P. Landrieu

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Phoneme perception in a neonate with a left sylvian infarct

G Dehaene-Lambertz, A. Christophe, G. Dehaene-Lambertz, 2004, Brain and Language.

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

Hans H. Jung, C. Tilikete, M. Koenig, 2018, JAMA neurology.

Schizencephaly, consequence of a developmental vasculopathy? A clinicopathological report.

C. Lacroix, P. Landrieu, 1994, Clinical neuropathology.

Congenital unilateral perisylvian syndrome: radiological basis and clinical correlations.

M. Tardieu, P. Landrieu, G. Sébire, 1996, Journal of Neurology Neurosurgery & Psychiatry.

Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts

C. Lacroix, P. Landrieu, M. Zérah, 1996, Neurology.

Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract.

P. Landrieu, M. Odiévre, D. Alagille, 1981, Archives of disease in childhood.

Obstetrical and neonatal characteristics vary with birthweight in a cohort of 100 term newborns with symptomatic arterial ischemic stroke.

B. Tardy, P. Landrieu, E. Saliba, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Developmental dilatation of Virchow-Robin spaces: a genetic disorder?

P. Landrieu, B. Husson, Anne-Laure Bruna, 2009, Pediatric neurology.

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

L. Lagae, A. Vanderver, K. Devriendt, 2015, American journal of medical genetics. Part A.

A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency

A. Munnich, D. Galanaud, N. Boddaert, 2010, Journal of Medical Genetics.

Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

H. Waterham, R. Wanders, W. Kuis, 2001, European Journal of Human Genetics.

Dominantly transmitted congenital indifference to pain

P. Landrieu, C. Allaire, G. Said, 1990, Annals of neurology.

Hereditary motor-sensory, motor, and sensory neuropathies in childhood.

P. de Jonghe, P. Landrieu, J. Baets, 2013, Handbook of clinical neurology.

Exhaustive analysis of BH 4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

Michael K. Hutchinson, M. Vidailhet, D. Grabli, 2009 .

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.

Michael K. Hutchinson, M. Vidailhet, D. Grabli, 2009, Brain : a journal of neurology.

Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.

A. Munnich, J. Melki, A. Verloes, 1996, The Journal of clinical investigation.

Ischaemic stroke from dissection of the craniocervical arteries in childhood: report of 12 patients.

M. Tardieu, P. Landrieu, P. Lasjaunias, 2003, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Stroke in Childhood: Outcome and Recurrence Risk by Mechanism in 59 Patients

M. Tardieu, P. Landrieu, P. Lasjaunias, 2000, Journal of child neurology.

Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

H. Waterham, R. Wanders, W. Kuis, 2001, European Journal of Human Genetics.

Allelic heterogeneity of SMARD1 at the IGHMBP2 locus

A. Munnich, J. Melki, L. Viollet, 2004, Human mutation.

Allelic Heterogeneity of SMARD1 at the IGHMBP2

A. Munnich, J. Melki, L. Viollet, 2004 .

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis

T. Eggermann, K. Huehne, B. Rautenstrauss, 2008, Neuromuscular Disorders.

Peripheral neuropathy with hypomyelination, chronic intestinal pseudo‐obstruction and deafness: A developmental “neural crest syndrome” related to a SOX10 mutation

C. Lacroix, S. Lyonnet, C. Faure, 2000, Annals of neurology.

Acute inflammatory demyelinating polyradiculopathy in children: Clinical and electrodiagnostic studies

S. Metral, C. Delanoé, P. Landrieu, 1998, Annals of neurology.

Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndrome.

P. Rustin, P. Landrieu, C. Rambaud, 1997, The Journal of pediatrics.

Nervous and Ocular Disorders in Children with Cholestasis and Vitamin A and E Deficiencies

P. Landrieu, M. Odiévre, D. Alagille, 2007, Hepatology.

Transient Cerebral Arteriopathy: A Disorder Recognized by Serial Angiograms in Children With Stroke

M. Tardieu, P. Landrieu, P. Lasjaunias, 1998, Journal of child neurology.

Sturge-Weber disease with repercussion on the prenatal development of the cerebral hemisphere.

P. Landrieu, P. Lasjaunias, B. Husson, 2002, AJNR. American journal of neuroradiology.

Aphasia Owing to Subcortical Brain Infarcts in Childhood

C. Grandin, P. Landrieu, A. Gout, 2005, Journal of child neurology.

Acute Transverse Myelitis in Children: Clinical Course and Prognostic Factors

M. Tardieu, P. Landrieu, G. Sébire, 2003, Journal of child neurology.

Efficacy of high dose steroid therapy in children with severe acute transverse myelitis

M. Tardieu, P. Landrieu, C. Nuttin, 2001, Journal of neurology, neurosurgery, and psychiatry.

Leukoencephalopathy with vanishing white matter caused by compound heterozygous mutations in mitochondrial complex I NDUFS1 subunit.

A. Legrand, P. Landrieu, A. Slama, 2010, Molecular genetics and metabolism.

Rapid screening for nuclear genes mutations in isolated respiratory chain complex I defects.

A. Legrand, P. Landrieu, A. Slama, 2009, Molecular genetics and metabolism.

Hematologic Involvement in Mitochondrial Cytopathies in Childhood: A Retrospective Study of Bone Marrow Smears

B. Bader-Meunier, P. Landrieu, G. Tchernia, 1999, Pediatric Research.

Prenatal Encephalopathies of Vascular Origin

P. Landrieu, 1994 .

Coma associated with intense bursts of abnormal movements and long-lasting cognitive disturbances: an acute encephalopathy of obscure origin.

J. Aicardi, M. Tardieu, P. Landrieu, 1992, The Journal of pediatrics.

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

Jonathan C. Fuller, D. Bonthron, E. Bertini, 2009, Nature Genetics.

Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

A. Green, D. Bonthron, E. Bertini, 2007, American journal of human genetics.

Central nervous system lesions in hypomclanosis of Ito: an MRI and pathological study

C. Lacroix, M. Tardieu, P. Landrieu, 1993, Journal of Neurology.

Refractory anaemia and mitochondrial cytopathy in childhood

A. Munnich, P. Rustin, B. Bader-Meunier, 1994, British journal of haematology.

A Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease

A. Goffinet, P. Landrieu, E. Giustina, 2004, Acta Neuropathologica.

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

A. Munnich, C. Fallet-Bianco, I. Gut, 2021, Journal of Medical Genetics.

Acute Cerebellar Atrophy in Encephalitis

P. Landrieu, B. Tabarki, B. Husson, 1998, Journal of child neurology.

PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome.

A. Munnich, D. Gozal, S. Lyonnet, 2008, American journal of respiratory and critical care medicine.

Giant axonal neuropathy locus refinement to a < 590 kb critical interval

M. Hamida, D. Callen, H. Topaloglu, 2000, European Journal of Human Genetics.

Aggregation of a subpopulation of vimentin filaments in cultured human skin fibroblasts derived from patients with giant axonal neuropathy.

J. Hauw, M. Basseville, P. Landrieu, 1996, Cell motility and the cytoskeleton.

Analysis of a splice-site mutation in the sap-precursor gene of a patient with metachromatic leukodystrophy.

K. Sandhoff, P. Landrieu, M. Vanier, 1996, American journal of human genetics.

Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event

C. Junien, P. Landrieu, M. Mannens, 1993, European journal of human genetics : EJHG.

Mechanisms underlying a life‐threatening skeletal muscle Na+ channel disorder

S. Bendahhou, D. Simkin, B. Fontaine, 2011, The Journal of physiology.

Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.

A. Munnich, P. Rustin, A. Rötig, 1994, The Journal of clinical investigation.

Bone marrow transplantation in metachromatic leukodystrophy caused by saposin-B deficiency: a case report with a 3-year follow-up period.

S. Metral, K. Sandhoff, P. Landrieu, 1998, The Journal of pediatrics.

Vitamin E deficiency is responsible for neurologic abnormalities in cholestatic children.

F. Alvarez, P. Landrieu, C. Féo, 1985, The Journal of pediatrics.

The association between developmental handicaps and traumatic brain injury during pregnancy: An issue that deserves more systematic evaluation

P. Landrieu, E. Papiernik, C. Bonnier, 2006, Brain injury.

Critical illness neuromuscular disease: clinical, electrophysiological, and prognostic aspects

P. Landrieu, P. V. D. Van den Bergh, G. Sébire, 2002, Archives of disease in childhood.

Vein of Galen aneurysmal malformations

P. Landrieu, K. terBrugge, P. Lasjaunias, 2007, Acta Neurochirurgica.

Short- and long-term prognostic value of the electroencephalogram in children with severe head injury.

P. Landrieu, Y Navelet, P Landrieu, 1989, Electroencephalography and clinical neurophysiology.

Treatment of vein of Galen aneurysmal malformation.

P. Landrieu, P. Lasjaunias, G. Rodesch, 1989, Journal of neurosurgery.

Early onset (childhood) monogenic neuropathies.

P. Landrieu, J. Baets, 2013, Handbook of clinical neurology.

Insidious peripheral neuropathy occurring under treatment in infantile MTHFR deficiency

P. Landrieu, J. Zittoun, F. Mesrati, 2009, Journal of Inherited Metabolic Disease.

[A spectacular and benign syndrome of neonatal convulsions: deep sleep myoclonus].

M. Tardieu, P. Landrieu, Y. Navelet, 1986, Archives francaises de pediatrie.

High dose methylprednisolone in severe acute transverse myelopathy

M. Tardieu, P. Landrieu, G. Sébire, 1997, Archives of Disease in Childhood.

Aqueductal Stenosis in X‐Linked Hydrocephalus: a Secondary Phenomenon?

P. Landrieu, G. Lyon, G. Ferrière, 1979, Developmental medicine and child neurology.

Ectopic secreting choroid plexus in the oropharynx.

P. Landrieu, P. Lasjaunias, J. Comoy, 1985, Pediatric neuroscience.

Heterozygous FIC1 deficiency: a new genetic predisposition to transient neonatal cholestasis.

P. Landrieu, M. Rio, E. Jacquemin, 2010, Journal of pediatric gastroenterology and nutrition.

Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathies

B. Gilbert-Dussardier, M. Gonzalès, B. Grandchamp, 2011, Neuromuscular Disorders.

MRI-neuropathological correlations in type 1 lissencephaly

C. Lacroix, P. Landrieu, D. Pariente, 1998, Neuroradiology.

SMN gene deletion in variant of infantile spinal muscular atrophy

A. Munnich, J. Melki, S. Lefebvre, 1995, The Lancet.

Motor Outcomes After Neonatal Arterial Ischemic Stroke Related to Early MRI Data in a Prospective Study

L. Hertz-Pannier, P. Landrieu, S. Chabrier, 2010, Pediatrics.

Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases

L. Vallée, O. Boespflug-Tanguy, M. Tardieu, 2004, Journal of Medical Genetics.

New insights (and new interrogations) in perinatal arterial ischemic stroke.

M. Dinomais, P. Landrieu, S. Chabrier, 2011, Thrombosis research.

Cerebral Proliferative Angiopathy: Clinical and Angiographic Description of an Entity Different From Cerebral AVMs

T. Krings, A. Ozanne, P. Landrieu, 2008, Stroke.

MR angiography findings in infants with neonatal arterial ischemic stroke in the middle cerebral artery territory: A prospective study using circle of Willis MR angiography.

L. Hertz-Pannier, C. Adamsbaum, M. Dinomais, 2016, European journal of radiology.

Central nervous system lesions in hypomelanosis of Ito: an MRI and pathological study.

C. Lacroix, M. Tardieu, P. Landrieu, 1993, Journal of neurology.

Haemorrhagic shock and encephalopathy syndrome: neurological course and predictors of outcome

P. Landrieu, G. Sébire, Y. Navelet, 1999, Intensive Care Medicine.

Club feet with congenital perisylvian polymicrogyria possibly due to bifocal ischemic damage of the neuraxis in utero

P. Landrieu, H. Bensahel, F. Kammoun, 2004, American journal of medical genetics. Part A.

Vein of Galen aneurysmal malformations. Report of 36 cases managed between 1982 and 1988.

P. Landrieu, K. terBrugge, P. Lasjaunias, 1989, Acta neurochirurgica.

Relations between molecular and biological abnormalities in 11 families from siblings affected with methylenetetrahydrofolate reductase deficiency

B. Echenne, J. Saudubray, P. Landrieu, 2003, European Journal of Pediatrics.

Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

L. Lagae, A. Vanderver, R. Schiffmann, 2016, Nature Genetics.

TUBERCULOUS MENINGITIS DUE TO BCG IN TWO PREVIOUSLY HEALTHY CHILDREN

M. Tardieu, P. Landrieu, C. Truffot-Pernot, 1988, The Lancet.

Unusual clinical expression and long survival of a pseudouridylate synthase (PUS1) mutation into adulthood

A. Munnich, A. Rötig, B. Bader-Meunier, 2014, European Journal of Human Genetics.

Peripheral neuropathy in type A Niemann-Pick disease

P. Landrieu, G. Saïd, 1984, Acta Neuropathologica.

Extensive macrogyri or no visible gyri

J. Aicardi, M. Tardieu, P. Landrieu, 1995, Neurology.

[Prevention of febrile convulsions and kinetics of diazepam per os].

M. Tardieu, P. Landrieu, A. Taburet, 1984, Archives francaises de pediatrie.

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.

I. Gut, M. Bayés, J. Melki, 2014, Human molecular genetics.

Prenatal Cytomegalovirus Disease and Cerebral Microgyria: Evidence for Perfusion Failure, not Disturbance of Histogenesis, as the Major Cause of Fetal Cytomegalovirus Encephalopathy

P. Landrieu, G. Lyon, G. Harmant-van Rijckevorsel, 1984, Neuropediatrics.

Familial isolated vitamin E deficiency. Extensive study of a large family with a 5-year therapeutic follow-up

P. Landrieu, J. Amiel, J. Mazière, 1995, Journal of Inherited Metabolic Disease.

[Schwann cell pathology and axonal reduction in a case of congenital neuropathy with hypomyelinization].

S. Metral, P. Landrieu, D. Cau, 1985, Archives francaises de pediatrie.

Submicroscopic deletions of 17p13.3 in type 1 Lissencephaly

M. Tardieu, P. Landrieu, N. Miladi, 1994, Human Genetics.

Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.

N. Romero, P. Landrieu, N. Monnier, 2001, Human molecular genetics.

[SPECT-identified hypoperfusion of the left temporomesial structures in a Kleine-Levin syndrome].

E. Durand, P. Landrieu, A. Prigent, 2002, Revue neurologique.

[Primary amenorrhea revealing congenital hydrocephalus].

P. Landrieu, M. Zérah, E. Thibaud, 1996, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Respiratory Chain Deficiency in Alpers Syndrome

A. Munnich, P. Rustin, A. Rötig, 2001, Neuropediatrics.

Anterior Spinal Artery Syndrome Mimicking Infantile Spinal Muscular Atrophy

S. Metral, C. Lacroix, P. Landrieu, 1993, American journal of perinatology.

[Sex-linked, nonprogressive, familial chorea].

M. Tardieu, P. Landrieu, J. Lapresle, 1984, Revue neurologique.

[Neurogenic bladder in children with acute transverse myelopathy].

M. Tardieu, P. Landrieu, G. Sébire, 1998, Archives de pédiatrie.

[Encephalopathy associated with severe bacterial infections: "presuppurative encephalitis" or "toxi-infectious disorder"?].

P. Nordmann, P. Landrieu, V. P. Thi, 2002, Revue neurologique (Paris).

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

M. Koenig, B. Tüysüz, H. Topaloglu, 2000, Nature Genetics.

Infantile neuropathy with unstable myelin: study of the Po protein

C. Lacroix, J. Deleuze, S. Peudenier, 1993, Journal of Neurology.

Progressive neuronal degeneration of childhood: prenatal diagnosis by MRI

C. Lacroix, P. Landrieu, N. Villeneuve, 2005, Prenatal Diagnosis.

[Cataplexy revealing an atypical form of Niemann-Pick disease type C].

P. Landrieu, M. Vanier, C. Rodriguez-Lafrasse, 1991, Archives francaises de pediatrie.

E Y cacy of high dose steroid therapy in children with severe acute transverse myelitis

P. Landrieu, C. Nuttin, G. Sébire, 2001 .

EYcacy of high dose steroid therapy in children with severe acute transverse myelitis

P. Landrieu, C. Nuttin, G. Sébire, 2001 .

Locked in syndrome with a favourable outcome

M. Tardieu, P. Landrieu, A. Menget, 1984, European Journal of Pediatrics.

Efficacy of high dose steroid therapy in children with severe acute transverse myelitis

M. Tardieu, P. Landrieu, C. Nuttin, 2001, Journal of neurology, neurosurgery, and psychiatry.

Peripheral nerve involvement in children with chronic cholestasis and vitamin E deficiency. A clinical, electrophysiological and morphological study.

F. Alvarez, S. Metral, P. Landrieu, 1985, Neuropediatrics.

Congenital unilateral perisylvian syndrome: radiological basis and clinical correlations.

M. Tardieu, P. Landrieu, G. Sébire, 1996, Journal of neurology, neurosurgery, and psychiatry.

A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency

D. Galanaud, N. Boddaert, A. Rötig, 2010, Journal of Medical Genetics.

Liver Peroxisome Damage during Acute Hepatic Failure in Partial Ornithine Transcarbamylase Deficiency

P. Landrieu, F. Hoof, G. Lyon, 1982, Pediatric Research.