17q11.2 and demonstrate maximum lod scores of 2.35 and 0.63 at recombination values of .1 and .2, respectively. The marker LL101 has been mapped to 17p13.105-17p13.100 and demonstrates a maximum lod score of 1.56 at a recombination value of .1. Our study confirms the localization of CMTD type IA to the pericentromeric region of chromosome 17.

Animals↗
PubMed1989

Study of C. burnetii human and animal seroprevalence in a rural population in Madrid community.

A pilot study on human seroprevalence of antibodies to C. burnetii in the Madrid region, initiated in a small rural population, shows a 15.4% positivity by the indirect immunofluorescence test. An urban sample shows an 8.8% positivity. Animal seroprevalence in livestock located in the village under study is 76.6% in caprine and 17.7% in bovine. A high risk epidemiological situation is detected.

Animals↗
PubMed1989

Spinal cord compression due to intradural extramedullary aspergilloma and cyst: a case report.

A case of thoracic spinal cord compression caused by intradural extramedullary cyst associated with aspergilloma is presented. The specific diagnosis was extremely difficult and required specialized tissue studies. Clinical suspicion of fungal infection, surgical intervention for spinal cord decompression, and tissue biopsy and relentless diagnostic laboratory studies are particular features of this case.

Adult↗
PubMed1989

Higher T-cell imbalance and growth factor receptor expression in B-cell chronic lymphocytic leukemia (B-CLL) as compared to monoclonal B-cell lymphocytosis of undetermined significance (B-MLUS).

The surface marker phenotype of lymphocytes derived from 12 patients with B-CLL was compared to that of lymphocytes from 10 patients with an other monoclonal but clinical benign form of B-cell proliferative disorder termed monoclonal B-cell lymphocytosis of undetermined significance (B-MLUS). A panel of well characterized monoclonal antibodies was used for the surface marker determinations. The mean total number of B cells (CD20) was 8.5 x 10(9)/1 in B-MLUS as compared to 44 x 10(9)/1 in B-CLL (p less than 0.001). B-CLL had a greater imbalance in T-cell subpopulations than B-MLUS and healthy controls. Total numbers of CD3+, CD8+ cells as well as cells expressing the NK-related antigens (CD16, Leu-7) and IL-2 receptor (CD25) bearing lymphocytes were statistically significant higher in B-CLL than in B-MLUS. Analyses of B-cell enriched populations showed that B-CLL represented B cells of an early maturation stage, whereas B cells from B-MLUS were more mature as judged by the loss of the CD21 surface marker. A larger fraction of B cells in B-CLL compared to B-MLUS exhibited a higher activation stage as revealed by the expression of the CD21, CD25 and CD35 structures as well as the FMC7 antigen.

Aged↗
PubMed1989

Central vestibular projections of primary cervical fibers in the frog.

The origin of cervicovestibular inputs was documented in frogs, as well as the number of fibers, site of projection, and their distribution within the nuclei. The first spinal nerve in 15 frogs was labeled with extracellular injections of horseradish peroxidase. The brain stem and the posterior root were sectioned serially. The trajectories of the fibers in the central nervous system were reconstructed, and the number and diameters of the fibers in the posterior root were determined. The average number of fibers in the first posterior root was 143 +/- 6.2, their number decreasing exponentially with increased diameter. After entering the spinal cord the fibers were located in the dorsal funiculus. The thick and medium-sized fibers coursed medially in relation to the thin ones, giving collaterals to the spinal cord and to the obex region. The thinnest fibers projected to the reticular formation and nucleus of the solitary tract. Only collaterals from fibers of medium and thick caliber reached the vestibular area in their trajectory to the cerebellum (spinocerebellar fibers). All the vestibular nuclei received collaterals and endings from the spinocerebellar fibers, the ventral nucleus being the most innervated. The total number of branches for the vestibular area, however, was very small. The results of this experiment are correlated with physiological and anatomical findings described in the literature.

Animals↗
PubMed1989

[Fluoridated amalgams. Bibliographic review].

A review on fluoride containing amalgam is reported in this paper. The inhibitory effects of fluoride on dental caries are well known for many years. Thus, the incorporation of fluoride to an amalgam restoration prevents the occurrence of marginal caries. Other physical properties of fluoride amalgams such as compressive strength, dimensional changes, creep and corrosion are also reviewed in this paper.

Dental Amalgam↗
PubMed1988

IgA nephropathy and polycystic kidney disease.

We report a patient with polycystic kidney disease, advanced renal failure, and nephrotic-range proteinuria. Kidney biopsy revealed IgA nephropathy with lesions of focal and segmental glomerular sclerosis. This association had not been previously described and is probably coincidental. This case supports the assumption that the nephrotic-range proteinuria observed in some polycystic patients could be the consequence of another superimposed glomerular disease. This glomerulopathy can worsen the course of azotemia in these patients.

Aged↗