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Biomedical subjects

F Zacchello

Publications and source records attributed to F Zacchello.

At least 127 records · Page 7Linked to original sources
PubMed1988

In-vitro production of HIV-specific antibody in children at risk of AIDS.

To improve on the early diagnosis of human immunodeficiency virus (HIV) infection, 37 children born to HIV-infected mothers and 22 controls were investigated for in-vitro synthesis of IgG antibody directed against HIV components. For 14 of 16 infected children western blot showed HIV-specific IgG in the supernatants of cultures of their peripheral blood lymphocyte cultures. HIV-specific IgG synthesis was detected in cultures from 4 out of 17 seropositive children aged under 15 months with no clinical or laboratory evidence of infection. No HIV-specific IgG production was observed in cultures from 4 uninfected children or 22 controls. The results show that the demonstration of in-vitro production of HIV-specific IgG may help in the early diagnosis of HIV infection in children.

Acquired Immunodeficiency Syndrome↗
PubMed1987

Modification of bronchial hyperreactivity during pollen season in children allergic to grass.

Ten children, sensitive to grass pollens with seasonal rhinitis and mild asthma, underwent bronchial challenge with carbachol in the pre-seasonal, seasonal, and post-seasonal period. According to pollen count, we observed significant differences between pre-seasonal, seasonal, and post-seasonal values. Also basal FEV1 values varied in the same fashion. Seven of the ten children also participated in a previous similar study in 1984, at which time they did not demonstrate significant variations to bronchial challenge. We wish to emphasize the importance of pollen concentration in the atmosphere as well as the existence of a threshold value of grass pollen necessary for a significant modification in bronchial reactivity to occur.

Asthma↗
PubMed1985

Hydroxyl negative chemical ionization mass spectrometry linked with collisionally activated decomposition. A modern analytical tool in inborn errors of metabolism.

Two kinds of inborn errors of metabolism, dicarboxylic aciduria and hyperoxaluria, have been studied by means of hydroxyl negative ion chemical ionization [NICI(OH-)], linked with collisionally activated decomposition experiments on the [M-H]- species of the pathognomonic organic acids. This method has led to non-controversial qualitative determinations of C4-C10 dicarboxylic acids and oxalic, glyceric and glyoxylic acids. NICI(OH-) linked with collisionally activated decomposition mass analysed ion kinetic energy spectrometry (CAD MIKES) is proposed herein for diagnostic purposes, as a valid mass spectrometric alternative to standard gas chromatographic/mass spectrometric analysis. The procedure is characterized by simplified sample treatment and by fast execution.

Gas Chromatography-Mass Spectrometry↗
PubMed1984

CAD MIKES: a new method for a rapid and unequivocal structural identification of organic acids in biological fluids. A first application to a case of methylmalonic aciduria.

A novel application of Collisionally Activated Decomposition Mass analysed Ion Kinetic Energy (CAD MIKE) spectrometry to separation and positive structural identification of urinary methylmalonic acid (MMA) (the pathognomonic compound for the diagnosis of methylmalonic acidurias) is presented. CAD MIKES scans of EI ionic species at m/z 119 ([M + H]+) and m/z 101 ([M-OH]+) have been obtained from a pure standard of MMA and from crude urinary acid fractions. With reference to the procedures employed so far, the advantages of the proposed method lie in fast and simplified sample pretreatment and in a quick non-controversial response to a clinical suspicion of serious, life-threatening inherited metabolic diseases.

Child, Preschool↗
PubMed1975

Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation.

The case is described of a malformed girl with partial trisomy for a segment of the long arm of chromsome (4q32 leads to qter) due to an unfavourable segregation of a maternal reciprocal translocation t(4;21) (q32q22). The clinical comparison between the child and patients previously described by other authors does not suggest the existence of a syndrome associated with trisomy 4q+.

Adult↗