J. Leroy

发表

Transgene expression kinetics after transfection with cationic phosphonolipids in hematopoietic non adherent cells.

C. Férec, C. Guillaume, J. Yaouanc, 1998, Biochimica et biophysica acta.

Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia.

N. Romero, L. Viollet, J. Leroy, 2003, Brain : a journal of neurology.

Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiency

G. Bassez, P. Carlier, P. Laforêt, 2003, Neuromuscular Disorders.

A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene

A. Lemainque, C. Bönnemann, N. Romero, 2002, Annals of neurology.

Improving Sun Protection Behaviour in Children: Study Design and Baseline Results of a Randomized Trial in Italian Elementary Schools

J. Utikal, C. Klemke, T. Waldmann, 2003, Dermatology.

The binding of some human antiendothelial cell antibodies induces endothelial cell apoptosis.

J. Piette, Y. Shoenfeld, Y. Levy, 1998, The Journal of clinical investigation.

Systemic administration of cationic phosphonolipids/DNA complexes and the relationship between formulation and lung transfection efficiency.

C. Férec, C. Guillaume, P. Delépine, 2000, Biochimica et biophysica acta.

Intravenous pulse cyclophosphamide therapy in myositis and Sjögren's syndrome.

P. Youinou, A. Drosos, J. Leroy, 1990, Arthritis and rheumatism.

A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis

N. Romero, J. Hogrel, P. Laforêt, 2006, Neuromuscular Disorders.

Severe renal involvement in primary Sjogren's syndrome.

J. Clèdes, J. Leroy, J. Hervé, 1989, Advances in experimental medicine and biology.

The origin of tubular aggregates in human myopathies

B. Eymard, J. Leroy, F. Chevessier, 2005, The Journal of pathology.

[Hyperimmunoglobulinemia D or periodic fever syndrome. Cutaneous manifestations in 3 cases].

H. Cartier, J. Leroy, D. Mottier, 1996, Annales de dermatologie et de venereologie.

Phosphonocationic lipids in protein delivery to mice lungs.

C. Férec, C. Guillaume, P. Delépine, 2000, Journal of pharmaceutical sciences.

Follow up study of labial salivary gland lesions in primary Sjögren's syndrome.

P. Youinou, J. Berthelot, J. Leroy, 1992, Annals of the rheumatic diseases.

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease.

B. Buendia, J. Rendu, O. Dubourg, 2016, Human molecular genetics.

MUSK, a new target for mutations causing congenital myasthenic syndrome.

C. Legay, L. Schaeffer, E. Goillot, 2004, Human molecular genetics.

Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.

N. Romero, J. Leroy, E. Lacène, 2006, Brain : a journal of neurology.

Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation

B. Eymard, J. Leroy, M. Fardeau, 2004, Neuromuscular Disorders.

The detection of Tel–TrkC chimeric transcripts is more specific than TrkC immunoreactivity for the diagnosis of congenital fibrosarcoma

M. Copin, P. Dubus, J. Coindre, 2001, The Journal of pathology.

A study of familial lupus erythematosus‐likes disease and hereditary angio‐oedema treated with danazol

P. Youinou, J. Clèdes, J. Leroy, 1983, The British journal of dermatology.

Zygomycosis caused by Cunninghamella bertholletiae in a kidney transplant recipient.

J. Leroy, B. Sassolas, B. Bourbigot, 2004, Medical mycology.

Respiratory failure associated with hydroxychloroquine neuromyopathy.

Y. le Tulzo, J. Leroy, C. Camus, 1995, European neurology.

Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiency

B. Eymard, J. Leroy, E. Krejci, 2003, Neuromuscular Disorders.

Comparison of labial and sublingual salivary gland biopsies in the diagnosis of Sjögren's syndrome.

P. Youinou, J. Leroy, P. Katsikis, 1990, Annals of the rheumatic diseases.

lesions in primary Sjögren ' s syndrome . Follow up study of labial salivary gland

P. Youinou, J. Berthelot, J. Leroy, 2022 .

Pigmented Purpuric Dermatitis Preceding the Diagnosis of Mycosis fungoides by 24 Years

J. Leroy, P. Le Roux, P. Plantin, 2003, Dermatology.

Lymphocytic infiltration of salivary ducts: a histopathologic lesion specific for primary Sjögren's syndrome?

P. Youinou, J. Leroy, Y. Pennec, 1992, Arthritis and rheumatism.

The antischistosomal activity of oltipraz.

J. Leroy, E. Bueding, P. Dolan, 1982, Research communications in chemical pathology and pharmacology.

[Subcutaneous mycosis due to Scopulariopsis brevicaulis in an aplasic patient].

L. Misery, J. Leroy, C. Berthou, 2003, Annales de dermatologie et de vénéréologie.

[Drug hypersensitivity syndrome during treatment with valproic acid].

H. Cartier, J. Leroy, P. Plantin, 1995, Presse medicale.

Lichen planus pigmentosus associated with acrokeratosis of Bazex

J. Leroy, A. Zagnoli, B. Sassolas, 1994, Clinical and experimental dermatology.

Aseptic Neutrophilic Abscess of the Vulva

L. Misery, J. Leroy, Y. Laurent, 2005, Dermatology.

[Neutrophilic dermatosis associated with propylthiouracil-induced p-ANCA (p-antineutrophil cytoplasmic antibodies)].

L. Misery, J. Leroy, I. Kupfer-Bessaguet, 2005, Annales de dermatologie et de venereologie.

[Candida albicans onychomadesis. Neonatal contamination].

C. Calligaris, J. Leroy, P. Plantin, 1992, Annales de dermatologie et de venereologie.

Systemic amyloidosis in the course of maintenance hemodialysis.

P. Youinou, M. Guillodo, J. Clèdes, 1985, Nephron.

Topical imiquimod treatment of lentigo maligna: clinical and histologic evaluation.

L. Misery, J. Leroy, I. Kupfer-Bessaguet, 2004, Journal of the American Academy of Dermatology.

Metabolism of oltipraz and glutathione reductase inhibition.

J. Leroy, T. Martens, M. Fleury, 1990, Biochemical Pharmacology.

Effect of oltipraz on the metabolism of glutathione in Schistosoma mansoni.

J. Leroy, M. Azoulay, F. Frappier, 1988, Biochemical pharmacology.

Reappraisal of tests for xerostomia.

P. Youinou, J. Leroy, Y. Pennec, 1993, Clinical and experimental rheumatology.

Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies.

F. Muntoni, C. Bönnemann, N. Romero, 2002, American journal of human genetics.

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J. Leroy, D. Mabin, T. Pamantung, 2001 .

[Localized recurrent light-induced Darier disease following Blaschko lines].

J. Leroy, P. Plantin, E. Le Noac'h, 1994, Annales de dermatologie et de venereologie.

AMP-deaminase in elasmobranch fish: a comparative histochemical and enzymatic study.

E. Gobin, J. Leroy, L. Izem, 2005, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

Role of dorsal vagal motor nucleus in angiotensin II-mediated tachycardia in the conscious trout Oncorhynchus mykiss

J. Leroy, J. C. Mével, D. Mabin, 1997, Brain Research.

A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia

L. Schaeffer, E. Goillot, A. Taly, 2013, PloS one.

[Universal dyschromatosis: a familial case].

J. Leroy, P. Plantin, P. Schoenlaub, 1998, Annales de dermatologie et de venereologie.

IgA isotyping of antigliadin antibodies. A possible clue for a less invasive diagnosis of coeliac disease.

G. Dacremont, M. D. de Baets, J. Leroy, 1989, Clinica chimica acta; international journal of clinical chemistry.

[Anterior thoracic and intervertebral erosive joint diseases associated with palmoplantar pustulosis].

J. Leroy, G. Guillet, P. Le Goff, 1985, Revue du rhumatisme et des maladies osteo-articulaires.

[Pyoderma gangrenosum, subcorneal IgA pustulosis and recurrent neutrophilic pleural and pulmonary diseases in a patient with IgA gammopathy].

H. Cartier, J. Leroy, P. Plantin, 1995, Annales de dermatologie et de venereologie.

Hodgkin's disease masquerading as fibrous thyroiditis: potential role of cytokines in in vivo and in vitro studies

J. Leroy, L. Sensébé, V. Kerlan, 2002, Clinical endocrinology.

Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes

A. Barois, B. Eymard, B. Hainque, 2003, Journal of medical genetics.

[Idiopathic eruptive macular pigmentation].

J. Leroy, A. Le Berre, P. Le Roux, 1993, Archives francaises de pediatrie.

Nevus oligemicus: a new case.

J. Leroy, P. Plantin, G. Guillet, 1992, Journal of the American Academy of Dermatology.

Collagen type III glomerulopathy: a new type of hereditary nephropathy

M. Gubler, A. Bensman, J. Leroy, 1993, Pediatric Nephrology.

Disposition of 14C-oltipraz in animals. Pharmacokinetics in mice, rats and monkeys. Comparison of the biotransformation in the infected mouse and in the schistosomes.

J. Leroy, M. Marlard, D. Heusse, 1985, Arzneimittel-Forschung.

Abnormal Distribution of Calcium-Handling Proteins: A Novel Distinctive Marker in Core Myopathies

K. Parain, N. Romero, J. Leroy, 2007, Journal of neuropathology and experimental neurology.

[Bi-symptomatic CINCA syndrome with inaugural urticaria and major articular lesions].

A. Prieur, J. Leroy, B. Sassolas, 1999, Annales de dermatologie et de venereologie.

Renal failure in the course of reactivation of varicella-zoster virus infection in a renal transplant recipient.

J. Clèdes, E. Hardy, J. Leroy, 1986, The Journal of infection.

[Disseminated granuloma annulare following puvatherapy].

J. Leroy, J. Dorval, R. Masse, 1979, Annales de dermatologie et de venereologie.

Cationic phosphonolipids as nonviral gene transfer agents in the lungs of mice.

C. Férec, J. Yaouanc, J. Clement, 1998, Human gene therapy.

Lymphoma with regression after methotrexate withdrawal in a patient with rheumatoid arthritis. Role for the Epstein-Barr virus.

A. Saraux, J. Leroy, P. Le Goff, 1998, Revue du rhumatisme.

TheStargazin-RelatedProtein7InteractswiththemRNA- BindingProteinHeterogeneousNuclearRibonucleoprotein A2andRegulatestheStabilityofSpecificmRNAs,Including

J. Leroy, F. Moss, 2008 .

[Deep morphea-type lesions, first manifestations of lymphocytic lymphoma].

J. Leroy, A. Le Berre, P. Plantin, 1996, Annales de dermatologie et de vénéréologie.

[Post-traumatic osteoid osteoma. Apropos of 2 cases and review of the literature].

J. Leroy, P. Le Goff, D. Baron, 1992, Revue du rhumatisme et des maladies osteo-articulaires.

Is Fibromyalgia a Variant of Sjӧgren’s Syndrome?

P. Youinou, J. Leroy, P. Goff, 2018 .

Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSK.

C. Legay, L. Schaeffer, E. Goillot, 2005, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus.

N. Romero, L. Viollet, P. Laforêt, 2005, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

[DRESS syndrome related to Hexaquine (quinine and thiamine)].

J. Leroy, B. Sassolas, M. Greco, 2006, Annales de dermatologie et de venereologie.

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease.

B. Buendia, J. Rendu, O. Dubourg, 2016, Human molecular genetics.

[Mytomycin C nephrotoxicity. 3 new cases and review of the literature].

K. Ang, J. Clèdes, J. Leroy, 1982, Nephrologie.