J. Julien

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Evidence of presence of poliovirus genomic sequences in cerebrospinal fluid from patients with postpolio syndrome

H. Kopecká, F. Fuchs, M. Aymard, 1996, Journal of clinical microbiology.

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family

E. Pegoraro, R. Petersen, P. Gambetti, 1997, Neurology.

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

P Brown, M. Tabaton, P. Cortelli, 1992, Science.

Extensive cerebral calcification and retinal changes in pseudohypoparathyroidism

X. Ferrer, J. Julien, E. Ellie, 1989, Journal of Neurology.

Unilateral diaphragmatic paralysis: an electrophysiological study.

R. Marthan, M. Barat, J. Julien, 1992, Journal of neurology, neurosurgery, and psychiatry.

Adrenomyeloneuropathy: demonstration of inclusions at the level of the peripheral nerve.

D. Darriet, J. Vallat, X. Ferrer, 1981, European neurology.

Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

A. Ducros, E. Tournier-Lasserve, X. Ferrer, 2001, Journal of Neurology.

Congenital insensitivity to pain with anhydrosis. Report of two unrelated cases.

G. Ponsot, A. Vital, J. Julien, 1998, Journal of the peripheral nervous system : JPNS.

Peripheral myelin modification in CMT1B correlates with MPZ gene mutations

G. L. Masson, P. Latour, I. Bernard, 1999, Neuromuscular Disorders.

IgM Demyelinative neuropathy with amyloidosis and biclonal gammopathy

J. Vallat, X. Ferrer, J. Julien, 1984, Annals of neurology.

The French FFI Cases

J. Julien, C. Vital, G. Géraud, 1998, Brain pathology.

Familial idiopathic striopallidodentate calcifications

X. Ferrer, J. Julien, E. Ellie, 1989, Neurology.

Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 cases

B. Guiraud-Chaumeil, A. Steck, M. Barat, 2000, Acta Neuropathologica.

Myelin modifications in 8 cases of peripheral neuropathy with Waldenström's macroglobulinemia and anti-MAG activity.

A. Steck, A. Vital, J. Julien, 1997, Ultrastructural pathology.

Neuropathy associated with “benign” anti-myelin-associated glycoprotein IgM gammopathy: Clinical, immunological, neurophysiological pathological findings and response to treatment in 33 cases

A. Steck, A. Vital, J. Julien, 2004, Journal of Neurology.

Morphological findings on peripheral nerve biopsies in 15 patients with human immunodeficiency virus infection

M. Beylot, A. Vital, J. Julien, 2004, Acta Neuropathologica.

[Neurologic manifestations of Lyme disease. Apropos of 25 cases].

J. Ragnaud, P. Morlat, J. Orgogozo, 1995, La Revue de medecine interne.

Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 cases.

K. Petry, J. Orgogozo, M. Barat, 2000, Ultrastructural pathology.

Widespread dilatation of perivascular spaces

J. Julien, C. Vital, 1997, Neurology.

Thrombotic thrombocytopenic purpura associated with ticlopidine.

J. Julien, E. Ellie, C. Durrieu, 1992, Stroke.

Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I

A. Vital, J. Julien, C. Vital, 2004, Acta Neuropathologica.

Postpolio syndrome: poliovirus persistence is involved in the pathogenesis

B. Lina, H. Kopecká, F. Fuchs, 1999, Journal of Neurology.

Polyneuropathy associated with IgM monoclonal gammopathy

A. Steck, A. Vital, J. Julien, 1989, Acta Neuropathologica.

Primary meningeal B lymphoma presenting as a subacute ascending polyradiculoneuropathy.

X. Ferrer, J. Julien, C. Vital, 1991, Journal of neurology, neurosurgery, and psychiatry.

Subacute inflammatory polyneuropathy: two cases with plasmacytoid histiocytes in the endoneurium.

A. Vital, J. Julien, C. Vital, 1998, Ultrastructural pathology.

Polyneuropathy in Waldenström's macroglobulinemia. Deposition of M component on myelin sheaths.

D. Darriet, J. Vallat, J. Julien, 1978, Archives of neurology.

Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and "fingerprint" inclusions.

J. Vallat, J. Julien, C. Vital, 1974, Journal of the neurological sciences.

Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects

P Brown, B. Ghetti, A. Giese, 1999, Annals of neurology.

Myopathy and cerebellar syndrome during acute poisoning with lithium carbonate.

J. Vallat, J. Julien, C. Vital, 1979, Muscle & nerve.

CT and high-field MRI in septic thrombosis of the cavernous sinuses

J. Drouillard, J. Julien, B. Houang, 2004, Neuroradiology.

Cavernous sinus syndrome due to lymphoma.

J. Drouillard, X. Ferrer, J. Julien, 1984, Journal of neurology, neurosurgery, and psychiatry.

Peripheral neuropathies and lymphoma without monoclonal gammopathy: a new classification

M. Barat, A. Vital, J. Julien, 1990, Journal of Neurology.

Jaw closing spasm--a form of focal dystonia? An electrophysiological study.

X. Ferrer, J. Julien, J. Demotes-Mainard, 1989, Journal of neurology, neurosurgery, and psychiatry.

[Our experience with acute necrotizing encephalitis. Demonstration of herpes virus by the electron microscope].

J. Julien, C. Vital, M. Duvert, 1968, La Presse medicale.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.

B. Dubois, M. Vérin, F. Viader, 1996, American journal of human genetics.

Clinical spectrum of CADASIL: a study of 7 families

B. Dubois, M. Krebs, H. Chabriat, 1995, The Lancet.

A transthyretin variant (alanine 49) associated with familial amyloidotic polyneuropathy in a French family.

J. Liepnieks, M. Benson, J. Julien, 1993, Journal of medical genetics.

Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features

Alexandra Durr, Charles Duyckaerts, Yves Agid, 1996, Annals of neurology.

Thalidomide neuropathy: An electrophysiologic study

J. Julien, A. Taieb, M. Doutre, 1986, Muscle & nerve.

[Ovular myopathy with primary hypogonadism. Mitochondrial abnormalities in ultrastructural study].

J. Vallat, J. Julien, C. Vital, 1973, Revue neurologique.

Inclusion body myositis Clinical, biological and ultrastructural study

J. Vallat, J. Julien, C. Vital, 1982, Journal of the Neurological Sciences.

[Autosomal dominant centronuclear myopathy].

X. Ferrer, J. Julien, C. Vital, 2020, Revue neurologique.

[Divry-Van Bogaert cortico-meningeal angiomatosis and Sneddon's syndrome. Nosological study. Apropos of 4 cases].

X. Ferrer, J. Julien, C. Vital, 1987, Revue neurologique.

Gonadotrophins, livedo reticularis, and strokes.

J. Julien, G. Le Masson, E. Ellie, 1990, Stroke.

Nuclear inclusions in oculopharyngeal dystrophy An ultrastructural study of six cases

J. Orgogozo, P. Loiseau, J. Vallat, 1983, Journal of the Neurological Sciences.

Presence of inclusion body myositis‐like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases

J. Julien, C. Vital, M. Coquet, 1990, Neuropathology and applied neurobiology.

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

J. Weissenbach, Y. Agid, R. Sherrington, 1996, Human molecular genetics.

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

F. Chédru, F. Tison, G. Ponsot, 1999, American journal of human genetics.

Expanding lacunae causing triventricular hydrocephalus.

J. Julien, C. Vital, 2000, Journal of neurosurgery.

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.

J. Mandel, A. Hanauer, V. Biancalana, 1992, Human molecular genetics.

Cervical cord compression by solitary osteochondroma of the atlas.

J. Julien, C. Vital, V. Riemens, 1978, Journal of neurology, neurosurgery, and psychiatry.

Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits

R. Petersen, P. Gambetti, X. Ferrer, 1998, Neuropathology and applied neurobiology.

Allelic origin of the abnormal prion protein isoform in familial prion diseases

E. Cochran, Shu G. Chen, P. Brown, 1997, Nature Medicine.

Clinical Features of Fatal Familial Insomnia: Phenotypic Variability in Relation to a Polymorphism at Codon 129 of the Prion Protein Gene

G. Plazzi, P. Cortelli, P. Avoni, 1998, Brain pathology.

High-frequency stimulation of the globus pallidus internalis in Parkinson's disease: a study of seven cases.

D. Guehl, B. Bioulac, T. Boraud, 1997, Journal of neurosurgery.

Guillain—Barré syndrome and Hodgkin's disease Ultrastructural study of a peripheral nerve

D. Darriet, J. Julien, C. Vital, 1980, Journal of the Neurological Sciences.

Epilepsy and agitated delirium caused by an astrocytoma of the amygdala.

J. Vallat, J. Julien, C. Vital, 1979, European neurology.

Isolated peripheral nerve relapse masquerading as Guillain-Barré syndrome in a patient with acute lymphoblastic leukemia.

A. Vital, J. Julien, C. Vital, 1993, Leukemia & lymphoma.

High‐grade B‐cell cerebral lymphoma in a patient with anti‐myelin‐associated glycoprotein IgM paraproteinemic neuropathy

A. Steck, A. Vital, J. Julien, 1995, Neurology.

Uncompacted myelin lamellae in two cases of peripheral neuropathy

J. Julien, C. Vital, A. Lagueny, 2004, Acta Neuropathologica.

Chronic demyelinating neuropathy with IgM‐producing lymphocytes in peripheral nerve and delayed appearance of “benign” monoclonal gammopathy

J. Vallat, J. Julien, C. Vital, 1984, Neurology.

Multiple sclerosis: an overview.

X. Ferrer, J. Julien, 1989, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[Post-radiotherapy anterior horn cell syndrome].

X. Ferrer, J. Julien, A. Lagueny, 1985, Revue neurologique.

La chorée-acanthocytose.

X. Ferrer, J. Julien, A. Lagueny, 1990 .

Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A

P. Latour, X. Ferrer, A. Vital, 2000, Journal of the peripheral nervous system : JPNS.

Jaw dystonia triggered by biting into hard food

P. Caix, J. Julien, A. Lagueny, 1991, Movement Disorders.

Parkinsonism in a patient with Leber hereditary optic neuropathy (LHON).

M. Martin-Négrier, X. Ferrer, A. Vital, 2015, Revue neurologique.

Involvement of respiratory muscles in adult‐onset dystonia: A clinical and electrophysiological study

G. L. Masson, P. Burbaud, X. Ferrer, 1995, Movement disorders : official journal of the Movement Disorder Society.

Enzyme immunoassay for myelin basic protein in cerebrospinal fluid.

V. Dousset, B. Brochet, J. Julien, 1997, Brain research. Brain research protocols.

Hereditary motor and sensory neuropathy type II with axonal lesions

X. Ferrer, J. Julien, C. Vital, 1988, Journal of Neurology.

[Myopathy in adults caused by acid maltase deficiency. A trial of treatment with high protein diet].

C. Desnuelle, X. Ferrer, T. Levade, 1992, La Revue de medecine interne.

Chronic relapsing idiopathic polyneuropathy with primary axonal lesions.

X. Ferrer, J. Julien, C. Vital, 1989, Journal of neurology, neurosurgery, and psychiatry.

Neuropathie a tomacula. Etude electrophysiologique

X. Ferrer, A. Vital, J. Julien, 1985 .

Idiopathic CD4+ T-cell lymphocytopenia and subacute inflammatory demyelinating polyradiculoneuropathy

X. Ferrer, J. Julien, C. Vital, 1995, Neurology.

Prion disease with octapeptide repeat insertion.

X. Ferrer, A. Vital, J. Julien, 1999, Clinical and experimental pathology.

[Paraneoplastic encephalomyelitis. Apropos of an anatomical and clinical observation].

J. Julien, C. Vital, 1969, Revue neurologique.

[De Quervain's tenosynovitis: a cause of compression of the superficial branch of the radial nerve].

J. Julien, A. Lagueny, R. Bullier, 1981, La Nouvelle presse medicale.

Delayed onset movement disorders as a complication of central pontine myelinolysis

F. Tison, J. Julien, X. Ferre, 1991, Movement disorders : official journal of the Movement Disorder Society.

[Neurogenic muscular hypertrophy. Association with abnormal electrophysiological activities].

X. Ferrer, J. Julien, C. Vital, 1987, Revue neurologique.

Inclusion body myositis Clinical, biological and ultrastructural study

J. Vallat, J. Julien, C. Vital, 1982, Journal of the Neurological Sciences.

[Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study].

J. Vallat, J. Julien, C. Vital, 1970, Revue neurologique (Paris).