| Prevention of vitamin K deficiency bleeding with three oral mixed micellar phylloquinone doses: results of a 6-year (2005-2011) surveillance in Switzerland | European journal of pediatrics | | | 2013 | 686 | 1 |
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| Incidence of severe hyperbilirubinaemia in Switzerland: a nationwide population-based prospective study | Archives of disease in childhood. Fetal and neonatal edition | | | 2011 | 665 | 0 |
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| Delayed recognition of Guillain-Barre syndrome in a child: a misleading respiratory distress | The Journal of emergency medicine | | | 2010 | 563 | 0 |
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| Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti-N-methyl-D-aspartate receptor encephalitis | Developmental medicine and child neurology | | | 2010 | 596 | 0 |
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| Prospective population-based study of RSV-related intermediate care and intensive care unit admissions in Switzerland over a 4-year period (2001-2005) | Infection | | | 2009 | 618 | 0 |
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| Alexander disease: early presence of cerebral MRI criteria | European journal of paediatric neurology | | | 2009 | 648 | 0 |
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| Is benign myoclonic epilepsy of infancy truly idiopathic and generalized? | Epileptic disorders | | | 2009 | 725 | 0 |
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| Neural tube defects in Switzerland from 2001 to 2007: are periconceptual folic acid recommendations being followed? | Schweizerische medizinische Wochenschrift | | | 2008 | 606 | 0 |
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| Three-year surveillance of intussusception in children in Switzerland | Pediatrics | | | 2007 | 552 | 0 |
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| MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother | Brain & development | | | 2007 | 585 | 0 |
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| Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report | Journal of neurosurgery | | | 2007 | 618 | 0 |
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| Food colourings, preservatives, and hyperactivity | Lancet | | | 2007 | 534 | 0 |
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| Freeman Miller, Steven J. Bachrach (eds): Cerebral palsy. A complete guide for caregiving, Second edition | European journal of pediatrics | | | 2007 | 671 | 314 |
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| Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children | Neuropediatrics | | | 2006 | 510 | 0 |
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| Speech delay due to a prelinguistic regression of epileptic origin | Neuropediatrics | | | 2004 | 576 | 0 |
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| Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument | Neuropediatrics | | | 2004 | 684 | 0 |
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| Food colourings and preservatives--allergy and hyperactivity | Lancet | | | 2004 | 559 | 1 |
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| Malaises, syncopes et autres pertes de connaissance chez l'enfant | Revue médicale de la Suisse romande | | | 2003 | 546 | 9 |
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| Comment investiguer une maladie musculaire? | Revue médicale de la Suisse romande | | | 2003 | 603 | 0 |
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| Early onset and rapidly progressive subacute sclerosing panencephalitis after congenital measles infection | European journal of pediatrics | | | 2002 | 528 | 0 |
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| Epileptic falls and gait disturbance in two young children with a sharp wave focus at the vertex: a variant of benign partial epilepsy of childhood? | European journal of paediatric neurology | | | 2002 | 512 | 0 |
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| A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene | Annals of neurology | | | 2002 | 725 | 0 |
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| Myocarditis associated with parvovirus B19 infection in two siblings with merosin-deficient congenital muscular dystrophy | European journal of pediatrics | | | 2000 | 530 | 0 |
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| T-type alpha 1H Ca2+ channels are involved in Ca2+ signaling during terminal differentiation (fusion) of human myoblasts | Proceedings of the National Academy of Sciences of the United States of America | | | 2000 | 633 | 0 |
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| Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases | Annals of neurology | | | 2000 | 534 | 0 |
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| Early fatal pontocerebellar hypoplasia in premature twin sisters | European journal of paediatric neurology | | | 2000 | 536 | 0 |
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| MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity | European journal of human genetics | | | 1999 | 527 | 207 |
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| Hyperactivité avec déficit de l'attention : le point de vue du neuropédiatre | Médecine et hygiène | | | 1999 | 521 | 1 |
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| Plant-induced seizures: reappearance of an old problem | Journal of neurology | | | 1999 | 677 | 0 |
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| Non-invasive epileptic focus localization using EEG-triggered functional MRI and electromagnetic tomography | Electroencephalography and clinical neurophysiology | | | 1998 | 661 | 1 |
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| PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy | Journal of medical genetics | | | 1998 | 546 | 0 |
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| Migraine : particularités sémiologiques chez l'enfant | Les dimensions de la douleur en ophtalmologie | | | 1998 | 418 | 0 |
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| Contribution of a non-inactivating potassium current to the resting membrane potential of fusion-competent human myoblasts | Journal of physiology | | | 1996 | 711 | 0 |
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