CH
Haenggeli, Charles-Antoine
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| 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 | 671 | 1 | ||
| Incidence of severe hyperbilirubinaemia in Switzerland: a nationwide population-based prospective study | Archives of disease in childhood. Fetal and neonatal edition | | 2011 | 655 | 0 | ||
| Delayed recognition of Guillain-Barre syndrome in a child: a misleading respiratory distress | The Journal of emergency medicine | | 2010 | 547 | 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 | 586 | 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 | 610 | 0 | ||
| Alexander disease: early presence of cerebral MRI criteria | European journal of paediatric neurology | | 2009 | 637 | 0 | ||
| Is benign myoclonic epilepsy of infancy truly idiopathic and generalized? | Epileptic disorders | | 2009 | 711 | 0 | ||
| Neural tube defects in Switzerland from 2001 to 2007: are periconceptual folic acid recommendations being followed? | Schweizerische medizinische Wochenschrift | | 2008 | 591 | 0 | ||
| Three-year surveillance of intussusception in children in Switzerland | Pediatrics | | 2007 | 540 | 0 | ||
| MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother | Brain & development | | 2007 | 575 | 0 | ||
| Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report | Journal of neurosurgery | | 2007 | 610 | 0 | ||
| Food colourings, preservatives, and hyperactivity | Lancet | | 2007 | 526 | 0 | ||
| Freeman Miller, Steven J. Bachrach (eds): Cerebral palsy. A complete guide for caregiving, Second edition | European journal of pediatrics |  | 2007 | 660 | 257 | ||
| Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children | Neuropediatrics | | 2006 | 502 | 0 | ||
| Speech delay due to a prelinguistic regression of epileptic origin | Neuropediatrics | | 2004 | 556 | 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 | 671 | 0 | ||
| Food colourings and preservatives--allergy and hyperactivity | Lancet | | 2004 | 544 | 1 | ||
| Malaises, syncopes et autres pertes de connaissance chez l'enfant | Revue médicale de la Suisse romande | | 2003 | 539 | 9 | ||
| Comment investiguer une maladie musculaire? | Revue médicale de la Suisse romande | | 2003 | 588 | 0 | ||
| Early onset and rapidly progressive subacute sclerosing panencephalitis after congenital measles infection | European journal of pediatrics | | 2002 | 518 | 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 | 495 | 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 | 711 | 0 | ||
| Myocarditis associated with parvovirus B19 infection in two siblings with merosin-deficient congenital muscular dystrophy | European journal of pediatrics | | 2000 | 522 | 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 | 623 | 0 | ||
| Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases | Annals of neurology | | 2000 | 525 | 0 | ||
| Early fatal pontocerebellar hypoplasia in premature twin sisters | European journal of paediatric neurology | | 2000 | 524 | 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 | 514 | 190 | ||
| Hyperactivité avec déficit de l'attention : le point de vue du neuropédiatre | Médecine et hygiène | | 1999 | 510 | 1 | ||
| Plant-induced seizures: reappearance of an old problem | Journal of neurology | | 1999 | 668 | 0 | ||
| Non-invasive epileptic focus localization using EEG-triggered functional MRI and electromagnetic tomography | Electroencephalography and clinical neurophysiology | | 1998 | 651 | 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 | 536 | 0 | ||
| Migraine : particularités sémiologiques chez l'enfant | Les dimensions de la douleur en ophtalmologie | | 1998 | 406 | 0 | ||
| Contribution of a non-inactivating potassium current to the resting membrane potential of fusion-competent human myoblasts | Journal of physiology | | 1996 | 700 | 0 |
