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Eva Andermann

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Todor Arsov; Katherine R Smith; John Damiano; Silvana Franceschetti; Laura Canafoglia; Catherine J Bromhead; Eva Andermann; Danya F Vears; Patrick Cossette; Sulekha Rajagopalan; Alan McDougall; Vito Sofia; Michael Farrell; Umberto Aguglia; Andrea Zini; Stefano Meletti; Michela Morbin; Saul Mullen; Frederick Andermann; Sara E Mole; Melanie Bahlo; Samuel F Berkovic
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.
Eva Andermann; Frederick Andermann
A life in epilepsy.
Leanne M Dibbens; R Michelucci; A Gambardella; Frederick Andermann; G Rubboli; M A Bayly; T Joensuu; D F Vears; S Franceschetti; L Canafoglia; R Wallace; A G Bassuk; D A Power; C A Tassinari; Eva Andermann; A E Lehesjoki; Samuel F Berkovic
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure.

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All Publications

2011: Todor Arsov; Katherine R Smith; John Damiano; Silvana Franceschetti; Laura Canafoglia; Catherine J Bromhead; Eva Andermann; Danya F Vears; Patrick Cossette; Sulekha Rajagopalan; Alan McDougall; Vito Sofia; Michael Farrell; Umberto Aguglia; Andrea Zini; Stefano Meletti; Michela Morbin; Saul Mullen; Frederick Andermann; Sara E Mole; Melanie Bahlo; Samuel F Berkovic
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.
American journal of human genetics 2011;88(5):566-73.
2010: Eva Andermann; Frederick Andermann
A life in epilepsy.
Epilepsia 2010;51 Suppl 1():101-3.
2009: Leanne M Dibbens; R Michelucci; A Gambardella; Frederick Andermann; G Rubboli; M A Bayly; T Joensuu; D F Vears; S Franceschetti; L Canafoglia; R Wallace; A G Bassuk; D A Power; C A Tassinari; Eva Andermann; A E Lehesjoki; Samuel F Berkovic
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure.
Annals of neurology 2009;66(4):532-6.
2008: An C Jansen; Eva Andermann; Florence Niel; Isabelle Creveaux; Odile Boespflug-Tanguy; Frederick Andermann
Leucoencephalopathy with vanishing white matter may cause progressive myoclonus epilepsy.
Epilepsia 2008;49(5):910-3.
2008: Samuel F Berkovic; Leanne M Dibbens; Alicia Oshlack; Jeremy D Silver; Marina Katerelos; Danya F Vears; Renate Lüllmann-Rauch; Judith Blanz; Ke Wei Zhang; Jim Stankovich; Renate M Kalnins; John P Dowling; Eva Andermann; Frederick Andermann; Enrico Faldini; Rudi D'Hooge; Lata Vadlamudi; Richard A Macdonell; Bree L Hodgson; Marta A Bayly; Judy Savige; John C Mulley; Gordon K Smyth; David A Power; Paul Saftig; Melanie Bahlo
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis.
American journal of human genetics 2008;82(3):673-84.
2007: An C M Jansen; Henian Cao; Paige Kaplan; Kenneth Silver; Gabriel Leonard; Linda De Meirleir; Willy Lissens; Inge Liebaers; Martin Veilleux; Frederick Andermann; Robert A Hegele; Eva Andermann
Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene.
Archives of neurology 2007;64(11):1629-34.
2007: Louise A Harkin; Jacinta M McMahon; Xenia Iona; Leanne M Dibbens; James T Pelekanos; Sameer M Zuberi; Lynette G Sadleir; Eva Andermann; Deepak Gill; Kevin Farrell; Mary Connolly; Thorsten Stanley; Michael Harbord; Frederick Andermann; Jing Wang; Sat Dev Batish; Jeffrey G Jones; William K Seltzer; Alison Gardner; Grant Sutherland; Samuel F Berkovic; John C Mulley; Ingrid E Scheffer
The spectrum of SCN1A-related infantile epileptic encephalopathies.
Brain : a journal of neurology 2007;130(Pt 3):843-52.
2006: An C Jansen; Ozgur Sancak; Maria Daniela D'Agostino; AmanPreet Badhwar; Penelope Roberts; Gabriella Gobbi; Ralph Wilkinson; Denis Melanson; Donatella Tampieri; Robert K Koenekoop; Mark Gans; anneke maat-kievit; Miriam A Goedbloed; Ans M W van den Ouweland; Mark Nellist; Massimo Pandolfo; Mary McQueen; Katherine Sims; Elizabeth A Thiele; François Dubeau; Frederick Andermann; David J Kwiatkowski; D J J Halley; Eva Andermann
Unusually mild tuberous sclerosis phenotype is associated with TSC2 R905Q mutation.
Annals of neurology 2006;60(5):528-39.
2006: Ruth H Walker; Adrian Danek; Carol Dobson-Stone; Renzo Guerrini; Hans H Jung; Anne-Louise Lafontaine; Luca Rampoldi; François Tison; Eva Andermann
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromes.
Movement disorders : official journal of the Movement Disorder Society 2006;21(11):1794-805.
2006: Maria Augusta Montenegro; Demet Kinay; Fernando Cendes; Andrea Bernasconi; Neda Bernasconi; AC Coan; Li Li; Marilisa M Guerreiro; Carlos A M Guerreiro; Iscia Lopes-Cendes; Eva Andermann; F Dubeau; F Andermann
Patterns of hippocampal abnormalities in malformations of cortical development.
Journal of neurology, neurosurgery, and psychiatry 2006;77(3):367-71.
2005: Carol Dobson-Stone; Antonio Velayos-Baeza; An Jansen; Frederick Andermann; François Dubeau; Francine Robert; Anne Summers; Anthony E Lang; Sylvain Chouinard; Adrian Danek; Eva Andermann; Anthony P Monaco
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis.
Neurogenetics 2005;6(3):151-8.
2005: Abdullah Al-Asmi; An C Jansen; AmanPreet Badhwar; François Dubeau; Donatella Tampieri; Chaim Shustik; Suha Mercho; Ghislaine Savard; Carol Dobson-Stone; Anthony P Monaco; Frederick Andermann; Eva Andermann
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis.
Epilepsia 2005;46(8):1256-63.
2005: An C Jansen; Gabriel Leonard; Alexandre C Bastos; Josée E Esposito-Festen; Donatella Tampieri; Kate Watkins; Frederick Andermann; Eva Andermann
Cognitive functioning in bilateral perisylvian polymicrogyria (BPP): clinical and radiological correlations.
Epilepsy & behavior : E&B 2005;6(3):393-404.
2005: Eliane Kobayashi; Andrew P Bagshaw; A Jansen; Frederick Andermann; Eva Andermann; Jean Gotman; François Dubeau
Intrinsic epileptogenicity in polymicrogyric cortex suggested by EEG-fMRI BOLD responses.
Neurology 2005;64(7):1263-6.
2005: Frederick Andermann; Eliane Kobayashi; Eva Andermann
Genetic focal epilepsies: state of the art and paths to the future.
Epilepsia 2005;46 Suppl 10():61-7.
2004: AmanPreet Badhwar; An Jansen; Frederick Andermann; Massimo Pandolfo; Eva Andermann
Striking intrafamilial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the FRDA1 gene.
Movement disorders : official journal of the Movement Disorder Society 2004;19(12):1424-31.
2004: Cary S Kogan; Armando Bertone; Kim Cornish; Isabelle Boutet; Vazken M Der Kaloustian; Eva Andermann; Jocelyn Faubert; Avi Chaudhuri
Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome.
Neurology 2004;63(9):1634-9.
2004: D D'Agostino; Matteo Bertelli; S Gallo; Stefano Cecchin; E Albiero; P G Garofalo; A Gambardella; J-M St Hilaire; H Kwiecinski; Eva Andermann; M Pandolfo
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy.
Neurology 2004;63(8):1500-2.
2004: An C Jansen; Eva Andermann; Frederick Andermann
Biparental inheritance in idiopathic generalized epilepsy.
Epilepsia 2004;45(10):1294-5.
2004: AmanPreet Badhwar; Samuel F Berkovic; John P Dowling; Michael Gonzales; Sridar Narayanan; Amy Brodtmann; Leon Berzen; John Caviness; Claudia Trenkwalder; Juliane Winkelmann; Jean Rivest; Marie Lambert; Otto Hernandez-Cossio; Stirling Carpenter; Frederick Andermann; Eva Andermann
Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorder.
Brain : a journal of neurology 2004;127(Pt 10):2173-82.
2004: Samuel F Berkovic; José M Serratosa; Hilary A Phillips; Lan Xiong; Eva Andermann; Fernando Díaz-Otero; Pilar Gómez-Garre; Mercedes Martín; Yolanda Fernández-Bullido; Frederick Andermann; Iscia Lopes-Cendes; Francois Dubeau; Richard Desbiens; Ingrid E Scheffer; Robyn H Wallace; John C Mulley; Massimo Pandolfo
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
Epilepsia 2004;45(9):1054-60.
2004: Maria Daniela D'Agostino; Alexandre C Bastos; C Piras; Andrea Bernasconi; T Grisar; V Gross Tsur; J Snipes; Csaba Juhász; Harry T Chugani; Renzo Guerrini; H Cross; Eva Andermann; François Dubeau; Jose Luis Montes; André Olivier; Frederick Andermann
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformation.
Neurology 2004;62(12):2214-20.
2004: Dominique J Verlaan; Sandra B Laurent; U Sure; Helmut Bertalanffy; Eva Andermann; Frederick Andermann; Guy Rouleau; Adrian M Siegel
CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.
Neurology 2004;62(7):1213-5.
2004: Lata Vadlamudi; Eva Andermann; C T Lombroso; S C Schachter; Roger L Milne; John L Hopper; Frederick Andermann; Samuel F Berkovic
Epilepsy in twins: insights from unique historical data of William Lennox.
Neurology 2004;62(7):1127-33.
2004: Orvar Eeg-Olofsson; Tomas Bergström; F Andermann; Eva Andermann; A Olivier; Bertil Rydenhag
Herpesviral DNA in brain tissue from patients with temporal lobe epilepsy.
Acta neurologica Scandinavica 2004;109(3):169-74.
2004: Cary S Kogan; Isabelle Boutet; Kim Cornish; Shahin Zangenehpour; Kathy T Mullen; Jeanette J A Holden; Vazken M Der Kaloustian; Eva Andermann; Avi Chaudhuri
Differential impact of the FMR1 gene on visual processing in fragile X syndrome.
Brain : a journal of neurology 2004;127(Pt 3):591-601.
2004: Jane R Richmond; Preetha Krishnamoorthy; Eva Andermann; Alice Benjamin
Epilepsy and pregnancy: an obstetric perspective.
American journal of obstetrics and gynecology 2004;190(2):371-9.
2003: Robyn H Wallace; Bree L Hodgson; Bronwyn E Grinton; R M Gardiner; R Robinson; V Rodriguez-Casero; Lynette G Sadleir; J Morgan; Louise A Harkin; Leanne M Dibbens; T Yamamoto; Eva Andermann; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.
Neurology 2003;61(6):765-9.
2003: Eliane Kobayashi; Maria Daniela D'Agostino; Iscia Lopes-Cendes; Eva Andermann; François Dubeau; Carlos A M Guerreiro; André A Schenka; Luciano S Queiroz; André Olivier; Fernando Cendes; Frederick Andermann
Outcome of surgical treatment in familial mesial temporal lobe epilepsy.
Epilepsia 2003;44(8):1080-4.
2003: E Kobayashi; M D D'Agostino; Iscia Lopes-Cendes; S F Berkovic; M L Li; Eva Andermann; F Andermann; Fernando Cendes
Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy.
Neurology 2003;60(3):405-9.
2003: Marco Fedi; David C Reutens; Frederick Andermann; Hidehiko Okazawa; Warren Boling; Carole White; François Dubeau; Akio Nakai; Donald Gross; Eva Andermann; Mirko Diksic
alpha-[11C]-Methyl-L-tryptophan PET identifies the epileptogenic tuber and correlates with interictal spike frequency.
Epilepsy research 2003;52(3):203-13.
2003: François Gros-Louis; Inge A Meijer; Collette K Hand; Marie-Pierre Dubé; Daune L MacGregor; Marie-Hélène Seni; Rebecca S Devon; Michael R Hayden; Frederick Andermann; Eva Andermann; Guy Rouleau
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred.
Annals of neurology 2003;53(1):144-5.
2002: Sarah E Heron; Kathryn M Crossland; Eva Andermann; Hilary A Phillips; Allison J Hall; Andrew F Bleasel; Michael Shevell; Suha Mercho; Marie-Hélène Seni; Marie-Christine Guiot; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer
Sodium-channel defects in benign familial neonatal-infantile seizures.
Lancet 2002;360(9336):851-2.
2002: AmanPreet Badhwar; Auli Siren; Eva Andermann; Frederick Andermann
Myoclonic status epilepticus: video presentation.
Movement disorders : official journal of the Movement Disorder Society 2002;17(2):409-11.
2001: Marco Fedi; David C Reutens; Hidehiko Okazawa; Frederick Andermann; Warren Boling; François Dubeau; Carole White; Akio Nakai; Donald Gross; Eva Andermann; Mirko Diksic
Localizing value of alpha-methyl-L-tryptophan PET in intractable epilepsy of neocortical origin.
Neurology 2001;57(9):1629-36.
2001: Andrea Bernasconi; V Martinez; Pedro Rosa-Neto; D D'Agostino; Neda Bernasconi; Samuel Berkovic; M MacKay; A Simon Harvey; André Palmini; Jaderson Costa DaCosta; Eduardo Paglioli; H I Kim; M Connolly; André Olivier; François Dubeau; Eva Andermann; Renzo Guerrini; WW Whisler; L de Toledo-Morrell; F Morrell; Frederick Andermann
Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate results.
Epilepsia 2001;42(9):1124-9.
2001: Volney L Sheen; Peter DIxon; JW Fox; Susan E Hong; L Kinton; S M Sisodiya; J S Duncan; F Dubeau; IE Scheffer; Steven C Schachter; Andrew Wilner; R Henchy; P Crino; K Kamuro; F DiMario; M Berg; R Kuzniecky; A J Cole; Edward B Bromfield; M Biber; Donald L Schomer; James W Wheless; K Silver; G H Mochida; SF Berkovic; F Andermann; Eva Andermann; William B Dobyns; Nicholas W Wood; Christopher Walsh
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.
Human molecular genetics 2001;10(17):1775-83.
2001: Rita Singh; Eva Andermann; W P Whitehouse; A Simon Harvey; D L Keene; Marie-Hélène Seni; Kathryn M Crossland; Frederick Andermann; Samuel F Berkovic; Ingrid E Scheffer
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
Epilepsia 2001;42(7):837-44.
2001: S Duncan; Suha Mercho; Iscia Lopes-Cendes; Marie-Hélène Seni; A Benjamin; François Dubeau; Frederick Andermann; Eva Andermann
Repeated neural tube defects and valproate monotherapy suggest a pharmacogenetic abnormality.
Epilepsia 2001;42(6):750-3.
2001: Marco Fedi; David C Reutens; François Dubeau; Eva Andermann; D D'Agostino; Frederick Andermann
Long-term efficacy and safety of piracetam in the treatment of progressive myoclonus epilepsy.
Archives of neurology 2001;58(5):781-6.
2001: Ruth Ann Marrie; Eric A Shoubridge; J P Antel; Douglas L Arnold; J Chen; Eva Andermann; Frederick Andermann
Unusual imaging findings in progressive myoclonus epilepsy.
Epilepsia 2001;42(3):430-2.
2000: Marilisa M Guerreiro; Eva Andermann; Renzo Guerrini; William B Dobyns; R Kuzniecky; K Silver; P Van Bogaert; C Gillain; P David; Giovanni Ambrosetto; A Rosati; F Bartolomei; A Parmeggiani; Ritva Paetau; O Salonen; Jaakko Ignatius; Renato Borgatti; Claudio Zucca; Alexandre C Bastos; André Palmini; W Fernandes; M A Montenegro; F Cendes; Frederick Andermann
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.
Annals of neurology 2000;48(1):39-48.
1999: L Xiong; M Labuda; D S Li; Thomas J Hudson; R Desbiens; G Patry; S Verret; P Langevin; Suha Mercho; Marie-Hélène Seni; Ingrid E Scheffer; François Dubeau; Samuel F Berkovic; Frederick Andermann; Eva Andermann; Massimo Pandolfo
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.
American journal of human genetics 1999;65(6):1698-710.
1999: Frederick Andermann; Eva Andermann; Alain Ptito; S Fontaine; M Joubert
History of Joubert syndrome and a 30-year follow-up of the original proband.
Journal of child neurology 1999;14(9):565-9.
1999: Dina Battino; Sunao Kaneko; Eva Andermann; Giuliano Avanzini; Maria Paola Canevini; Raffaele Canger; Danilo Croci; Cristina Fumarola; L Guidolin; Daniela Mamoli; F Molteni; Giorgio Pardi; Aglaia Vignoli; Y Fukushima; R Kan; A Takeda; Y Nakane; Y Ogawa; L Dansky; M Oguni; I Lopez-Ciendas; A Sherwin; Frederick Andermann; Marie-Hélène Seni; M Goto
Intrauterine growth in the offspring of epileptic women: a prospective multicenter study.
Epilepsy research 1999;36(1):53-60.
1999: Sunao Kaneko; Dina Battino; Eva Andermann; Kazumaru Wada; R Kan; A Takeda; Y Nakane; Y Ogawa; Giuliano Avanzini; Cristina Fumarola; Tiziana Granata; F Molteni; Giorgio Pardi; Lorella Minotti; Raffaele Canger; L Dansky; M Oguni; I Lopes-Cendas; A Sherwin; Frederick Andermann; Marie-Hélène Seni; Motohiro Okada; T Teranishi
Congenital malformations due to antiepileptic drugs.
Epilepsy research 1999;33(2-3):145-58.
1999: Joseph G Gleeson; Sharon Minnerath; JW Fox; Kristina M Allen; R F Luo; Susan E Hong; M J Berg; R Kuzniecky; Pamela Reitnauer; Renato Borgatti; A P Mira; Renzo Guerrini; Gregory L Holmes; C M Rooney; SF Berkovic; IE Scheffer; edward cooper; S Ricci; R Cusmai; Thomas Crawford; R Leroy; Eva Andermann; James W Wheless; William B Dobyns; Christopher Walsh
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
Annals of neurology 1999;45(2):146-53.
1999: C Gurses; Donald Gross; Frederick Andermann; Alexandre C Bastos; François Dubeau; M Calay; M Eraksoy; S Bezci; Eva Andermann; Denis Melanson
Periventricular leukomalacia and epilepsy: incidence and seizure pattern.
Neurology 1999;52(2):341-5.
1998: Adrian M Siegel; Frederick Andermann; AmanPreet Badhwar; Guy Rouleau; M Dam; H C Hopf; J Dichgans; M Sturzenegger; N J Hopf; N Yasui; Frank Stepper; M Killer; J A Vanneste; Nicola Acciarri; P Drigo; J Christensen; V Braun; Dilek Könü; Eva Andermann
Anticipation in familial cavernous angioma: ascertainment bias or genetic cause.
Acta neurologica Scandinavica 1998;98(6):372-6.
1998: Adrian M Siegel; Eva Andermann; AmanPreet Badhwar; Guy Rouleau; G L Wolford; Frederick Andermann; K Hess
Anticipation in familial cavernous angioma: a study of 52 families from International Familial Cavernous Angioma Study. IFCAS Group.
Lancet 1998;352(9141):1676-7.
1998: Marilisa M Guerreiro; Frederick Andermann; Eva Andermann; André Palmini; Peter Hwang; H J Hoffman; Hiroshi Otsubo; Alexandre C Bastos; François Dubeau; G Jackson Snipes; André Olivier; T Rasmussen
Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patients.
Neurology 1998;51(5):1263-9.
1998: Hilary A Phillips; Ingrid E Scheffer; Kathryn M Crossland; K P Bhatia; D R Fish; CD Marsden; S J Howell; John B P Stephenson; John Tolmie; G Plazzi; Orvar Eeg-Olofsson; Rita Singh; Iscia Lopes-Cendes; Eva Andermann; Frederick Andermann; Samuel F Berkovic; John C Mulley
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24.
American journal of human genetics 1998;63(4):1108-16.
1998: Andrea Bernasconi; F Cendes; E A Shoubridge; Eva Andermann; Li Li; Douglas L Arnold; Frederick Andermann
Spectroscopic imaging of frontal neuronal dysfunction in hyperekplexia.
Brain : a journal of neurology 1998;121 ( Pt 8)():1507-12.
1998: Andrea Bernasconi; Frederick Andermann; F Cendes; François Dubeau; Eva Andermann; André Olivier
Nocturnal temporal lobe epilepsy.
Neurology 1998;50(6):1772-7.
1998: F Cendes; Iscia Lopes-Cendes; Eva Andermann; Frederick Andermann
Familial temporal lobe epilepsy: a clinically heterogeneous syndrome.
Neurology 1998;50(2):554-7.
1998: Carol Macmillan; T Kirkham; K Fu; V Allison; Eva Andermann; D Chitayat; D Fortier; Mark Gans; H Hare; N Quercia; D Zackon; Eric A Shoubridge
Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.
Neurology 1998;50(2):417-22.
1998: Hannah M Mitchison; Hofmann Sandra; C H Becerra; Patricia B Munroe; BD Lake; Yanick J Crow; John B P Stephenson; Ruth E Williams; IL Hofman; Peter E M Taschner; J J Martin; M Philippart; Eva Andermann; F Andermann; Sara E Mole; R Mark Gardiner; AM O'Rawe
Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits.
Human molecular genetics 1998;7(2):291-7.
1997: M Melanson; Josephine Nalbantoglu; Samuel Berkovic; C Melmed; Eva Andermann; L J Roberts; S Carpenter; G Jackson Snipes; Frederick Andermann
Progressive myoclonus epilepsy in young adults with neuropathologic features of Alzheimer's disease.
Neurology 1997;49(6):1732-3.
1997: L Montermini; Eva Andermann; M Labuda; Andrea Richter; Massimo Pandolfo; F Cavalcanti; Luigi Pianese; L Iodice; G Farina; Antonella Monticelli; Mimmo Turano; Alessandro Filla; Giuseppe De Michele; Sergio Cocozza
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.
Human molecular genetics 1997;6(8):1261-6.
1997: L Montermini; Andrea Richter; Kenneth Morgan; C M Justice; D Julien; Barbara Castellotti; Jocelyne Mercier; J Poirier; F Capozzoli; Jean-Pierre Bouchard; B Lemieux; Jean Mathieu; Michel Vanasse; Marie-Hélène Seni; G Graham; Frederick Andermann; Eva Andermann; SB Melançon; Bronya J B Keats; Stefano Di Donato; Massimo Pandolfo
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion.
Annals of neurology 1997;41(5):675-82.
1997: M Elizabeth Ross; Kristina M Allen; A K Srivastava; T Featherstone; Joseph G Gleeson; B Hirsch; B N Harding; Eva Andermann; R Abdullah; M Berg; D Czapansky-Bielman; D J Flanders; Renzo Guerrini; J Motté; A P Mira; IE Scheffer; SF Berkovic; F Scaravilli; R A King; David Ledbetter; David Schlessinger; William B Dobyns; Christopher Walsh
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.
Human molecular genetics 1997;6(4):555-62.
1997: Ronald G Lafrenière; Daniel Rochefort; N Chrétien; Johanna M Rommens; J I Cochius; Reetta Kälviäinen; U Nousiainen; G Patry; K Farrell; B Söderfeldt; A Federico; B R Hale; O H Cossio; T Sørensen; M A Pouliot; T Kmiec; P Uldall; J Janszky; M R Pranzatelli; F Andermann; Eva Andermann; Guy Rouleau
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
Nature genetics 1997;15(3):298-302.
1997: AM O'Rawe; Hannah M Mitchison; Ross Williams; R Wheeler; Eva Andermann; F Andermann; Y M Hart; J J Martin; M Philippart; John B P Stephenson; R Mark Gardiner; Sara E Mole
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic deposits.
Neuropediatrics 1997;28(1):21-2.
1996: Ronald G Lafrenière; Daniel Rochefort; Zoha Kibar; E A Fon; Fei-Yu Han; J Cochius; X Kang; S Baird; R G Korneluk; Eva Andermann; Johanna M Rommens; Guy Rouleau
Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3.
Genomics 1996;38(3):264-72.
1996: A Gambardella; André Palmini; Frederick Andermann; François Dubeau; Jaderson Costa DaCosta; L Felipe Quesney; Eva Andermann; A Olivier
Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy.
Electroencephalography and clinical neurophysiology 1996;98(4):243-9.
1996: David C Reutens; Frederick Andermann; A Olivier; Eva Andermann; François Dubeau
Unusual features of supplementary sensorimotor area epilepsy: cyclic pattern, unusual sensory aura, startle sensitivity, anoxic encephalopathy, and spontaneous remission.
Advances in neurology 1996;70():293-300.
1996: Isabel Silveira; Iscia Lopes-Cendes; Stephen J Kish; Patrícia Maciel; Claudia Gaspar; Paula Coutinho; MI Botez; H Teive; Walter Oleschko Arruda; C E Steiner; W Pinto-Júnior; J A Maciel; S Jerin; GEORGE SACK; Eva Andermann; L Sudarsky; Roger Rosenberg; P MacLeod; D Chitayat; R Babul; Jorge Sequeiros; Guy Rouleau
Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
Neurology 1996;46(1):214-8.
1996: L K Casaubon; M Melanson; Iscia Lopes-Cendes; Claude Marineau; Eva Andermann; Frederick Andermann; J Weissenbach; C Prévost; J P Bouchard; J Mathieu; Guy Rouleau
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.
American journal of human genetics 1996;58(1):28-34.
1995: Iscia Lopes-Cendes; Hilary A Phillips; Ingrid E Scheffer; John C Mulley; R Desbiens; Eva Andermann; F Cendes; S Verret; Frederick Andermann; S F Berkovic
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locus.
Epilepsy research 1995;22(3):227-33.
1995: François Dubeau; Donatella Tampieri; N Lee; Eva Andermann; S Carpenter; Richard LeBlanc; A Olivier; R Radtke; J G Villemure; Frederick Andermann
Periventricular and subcortical nodular heterotopia. A study of 33 patients.
Brain : a journal of neurology 1995;118 ( Pt 5)():1273-87.
1995: André Palmini; A Gambardella; Frederick Andermann; François Dubeau; Jaderson Costa DaCosta; A Olivier; Donatella Tampieri; P Gloor; F Quesney; Eva Andermann
Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results.
Annals of neurology 1995;37(4):476-87.
1995: Ingrid E Scheffer; K P Bhatia; Iscia Lopes-Cendes; D R Fish; CD Marsden; Eva Andermann; Frederick Andermann; R Desbiens; D Keene; F Cendes
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder.
Brain : a journal of neurology 1995;118 ( Pt 1)():61-73.
1994: J Cochius; S Carpenter; Eva Andermann; Guy Rouleau; U Nousiainen; R Kalviainen; K Farrell; Frederick Andermann
Sweat gland vacuoles in Unverricht-Lundborg disease: a clue to diagnosis?
Neurology 1994;44(12):2372-5.
1994: Eva Andermann; Frederick Andermann; K Silver; S Levin; D Arnold
Benign familial nocturnal alternating hemiplegia of childhood.
Neurology 1994;44(10):1812-4.
1994: André Palmini; Eva Andermann; Frederick Andermann
Prenatal events and genetic factors in epileptic patients with neuronal migration disorders.
Epilepsia 1994;35(5):965-73.
1994: Iscia Lopes-Cendes; Eva Andermann; E Attig; F Cendes; S Bosch; M Wagner; F Gerstenbrand; Frederick Andermann; Guy Rouleau
Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.
American journal of human genetics 1994;54(5):774-81.
1994: Iscia Lopes-Cendes; Eva Andermann; Guy Rouleau
Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus.
Genomics 1994;21(1):270-4.
1994: Frederick Andermann; S Ohtahara; Eva Andermann; P Camfield; K Kobayashi
Infantile hypotonia and paroxysmal dystonia: a variant of alternating hemiplegia of childhood?
Movement disorders : official journal of the Movement Disorder Society 1994;9(2):227-9.
1994: Ingrid E Scheffer; K P Bhatia; Iscia Lopes-Cendes; D R Fish; CD Marsden; Frederick Andermann; Eva Andermann; R Desbiens; F Cendes; J I Manson
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder.
Lancet 1994;343(8896):515-7.
1993: F Cendes; Frederick Andermann; P Gloor; Iscia Lopes-Cendes; Eva Andermann; Denis Melanson; Marilyn Jones-Gotman; Yvonne Robitaille; A Evans; T Peters
Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?
Annals of neurology 1993;34(6):795-801.
1993: F Cendes; François Dubeau; A Olivier; A Cukiert; Eva Andermann; L Felipe Quesney; Frederick Andermann
Increased neocortical spiking and surgical outcome after selective amygdalo-hippocampectomy.
Epilepsy research 1993;16(3):195-206.
1993: B Abou-Khalil; Eva Andermann; Frederick Andermann; A Olivier; L Felipe Quesney
Temporal lobe epilepsy after prolonged febrile convulsions: excellent outcome after surgical treatment.
Epilepsia 1993;34(5):878-83.
1993: F Cendes; Frederick Andermann; François Dubeau; P Gloor; A Evans; Marilyn Jones-Gotman; A Olivier; Eva Andermann; Yvonne Robitaille; Iscia Lopes-Cendes
Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric study.
Neurology 1993;43(6):1083-7.
1993: André Palmini; Frederick Andermann; H de Grissac; Donatella Tampieri; Yvonne Robitaille; P Langevin; R Desbiens; Eva Andermann
Stages and patterns of centrifugal arrest of diffuse neuronal migration disorders.
Developmental medicine and child neurology 1993;35(4):331-9.
1992: Peter Hechtman; B Boulay; Marc de Braekeleer; Eva Andermann; SB Melançon; J Larochelle; C Prevost; Feige Kaplan
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada.
Human genetics 1992;90(4):402-6.
1992: Eva Andermann; Frederick Andermann
The children of mothers with epilepsy: recent trends in research, management and prospect.
Brain & development 1992;14(6):423.
1992: M Oguni; L Dansky; Eva Andermann; A Sherwin; Frederick Andermann
Improved pregnancy outcome in epileptic women in the last decade: relationship to maternal anticonvulsant therapy.
Brain & development 1992;14(6):371-80.
1992: Marc de Braekeleer; Peter Hechtman; Eva Andermann; Feige Kaplan
The French Canadian Tay-Sachs disease deletion mutation: identification of probable founders.
Human genetics 1992;89(1):83-7.
1992: François Dubeau; A Sherwin; A Olivier; J Villemure; R Leblanc; L Felipe Quesney; Eva Andermann; Frederick Andermann
Excitatory amino acids modulate phosphoinositide signal transduction in human epileptic neocortex.
Epilepsia 1992;33(2):255-62.
1992: Frederick Andermann; Eva Andermann
Migraine and epilepsy, with special reference to the benign epilepsies of childhood.
Epilepsy research. Supplement 1992;6():207-14.
1992: André Palmini; Frederick Andermann; Donatella Tampieri; Eva Andermann; Yvonne Robitaille; A Olivier
Epilepsy and cortical cytoarchitectonic abnormalities: an attempt at correlating basic mechanisms with anatomoclinical syndromes.
Epilepsy research. Supplement 1992;9():19-29; discussion 29-30.
1991: André Palmini; Frederick Andermann; A Olivier; Donatella Tampieri; Yvonne Robitaille; Eva Andermann; G Wright
Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patients.
Annals of neurology 1991;30(6):741-9.
1991: S F Berkovic; Frederick Andermann; Eric A Shoubridge; S Carpenter; Yvonne Robitaille; Eva Andermann; C Melmed; George Karpati
Mitochondrial dysfunction in multiple symmetrical lipomatosis.
Annals of neurology 1991;29(5):566-9.
1990: Peter Hechtman; Feige Kaplan; J Bayleran; B Boulay; Eva Andermann; Marc de Braekeleer; SB Melançon; Marie Lambert; M Potier; R Gagné
More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians.
American journal of human genetics 1990;47(5):815-22.
1990: L A Goossens; Frederick Andermann; Eva Andermann; G M Remillard
Reflex seizures induced by calculation, card or board games, and spatial tasks: a review of 25 patients and delineation of the epileptic syndrome.
Neurology 1990;40(8):1171-6.
1989: Peter Hechtman; B Boulay; J Bayleran; Eva Andermann
The mutation mechanism causing juvenile-onset Tay-Sachs disease among Lebanese.
Clinical genetics 1989;35(5):364-75.
1989: Frederick Andermann; S Berkovic; S Carpenter; Eva Andermann
The Ramsay Hunt syndrome is no longer a useful diagnostic category.
Movement disorders : official journal of the Movement Disorder Society 1989;4(1):13-7.
1988: O Eeg-Olofsson; C K Osterland; R D Guttmann; Frederick Andermann; J F Prchal; Eva Andermann; N A Janjua
Immunological studies in focal epilepsy.
Acta neurologica Scandinavica 1988;78(5):358-68.
1988: A Sherwin; Yvonne Robitaille; F Quesney; A Olivier; J Villemure; R Leblanc; William Feindel; Eva Andermann; Jean Gotman; Frederick Andermann
Excitatory amino acids are elevated in human epileptic cerebral cortex.
Neurology 1988;38(6):920-3.
1988: S F Berkovic; S Carpenter; Frederick Andermann; Eva Andermann; L S Wolfe
Kufs' disease: a critical reappraisal.
Brain : a journal of neurology 1988;111 ( Pt 1)():27-62.
1988: Eva Andermann; J C Jacob; Frederick Andermann; S Carpenter; L Wolfe; S F Berkovic
The Newfoundland aggregate of neuronal ceroid-lipofuscinosis.
American journal of medical genetics. Supplement 1988;5():111-6.
1988: S F Berkovic; Frederick Andermann; Eva Andermann; S Carpenter; L Wolfe
Kufs disease: clinical features and forms.
American journal of medical genetics. Supplement 1988;5():105-9.
1988: Frederick Andermann; Eva Andermann
Startle disorders of man: hyperekplexia, jumping and startle epilepsy.
Brain & development 1988;10(4):213-22.
1986: O Eeg-Olofsson; N A Janjua; Eva Andermann; R D Guttmann; K Osterland
Immunological and genetic studies in primary generalized corticoreticular epilepsy.
Acta neurologica Scandinavica 1986;74(6):425-31.