Zobrazeno 1 - 10
of 155
pro vyhledávání: '"J Mises"'
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 8:45-53
Summary Since 1973 the authors have studied the EEG appearances in hyperphenylalaninaemia : 82 children were studied, comprising : 68 children with phenylketonuria, 33 of whom had been treated within the first 3 months of life, whilst 35 had only sta
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 8:102-106
Summary 12 cases of non-ketotic hyperglycinemia in neonates diagnosed at a time of neurological distress were studied. A characteristic tracing was observed permitting correct diagnosis in 6 cases. It consisted of a burst suppression characterized by
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 13:240-244
Summary This article is devoted to a consideration of the clinical prognostic significance of “trace discontinu”. The authors first distinguish “trace discontinu” from the “trace paroxystique” and “trace alternant” patterns in the new
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 8:456-463
Summary A study of the E.E.G. abnormalities observed in 15 children with herpes encephalitis demonstrated typical periodic complexes in 12 of the recordings, which is in conformity with the data in the published literature concerning findings in adul
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 7:410-415
Summary The purpose of this study was to evaluate the prognostic value of neonatal E.E.G. tracings in children born at term. The clinical course of 45 children was followed and related to E.E.G. abnormalities reported during the first 5 days of life.
Autor:
F. Moussali-Salefranques, Hélène Ogier, M. L. Laroque, J. Mises, F X Coude, Jean-Marie Saudubray, C. Charpentier
Publikováno v:
Journal of Inherited Metabolic Disease. 5:117-120
The periodic EEG pattern during the first week associated with lethargy and myoclonic jerks is the major clinical sign in non-ketotic hyperglycinaemia. The blood and urine glycine level may be at the upper limit of the normal range in some cases. Dia
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 17:301-308
Resume 27 cas d'abces cerebraux neo-nataux enregistres precocement ont ete etudies. Deux groupes ont ete distingues: nouveau-nes ayant convulse (20 cas), nouveau-nes n'ayant pas convulse (7 cas). Les auteurs etudient les differents aspects de l'EEG i
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 8:71-77
The EEG study was carried out on 8 cases of methylmalonic acidaemia, in the neonatal period (3 cases), developing later with a ketotic coma, hyperglycinemia, hyperammonaemia, leucopenia and thrombocytopenia (3 cases) and detected before birth (2 case
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 11:445-449
Summary Fifteen children between the age of 3 and 7 years who had had unilateral seizure followed by a transitory hemiplegia (without fever) were observed. This seizure was the only one in 13 of the children; a second fit appeared in 2 others. The av
Publikováno v:
Revue d&'apos;Electroencéphalographie et de Neurophysiologie Clinique. 11:379-384
Summary Of 61 newborns with disorders in amino acid metabolism, 20 had seizures; 15 of them have been recorded. Clinically, seizures are mostly partial clonic jerks. There seems to be some homogeneity of EEG features in relation to causal amino acido