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Biomedical subjects

C Fiore

Publications and source records attributed to C Fiore.

At least 55 records · Page 3Linked to original sources

[Retrobulbar injection of chlorpromazine in the absolute glaucoma (author's transl)].

The retrobulbar injection of a mixture of 2,5% of chlorpromazine + 2 % of novocaïne in blind and severely painful eyes was followed by a marked improvement of the subjective simptomatology in 82,5 % of the 63 subjects tested. The averaged follow-up was 2,6 years (range within 4 months and 8 years). Safe, simple and lacking in systemic involvement, the treatment with chlorpromazine can be proposed like a valide alternative to enucleation.

Adult↗

The effect of the epidermal growth factor (EGF) on the corneal epithelium in humans.

Epidermal growth factor (EGF) is a polypeptide hormone present in mammalian organs. In vivo, it shortens the time course of the corneal reepithelialization by stimulating a marked cell proliferation of the corneal epithelium. A further direct effect in vivo has been confirmed on human corneal epithelium and epidermis in culture. Tests in several nondystrophic diseases of the corneal epithelium confirmed the observations previously made in the rabbit that EGF accelerates the process of epithelial healing. The integrity of the corneal stroma is prejudicial for the maximum effect of the EGF, in the sense that the deeper the stroma is damaged, the less EGF acts. In herpetic lesions EGF is effective within 48 h only when the virus-affected area of the corneal epithelium has been scraped off. EGF is proposed as a new and efficacious agent for increasing the restorative process of the corneal epithelium in many nondystrophic diseases.

Adolescent↗

[Degenerative ocular retinal albinism in a girl ten years old (author's transl)].

Ocular albinism with myopia and impaired vision (R.E. 0.2; L.E. 0.6), but without nystagmus, were observed in a 10-year-old girl. The electrophysiological tests indicate, in addition, the presence of a tapetoretinal degeneration. It is assumed that the patient is carrier of two genes, a sex-linked one responsible for albinismus solum fundi and a second one of autosomal-recessive type, responsible for the tapetoretinal degenerartion.

Albinism↗

[Goldmann-Favre hyaloido-tapetoretinal degeneration].

In a sister and brother we found a case of vitreo-tapeto-retinal degeneration (macular retinoschisis, night-blindness, vitreous micro-fibrillose degeneration, abolished E.R.G., very pathological E.O.G.) and a "fruste" form of tapeto-retinal degeneration (De Lange's curve and flicker-E.R.G. both modified, E.R.G. subnormal and slight pathological changes in adaptometry). The father of these two patients suffered from tapeto-retinal degeneration which had caused complete blindness. Basing their suppositions on their personal experience and medical literature, the authors believe that the type of vitreo-retinal degeneration is best determined after examination of the mode of hereditary transmission. In the family which is presented, they believe that it is a form of Goldmann-Favre's disease with pseudo-dominance.

Adaptation, Ocular↗

[Value of functional and electrophysiological studies in amblyopia].

In a group of patients suffering from amblyopia, the authors confront the results after orthoptic treatment with data provided by functional and electrophysiological examination. In 37 patients the clinical diagnosis of functional amblyopia had been made, but in 8 of these cases complimentary functional and electrophysiological examinations showed organic perturbations. This explains the failure, in these cases, of the orthoptic treatment. In the remaining 29 patients, clinical forms of functional amblyopia were found. In this group, the authors studied 20 cases showing no improvement with treatment: in 15 out of the 20 the VERs were pathological. In the 9 remaining cases which have showed improvement the VER'S were never abnormal. VER study can be undertaken, without general anaesthesia, as from 3 to 4 years of age. The authors conclude that all clinical forms of amblyopia should undergo VER investigation: patients showing pathological changes should be excluded from orthoptic treatment, from which they have no possibility of deriving benefit.

Amblyopia↗

[Evoked visual potentials in tapeto-retinal degeneration].

A study of the behaviour of V.E.P. latencies and amplitudes in 247 eyes suffering from different clinical forms of chorio-retinal degenerations is presented. In 147 eyes the E.R.G. and the V.E.R. were simultaneously recorded, and this group was used for studying the relation ship between E.R.G., V.E.P. and visual acuity. The authors are of the opinion that the V.E.P., in that it investigates particularly the macular region, provides a clinical test of real interest in the prognosis of visual acuity in a known clinical context.

Choroid↗

[Genetic counseling in retinoblastoma].

The author reviews the literature about the inheritance of retinoblastoma and notes an increase of both the frequency of the affection and the chance of survival. He then estimates the genetic risks for the descendency in all cases of sporadic and familial retinoblastoma.

Chromosome Deletion↗