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Biomedical subjects

A Cabello

Publications and source records attributed to A Cabello.

At least 109 records · Page 6Linked to original sources
PubMed1989

Bacteriophage lambda-mediated transposon mutagenesis of phytopathogenic and epiphytic Erwinia species is strain dependent.

Using transformation and conjugal mobilization, plasmids carrying the lamB gene of Escherichia coli were transferred to a range of Erwinia strains. The resultant strains were infected with lambda 467, and kanamycin resistant transductants were screened for various mutant phenotypes including auxotrophy and altered extracellular enzyme activities. Reversion analysis suggested that most mutant phenotypes were due to Tn5 insertion. The applicability of the techniques was highly strain dependent. However a rapid and simple route to mutant isolation was obtained, which could allow the use of other lambda-related genetic techniques in several important species which, to date, have not been genetically manipulated.

Bacteriophage lambda↗
PubMed1989

[Post-cesarean uterine scar].

The American College of Obstetricians and Gynecologists recommends that women with one previous cesarean section be allowed a trial of labor. One of the exclusions to this recommendation are women with 2 or more previous cesarean section because of the risk of uterine dehiscence. We measured fibrosis in a sample obtained from the uterine scar region, finding the higher rate of fibrosis (35.7%) for the group with one previous cesarean section. We conclude that uterine scar shows no clear differences after one, two or more cesarean sections, so the risk of uterine scar dehiscence could be similar.

Adult↗
PubMed1989

[Myopathy associated to human immunodeficiency virus (HIV) infection].

Myopathy associated with HIV infection is rare and generally appears before the manifestations of other symptoms of AIDS. Its first symptoms are proximal weakness and myalgias, together with increased CPK. Electromyographic studies show either a myopathic pattern or the mixed pattern characteristics of inflammatory myopathies. Histologically they can be classified into three groups: 1) cases which present only with necrosis and regeneration of fibers; 2) those which associate to the above findings, inflammatory infiltrates, and 3) cases whose predominant characteristics is the presence of nemaline structures, with or without inflammation. The etiology of the AIDS associated myopathy is unknown, but most factors indicate an autoimmune mechanism in the pathogenesis of the disease.

Acquired Immunodeficiency Syndrome↗
PubMed1988

[Congenital muscular dystrophy. Apropos of 4 cases].

Four cases of congenital muscular dystrophy are reported. Muscular weakness and hypotonia, with different clinical severity, was present from birth in three patients; in the fourth one, it began at two months old. Three cases had joint contractures. One patient died by respiratory infection. Serum CK level was very high in all of them. Muscle biopsies showed pathologic changes consistent with muscular dystrophy with endomysial and perimysial fibrosis and fatty infiltration. Authors analysed this illness emphasizing clinical and biochemical (CK) data so that an early diagnosis can be suspected.

Biopsy↗
PubMed1987

Chromatolytic changes in the central nervous system of patients with the toxic oil syndrome.

Five patients died of a severe neuromyopathy months after the ingestion of adulterated rapeseed oil. These patients were selected for this study due to the presence of striking chromatolytic lesions in symmetric and scattered nuclei of the brain stem, including the locus coeruleus, midline raphe, lateral reticular nuclei of the medulla and cuneate nuclei. Two of the five cases, in addition to these topographic levels of involvement, had remarkable chromatolysis, vacuolar degeneration and heavy silver impregnation of the swollen perykarya and proximal dendrites in the nuclei of the basis pontis. In this paper we analyze the features of the chromatolytic lesion and suggest that the neuronal pathology observed in these cases is an example of irreversible chromatolysis involving vacuolization and filamentous proliferation as final events of the chromatolytic process. The cause of the cell degeneration in the toxic oil syndrome (TOS) is yet undetermined. Chromatolysis in this disease may be the result of a neurotoxic action of the toxic factor in the adulterated oil.

Brassica↗
PubMed1987

Subcortical arteriosclerotic encephalopathy (Binswanger's disease): a report of five patients.

Five patients with variable clinical symptoms were diagnosed as having--subcortical arteriosclerotic encephalopathy (Binswanger disease) based on the presence of lacunar infarcts in basal ganglia, various abnormalities of subcortical white matter and severe thickening and hyalinization of penetrating arteries and arterioles. One case had a classical clinical picture while in the others the course of the disease was short and was associated with severe systemic abnormalities. The variability of the clinical features, the identify of "classical" clinical symptoms with other forms of cerebral arteriosclerosis, the similarity between "atypical" cases and other entities, and the high frequency of associated conditions makes it difficult to characterize the clinical pathological entity called subcortical arteriosclerotic encephalopathy.

Aged↗
PubMed1986

Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family.

A family with hereditary motor and sensory neuropathy (HMSN) type II is described in which 10 affected and 17 unaffected members in three generations were examined. The peak age of onset was in the second decade. In the youngest generation, the proportion of affected to unaffected individuals at risk significantly differed from the expected 50%. There was slight slowing of conduction velocities in 36% of nerves; however, only 3 out of 10 affected members had entirely normal conduction studies. The amplitude of the sensory potentials of median and peroneal nerves was almost uniformly reduced. In all affected patients electromyography of anterior tibial muscles showed signs of neurogenic involvement. Histological study of two sural nerves and a sciatic nerve and its branches revealed loss of myelinated fibres with a proximal-to-distal gradient in this fibre loss, clusters of small regenerating fibres, and atrophic axons. Postmortem study of the proband showed loss of anterior horn and dorsal root ganglion neurons in the lumbar and sacral segments and degeneration of the fasciculus gracilis. Morphometric evaluation of L5 ventral and dorsal roots revealed a normal number of myelinated fibres, diameter histograms being shifted to the left because of a significant loss of large myelinated fibres and regeneration. These anatomical findings are consistent with the hypothesis that HMSN type II represents a primary neuronopathy affecting motor and sensory neurons.

Adult↗
PubMed1986

A study of IgE in immunoglobulin preparations for intravenous administration. I. IgE in intravenous IgG.

We have studied the IgE content of different lots of commercial intravenous IgG preparations used in our day hospital as replacement therapy for patients with agammaglobulinemia. Two enzymatic methods were used: Phadezym and FAST. The average amounts of IgE detected in Endobulin and Sandoglobulin lots were very high with respect to serum values in the general population. In some lots we found low titers of specific IgE (RAST class 1) to house dust mite, rye grass and cow's milk. We also found in most preparations the presence of IgG anti-IgE which are usually present in sera from atopic patients. Despite a low post-infusion increase of serum IgE and the absence of sensitization or adverse reactions observed, a careful selection of donors with normal IgE levels may need to be recommended to manufacturers in the future.

Agammaglobulinemia↗
PubMed1984

Toxic epidemic syndrome: musculoskeletal manifestations.

The musculoskeletal manifestations of a new systemic disease that developed after toxic oil consumption are described. Clinically, it was characterized by the presence of arthralgias, sometimes arthritis, extensive muscle atrophy, severe neuropathy and a scleroderma-like skin involvement. Radiologically, different types of osteopenia could be seen in the absence of joint space narrowing or erosions. Neither hypertrophy, nor hyperplasia of synoviocytes were seen on microscopic examination. A non-necrotizing vasculitis and increase in fibrous tissue were observed at different levels.

Adolescent↗
PubMed1983

Paraganglioma of the cauda equina.

The authors present two cases of paraganglioma located in the cauda equina. Diagnosis was suspected by light microscopy and confirmed with the identification of characteristic neurosecretory vesicles. The presence of cytoplasmic filaments in both of our cases and of cilia in one case are very unusual findings in paraganglioma and seem to be characteristic of this location. The cauda equina is a extremely rare location for this type of tumor and, as far is known, only ten other cases have been reported. Paraganglioma should be considered as a diagnostic possibility in order not only to make a correct diagnosis, but also to prepare tissues for special stains and biological and electronmicroscopic studies.

Adult↗
PubMed1983

Dominantly inherited motor and sensory neuropathy type I. Genetic, clinical, electrophysiological and pathological features in four families.

This report describes the genetic, clinical, electrophysiological and sural nerve biopsy features in 26 affected members and 21 unaffected relatives from 4 families with autosomal dominant inherited motor and sensory neuropathy (HMSN), Type I. In all age categories, the proportion of affected to unaffected individuals at risk did not significantly differ from the expected 50%. The peak age of onset was in the first decade. There was a complete concordance between nerve conduction velocity in the propositi and that in their affected relatives within each family. Marked slowing of conduction velocities was present as early as the age of 2.5 years, while precocious clinical signs and symptoms were quite subtle. Determination of conduction velocity is a valuable aid aid to the early diagnosis of the disease.

Biopsy↗