C. Haenggeli

发表

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

A. Lemainque, C. Bönnemann, N. Romero, 2002, Annals of neurology.

Food colourings and preservatives—allergy and hyperactivity

P. Eigenmann, C. Haenggeli, 2004, The Lancet.

Computed tomography in white-matter disease.

B. Drayer, P. Crumrine, M. Painter, 1979, Radiology.

Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti‐N‐methyl‐d‐aspartate receptor encephalitis

V. Ricotti, C. Korff, M. King, 2009, Developmental medicine and child neurology.

Plant-induced seizures: reappearance of an old problem

T. Landis, P. Burkhard, K. Burkhardt, 1999, Journal of Neurology.

Early fatal pontocerebellar hypoplasia in premature twin sisters.

A. Bottani, A. Maret, S. Hanquinet, 2000, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Multi‐minicore disease–searching for boundaries: Phenotype analysis of 38 cases

A. Toutain, N. Romero, B. Estournet, 2000, Annals of neurology.

Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report.

D. Rüfenacht, J. Delavelle, A. Bottani, 2007, Journal of neurosurgery.

Non-invasive epileptic focus localization using EEG-triggered functional MRI and electromagnetic tomography.

T Landis, M Seeck, X Golay, 1998, Electroencephalography and clinical neurophysiology.

Pyridoxine-dependent seizures, clinical and therapeutic aspects

E. Girardin, L. Paunier, C. Haenggeli, 1991, European Journal of Pediatrics.

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

J. Tolmie, Y. Crow, D. Hadley, 2004, Neuropediatrics.

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.

V. Frey, J. Harpey, C. Cruaud, 1998, Journal of medical genetics.

Incidence of First Epileptic Seizures in the Canton of Geneva, Switzerland

P. Jallon, A. Morabia, C. Haenggeli, 1997, Epilepsia.

Early onset and rapidly progressive subacute sclerosing panencephalitis after congenital measles infection

F. Picard, J. Delavelle, Laurent Roux, 2002, European Journal of Pediatrics.

LOPERAMIDE OVERDOSE MANAGED BY NALOXONE

C. Haenggeli, Gillian Friedli, 1980, The Lancet.

Guillain-Barré syndrome following immunisation withHaemophilus influenzae type b conjugate vaccine

S. Suter, A. Gervaix, C. Haenggeli, 1993, European Journal of Pediatrics.

Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation

A. Schnitzler, J. Volkmann, L. Timmermann, 2010, Brain : a journal of neurology.

Locked-in syndrome in an adolescent patient with pneumococcal meningitis.

J. Delavelle, W. Habre, C. Haenggeli, 1996, Neuropediatrics.

Neuropsychological Problems after Paediatric Stroke: Two Year Follow-Up of Swiss Children

E. Boltshauser, E. Roulet Perez, G. Ramelli, 2006, Neuropediatrics.

MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother

S. Antonarakis, M. Morris, I. Bouchardy, 2007, Brain and Development.

Is benign myoclonic epilepsy of infancy truly idiopathic and generalized?

C. Michel, M. Seeck, C. Korff, 2009, Epileptic disorders : international epilepsy journal with videotape.

Food colourings, preservatives, and hyperactivity

P. Eigenmann, C. Haenggeli, 2007, The Lancet.

CT in Wilson disease

L. Paunier, C. Haenggeli, H. Hauser, 1981, Neurology.

Alexander disease: early presence of cerebral MRI criteria.

C. Korff, J. Delavelle, M. S. van der Knaap, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Operculum syndrome: unusual feature of herpes simplex encephalitis.

C. Haenggeli, J. C. van der Poel, W. Overweg-Plandsoen, 1995, Pediatric neurology.

Contribution of a non‐inactivating potassium current to the resting membrane potential of fusion‐competent human myoblasts.

C. Bader, M. Hamann, L. Bernheim, 1996, The Journal of physiology.

MEHMO, a novel syndrome: assignment of disease locus to Xp21.1–p22.13

A. Bottani, C. DeLozier-Blanchet, C. Haenggeli, 1999, European Journal of Human Genetics.

Connatal Pelizaeus‐Merzbacher Disease

C. Haenggeli, G. Pizzolato, Charles‐A. Haenggeli, 1989, Developmental medicine and child neurology.

T-type alpha 1H Ca2+ channels are involved in Ca2+ signaling during terminal differentiation (fusion) of human myoblasts.

C. Bader, P. Bijlenga, L. Bernheim, 2000, Proceedings of the National Academy of Sciences of the United States of America.

T-type a1H Ca21 channels are involved in Ca21 signaling during terminal differentiation (fusion) of human myoblasts

C. Bader, P. Bijlenga, L. Bernheim, 2000 .