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The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factors

Neuropediatrics, 2005-04, Vol.36 (2), p.90-97

2005

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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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Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants–a Population Based Analysis

Pediatric research, 2018-11, Vol.84 (5), p.632-638

2018

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BECTS evolving to Landau–Kleffner Syndrome and back by subsequent recovery: A longitudinal language reorganization case study using fMRI, source EEG, and neuropsychological testing

Epilepsy & behavior, 2013-04, Vol.27 (1), p.107-114

2013

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Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series

Swiss medical weekly, 2006-03, Vol.136 (11-12), p.189

2006

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Swelling of the third nerve in a child with transient oculomotor paresis: a possible cause of ophthalmoplegic migraine

Neuropediatrics, 2000-06, Vol.31 (3), p.145-147

2000

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Dystrobrevin isoform expression in patients with neuromuscular disease

Clinical neuropathology, 2010-07, Vol.29 (4), p.254-261

Ramelli, G P

2010

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Non-infectious causes of uveitis in 70 Swiss children

Acta Paediatrica, 2000-08, Vol.89 (8), p.955-958

2000

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Precipitants in 42 cases of erythema multiforme

European journal of pediatrics, 1999-11, Vol.158 (11), p.929-932

1999

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Ganglion cyst of the peroneal nerve : A differential diagnosis of peroneal nerve entrapment neuropathy

European neurology, 1999, Vol.41 (1), p.56-58

1999

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Congenital pseudarthrosis of the ulna and radius in two cases of neurofibromatosis type 1

Pediatric surgery international, 2001-03, Vol.17 (2-3), p.239-241

2001

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Circulating antineutrophil autoantibodies in a child with isolated central nervous system vasculitis

Neuropediatrics, 1999-10, Vol.30 (5), p.268-269

1999

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A novel insert mutation in gamma-sarcoglycan gene leads to severe childhood autosomal recessive muscular dystrophy

Journal of neurology, 2002-11, Vol.249 (11), p.1608-1611

2002

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Concomitance of Childhood Absence and Rolandic Epilepsy

Clinical EEG electroencephalography, 1998-10, Vol.29 (4), p.177-180

1998

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Urinary chloride excretion distinguishes between renal and extrarenal metabolic alkalosis

European journal of pediatrics, 1995-12, Vol.154 (12), p.979-982

1995

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Nervous system dysfunction in Henoch–Schönlein syndrome: systematic review of the literature

Rheumatology (Oxford, England), 2009-12, Vol.48 (12), p.1524-1529

2009

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Dapsone in cutaneous Henoch-Schönlein syndrome-worth a trial

Acta Paediatrica, 1997-03, Vol.86 (3), p.337-337

1997

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Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006–2015: a population-based analysis

Archives of disease in childhood. Fetal and neonatal edition, 2018-07, Vol.103 (4), p.F337-F342

2018

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Plasma ionized magnesium in tubular disorders with and without total hypomagnesemia

Pediatric nephrology (Berlin, West), 1999-01, Vol.13 (1), p.50-53

1999

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Outcome at two years of age in a Swiss national cohort of extremely preterm infants born between 2000 and 2008

BMC pediatrics, 2012-12, Vol.12 (1), p.198-198, Article 198

2012

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Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation

Genetic counseling, 2002, Vol.13 (2), p.151

2002

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Rhabdomyolysis and anesthesia: A report of two cases and review of the literature

Pediatric neurology, 1996-10, Vol.15 (3), p.254-257

1996

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Short-term neurological improvement in neonates with hypoxic-ischemic encephalopathy predicts neurodevelopmental outcome at 18-24 months

Journal of perinatal medicine, 2020-03, Vol.48 (3), p.296-303

2020

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Neurodevelopmental outcome at early school age in a Swiss national cohort of very preterm children

Swiss medical weekly, 2019-06, Vol.149, p.w20084

2019

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The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factors

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

Quality of life after paediatric ischaemic stroke

Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants–a Population Based Analysis

BECTS evolving to Landau–Kleffner Syndrome and back by subsequent recovery: A longitudinal language reorganization case study using fMRI, source EEG, and neuropsychological testing

Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series

Swelling of the third nerve in a child with transient oculomotor paresis: a possible cause of ophthalmoplegic migraine

Dystrobrevin isoform expression in patients with neuromuscular disease

Non-infectious causes of uveitis in 70 Swiss children

Precipitants in 42 cases of erythema multiforme

Ganglion cyst of the peroneal nerve : A differential diagnosis of peroneal nerve entrapment neuropathy

Congenital pseudarthrosis of the ulna and radius in two cases of neurofibromatosis type 1

Circulating antineutrophil autoantibodies in a child with isolated central nervous system vasculitis

A novel insert mutation in gamma-sarcoglycan gene leads to severe childhood autosomal recessive muscular dystrophy

Concomitance of Childhood Absence and Rolandic Epilepsy

Urinary chloride excretion distinguishes between renal and extrarenal metabolic alkalosis

Nervous system dysfunction in Henoch–Schönlein syndrome: systematic review of the literature

Dapsone in cutaneous Henoch-Schönlein syndrome-worth a trial

Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006–2015: a population-based analysis

Plasma ionized magnesium in tubular disorders with and without total hypomagnesemia

Outcome at two years of age in a Swiss national cohort of extremely preterm infants born between 2000 and 2008

Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation

Rhabdomyolysis and anesthesia: A report of two cases and review of the literature

Short-term neurological improvement in neonates with hypoxic-ischemic encephalopathy predicts neurodevelopmental outcome at 18-24 months

Neurodevelopmental outcome at early school age in a Swiss national cohort of very preterm children

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