J. Mussini

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J. Mussini, J M Mussini, 1982, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris.

Treatment of graft-versus-host disease by extracorporeal photochemotherapy: a pilot study.

B. Mahé, N. Milpied, J. Mussini, 1997, Transplantation.

Macrophagic myofasciitis: an emerging entity

P. Laforêt, F. Authier, M. Fardeau, 1998, The Lancet.

Sjögren's syndrome-associated myositis with germinal centre-like structures.

A. Néel, A. Masseau, M. Hamidou, 2017, Autoimmunity reviews.

[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].

D. Hannequin, A. Toutain, V. Drouin‐Garraud, 2005, Revue neurologique.

The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy

M. Lathrop, A. Nègre-Salvayre, P. Laforêt, 2007, Nature Genetics.

A prospective study of criteria for the diagnosis of toxoplasmic encephalitis in 186 AIDS patients

P. Morlat, F. Raffi, C. Michelet, 1997, AIDS.

Long-term efficacy of mycophenolate mofetil in a case of refractory antisynthetase syndrome.

A. Masseau, M. Hamidou, J. Mussini, 2009, Joint, bone, spine : revue du rhumatisme.

Muscle biopsy in anti-neutrophil cytoplasmic antibody-associated vasculitis: diagnostic yield depends on anti-neutrophil cytoplasmic antibody type, sex and neutrophil count.

C. Volteau, A. Néel, A. Masseau, 2020, Rheumatology.

Neurotoxicological Assessment After Intracisternal Injection of Liposomal Bupivacaine in Rabbits

D. Benhamou, M. Pinaud, G. Couarraze, 1997, Anesthesia and analgesia.

Adult sphingomyelinase deficiency

J. Hauw, M. Auclair, J. Mazière, 1990, Neurology.

Long-term prognosis of 69 patients with dermatomyositis or polymyositis.

J. Berthelot, Y. Maugars, A. Prost, 1996, Clinical and experimental rheumatology.

Immunofluorescence studies of intra cytoplasmic immunoglobulin binding lymphoid cells (CILC) in the central nervous system. Report of 32 cases including 19 multiple sclerosis

J. Hauw, R. Escourolle, J. Mussini, 1977, Acta Neuropathologica.

ACUTE LYMPHOBLASTIC LEUKEMIA ASSOCIATED WITH DERMATOMYOSITIS IN A CHILD

J. Harousseau, J. Stalder, F. Millot, 1993, Pediatric dermatology.

Is Ketamine or Its Preservative Responsible for Neurotoxicity in the Rabbit?

J. Mussini, J. Malinovsky, J. Lepage, 1993, Anesthesiology.

Ketamine and midazolam neurotoxicity in the rabbit.

M. Pinaud, J. Mussini, J. Malinovsky, 1991, Anesthesiology.

Distal inflammatory myopathy: Unusual presentation of polymyositis or new entity?

T. Maisonobe, O. Dubourg, P. Laforêt, 2008, Neuromuscular Disorders.

Use of Muscle Biopsies for Diagnosis of Systemic Vasculitides

A. Masseau, M. Hamidou, J. Mussini, 2011, The Journal of Rheumatology.

Intracytoplasmic immunoglobulin-binding lymphoid cells (IgGLC) of the cerebrospinal fluid in multiple sclerosis and other neurological disorders.

J. Hauw, R. Escourolle, J. Mussini, 1980, Annales d'immunologie.

Combined Nomarski interference contrast and immunofluorescent study of neuropathological specimens: CSF sediments and paraffin embedded brain tissues.

J. Hauw, R. Escourolle, J. Mussini, 1977, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

[Heart arrest during general anesthesia in a child with unrecognized Duchenne's dystrophy].

A. Bigot, J. Mussini, J. Arnould, 1986, Annales francaises d'anesthesie et de reanimation.

Pathology of the Central Nervous System in Chester‐Erdheim Disease: Report of Three Cases

H. Adle-Biassette, J. Chetritt, F. Gray, 1997, Journal of neuropathology and experimental neurology.

Chester-Erdheim disease: a neoplastic disorder.

V. Paradis, P. Bedossa, C. Maurage, 1999, Human pathology.

Skin patch, polyneuropathy, and paraproteinemia.

P. Moreau, S. Barbarot, L. Musset, 2012, The American journal of medicine.

A Monoclonal Antibody to O-Acetyl-GD2 Ganglioside and Not to GD2 Shows Potent Anti-Tumor Activity without Peripheral Nervous System Cross-Reactivity

F. Paris, J. Barbet, T. Chaumette, 2011, PloS one.

Use of 1-Pyrenedecanoic Acid for Demonstrating the Catabolic Block of Cytoplasmic Triacylglycerols in a Lymphoid Cell Line Established from a Patient Affected with Multisystemic Lipid Storage Myopathy (Type 3)

M. Vuillaume, R. Salvayre, A. Maret, 1988 .

Neurophysiological investigation of neurological complication after regional anaesthesia.

Y. Péréon, J. Mussini, J. Malinovsky, 2002, Anaesthesia.

Becker‐type muscular dystrophy

W. Bradley, P. Fawcett, J. Mussini, 1978, Muscle & nerve.

CHLORBUTANOL IS RESPONSIBLE FOR KETAMINE NEUROTOXICITY IN RABBITS

M. Pinaud, J. Mussini, J. Malinovsky, 1991 .

Rigid spine syndrome: histological examinations of male and female cases.

J. Hauw, A. Prost, F. Gray, 1981, Acta neuropathologica. Supplementum.

[Rigid-spine syndrome in a female patient (author's transl)].

A. Prost, J. Mathé, F. Gray, 1982, Revue neurologique.

Two novel variants in CNTNAP1 in two siblings presenting with congenital hypotonia and hypomyelinating neuropathy

S. Küry, C. Bénéteau, B. Cogné, 2016, European Journal of Human Genetics.

Extracorporeal photochemotherapy for secondary chronic progressive multiple sclerosis: a pilot study

B. Dupas, J. Mussini, D. Chabannes, 2002, Photodermatology, photoimmunology & photomedicine.

A new MPZ mutation associated with a mild CMT1 phenotype presenting with recurrent nerve compression

P. Guiheneuc, Y. Péréon, P. Latour, 2008, Muscle & nerve.

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

A. Munnich, D. Figarella-Branger, S. Küry, 2015, Orphanet Journal of Rare Diseases.

Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis.

R. Redon, A. Munnich, B. Keavney, 2013, American journal of human genetics.

A severe congenital myasthenic syndrome with ” dropped head ” caused by novel MUSK mutations

B. Isidor, A. Magot, X. Ferrer, 2017 .

Muscle magnetic resonance imaging abnormalities in X‐linked myopathy with excessive autophagy

S. Mercier, Y. Péréon, B. Isidor, 2015, Muscle & nerve.

Crushed and Injected Buprenorphine Tablets: Characteristics of Princeps and Generic Solutions

P. Jolliet, J. Mussini, C. Victorri-Vigneau, 2014, PloS one.

[Cerebral radionecrosis discovered 32 years after conventional irradiation therapy for a pituitary adenoma (author's transl)].

C. Magne, J. Mathé, J. Mussini, 1980, Revue neurologique (Paris).

Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series

J. Lefaucheur, G. Bassez, B. Eymard, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia

S. Küry, Y. Péréon, S. Barbarot, 2017, Clinical genetics.

Malignant sellar, parasellar and skull base tumors

D. Khayat, B. Dupas, B. Charbonnel, 1998 .

[Vascular manifestation of thoracic outlet syndrome. Prospective study of 104 patients].

B. Planchon, P. de Faucal, J. Mussini, 1991, Journal des maladies vasculaires.

Is there a maturation defect related to calcium in muscle mitochondria from dystrophic mice and Duchenne and Becker muscular dystrophy patients?

J. Mussini, B. Lucas-Héron, B. Ollivier, 1989, Journal of the Neurological Sciences.

The Spectrum of Renal Involvement in Patients With Inflammatory Myopathies

E. Hachulla, M. Laville, P. Rémy, 2014, Medicine.

A case of myelofibrosis with aberrant myelogenesis in neuromuscular biopsy

M. Leporrier, J. Mussini, M. Poisson, 1979, Muscle and Nerve.

[Quantitative study of the peripheral nerve in semi-thin section by the Nomarski interference contrast technic].

B. Vanderkelen, J. Hauw, R. Escourolle, 1977, Revue neurologique.

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.

[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)].

T. Maisonobe, P. Laforêt, B. Eymard, 2000, Presse medicale.

[Macrophagic myofasciitis: description and etiopathogenic hypotheses. Study and Research Group on Acquired and Dysimmunity-related Muscular Diseases (GERMMAD) of the French Association against Myopathies (AFM)].

T. Maisonobe, P. Laforêt, F. Authier, 1999, La Revue de medecine interne.

Biochemical and ultrastructural features of human fibroblasts cultured from a new variant of type 3 lipid storage myopathy

S. Billaudel, R. Salvayre, A. Maret, 1988, Biology of the cell.

[Antisynthetase syndrome. Three cases and a review of the literature].

M. Hamidou, C. Agard, J. Mussini, 2003, Annales de medecine interne.

Subversion of human intestinal mucosa innate immunity by a Crohn’s disease-associated E. coli

N. Caroff, A. Jarry, J. Mosnier, 2014, Mucosal Immunology.

Atypical nuclear abnormalities in a patient with Brody disease

Y. Péréon, A. Magot, D. Sternberg, 2015, Neuromuscular Disorders.

Stabilisation of a severe case of P.O.E.M.S. syndrome after tamoxifen administration.

J. Brisseau, J. Mussini, J. Barrier, 1989, Journal of neurology, neurosurgery, and psychiatry.

Intravenous cyclophosphamide in refractory polyneuropathy associated with IgM monoclonal gammopathy: an uncontrolled open trial.

M. Hamidou, J. Mussini, S. Wiertlewsky, 2005, The American journal of medicine.

Polymyositis with infiltration by lymphoid follicles.

J. Hauw, A. Buge, R. Escourolle, 1981, Archives of neurology.

Abnormalities of the intracerebral vasculature in a case of neurofibromatosis.

L. Picard, J. Mussini, Y. Lajat, 1980, Journal of neuroradiology. Journal de neuroradiologie.

In situ immunophenotype of the inflammatory infiltrate in eosinophilic fasciitis.

A. Jarry, S. Barbarot, K. Renaudin, 2003, Journal of Rheumatology.

[Primary Gougerot-Sjögren syndrome with necrotizing polymyositis: favorable effect of hydroxychloroquine].

J. Mussini, S. Cottin, J. Grolleau, 1987, Revue neurologique.

Interstitial nephritis in a case of phenylbutazone hypersensitivity.

J. Walls, G. Russell, J. Mussini, 1978, British medical journal.