CH
Haenggeli, Charles-Antoine
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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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 | 597 | 1 | |||
Incidence of severe hyperbilirubinaemia in Switzerland: a nationwide population-based prospective study | Archives of disease in childhood. Fetal and neonatal edition | 2011 | 570 | 0 | |||
Delayed recognition of Guillain-Barre syndrome in a child: a misleading respiratory distress | The Journal of emergency medicine | 2010 | 486 | 0 | |||
Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti-N-methyl-D-aspartate receptor encephalitis | Developmental medicine and child neurology | 2010 | 511 | 0 | |||
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 | 564 | 0 | |||
Alexander disease: early presence of cerebral MRI criteria | European journal of paediatric neurology | 2009 | 576 | 0 | |||
Is benign myoclonic epilepsy of infancy truly idiopathic and generalized? | Epileptic disorders | 2009 | 599 | 0 | |||
Neural tube defects in Switzerland from 2001 to 2007: are periconceptual folic acid recommendations being followed? | Schweizerische medizinische Wochenschrift | 2008 | 542 | 0 | |||
Three-year surveillance of intussusception in children in Switzerland | Pediatrics | 2007 | 504 | 0 | |||
MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother | Brain & development | 2007 | 515 | 0 | |||
Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report | Journal of neurosurgery | 2007 | 543 | 0 | |||
Food colourings, preservatives, and hyperactivity | Lancet | 2007 | 497 | 0 | |||
Freeman Miller, Steven J. Bachrach (eds): Cerebral palsy. A complete guide for caregiving, Second edition | European journal of pediatrics | 2007 | 609 | 207 | |||
Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children | Neuropediatrics | 2006 | 453 | 0 | |||
Speech delay due to a prelinguistic regression of epileptic origin | Neuropediatrics | 2004 | 490 | 0 | |||
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 | 578 | 0 | |||
Food colourings and preservatives--allergy and hyperactivity | Lancet | 2004 | 500 | 1 | |||
Malaises, syncopes et autres pertes de connaissance chez l'enfant | Revue médicale de la Suisse romande | 2003 | 490 | 9 | |||
Comment investiguer une maladie musculaire? | Revue médicale de la Suisse romande | 2003 | 529 | 0 | |||
Early onset and rapidly progressive subacute sclerosing panencephalitis after congenital measles infection | European journal of pediatrics | 2002 | 470 | 0 | |||
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 | 457 | 0 | |||
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 | 605 | 0 | |||
Myocarditis associated with parvovirus B19 infection in two siblings with merosin-deficient congenital muscular dystrophy | European journal of pediatrics | 2000 | 489 | 0 | |||
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 | 564 | 0 | |||
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases | Annals of neurology | 2000 | 451 | 0 | |||
Early fatal pontocerebellar hypoplasia in premature twin sisters | European journal of paediatric neurology | 2000 | 476 | 0 | |||
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 | 471 | 173 | |||
Hyperactivité avec déficit de l'attention : le point de vue du neuropédiatre | Médecine et hygiène | 1999 | 440 | 1 | |||
Plant-induced seizures: reappearance of an old problem | Journal of neurology | 1999 | 581 | 0 | |||
Non-invasive epileptic focus localization using EEG-triggered functional MRI and electromagnetic tomography | Electroencephalography and clinical neurophysiology | 1998 | 532 | 1 | |||
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 | 478 | 0 | |||
Migraine : particularités sémiologiques chez l'enfant | Les dimensions de la douleur en ophtalmologie | 1998 | 361 | 0 | |||
Contribution of a non-inactivating potassium current to the resting membrane potential of fusion-competent human myoblasts | Journal of physiology | 1996 | 661 | 0 |