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1.
Nature ; 616(7955): 50-55, 2023 04.
Article in English | MEDLINE | ID: mdl-36949196

ABSTRACT

The ambition of harnessing the quantum for computation is at odds with the fundamental phenomenon of decoherence. The purpose of quantum error correction (QEC) is to counteract the natural tendency of a complex system to decohere. This cooperative process, which requires participation of multiple quantum and classical components, creates a special type of dissipation that removes the entropy caused by the errors faster than the rate at which these errors corrupt the stored quantum information. Previous experimental attempts to engineer such a process1-7 faced the generation of an excessive number of errors that overwhelmed the error-correcting capability of the process itself. Whether it is practically possible to utilize QEC for extending quantum coherence thus remains an open question. Here we answer it by demonstrating a fully stabilized and error-corrected logical qubit whose quantum coherence is substantially longer than that of all the imperfect quantum components involved in the QEC process, beating the best of them with a coherence gain of G = 2.27 ± 0.07. We achieve this performance by combining innovations in several domains including the fabrication of superconducting quantum circuits and model-free reinforcement learning.

2.
Folia Morphol (Warsz) ; 76(4): 603-607, 2017.
Article in English | MEDLINE | ID: mdl-28553853

ABSTRACT

The present research used immunohistochemistry to analyse the detection and localisation of nitric oxide synthase (NOS) isoforms in the ductuli efferentes and epididymis of prepubertal and adult alpaca. In the ductuli efferentes and epididymis of prepubertal and adult animals, nNOS and eNOS were similarly expressed in epithelial lining cells, conversely differences were observed in the immunopresence of iNOS. Our data provide evidence that NOS isoforms may have roles in reproductive functions and in the developmental processes of the excurrent duct system in the alpaca.

3.
Biochim Biophys Acta ; 1290(2): 184-90, 1996 Jun 04.
Article in English | MEDLINE | ID: mdl-8645722

ABSTRACT

In this paper we describe the purification to molecular homogeneity of the enzyme that cleaves the synthetic epidermal mitosis-inhibiting pentapeptide (pyroGlu-Glu-Asp-Ser-Gly; EPP) from swine serum. Biochemical characterisation of the enzyme shows a glycoprotein with apparent molecular mass of 200 kDa. The Km and Kcat values for EPP hydrolysis are 0.624 mM and 694 s-1, respectively. Use of proteinase inhibitors shows the enzyme's metalloendopeptidase character. Moreover, captopril and lisinopril prevent the cleavage of EPP. The N-terminal amino-acid sequence of the purified protein corresponds to the N-terminal amino-acid sequence of swine kidney angiotensin-converting enzyme, a dipeptidyl carboxypeptidase (EC 3.4.15.1).


Subject(s)
Carboxypeptidases/blood , Growth Inhibitors/metabolism , Oligopeptides/metabolism , Peptidyl-Dipeptidase A/metabolism , Amino Acid Sequence , Angiotensin-Converting Enzyme Inhibitors/pharmacology , Animals , Captopril/pharmacology , Carboxypeptidases/chemistry , Enzyme Inhibitors/pharmacology , Glycoproteins/chemistry , Growth Inhibitors/blood , Kinetics , Lisinopril/pharmacology , Molecular Sequence Data , Pyrrolidonecarboxylic Acid/analogs & derivatives , Substrate Specificity , Swine
4.
Biol Psychiatry ; 47(4): 332-7, 2000 Feb 15.
Article in English | MEDLINE | ID: mdl-10686268

ABSTRACT

BACKGROUND: Multiple groups have reported on the use of repetitive transcranial magnetic stimulation (rTMS) in treatment-resistant major depression. The purpose of this study is to assess the efficacy of rTMS in unmedicated, treatment-resistant patients who meet criteria for major depression. METHODS: Depressed subjects, who had failed to respond to a median of four treatment trials, were assigned in a randomized double-blind manner to receive either active (n = 10; 20 2-sec trains of 20 Hz stimulation with 58-sec intervals; delivered at 80% motor threshold with the figure-of-eight coil positioned over the left dorsolateral prefrontal cortex) or sham (n = 10; similar conditions with the coil elevated and angled 45 degrees tangentially to the scalp) rTMS. These sequences were applied during 10 consecutive weekdays. Continuous electroencephalogram sampling and daily motor threshold determinations were also obtained. RESULTS: The group mean 25-item Hamilton Depression Rating Scale (HDRS) score was 37.2 (+/- 2.0 SEM) points. Adjusted mean decreases in HDRS scores were 14.0 (+/- 3.7) and 0.2 (+/- 4.1) points for the active and control groups, respectively (p <.05). One of 10 subjects receiving active treatment demonstrated a robust response (i.e., HDRS decreased from 47 to 7 points); three other patients demonstrated 40-45% decreases in HDRS scores. No patients receiving sham treatment demonstrated partial or full responses. CONCLUSIONS: A 2-week course of active rTMS resulted in statistically significant but clinically modest reductions of depressive symptoms, as compared to sham rTMS in a population characterized by treatment resistance.


Subject(s)
Depressive Disorder, Major/therapy , Prefrontal Cortex/physiology , Adolescent , Adult , Aged , Depressive Disorder, Major/diagnosis , Double-Blind Method , Electroencephalography , Electromagnetic Phenomena/methods , Female , Humans , Male , Middle Aged , Periodicity , Psychiatric Status Rating Scales , Severity of Illness Index , Skull/physiology , Treatment Outcome
5.
FEBS Lett ; 291(1): 67-70, 1991 Oct 07.
Article in English | MEDLINE | ID: mdl-1936253

ABSTRACT

The pentapeptide pyroGlu-Ala-Glu-Ser-Asn has been synthetized and phosphorylated in vitro at level of serine by protein kinase NII isolated from calf thymus chromatin. It is noteworthy that the calf thymus kinase NII shows a remarkable affinity for this peptide. The [32P]peptide is able to bind to several DNAs in the presence of Mg2+ (lambda phage, calf thymus, pBR540 plasmid). This binding appears not specific with regard to the type of DNA and its base sequence. These data support the hypothesis that phosphorylated acidic domains of nuclear nonhistone proteins could bind directly to DNA in the presence of Mg2+ cations.


Subject(s)
DNA/metabolism , Magnesium/metabolism , Peptides/metabolism , Protein Kinases/metabolism , Amino Acid Sequence , Animals , Cattle , Chromatography, Thin Layer , Electrophoresis, Polyacrylamide Gel , Hydrogen-Ion Concentration , Kinetics , Molecular Sequence Data , Oligopeptides/metabolism , Phosphorylation
6.
J Endocrinol ; 152(1): 141-6, 1997 Jan.
Article in English | MEDLINE | ID: mdl-9014849

ABSTRACT

The presence of pituitary adenylate cyclase-activating peptide (PACAP) 38-immuno-like material (PACAP 38-IL) in the brain and ovary of the crested newt, Triturus carnifex, and its action on ovarian steroidogenesis and prostaglandin synthesis were evaluated. The HPLC, brain and ovary extract peaks that eluted like PACAP 38 were considered PACAP 38-like material. The concentrations of PACAP 38-II in the HPLC extracts were measured by RIA. T. carnifex ovary was incubated with PACAP 38, brain and ovary PACAP 38-IL, and inhibitors of cyclooxygenase (COX), adenylate cyclase (AC) and phospholipase C (PLC) for 30 and 60 min. PACAI 38, and brain and ovary PACAP 38-IL increased prostaglandin E2 (PGE2) (30 and 60 min), and progesterone and corticosterone (60 min), but decreased oestradiol-17 beta (60 min). COX and PLC inhibitors counteracted the increases in PGE2, progesterone and corticosterone and the decrease in oestradiol-17 beta, and the AC, inhibitor also counteracted them except for PGE2. These results suggest that PACAP 38-IL, present in T. carnifex brain and ovary, acts on PLC, inducing the increase of PGE2 which, in turn, acting on AC, induces increases in progesterone and corticosterone and a decrease in oestradiol-17 beta.


Subject(s)
Brain/metabolism , Neuropeptides/metabolism , Neurotransmitter Agents/metabolism , Ovary/metabolism , Salamandridae/metabolism , Adenosine/analogs & derivatives , Adenosine/pharmacology , Adenylyl Cyclase Inhibitors , Animals , Aspirin/pharmacology , Brain Chemistry , Chromatography, High Pressure Liquid , Corticosterone/biosynthesis , Cyclooxygenase Inhibitors/pharmacology , Dinoprostone/biosynthesis , Female , Neuropeptides/analysis , Neurotransmitter Agents/analysis , Organ Culture Techniques , Ovary/chemistry , Pituitary Adenylate Cyclase-Activating Polypeptide , Progesterone/biosynthesis , Radioimmunoassay , Type C Phospholipases/antagonists & inhibitors , p-Methoxy-N-methylphenethylamine/pharmacology
7.
Peptides ; 15(1): 7-13, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8015983

ABSTRACT

We previously reported the isolation of low molecular weight phosphorylated peptides from the chromatin of several tissues. The chromatin peptides show a regulatory activity on DNA in vitro transcription and on cell growth and differentiation. In this paper, we report a molecular model of the native peptides designed according to the structural information obtained by means of biochemical and mass spectrometry analysis: pyroGlu-Ala-Gly-Glu-Asp-Ser(P)-Asp-Glu-Glu-Asn. This or very similar sequences are present in many transcription factors; on the basis of the structural model we presented and of related protein sequences, we have synthesized the peptide pyroGlu-Asp-Asp-Ser-Asp-Glu-Glu-Asn. This peptide affects transcription rate in reconstituted systems in vitro and in isolated nuclei; moreover, it inhibits the growth of HL60 cells with a parallel stimulus of differentiation.


Subject(s)
Cell Differentiation/physiology , Cell Division/physiology , Chromatin/chemistry , Models, Molecular , Peptides/chemistry , Transcription, Genetic , Amino Acid Sequence , Animals , Cell-Free System , Mass Spectrometry , Molecular Sequence Data , Molecular Weight , PC12 Cells , Phosphorylation , Structure-Activity Relationship , Trout
8.
Regul Pept ; 102(2-3): 111-7, 2001 Dec 15.
Article in English | MEDLINE | ID: mdl-11730983

ABSTRACT

A fluorescent analog of epidermal mitosis-inhibiting pentapeptide (pGlu-Glu-Asp-Ser-Gly) was synthesized by reacting tetramethylrhodamine isothiocyanate with ring-opened epidermal mitosis-inhibiting pentapeptide. The ring-opening reaction of the pyrrolidone moiety was performed with mild acidic hydrolysis and the product purified by reversed-phase high-performance liquid chromatography. Tetramethylrhodaminethiocarbamoyl-(Glu(1))-epidermal mitosis-inhibiting pentapeptide was purified by chromatography on Sephadex G-25 and reversed-phase high-performance liquid chromatography. After characterization by amino acid analysis, the analog was incubated in presence of A431 cell line to visualize the cellular localization of the epidermal mitosis-inhibiting pentapeptide. The data gave negative results.


Subject(s)
Glutamic Acid/chemical synthesis , Glutamic Acid/pharmacology , Mitosis/drug effects , Peptides/chemical synthesis , Peptides/pharmacology , Rhodamines/chemical synthesis , Rhodamines/pharmacology , Cell Adhesion/drug effects , Chromatography, Gel , Chromatography, High Pressure Liquid , Chromatography, Thin Layer , Fluorescent Dyes/metabolism , Glutamic Acid/analogs & derivatives , Glutamic Acid/isolation & purification , Humans , Microscopy, Confocal , Peptides/chemistry , Peptides/isolation & purification , Rhodamines/isolation & purification , Rhodamines/metabolism , Spectrophotometry, Ultraviolet , Tumor Cells, Cultured
9.
Regul Pept ; 111(1-3): 199-205, 2003 Mar 28.
Article in English | MEDLINE | ID: mdl-12609769

ABSTRACT

The degradation of thymic humoral factor-gamma2 (THF-gamma2), an immunoregulatory octapeptide important for T-lymphocyte regulation, by enzymes present in human plasma, was investigated. THF-gamma2 was metabolized through two steps that involved the detaching of N-terminal amino acid leucine followed by hydrolysis of the Lys(6)-Phe(7) bond. The THF-gamma2 cleavages were sensitive to aminopeptidase and metalloproteinase inhibitors. The degradation was completely blocked by amastatin and specific inhibitors of angiotensin converting enzyme (ACE). The cleavages occurred independently, with two different kinetics, faster for the N-terminal hydrolysis than for that of the Lys(6)-Phe(7) bond. Purified human plasma ACE was used to characterize the hydrolysis of Lys(6)-Phe(7) bond. The K(m) and K(cat) values for THF-gamma2 hydrolysis were 0.273 mM and 107 s(-1), respectively. The optimum of chloride concentration was 300 mM, while that of pH was 7.6. The presence of ACE in circulating mononuclear cells raises the possibility that it may play a role in modulating the THF-gamma2 activity.


Subject(s)
Oligopeptides/blood , Peptidyl-Dipeptidase A/blood , Amino Acid Sequence , Amino Acids/analysis , Animals , Cattle , Humans , Hydrogen-Ion Concentration , Hydrolysis , Kinetics , Leucyl Aminopeptidase/metabolism , Peptide Fragments/analysis , Peptide Fragments/chemistry , Protease Inhibitors/pharmacology , Sodium Chloride/pharmacology
10.
Pediatr Pulmonol ; 7(3): 145-52, 1989.
Article in English | MEDLINE | ID: mdl-2797928

ABSTRACT

We evaluated the effects of an 8-week aerobic training (1 hr, three times a week) on physical performance of ten patients with cystic fibrosis (CF) (median age, 12.5 yr; range 11.1-15.3 yr), with mild airway obstruction (FEV1 = 77 +/- 22% pred.), and ten healthy age-matched children (CONTR) (median age, 12.7 yr; range 12.2-15.2 yr). Physical performance was tested with maximal incremental (MAX) and submaximal (SMAX) (fixed workload of 1.7 W/kg during 6 min) exercise tests on a cycle ergometer. These and standard spirometric and anthropometric measurements were performed at the beginning and end of a period with usual daily activity and one with the training program. The kinetics of ventilatory parameters at the onset and end of SMAX were displayed by fitting data on oxygen uptake and minute ventilation by monoexponential curves (least-squares method). At the start and the end of the training period, all children were timed for endurance run to voluntary exhaustion and for sprinting through an obstacle course. A pattern of relative hyperventilation during SMAX and of poor performance in endurance and obstacle runs were evident at the start of the training period in patients with CF. The effects of training on MAX and SMAX were small and partial; the improvement in field test performances was significant only for CF and could be attributed to improvement of skill and motivation.


Subject(s)
Airway Obstruction/physiopathology , Cystic Fibrosis/physiopathology , Exercise , Physical Education and Training , Physical Endurance , Adolescent , Child , Cystic Fibrosis/therapy , Female , Forced Expiratory Flow Rates , Forced Expiratory Volume , Heart Rate , Humans , Male , Oxygen Consumption , Vital Capacity
11.
J Physiol Biochem ; 59(4): 269-76, 2003 Dec.
Article in English | MEDLINE | ID: mdl-15164946

ABSTRACT

The aim of the present study was to purify and characterize angiotensin-converting enzyme (ACE) present in frog ovary (Rana esculenta). Detergent and trypsin-extracted enzymes were purified using a one-step process, consisting of affinity chromatography on lisinopril coupled to Sepharose 6B. The molecular mass was 150 kDa for both detergent-extracted and trypsin-extracted enzyme. The specific activity of detergent-extracted and trypsin-extracted ACE was 294 U mg(-1) and 326 U mg(-1) respectively. The optimum pH range was from 7-8.5 at 37 degrees C and the optimum temperature was 50 degrees C. Optimum chloride concentration was about 200 mM for synthetic substrate FAPGG (N-[3-(2-furyl)acryloyl] L-phenylalanyl glycyl glycine) and angiotensin I, and 10 mM for bradykinin. The Km and Kcat values for FAPGG were 0.608 +/- 0.07 mM and 249 sec(-1) respectively and I50 values for captopril and lisinopril, two specific ACE inhibitors, were 68 +/- 12.55 nM and 6.763 +/- 0.66 nM respectively. Frog ovary tissue from prereproductive period was incubated in vitro in the presence of frog ovary ACE (2.5 mU/ml), captopril (0.1 mM), and lisinopril (0.1 mM). Production of 17beta-estradiol, progesterone, and prostaglandins E2 and F2alpha was determined. The data showed a modulation of 17beta-estradiol, progesterone and prostaglandin E2 production by ovary ACE.


Subject(s)
Ovary/enzymology , Rana esculenta/metabolism , Renin/isolation & purification , Steroids/biosynthesis , Angiotensin I/metabolism , Angiotensin-Converting Enzyme Inhibitors/metabolism , Animals , Bradykinin/metabolism , Captopril/metabolism , Female , Hydrogen-Ion Concentration , Lisinopril/metabolism , Oligopeptides/metabolism , Rana esculenta/anatomy & histology , Renin/metabolism , Sodium Chloride/metabolism , Temperature
12.
Acta Paediatr Suppl ; 412: 29-35, 1996 May.
Article in English | MEDLINE | ID: mdl-8783752

ABSTRACT

BACKGROUND: Recent studies suggest that coeliac disease (CD) is one of the commonest, life-long disorders in Italy. The aims of this multicentre work were: (a) to establish the prevalence of CD on a nationwide basis; and (b) to characterize the CD clinical spectrum in Italy. PATIENTS AND METHODS: Fifteen centres screened 17,201 students aged 6-15 years (68.6% of the eligible population) by the combined determination of serum IgG- and IgA-antigliadin antibody (AGA) test; 1289 (7.5%) were IgG and/or IgA-AGA positive and were recalled for the second-level investigation; 111 of them met the criteria for the intestinal biopsy: IgA-AGA positivity and/or AEA positivity or IgG-AGA positivity plus serum IgA deficiency. RESULTS: Intestinal biopsy was performed on 98 of the 111 subjects. CD was diagnosed in 82 subjects (75 biopsy proven, 7 not biopsied but with associated AGA and AEA positivity). Most of the screening-detected coeliac patients showed low-grade intensity illness often associated with decreased psychophysical well-being. There were two AEA negative cases with associated CD and IgA deficiency. The prevalence of undiagnosed CD was 4.77 x 1000 (95% CI 3.79-5.91), 1 in 210 subjects. The overall prevalence of CD, including known CD cases, was 5.44 x 1000 (95% CI 4.57-6.44), 1 in 184 subjects. The ratio of known to undiagnosed CD cases was 1 in 7. CONCLUSIONS: These findings confirm that, in Italy, CD is one of the most common chronic disorders showing a wide and heterogeneous clinical spectrum. Most CD cases remain undiagnosed unless actively searched.


Subject(s)
Celiac Disease/diagnosis , Mass Screening/methods , Adolescent , Antibodies/blood , Antibodies/immunology , Autoimmunity , Biomarkers/blood , Celiac Disease/complications , Celiac Disease/epidemiology , Celiac Disease/immunology , Child , Female , Follow-Up Studies , Gliadin/immunology , HLA-D Antigens/genetics , Humans , Immunoglobulin A/blood , Immunoglobulin A/immunology , Immunoglobulin G/blood , Immunoglobulin G/immunology , Italy , Male , Prevalence , Sensitivity and Specificity , Serologic Tests/methods
13.
Physiol Chem Phys Med NMR ; 24(2): 109-17, 1992.
Article in English | MEDLINE | ID: mdl-1508987

ABSTRACT

A variety of evidence suggests that a family of chromatin peptides (CPs), characterized by 1000D molecular weight, a pH dependent association to DNA and a prevailing presence of acidic amino acids in their structure, is involved in the regulation of genes expression. Nevertheless their action mechanism is still unknown. In our in vitro specific RNA transcription systems the CPs affect the initiation and not the elongation. Furthermore they inhibit the RNA transcription by interaction with the DNA rather than with the enzyme. The phagic in vitro specific RNA transcription is less affected by CPs than the eubacteric system, suggesting a kind of selectivity for target DNA sequences involved in the initiation of transcription.


Subject(s)
Chromatin/physiology , DNA-Directed RNA Polymerases/metabolism , Peptides/pharmacology , Plasmids , Transcription, Genetic/drug effects , Triticum/physiology , Chromatin/chemistry , Escherichia coli/enzymology , Kinetics , Molecular Weight , Nucleic Acid Denaturation , Peptides/isolation & purification , Seeds , T-Phages/enzymology , Templates, Genetic
14.
Physiol Chem Phys Med NMR ; 24(2): 97-107, 1992.
Article in English | MEDLINE | ID: mdl-1508994

ABSTRACT

RNA synthesis in cell and cell-free systems is inhibited by a family of acidic, low molecular weight chromatin peptides (CPs). These peptides were extracted from deproteinized DNA of prokaryotic and eukaryotic cells, but the low yield of purified material by this procedure hinders efforts aimed at understanding their action mechanism in gene regulation. In this report we describe two purification methods of CPs from an easily available source, wheat germ. A comparison is made between the method starting from deproteinized DNA and the method from purified chromatin. The biological effects (inhibition of L1210 cell growth and DNA in vitro transcription) of CPs from wheat germ together with their chemical characteristics (molecular weight, amino acid composition and presence of phosphoserine) show strong homology with those of CPs from other sources. These results suggest a possible role of these chromatin peptides in controlling gene expression.


Subject(s)
Cell Division/drug effects , Chromatin/physiology , DNA, Neoplasm/metabolism , Peptides/isolation & purification , Transcription, Genetic/drug effects , Triticum/physiology , Amino Acids/analysis , Animals , Cattle , Chromatin/chemistry , Chromatography, Gel , Chromatography, High Pressure Liquid , DNA/metabolism , DNA, Neoplasm/drug effects , DNA-Directed RNA Polymerases/metabolism , Escherichia coli/enzymology , Kinetics , Leukemia L1210 , Mice , Peptides/pharmacology , Seeds , Thymus Gland , Tumor Cells, Cultured
15.
Physiol Chem Phys Med NMR ; 20(2): 91-108, 1988.
Article in English | MEDLINE | ID: mdl-3065801

ABSTRACT

Low molecular weight peptides are linked to the chromatin DNA of several tissues, from which they can be dissociated by alkaline extraction. They show very high specific activity in the control of transcription "in vitro". In this work the biochemical properties of controlling transcription peptide effectors isolated from trout testis DNA are reported. The purified peptides prevailingly contain glutamic acid, serine, aspartic acid, glycine and alanine. Studies of the peptide structure by N-terminal analysis using the dansyl chloride procedure was unsuccessful, suggesting the presence of a blocked NH2 group. At the same time the active peptides cannot be digested by carboxypeptidases. The gel filtration of the chromatin peptidic fractions on Sephadex G-25, Trisacryl GF05 or Sephadex G-15 shows that the active peptides elute as a single major peak with an elution volume corresponding to a molecular weight of about 1000. The paper electrophoresis performed at different pH and ionic strength shows that the chromatin peptides are separated in two fractions. One of them is strongly acidic and migrates towards the positive pole until pH 1.9, indicating the presence of phosphoric residues which probably exert an important role in the control of transcription "in vitro". The chromatin peptides are further purified by Sephadex G-10 and high performance liquid chromatography. The amino acid analysis of the purified peptides are reported.


Subject(s)
Chromatin/metabolism , DNA/genetics , Phosphopeptides/isolation & purification , Testis/metabolism , Transcription, Genetic , Amino Acids/analysis , Animals , Chromatography, Gel , Chromatography, High Pressure Liquid , Chromatography, Thin Layer , DNA-Directed RNA Polymerases/metabolism , Escherichia coli/enzymology , Male , Phosphopeptides/physiology , Trout
16.
Physiol Chem Phys Med NMR ; 21(4): 289-94, 1989.
Article in English | MEDLINE | ID: mdl-2535125

ABSTRACT

Minimum substrate requirements for nuclear NII kinase (casein II kinase) were analyzed with synthetic peptides modeled according to amino acid composition of phosphopeptides isolated from chromatin. Uncharged blocked peptide termini decreased the requirement for acidic clusters neighboring the phosphate acceptor amino acid (serine) such that only one group immediately N-terminal to serine was sufficient for kinase activity. Studies on peptide interaction with DNA showed that the model phosphopeptides bound to DNA only in the phosphorylated form suggesting involvement of phosphorylation in protein-DNA interactions yet to be identified.


Subject(s)
DNA/chemistry , Peptides/chemistry , Protein Kinases/metabolism , Amino Acid Sequence , Bacteriophage lambda/metabolism , Cations , DNA, Viral/metabolism , Models, Chemical , Molecular Sequence Data , Phosphorylation , Phosphoserine/chemistry , Transcription, Genetic
17.
Pediatr Med Chir ; 5(4): 157-60, 1983.
Article in Italian | MEDLINE | ID: mdl-6647075

ABSTRACT

Patients suffering from chronic lung infections are a major problems in therapy of cystic fibrosis (CF). Resistance frequently occurs with great rapidity among isolates of Staphylococcus aureus and Pseudomonal aeruginosa. The rational for the use of frequent antibiotics (reduction of bacterial count), and the principle to follow while using antibiotics in CF patients are discussed. Research on amikacin peak levels and its average levels in serum, saliva and sputum is presented.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Cystic Fibrosis/complications , Respiratory Tract Infections/drug therapy , Amikacin/metabolism , Anti-Bacterial Agents/metabolism , Drug Resistance, Microbial , Drug Therapy, Combination , Humans , Tissue Distribution
18.
Pediatr Med Chir ; 4(5): 563-4, 1982.
Article in Italian | MEDLINE | ID: mdl-6927359

ABSTRACT

A case of subcutaneous fat necrosis (S.F.N.) with hypercalcemia and hyperlipemia in a newborn infant is reported. On the basis of previous reports it is impossible to definite the pathogenesis of hypercalcemia and hyperlipemia in subcutaneous fat necrosis. Moreover the Authors point out that in a newborn with S.F.N. plasma levels of calcium and lipids and, if it is possible, urinary prostaglandin E and serum PTH and 250HD3 should be determined.


Subject(s)
Fat Necrosis/complications , Hypercalcemia/complications , Hyperlipidemias/complications , Necrosis/complications , Female , Humans , Infant, Newborn , Pregnancy , Pregnancy in Diabetics/complications
19.
Pediatr Med Chir ; 12(6): 669-74, 1990.
Article in Italian | MEDLINE | ID: mdl-2093890

ABSTRACT

The study intends to value results of follow-up of risk neonates hospitalized for the period 1980-88 at Neonatal Intensive Care Unit of Bufalini Hospital Cesena and the course with time of neurologic and neuropsychological alterations, reported to the birth-rate of territory in which operates the Neonatal Intensive Care Unit. The survivor infants attended in follow up have been 419: 63 of neonatal weight less than or equal to 1500 g (group A), 117 of weight 1501-2000 g (group B), 239 of weight greater than 2000 g (group C). The follow-up provided at first 12 months of life a pediatric examination together with motoscopic examination to Milani-Comparetti every two months, at 3 years--4 years and 6 months, 7 years a pediatric examination with evaluation of Intelligence Quotient (N.E.M.I.), at last two months of 1st Primary School evaluation of acquired scholastic learning capacities by reading test of Inizan and calculation test of Meljac. Diagnosis of cerebral palsy (C.P.) has been always placed at first 12 months of life. All the survivors have been executed pediatric checks as foreseen at first 12 months of life. The subjects with CP are 26 (%); of these 13 have an I.Q. less than or equal to 70. The risk to develop CP seems to depend strictly by hypoxic perinatal stress (21/26 infants). The type of CP seems to be conditioned by neonatal weight, in particular as regards spastic paraplegia (10/12 infants of weight less than or equal to 2000 g), but hemiplegia and tetraplegia are with equality distributed (7/14 infants of weight less than or equal to 2000 g).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Cerebral Palsy/etiology , Infant, Newborn, Diseases , Child , Child, Preschool , Follow-Up Studies , Humans , Infant , Infant, Newborn , Intelligence Tests , Risk Factors , Time Factors
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