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Détail de l'auteur
Auteur Jürg LUTSCHG |
Documents disponibles écrits par cet auteur (3)



Benign migraine-like syndrome with CSF pleocytosis in children / Livia N. ROSSI in Developmental Medicine & Child Neurology, 27-2 (April 1985)
[article]
Titre : Benign migraine-like syndrome with CSF pleocytosis in children Type de document : Texte imprimé et/ou numérique Auteurs : Livia N. ROSSI, Auteur ; Jürg LUTSCHG, Auteur ; Franco VASSELLA, Auteur ; Oton BAJC, Auteur ; Otmar TONZ, Auteur ; Marco MUMENTHALER, Auteur Année de publication : 1985 Article en page(s) : p.192-198 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Four children with symptoms consistent with complicated migraine had CSF pleocytosis, in three cases lymphocytic and in the fourth polymorphonuclear. In one case the CSF abnormality was found during two separate attacks of complicated migraine. On the basis of the 23 cases reported in the literature and these four personal cases, the authors conclude that, as a rule, pleocytosis is a secondary phenomenon of an attack of complicated migraine. However, in exceptional cases an infectious disease might produce both a migraine attack and CSF pleocytosis. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=588
in Developmental Medicine & Child Neurology > 27-2 (April 1985) . - p.192-198[article] Benign migraine-like syndrome with CSF pleocytosis in children [Texte imprimé et/ou numérique] / Livia N. ROSSI, Auteur ; Jürg LUTSCHG, Auteur ; Franco VASSELLA, Auteur ; Oton BAJC, Auteur ; Otmar TONZ, Auteur ; Marco MUMENTHALER, Auteur . - 1985 . - p.192-198.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-2 (April 1985) . - p.192-198
Index. décimale : PER Périodiques Résumé : Four children with symptoms consistent with complicated migraine had CSF pleocytosis, in three cases lymphocytic and in the fourth polymorphonuclear. In one case the CSF abnormality was found during two separate attacks of complicated migraine. On the basis of the 23 cases reported in the literature and these four personal cases, the authors conclude that, as a rule, pleocytosis is a secondary phenomenon of an attack of complicated migraine. However, in exceptional cases an infectious disease might produce both a migraine attack and CSF pleocytosis. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=588 Hereditary motor sensory neuropathies in childhood / Livia N. ROSSI in Developmental Medicine & Child Neurology, 25-1 (February 1983)
[article]
Titre : Hereditary motor sensory neuropathies in childhood Type de document : Texte imprimé et/ou numérique Auteurs : Livia N. ROSSI, Auteur ; C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; Franco VASSELLA, Auteur Année de publication : 1983 Article en page(s) : p.19-31 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Clinical data on 24 patients with hereditary motor sensory neuropathies, with onset in the paediatric period, and of their relatives, is reported. Electrophysiological studies were done in all patients and in 15 relatives. The patients were divided into two groups (Types I and II) and their hereditary trait was determined. In 11 patients a sural nerve biopsy was performed and revealed different patterns of histological alterations. The nerve biopsy always confirmed the value of conduction velocity in distinguishing between Types I and II. A genetic discordance was observed, both in regard to the phenotype and the conduction velocity, and there was increased slowing of the conduction velocity as individuals grew older. Thus the classification of these disorders in childhood can be particularly difficult. The rôle of sural nerve biopsy is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559
in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.19-31[article] Hereditary motor sensory neuropathies in childhood [Texte imprimé et/ou numérique] / Livia N. ROSSI, Auteur ; C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; Franco VASSELLA, Auteur . - 1983 . - p.19-31.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.19-31
Index. décimale : PER Périodiques Résumé : Clinical data on 24 patients with hereditary motor sensory neuropathies, with onset in the paediatric period, and of their relatives, is reported. Electrophysiological studies were done in all patients and in 15 relatives. The patients were divided into two groups (Types I and II) and their hereditary trait was determined. In 11 patients a sural nerve biopsy was performed and revealed different patterns of histological alterations. The nerve biopsy always confirmed the value of conduction velocity in distinguishing between Types I and II. A genetic discordance was observed, both in regard to the phenotype and the conduction velocity, and there was increased slowing of the conduction velocity as individuals grew older. Thus the classification of these disorders in childhood can be particularly difficult. The rôle of sural nerve biopsy is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 Progressive neural muscular atrophy in a case of phenylketonuria / C. MEIER in Developmental Medicine & Child Neurology, 17-5 (October 1975)
[article]
Titre : Progressive neural muscular atrophy in a case of phenylketonuria Type de document : Texte imprimé et/ou numérique Auteurs : C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; F. VASELLA, Auteur ; A. BISCHOFF, Auteur Année de publication : 1975 Article en page(s) : p.625-630 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442
in Developmental Medicine & Child Neurology > 17-5 (October 1975) . - p.625-630[article] Progressive neural muscular atrophy in a case of phenylketonuria [Texte imprimé et/ou numérique] / C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; F. VASELLA, Auteur ; A. BISCHOFF, Auteur . - 1975 . - p.625-630.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 17-5 (October 1975) . - p.625-630
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442