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C. Haenggeli · SciRah

Researcher profile · Semantic Scholar

C. Haenggeli

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C. Haenggeli — researcher profile on SciRah

h-index: 22
Works: 44
Citations: 2,087

Most-cited papers

Non-invasive epileptic focus localization using EEG-triggered functional MRI and electromagnetic tomography.
M. Seeck, F. Lazeyras, C. Michel, O. Blanke +7 more
1998Electroencephalography and Clinical Neurophysiology266 citations Open access
Semantic Scholar
T-type alpha 1H Ca2+ channels are involved in Ca2+ signaling during terminal differentiation (fusion) of human myoblasts.
Philippe Bijlenga, Jian-Hui Liu, Estelle Espinos, C. Haenggeli +3 more
2000Proceedings of the National Academy of Sciences of the United States of America207 citations Open access
Semantic Scholar
Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation
L. Timmermann, K. Pauls, K. Wieland, R. Jech +20 more
2010Brain : a journal of neurology202 citations Open access
Semantic Scholar
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. Ferreiro, N. Monnier, N. Romero, J. Leroy +11 more
2002Annals of Neurology189 citations Open access
Semantic Scholar
Plant-induced seizures: reappearance of an old problem
P. Burkhard, K. Burkhardt, C. Haenggeli, T. Landis
1999Journal of Neurology125 citations Open access
Semantic Scholar
Neuropsychological Problems after Paediatric Stroke: Two Year Follow-Up of Swiss Children
J. Pavlovic, F. Kaufmann, E. Boltshauser, A. C. Mori +10 more
2006Neuropediatrics121 citations Open access
Semantic Scholar
Computed tomography in white-matter disease.
E. Heinz, B. Drayer, C. Haenggeli, M. Painter +1 more
1979Radiology106 citations
Semantic Scholar
Multi‐minicore disease–searching for boundaries: Phenotype analysis of 38 cases
A. Ferreiro, B. Estournet, D. Château, N. Romero +11 more
2000Annals of Neurology101 citations Open access
Semantic Scholar
Incidence of First Epileptic Seizures in the Canton of Geneva, Switzerland
P. Jallon, Michel Goumaz, C. Haenggeli, A. Morabia
1997Epilepsia101 citations
Semantic Scholar
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
Y. Crow, J. McMenamin, C. Haenggeli, D. Hadley +6 more
2004Neuropediatrics82 citations
Semantic Scholar
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.
P. Guicheney, N. Vignier, Xu Zhang, Yi He +16 more
1998Journal of Medical Genetics55 citations Open access
Semantic Scholar
Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti‐N‐methyl‐d‐aspartate receptor encephalitis
C. Poloni, C. Korff, V. Ricotti, M. King +4 more
2009Developmental Medicine & Child Neurology51 citations
Semantic Scholar
Pyridoxine-dependent seizures, clinical and therapeutic aspects
C. Haenggeli, E. Girardin, L. Paunier
1991European Journal of Pediatrics50 citations
Semantic Scholar
MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.
A. Dayer, A. Bottani, I. Bouchardy, J. Fluss +3 more
2007Brain & development (Tokyo. 1979)47 citations Open access
Semantic Scholar
Early onset and rapidly progressive subacute sclerosing panencephalitis after congenital measles infection
D. Cruzado, V. Masserey-Spicher, Laurent Roux, J. Delavelle +2 more
2002European Journal of Pediatrics47 citations Open access
Semantic Scholar
Food colourings and preservatives--allergy and hyperactivity.
P. Eigenmann, C. Haenggeli
2004The Lancet46 citations Open access
Semantic Scholar
Early fatal pontocerebellar hypoplasia in premature twin sisters.
V. Chaves-Vischer, G. Pizzolato, S. Hanquinet, Alexandre Maret +2 more
2000European journal of paediatric neurology35 citations Open access
Semantic Scholar
Contribution of a non‐inactivating potassium current to the resting membrane potential of fusion‐competent human myoblasts.
L. Bernheim, Jian‐Hui Liu, M. Hamann, C. Haenggeli +2 more
1996Journal of Physiology35 citations Open access
Semantic Scholar
Loperamide overdose managed by naloxone.
Gillian Friedli, C. Haenggeli
1980The Lancet34 citations
Semantic Scholar
Operculum syndrome: unusual feature of herpes simplex encephalitis.
J. C. van der Poel, C. Haenggeli, W. Overweg-Plandsoen
1995Pediatric Neurology30 citations
Semantic Scholar
Food colourings, preservatives, and hyperactivity.
P. Eigenmann, C. Haenggeli
2007The Lancet26 citations Open access
Semantic Scholar
T-type a1H Ca21 channels are involved in Ca21 signaling during terminal differentiation (fusion) of human myoblasts
Philippe Bijlenga, Jian‐Hui Liu, E. Espinos, C. Haenggeli +3 more
200022 citations
Semantic Scholar
Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report.
B. Jenny, I. Radovanovic, C. Haenggeli, J. Delavelle +5 more
2007Journal of Neurosurgery20 citations Open access
Semantic Scholar
MEHMO, a novel syndrome: assignment of disease locus to Xp21.1–p22.13
C. DeLozier-Blanchet, C. Haenggeli, A. Bottani
1999European Journal of Human Genetics15 citations Open access
Semantic Scholar
Guillain-Barré syndrome following immunisation withHaemophilus influenzae type b conjugate vaccine
A. Gervaix, Marianne Caflisch, S. Suter, C. Haenggeli
1993European Journal of Pediatrics12 citations
Semantic Scholar
Connatal Pelizaeus‐Merzbacher Disease
C. Haenggeli, E. Engel, G. Pizzolato
1989Developmental Medicine & Child Neurology12 citations
Semantic Scholar
Speech delay due to a prelinguistic regression of epileptic origin.
C. Dubois, D. Gianella, V. Chaves-Vischer, C. Haenggeli +2 more
2004Neuropediatrics11 citations Open access
Semantic Scholar
Locked-in syndrome in an adolescent patient with pneumococcal meningitis.
W. Habre, Marianne Caflisch, V. Chaves-Vischer, J. Delavelle +1 more
1996Neuropediatrics9 citations
Semantic Scholar
Alexander disease: early presence of cerebral MRI criteria.
C. Poloni, S. Ferey, C. Haenggeli, J. Delavelle +4 more
2009European journal of paediatric neurology8 citations Open access
Semantic Scholar
Is benign myoclonic epilepsy of infancy truly idiopathic and generalized?
C. Korff, P. Jallon, A. Lascano, C. Michel +2 more
2009Epileptic disorders7 citations Open access
Semantic Scholar
Freeman Miller, Steven J. Bachrach (eds): Cerebral palsy. A complete guide for caregiving, Second edition
C. Haenggeli, Susanne Suter-Stricker
2007European Journal of Pediatrics5 citations Open access
Semantic Scholar
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?
V. C. Vischer, M. Maeder‐Ingvar, F. Picard, C. Dubois +4 more
2002European journal of paediatric neurology4 citations Open access
Semantic Scholar
[Assisted ventilation in chronic neuromuscular diseases. The Vincre Group].
A. Kohler, J. Janssens, C. Haenggeli, J. Rossi +1 more
1997Revue medicale de la Suisse romande2 citations
Semantic Scholar
CT in Wilson disease
C. Haenggeli, H. Hauser, L. Paunier
1981Neurology2 citations
Semantic Scholar
[How should a muscular disease be studied?].
A. Kohler, C. Bader, L. Bernheim, A. Bottani +5 more
2003Revue medicale de la Suisse romande1 citations
Semantic Scholar
Sinus venous thrombosis in Swiss children
J. Pavlovic, M. Steinlin, F. Kaufmann, E. Boltshauser +8 more
20060 citations
Semantic Scholar
Speech Delay due to a Prelinguistic Regression of Epileptic Origin
C. Dubois, D. Gianella, V. Chaves-Vischer, C. Haenggeli +2 more
20040 citations Open access
Semantic Scholar
[Dizziness, syncope, and other consciousness loss in children].
C. Haenggeli
2003Revue medicale de la Suisse romande0 citations
Semantic Scholar
405 Duchenne muscular dystrophy with mental retardation and a peculiar phenotype associated with glycerol kinase deficiency
R. Schmid, A. Bottani, F. Picard, C. Haenggeli
19990 citations
Semantic Scholar
Locked-In Syndrome in an Adolescent Patient with Pneumococcal Meningitis
W. Habre, M. Caflisch, V. Chaves-Vischer, J. Delavelle +1 more
19960 citations
Semantic Scholar
Severe brain malformations in previously undescribed 4-nucleotide deletion in exon 10 of pyruvate dehydrogenase E1-alpha gene
C. Haenggeli, A. Bottani
19940 citations
Semantic Scholar
[The epileptic child and participation in sports].
C. Haenggeli
1988Helvetica paediatrica acta0 citations
Semantic Scholar
[Current neuropediatric aspects: the extraordinary "saga" of Rett's syndrome].
T. Deonna, C. Haenggeli
1985Revue medicale de la Suisse romande0 citations
Semantic Scholar
CT SCANNING AND NEURO-DEGENERATIVE DISEASES IN CHILDREN
C. Haenggeli, E. Heinz, M. Painter, T. Foley
1977Pediatric Research0 citations
Semantic Scholar

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