J. Fluss

M. Hawkes, S. Blaser, I. Kitai, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families

V. Fraix, L. Kremer, M. Koenig, 2021, Genetics in Medicine.

Herpes simplex encephalitis as a complication of neurosurgical procedures: report of 3 cases and review of the literature

M. Vargas, L. Kaiser, A. L'Huillier, 2016, Virology Journal.

MRI with fibre tracking in Cogan congenital oculomotor apraxia

L. Merlini, M. Vargas, R. D. Haller, 2010, Pediatric Radiology.

Recognition, identification, and diagnosis announcement of neonatal arterial ischemic stroke: A combined exploratory quantitative and qualitative study on parents' lived experiences.

J. Fluss, S. Chabrier, Cindy Leal Martins, 2021, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Stroke-like Phenomena Revealing Multifocal Cerebral Vasculitis in Pediatric Lyme Neuroborreliosis

V. Pereira, M. Vargas, J. Fluss, 2015, Journal of child neurology.

Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy

G. Carvill, I. Scheffer, H. Mefford, 2016, European Journal of Human Genetics.

Title : Pediatric stroke related to Lyme neuroborreliosis : Data from the Swiss NeuroPaediatric Stroke Registry and literature review

J. Fluss, M. Regényi, É. Roulet-Perez, 2018 .

Pediatric stroke related to Lyme neuroborreliosis: Data from the Swiss NeuroPaediatric Stroke Registry and literature review.

J. Fluss, M. Regényi, É. Roulet-Perez, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Vitamin D deficiency: A forgotten treatable cause of motor delay and proximal myopathy

J. Fluss, H. Chehade, G. D. Coulon, 2014, Brain and Development.

Deciphering the natural history of SCA7 in children

A. Durr, D. Devos, C. Cazeneuve, 2020, European journal of neurology.

Mid-hindbrain Malformations Due to Drugs Taken During Pregnancy

L. Merlini, M. Vargas, M. Becker, 2014, Journal of child neurology.

Molar Tooth Sign in Fetal Brain Magnetic Resonance Imaging Leading to the Prenatal Diagnosis of Joubert Syndrome and Related Disorders

D. Chitayat, S. Blaser, C. Raybaud, 2006, Journal of child neurology.

Risk Factors for Postprocedural Arterial Ischemic Stroke in Children With Cardiac Disease

J. Fluss, N. Sekarski, M. Regényi, 2020, Stroke.

[Current management of post-varicella stroke in children: a literature review].

S. Chabrier, J. Fluss, O. Monteventi, 2013, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Transient Cerebral Arteriopathy, Postvaricella Arteriopathy, and Focal Cerebral Arteriopathy or the Unique Susceptibility of the M1 Segment in Children With Stroke.

J. Fluss, G. Sébire, S. Chabrier, 2016, Stroke.

Specific language impairment versus Landau‐Kleffner syndrome

C. Billard, J. Fluss, F. Pinton, 2009, Epilepsia.

Feasibility, safety, and outcome of recanalization treatment in childhood stroke

J. Weber, J. Kaesmacher, J. Gralla, 2018, Annals of neurology.

Look for the nerves! MR neurography adds essential diagnostic value to routine MRI in pediatric practice: a pictorial overview.

M. Viallon, L. Merlini, M. Vargas, 2011, Journal of neuroradiology. Journal de neuroradiologie.

Mild influenza-associated encephalopathy/encephalitis with a reversible splenial lesion in a Caucasian child with additional cerebellar features.

J. Delavelle, M. Vargas, P. van Bogaert, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Cerebral sinovenous thrombosis and idiopathic nephrotic syndrome in childhood: report of four new cases and review of the literature

D. Geary, G. deVeber, J. Fluss, 2006, European Journal of Pediatrics.

Perinatal stroke syndromes: Similarities and diversities in aetiology, outcome and management.

M. Dinomais, J. Fluss, S. Chabrier, 2019, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Primary Leptomeningeal Melanocytosis in a 10-Year-Old Girl

M. Ansari, R. D. Haller, J. Lobrinus, 2011, Journal of child neurology.

ABCB1 polymorphisms and neuropsychiatric adverse events in oseltamivir-treated children during influenza H1N1/09 pandemia.

P. Dayer, C. Korff, J. Desmeules, 2011, Pharmacogenomics.

Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder

S. Antonarakis, A. Poretti, P. Makrythanasis, 2017, Neuropediatrics.

Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother

S. Antonarakis, S. Gimelli, Nelle Lambert, 2018, Journal of Human Genetics.

An unusual intraorbital abscess in a neonate.

S. Suter, K. Posfay-Barbe, J. Fluss, 2002, Journal of pediatric ophthalmology and strabismus.

De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features

S. Gimelli, F. Béna, P. Makrythanasis, 2010, Clinical genetics.

Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders

D. Goldstein, K. Roche, J. Baptista, 2021, Genetics in Medicine.

Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate

J. Fluss, F. Boehlen, Méryle Laurent, 2018, Child neurology open.

Making sense of missense variants in TTN-related congenital myopathies

F. Muntoni, M. Gautel, I. Richard, 2021, Acta Neuropathologica.

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections.

L. Lagae, J. Casanova, G. Mortier, 2017, The Journal of clinical investigation.

Late diagnosis of fucosidosis in a child with progressive fixed dystonia, bilateral pallidal lesions and red spots on the skin.

L. Merlini, M. Gautschi, J. Fluss, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Late discovery of infantile facial nerve schwannoma in a 10-year-old girl

B. Papsin, M. Shroff, S. Cushing, 2006 .

EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations

T. Hortobágyi, F. Baas, E. Aronica, 2014, Orphanet Journal of Rare Diseases.

EPNS/SFNP guideline on the anticoagulant treatment of cerebral sinovenous thrombosis in children and neonates.

L. D. de Vries, M. Tardieu, U. Nowak‐Göttl, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Multimodal Outcome at 7 Years of Age after Neonatal Arterial Ischemic Stroke.

G. Dray, M. Dinomais, J. Lefranc, 2016, The Journal of pediatrics.

Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy

Anne de Saint Martin, A. Afenjar, P. Berquin, 2021, Epilepsy & Behavior.

A Functionally Guided Approach to the Morphometry of Occipitotemporal Regions in Developmental Dyslexia: Evidence for Differential Effects in Boys and Girls

Franck Ramus, Ghislaine Dehaene-Lambertz, Irene Altarelli, 2013, The Journal of Neuroscience.

Cortical networks for vision and language in dyslexic and normal children of variable socio-economic status

Stanislas Dehaene, Ghislaine Dehaene-Lambertz, Karla Monzalvo, 2012, NeuroImage.

Numerical Abilities in Children With Congenital Hemiplegia: An Investigation of the Role of Finger Use in Number Processing

O. Renaud, J. Fluss, Caroline Castel, 2014, Developmental neuropsychology.

Factors affecting cognitive outcome in early pediatric stroke

E. Boltshauser, T. Heinks, G. Ramelli, 2014, Neurology.

Acute ischemic stroke in children versus young adults

E. Boltshauser, P. Jeannet, H. Mattle, 2011, Annals of neurology.

Incidence and Outcomes of Symptomatic Neonatal Arterial Ischemic Stroke

E. Boltshauser, G. Ramelli, O. Maier, 2015, Pediatrics.

Long-term outcome after arterial ischemic stroke in children and young adults

H. Mattle, J. Gralla, M. Arnold, 2015, Neurology.

Perinatal arterial ischemic stroke related to carotid artery occlusion.

J. Fluss, S. Ferey, S. Lebon, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects.

Tommaso Mazza, Jessica Rosati, William B Dobyns, 2017, American journal of human genetics.

Author's response: Extracerebral thrombi in symptomatic neonatal arterial ischemic stroke.

J. Fluss, S. Chabrier, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Impact of stroke volume on motor outcome in neonatal arterial ischemic stroke.

M. Mackay, C. Weisstanner, G. Ramelli, 2019, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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

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

Poor Reading in French Elementary School: The Interplay of Cognitive, Behavioral, and Socioeconomic Factors

Joel Fluss, Johannes C Ziegler, J. Ziegler, 2009, Journal of developmental and behavioral pediatrics : JDBP.

Reading, spelling and comprehension level in low socioeconomic backgrounds: outcome and predictive factors.

J. Ziegler, C. Billard, J. Fluss, 2010 .

Thalamic Hemorrhagic Stroke in the Term Newborn: A Specific Neonatal Syndrome With Non-uniform Outcome

L. Merlini, J. Fluss, S. Hanquinet, 2017, Journal of child neurology.

Structural brain abnormalities in epilepsy with myoclonic atonic seizures

P. Hagmann, C. Korff, J. Fluss, 2021, Epilepsy Research.

When should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?

C. Korff, J. Fluss, L. Bonafė, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Benzodiazepines in the acute management of seizures with autonomic manifestations: Anticipate complications!

A. Gervaix, L. Lacroix, C. Korff, 2011, Epilepsia.

SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum

Caitlin V. Miller, E. Bertini, R. Borgatti, 2021, Journal of Medical Genetics.

Cognitive and academic profiles in children with cerebral palsy: a narrative review.

K. Lidzba, J. Fluss, 2020, Annals of physical and rehabilitation medicine.

From congenial paralysis to post-early brain injury developmental condition: Where does cerebral palsy actually stand?

S. Brochard, M. Dinomais, Y. Bleyenheuft, 2020, Annals of physical and rehabilitation medicine.

MRI of the first event in pediatric acquired demyelinating syndromes with antibodies to myelin oligodendrocyte glycoprotein

K. Rostásy, A. Blaschek, C. Lechner, 2018, Journal of Neurology.

Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies

A. Munnich, G. Lenaers, N. Leboucq, 2022, European journal of neurology.

[Deficits in reading acquisition in primary school: cognitive, social and behavioral factors studied in a sample of 1062 children].

J. Ziegler, C. Billard, J. Fluss, 2009, Revue d'epidemiologie et de sante publique.

[Evolution of competence in reading, spelling and comprehension levels in low socioeconomic environments and impact of cognitive and behavioral factors on outcome in two years].

J. Ziegler, C. Billard, J. Fluss, 2010, Revue d'epidemiologie et de sante publique.

Severe and Progressive Fetal Ventriculomegaly Leading to the Diagnosis of Periventricular Nodular Heterotopias with Good Outcome

C. Garel, N. Bahi-Buisson, J. Fluss, 2015, Neuropediatrics.

Mirror therapy in children with hemiparesis: a randomized observer‐blinded trial

J. Fluss, C. Newman, S. Grunt, 2016, Developmental medicine and child neurology.

[Prevalence of reading disabilities in early elementary school: impact of socioeconomic environment on reading development in 3 different educational zones].

J. Ziegler, C. Billard, J. Fluss, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke

E. Boltshauser, P. Jeannet, H. Mattle, 2010 .

Anti-NMDA receptor encephalitis: the importance of early diagnosis and aggressive immunotherapy in tumor negative pediatric patients.

C. Korff, J. Fluss, M. Kurian, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Manual dexterity, but not cerebral palsy, predicts cognitive functioning after neonatal stroke

M. Dinomais, D. Brouillet, J. Fluss, 2018, Developmental medicine and child neurology.

Dexterity and Finger Sense: A Possible Dissociation in Children With Cerebral Palsy

J. Fluss, Catherine Thevenot, Nolwenn Guedin, 2018, Perceptual and motor skills.

Partial Rhombencephalosynapsis and Chiari Type II Malformation in a Child: a True Association Supported by DTI Tractography

C. Korff, L. Merlini, J. Fluss, 2012, The Cerebellum.

SERPINI1 pathogenic variants: An emerging cause of childhood‐onset progressive myoclonic epilepsy

S. Antonarakis, C. Korff, M. Pittet, 2017, American journal of medical genetics. Part A.

Modalities of reading acquisition in three siblings with infantile-onset saccade initiation delay (Cogan congenital ocular motor apraxia): A longitudinal study.

P. Zesiger, L. Merlini, J. Fluss, 2019, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Successful heart transplant in a child with congenital core myopathy and delayed‐onset restrictive cardiomyopathy due to recessive mutations in the titin (TTN) gene

M. Gautel, H. Jungbluth, J. Lobrinus, 2023, Pediatric transplantation.

Bi‐allelic loss of ERGIC1 causes relatively mild arthrogryposis

R. Hà-Vinh Leuchter, M. Abramowicz, A. Vannier, 2021, Clinical genetics.

Preliminary CommuniCation

P. Dayer, J. Desmeules, A. L'Huillier, 2009 .

Inflammatory Type Focal Cerebral Arteriopathy of the Posterior Circulation in Children: A Comparative Cohort Study

O. Maier, J. Fluss, S. Grunt, 2023, medRxiv.

MCF2 is linked to a complex perisylvian syndrome and affects cortical lamination

M. Guipponi, J. Fluss, A. Dayer, 2019, bioRxiv.

A Functionally Guided Approach to the Morphometry of Occipitotemporal Regions in Developmental Dyslexia: Evidence for Differential Effects in Boys and Girls

F. Ramus, G. Dehaene-Lambertz, Irene Altarelli, 2013, The Journal of Neuroscience.

Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects.

E. Bertini, L. Di Marcotullio, T. Mazza, 2017, American journal of human genetics.

Mild influenza-associated encephalopathy/encephalitis with a reversible splenial lesion in a Caucasian child with additional cerebellar features.

J. Delavelle, M. Vargas, P. van Bogaert, 2010, European journal of paediatric neurology.

EPNS/SFNP guideline on the anticoagulant treatment of cerebral sinovenous thrombosis in children and neonates.

L. D. de Vries, M. Tardieu, A. Lebas, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The effects of dual tasks on gait in children with cerebral palsy.

K. Aminian, N. Valenza, G. Allali, 2019, Gait & posture.

MRI of the first event in pediatric acquired demyelinating syndromes with antibodies to myelin oligodendrocyte glycoprotein

K. Rostásy, A. Blaschek, C. Lechner, 2018, Journal of Neurology.