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Biomedical subjects

M Martelli

Publications and source records attributed to M Martelli.

At least 109 records · Page 6Linked to original sources

[The popularity of bran].

After a brief introduction on the nature of the fibers either naturally present in or artificially added to the diet and their physiological functions, the pathological conditions in which fiber is added to the diet for therapeutic purposes are reviewed. Unfortunately high fiber diets have only had a beneficial effect on cases of constipation and diabetes mellitus. The irrational addition of uncommon fibres to the diet as popularly recommended for a wide variety of diseases is therefore criticised.

Colonic Neoplasms↗

Sequential combination of systemic high-dose ara-C and asparaginase for the treatment of central nervous system leukemia and lymphoma.

Eight patients with overt central nervous system (CNS) leukemia and lymphoma were treated with sequential administration of systemic high-dose cytosine arabinoside (HiDAC) and asparaginase (ASP) with no direct CNS therapy. Complete clearing of the cerebrospinal fluid (CSF) was achieved in six (86%) of seven patients with meningeal disease, generally after the first course of therapy. Two patients presented with evidence of extensive intracerebral disease; both responded with a greater than 50% regression of the tumor infiltrates. Concomitant extraneurologic localizations responded equally well to HiDAC/ASP: responses were seen in four of five patients, including complete remission in three of four patients who presented with marrow involvement. Toxicity was generally moderate and limited to myelosuppression (eight of eight patients), tolerable nausea and vomiting (eight of eight patients), mild hepatotoxicity (two of eight patients), and oral mucositis (one of eight patients). These results indicate that HiDAC/ASP is a tolerable and highly effective treatment modality for CNS leukemia and lymphoma and suggest its potential role for sanctuary chemoprophylaxis.

Adult↗

Have a health fair!

Have a Health Fair! It is an excellent mechanism for teaching health, disease prevention, and safety to young children. It also provides many benefits to parents, nurses, hospital staff and members of the community.

Child Health Services↗

Eosinophilic leukemia with prominent visceral involvement: histopathological and histochemical observations.

Evidence supporting the view that eosinophilic leukemia exists as a separate entity among myeloproliferative disorders was found in the pathological and histochemical findings in a case of hypereosinophilic disease. Blast cells and eosinophils in all stages of maturity, including unusual atypical eosinophil precursors, were seen in a prominent infiltration of the spleen and the liver. Blasts were far more numerous in the viscera, especially in the liver, than in the marrow and peripheral blood. Enzyme histochemical studies of plastic sections showed that blasts were reactive for cyanide-resistant peroxidase, which is specific for eosinophils, and could therefore be regarded as part of an eosinophilic leukemic proliferation. Some eosinophils showed aberrant reactivity for chloroacetate esterase. The existence of a neoplastic proliferation of eosinophils is consistent with the view that eosinophils represent a distinct marrow line. The possibility that hypereosinophilic patients may harbor a far more prominent blastosis in the viscera than is apparent from marrow and blood picture is also stressed. Finally, a chromosomic abnormality previously described in acute nonlymphocytic leukemia with atypical eosinophils in the marrow is for the first time reported in a patient with hypereosinophilic disease.

Adult↗

[Therapeutic use of prostacyclin in cardiovascular pathology].

After a brief survey of the already well known functions of tromboxane and prostacyclin both in physiological and pathological conditions, the data found in the literature on the therapeutical use of prostacyclin are discussed. The positive results obtained in the treatment of arteriosclerosis obliterans of the lower limbs, of Raynaud's syndrome, of ischaemic stroke and of ischaemic heart diseases, together with the very modest side effects of prostacyclin, suggest to continue with prostacyclin therapy even if its mechanism of action is not yet clear.

Arachidonic Acid↗

[The proteolytic etiopathogenesis of pulmonary emphysema].

Laennec and later workers attributed the aetiopathogenesis of emphysema to mechanical causes. This view has been superseded by the current proteolytic theory. It is now believed that the destruction of the pulmonary parenchyma in emphysema occurs when the homeostatic equilibrium between cellular proteases (polymorphonucleates and macrophages) and serum antiproteases (primarily alpha-1-antitrypsin) which protects the respiratory ways, is disturbed. This imbalance not only produces idiopathic emphysema due to alpha-1-antitrypsin but also post-bronchitic forms due to increased protease release.

Humans↗

[Idiopathic mitral valve prolapse].

Current knowledge concerning idiopathic prolapse of the mitral valve is illustrated. The histopathological cause is myxoid degeneration of the mitral cusps, which sometimes extends to the tendinous cords, the valve implant ring, and the apex of the papillary muscles. Primary damage to these structures, whose intactness is essential for correct closure of the ostium, causes protrusion of the ventricular cusps into the left atrium during ventricular systole (i.e. prolapse). The reason for this degeneration is not known. The high familial incidence of prolapse lends credit to the most widely held suggestion, namely a hereditary defect. The clinical progress is benign in the great majority of cases ("crystallized" form) and is often asymptomatic. Complications are possible, however, and must always be borne in mind. They include progressive and acute mitral insufficiency, infective endocarditis, arrhythmias, motor or sensitive neurological complications, and sudden death. Particular attention must be paid to the path to be followed to arrive at the correct diagnosis. Careful evaluation of some of the clinical signs arousing suspicion in the previous history and/or objective examination enable a diagnosis to be formed with relatively simple, non-invasive instrumental techniques, such as echocardiography and polycardiography, provided other forms of prolapse secondary to ischaemic heart disease, mitral endocarditis, etc. are excluded. "Therapy is obviously necessary in the presence of complications; however, even in "crystallized" form, in the presence of subjective symptoms, tranquillizers and possibly beta-blockers may be necessary".

Adrenergic beta-Antagonists↗

[Marfan's syndrome].

Marfan's disease is a hereditary condition (usually dominant) characterised by variously significant skeletal muscle, ocular, cardiac and above all respiratory alterations attributable to congenital disorder of the fibrous support proteins (particularly of collagen and elastin). Sporadic forms whose interpretation is uncertain, however may, also be observed. The exact nature of the biochemical error responsible for the syndrome, however, is not known. In the absence of fully indicative laboratory tests, diagnosis is based on recognition of he typical lesions and their systemic nature. Careful symptomatological examination of suspected subjects may lead to the detection of less common sites such as the respiratory system. Personal experience shows that it can also reveal clinically obsolete lesions, such as heart impairment discovered in some cases solely through elevation of the polycardiographic telediastolic index (in inverse relation to the pattern of the echocardiographic telediastolic volume), which is an expression of reduced ventricular compliance, and the presence of areas with a low thallium uptake, offering scintigraphic evidence of fibrosis replacing destroyed muscle fibres. Prognosis depends on the clinical expressiveness of the disease, i.e. the apparatuses involved and the extent of their damage. Heart alterations and their extent are undoubtedly an aggravating factor quoad vitam. The current position with regard to both drug management and possible surgical treatment is also discussed.

Adolescent↗

[Sarcoidosis].

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Adult↗

Healing of hyaluronic acid-enriched wounds: histological observations.

The influence of an exogenous supply of Na hyaluronate (HA) on the healing of superficial skin wounds in healthy and alloxan-induced diabetic rats was histologically assessed. Rats were treated by topical application on the wound site of a 2% Na hyaluronate solution. A facilitating effect of the HA-enrichment on wound repair processes (particularly epithelial migration and differentiation) was markedly evident in wounded diabetic rats. This result is discussed in terms of a possible favorable influence of an HA-enriched wound environment on cell migratory processes occurring during wound healing.

Animals↗

Chemical characterization of the hen eggshell matrix: isolation of an alkali-resistant peptide.

The eggshell matrix was obtained from hen eggshells using EDTA solutions. The water-soluble organic material was separated on a DEAE-cellulose column equilibrated with 8 M urea using Tris-hydrochloric acid buffer as eluent with a linear gradient of sodium chloride. Five main fractions were obtained which differ in amino acid composition and sugar contents. As is shown from the uronic acid content, the first two fractions eluted from the column are glycoproteins, while the other three contain proteins and glycosaminoglycans From the alkaline hydrolysate of the eggshell matrix, a peptide was isolated which is composed of aspartic acid, threonine, serine, glutamic acid, proline, glycine and alanine in a molar ratio of 2:1:3:7:1:3:1 with a minimum molecular weight of 2158 daltons. The calcium ion binding to this peptide was studied, at different pH values, with both free and blocked carboxyl groups, using murexide as an indicator of free Ca2+. The importance of this acidic peptide in the calcification process of the eggshell matrix is discussed.

Amino Acids↗

B-cell acute lymphoid leukemia (ALL) with lymphoblasts expressing surface immunoglobulins only at relapse.

Morphological, cytogenetic and immunological studies were performed on lymphoblasts of two patients with acute lymphoid leukemia at onset and at relapse. At onset and before any treatment lymphoblasts had L3-FAB morphology, a 14q+ chromosome abnormality due to a 8;14 translocation in the absence of expression of specific immunologic markers (E-rosette, C3-receptor, surface immunoglobulins). The clinical behaviour of the two patients was characterized by a very short first complete remission and by a short survival. At relapse SIg was expressed by lymphoblasts of both patients. This evolution in immunological phenotype of the dominant blast populations from onset to relapse provides evidence that in vivo, during the course of the leukemic disease, phenotype changes take place that seem to be cell differentiation.

Adolescent↗