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67 results on '"PAOLOZZI C"'

5. [Remote sequelae of hemolytic disease of the newborn (clinico-statistical study)]

Author

APPONI BATTINI G, DI TULLIO MT, RICCIARDI C, PAOLOZZI C, SALVATI G, SAPIO M., PERRONE, Laura, APPONI BATTINI, G, DI TULLIO, Mt, Ricciardi, C, Paolozzi, C, Salvati, G, Perrone, Laura, and Sapio, M.

Subjects
Erythroblastosis, Fetal, Male, Brain Diseases, Muscular Diseases, Pregnancy, Child, Preschool, Humans, Muscle Hypotonia, Female, Child Behavior Disorders, Anxiety, Child, Speech Disorders
Published
1980

10. Progressive rubella panencephalitis. Follow-up EEG study of a case

Author

Guizzaro, A., Volpe, E., Giacomo Lus, Bravaccio, F., Cotrufo, R., Paolozzi, C., Guizzaro, A, Volpe, E, Lus, Giacomo, Bravaccio, F, Cotrufo, R, and Paolozzi, C.

Subjects
Adult, Diagnosis, Differential, Male, Epilepsy, Time Factors, Mental Disorders, Encephalitis, Humans, Electroencephalography, Subacute Sclerosing Panencephalitis, Rubella, Follow-Up Studies
Abstract

Progressive rubella panencephalitis is a very rare slow virus disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.

11. [Nonpharmacological, ubiquitous, rapid, fused graphic elements in the electroencephalographic pattern of 2 sisters with type A sulfatidosis and ponto-cerebellar systemic atrophy]

Author

Paolozzi C, antonio federico, and Guazzi G

Subjects
Adult, Cerebral Cortex, Adolescent, Cerebellum, Pons, Humans, Electroencephalography, Female, Leukodystrophy, Metachromatic, Atrophy
Abstract

Two sisters, affected by late infantile type Sulfatidosis A, died at 22 and 15 years old respectively, presented, after autoptic examination, also a ponto-cerebellar athrophy. The EEG finding was characterized by few bioelectric abnormalities in the earlier studies of the disease and, afterwards, a progressive slower electric activities, with isolated asymmetric spikes. The typical aspects in the EEG recordings of our two patients were the presence of many rapid and diffuse elements, shay wawes without any pharmacological treatment. The significance of these peculiar recordings is there discussed.

Published
1976

13. [Aicardi's syndrome. Report of 2 cases]

Author

C, Paolozzi, G, di Iorio, V, Petretta, M R, Tata, E, Volpe, G C, Guazzi, Paolozzi, C, DI IORIO, Giuseppe, Petretta, V, Tata, Mr, Volpe, E, and Guazzi, Gc

Subjects
Child, Preschool, Humans, Infant, Electroencephalography, Female, Syndrome, Agenesis of Corpus Callosum, Child, Pedigree
Published
1978

14. Progressive rubella panencephalitis. Follow-up EEG study of a case.

Author

Guizzaro A, Volpe E, Lus G, Bravaccio F, Cotrufo R, and Paolozzi C

Subjects
Adult, Diagnosis, Differential, Electroencephalography, Encephalitis diagnosis, Encephalitis physiopathology, Encephalitis psychology, Epilepsy microbiology, Follow-Up Studies, Humans, Male, Mental Disorders microbiology, Subacute Sclerosing Panencephalitis diagnosis, Time Factors, Encephalitis microbiology, Rubella complications
Abstract

Progressive rubella panencephalitis is a very rare slow virus disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.

Published
1992

15. [Possibilities of error in EEG in sleep and consciousness (electroencephalographic observations in 153 children)].

Author

Paolozzi C, Bravaccio F, and Rossana Tata M

Subjects
Child Behavior Disorders etiology, Child, Preschool, Diagnostic Errors, Epilepsy diagnosis, Female, Humans, Infant, Intellectual Disability diagnosis, Male, Psychomotor Disorders etiology, Risk, Seizures, Febrile diagnosis, Brain Diseases diagnosis, Electroencephalography, Mental Disorders diagnosis
Abstract

The study concerns the EEG records of 153 children, aged within 1 and 4 and suffering from different neuropsychiatric disorders. Particularly during the first stages of sleep, graphoelements of epileptogenic morphology have been recorded in considerable amount. Obviously they were present in the records of clinically epileptic patients but they appeared also in the records of several patients having never suffered from epileptic seizures. The Authors suggest extreme caution in considering "epileptogenic" EEG patterns evoked by sleep in those children who are not clinically epileptic.

Published
1977

16. [Serial electroencephalographic study of 3 siblings with agenesis of the interhemispheric great commissurae, cortical neuronal immaturity and hypoplasia of the optico-pyramidal tracts].

Author

Paolozzi C and Guazzi G

Subjects
Abnormalities, Multiple genetics, Agenesis of Corpus Callosum, Blindness etiology, Cerebral Cortex abnormalities, Child, Female, Humans, Infant, Intellectual Disability, Male, Pedigree, Psychomotor Disorders etiology, Pyramidal Tracts abnormalities, Seizures etiology, Brain abnormalities, Optic Nerve abnormalities
Abstract

Three children, two females and one male, born from unrelated parents show brachycephaly, ogival palate, blindness from 5-6 months and progressive piramidal symptoms. Two subjects had since sixth monthy epileptic seizures, the other one died at 5 th month. In one subject died at 28 month age, central nervous system autoptic examination shows neuronal cortical immaturity, lack of corpus callosum, visual and piramidal patways hypoplasia. The serial EEG recording shows three caracteristic aspects: a) altough a marked changes, the organization of the electric cerebral activity was partially preserved; b) a epileptogenic potentiality was present, that is caracteristic of electro-clinic immage of this subject; c) a suggestive and peculiar tendency to asincrony and asimmetry of epileptic tendency in two hemispheres.

Published
1975

25. [Aicardi's syndrome. Report of 2 cases].

Author

Paolozzi C, di Iorio G, Petretta V, Tata MR, Volpe E, and Guazzi GC

Subjects
Child, Child, Preschool, Electroencephalography, Female, Humans, Infant, Pedigree, Syndrome, Agenesis of Corpus Callosum
Published
1978

26. [Pathogenetic, clinical and therapeutic considerations on a case of the stiff man syndrome].

Author

Bravaccio F, Sanna G, Volpe E, and Paolozzi C

Subjects
Adult, Anti-Bacterial Agents therapeutic use, Carbamazepine therapeutic use, Female, Humans, Immunization, Passive, Syndrome, gamma-Aminobutyric Acid therapeutic use, Muscular Diseases diagnosis, Muscular Diseases drug therapy
Abstract

The AA. describe the clinical features of a woman (fourty-one years old) suffering from Stiff-man syndrome. The treatment with diazepam and baclophene improuved the symptoms in a very satisfactory manner. The Author's opinion is that syndrome could be due to abnormal activity of neurotransmitters.

Published
1975

28. [Roussy-Levi disease (Study of a familial nucleus)].

Author

Paolozzi C, Ammendola A, Bravaccio F, Tata MR, Volpe E, and De Angelis G

Subjects
Adult, Aged, Female, Humans, Male, Middle Aged, Pedigree, Syndrome, Clubfoot genetics, Movement Disorders genetics, Reflex, Stretch
Published
1977

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