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Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children

Neuropediatrics, 2006-02, Vol.37 (1), p.13

2006

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Quality of life after paediatric ischaemic stroke

Developmental medicine and child neurology, 2017-01, Vol.59 (1), p.45-51

2017

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Apparent life-threatening event in infants: think about star anise intoxication!

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2011-07, Vol.18 (7), p.750

2011

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Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome

Neuropediatrics, 1993-04, Vol.24 (2), p.83

1993

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Malaise du nourrisson pensez à une intoxication à l’anis étoilé

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2011-07, Vol.18 (7), p.750-753

2011

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IAP08 Acute frontal lobe encephalopathy: a new entity?

European journal of paediatric neurology, 2007, Vol.11, p.57-57

2007

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Sleep spindle activity in double cortex syndrome: a case report

Epileptic disorders, 2010-09, Vol.12 (3), p.228-231

2010

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Increased focal interictal discharges during specific cognitive tasks

Neurocase, 1999-01, Vol.5 (1), p.13-19

1999

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The spectrum of acquired cognitive disturbances in children with partial epilepsy and continuous spike-waves during sleep. A 4-year follow-up case study with prolonged reversible learning arrest and dysfluency

European journal of paediatric neurology, 1997, Vol.1 (1), p.19-29

1997

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Ocular phenotype in a child with chondrodysplasia punctata, rhizomelic form

Klinische Monatsblätter für Augenheilkunde, 1997-05, Vol.210 (5), p.329

1997

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Myotonic dystrophy with a variable symptomatology and favorable clinical prognosis in a large family

Revue medicale de la Suisse romande, 1978-08, Vol.98 (8), p.431

1978

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Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)

Journal de genetique humaine, 1978-09, Vol.26 (3), p.237

Marcoz, J P

1978

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Current genetic problems of hemophilia and detection of carriers (author's transl)

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 1977-07, Vol.66 (27), p.830

Marcoz, J P

1977

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Neonatal case finding in hip abnormalities

Revue medicale de la Suisse romande, 1980-05, Vol.100 (5), p.409

1980

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Factitious epilepsy: Münchausen syndrome by proxy. Another aspect of child abuse: recurrent coma in a 4-year-old child caused by nonaccidental poisoning

Revue medicale de la Suisse romande, 1985-11, Vol.105 (11), p.995

1985

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Study of two brothers with XYY karyotype including one with mosaicism

Archiv fur Genetik, 1978, Vol.51 (2), p.63

1978

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Final results of a clinical, genetic and cytogenetic study of 182 oligophrenic patients in a medico-educational institution. 1

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 1982-07, Vol.71 (28), p.1150

1982

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Do all cases of trisomy 18 with long survival (beyond 10 years) show mosaicism in fibroblasts? (author's transl)

Journal de genetique humaine, 1978-06, Vol.26 (2), p.145

1978

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Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children

Quality of life after paediatric ischaemic stroke

Apparent life-threatening event in infants: think about star anise intoxication!

Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome

Malaise du nourrisson pensez à une intoxication à l’anis étoilé

IAP08 Acute frontal lobe encephalopathy: a new entity?

Sleep spindle activity in double cortex syndrome: a case report

Increased focal interictal discharges during specific cognitive tasks

The spectrum of acquired cognitive disturbances in children with partial epilepsy and continuous spike-waves during sleep. A 4-year follow-up case study with prolonged reversible learning arrest and dysfluency

Ocular phenotype in a child with chondrodysplasia punctata, rhizomelic form

Myotonic dystrophy with a variable symptomatology and favorable clinical prognosis in a large family

Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)

Current genetic problems of hemophilia and detection of carriers (author's transl)

Neonatal case finding in hip abnormalities

Factitious epilepsy: Münchausen syndrome by proxy. Another aspect of child abuse: recurrent coma in a 4-year-old child caused by nonaccidental poisoning

Study of two brothers with XYY karyotype including one with mosaicism

Final results of a clinical, genetic and cytogenetic study of 182 oligophrenic patients in a medico-educational institution. 1

Do all cases of trisomy 18 with long survival (beyond 10 years) show mosaicism in fibroblasts? (author's transl)

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