Full Text Journal Articles by
Author Jean Louis Dupond

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Long-term outcomes of 118 patients with eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) enrolled in two prospective trials.

Maxime Samson, Xavier Puéchal, Hervé Devilliers, Camillo Ribi, Pascal Cohen, Marc Stern, Christian Pagnoux, Luc Mouthon, Loïc Guillevin, ,

The purpose of this study was to assess the outcomes of 118 patients with eosinophilic granulomatosis with polyangiitis (EGPA) enrolled in 2 prospective, randomized, open-label clinical trials (1994-2005), with or without Five-Factor Score (FFS)-defined poor-prognosis factors, focusing on survival, disease-free survival, relapses, clinical and laboratory findings, therapeutic responses, and factors ... Read more >>

J. Autoimmun. (Journal of autoimmunity)
[2013, 43:60-69]

Cited: 44 times

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Fatigue in patients with rheumatic diseases.

Jean-Louis Dupond,

Fatigue is a prominent symptom in many rheumatic diseases. Numerous factors contribute to cause fatigue, which can be a source of frustration for the patients and physicians, as the treatment often fails to produce the desired improvement. Diagnostic guidelines direct insufficient attention to the various semiological patterns of fatigue seen ... Read more >>

Joint Bone Spine (Joint bone spine)
[2011, 78(2):156-160]

Cited: 15 times

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Plasma VEGF determination in disseminated lymphangiomatosis-Gorham-Stout syndrome: a marker of activity? A case report with a 5-year follow-up.

Jean-Louis Dupond, Laurent Bermont, Michel Runge, Marjolaine de Billy,

Disseminated lymphangiomatosis and Gorham-Stout disease are being considered as two forms of a single rare disease, characterized by a proliferation of lymphatic vessels, triggered by lymphangiogenic factors. There is no biological marker of the disease. Plasma VEGF might be a useful tool since the recent demonstration of its pivotal role ... Read more >>

Bone (Bone)
[2010, 46(3):873-876]

Cited: 27 times

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Management of infectious pneumonia: value of C-reactive protein.

Helder Gil, Nadine Meaux Ruault, Chafika Hafsaoui, Jean-Louis Dupond, Nadine Magy-Bertrand,

Am J Med (The American journal of medicine)
[2009, 122(5):e11; author reply e13]

Cited: 0 times

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Inaugural cervical vertebral sarcoidosis.

Daniel Wendling, Hélène Desmurs, Françoise Royer, Helder Gil, Jean-Louis Dupond,

J. Rheumatol. (The Journal of rheumatology)
[2008, 35(2):362-365]

Cited: 5 times

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Detection of a mesenchymal tumor responsible for hypophosphatemic osteomalacia using FDG-PET.

Jean-Louis Dupond, Hakim Mahammedi, Nadine Magy, Olaf Blagosklonov, Nadine Meaux-Ruault, Bernadette Kantelip,

We report a case of oncogenic osteomalacia (OO) in a 71-year-old man. The tumor, which was localized in the left lower mandible, was not found by CT, MRI, or 111-indium octreotide scintigraphy but was easily detected by FDG-PET. The use of this technique in OO has never been reported. ... Read more >>

Eur. J. Intern. Med. (European journal of internal medicine)
[2005, 16(6):445-446]

Cited: 15 times

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Systemic mastocytosis: predictable factors of poor prognosis present at the onset of the disease.

Katia Stankovic, Françoise Sarrot-Reynauld, Marie Puget, Christian Massot, Jacques Ninet, Bernard Lorcerie, Jean-Louis Dupond, Gilles Salles, Isabelle Durieu, Denis Vital Durand, Hugues Rousset,

Systemic mastocytosis (SM) refers to a group of heterogeneous diseases that can be divided into indolent SM, for which prognosis is favorable, and malignant SM, which has a poor prognosis. While the diagnosis of SM is often a challenge since clinical and biological abnormalities are not specific, prognosis is even ... Read more >>

Eur. J. Intern. Med. (European journal of internal medicine)
[2005, 16(6):387-390]

Cited: 2 times

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Observational study of potential risk factors of medication administration errors.

Edgar Tissot, Christian Cornette, Samuel Limat, Jean-Louis Mourand, Michële Becker, Joseph-Philippe Etievent, Jean-Louis Dupond, Micheline Jacquet, Marie-Christine Woronoff-Lemsi,

OBJECTIVE:Medication administration errors (MAEs) are the second most frequent type of medication errors, as has been shown in different studies in the literature. The aims of this observational study were to assess the rate and the potential clinical significance of MAEs and to determine the associated risk factors. DESIGN:In two ... Read more >>

Pharm World Sci (Pharmacy world & science : PWS)
[2003, 25(6):264-268]

Cited: 55 times

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Reactive hemophagocytic syndrome in adult systemic disease: report of twenty-six cases and literature review.

Robin Dhote, Jeanne Simon, Thomas Papo, Bruno Detournay, Laurent Sailler, Marie-Helene Andre, Jean-Louis Dupond, Claire Larroche, Anne-Marie Piette, Didier Mechenstock, Jean-Marc Ziza, Jean Arlaud, Anne-Sophie Labussiere, Agnes Desvaux, Vincent Baty, Philippe Blanche, Annette Schaeffer, Jean-Charles Piette, Loïc Guillevin, Alain Boissonnas, Boyan Christoforov,

OBJECTIVE: To analyze specific clinical findings, underlying disorders, treatments, outcomes, and prognostic factors for reactive hemophagocytic syndrome (RHS) in systemic disease. METHODS: Data were collected using standardized forms as part of a French national survey. Adult cases without an underlying malignancy, diagnosed on bone marrow or lymph node biopsy, were ... Read more >>

Arthritis Rheum. (Arthritis and rheumatism)
[2003, 49(5):633-639]

Cited: 157 times

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A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.

Nadine Magy, Juris J Liepnieks, Helder Gil, Bernadette Kantelip, Jean-Louis Dupond, Barbara Kluve-Beckerman, Merrill D Benson,

BACKGROUND:More than 80 transthyretin (TTR) mutations have been described, most associated with amyloidosis. Peripheral neuropathy is the most common clinical presentation in TTR amyloidosis although the carpal tunnel syndrome (CTS) may be the first symptom and skin can be involved, as transthyretin amyloidosis is a systemic disease. CASE REPORT:The 78 ... Read more >>

Amyloid (Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis)
[2003, 10(1):29-33]

Cited: 7 times

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[Mondor's thrombophlebitis and antiphospholipid antibodies].

Nadine Magy, Helder Gil, Evelyne Racadot, Jean-Louis Dupond,

Presse Med (Presse medicale (Paris, France : 1983))
[2003, 32(2):70-71]

Cited: 2 times

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Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.

Nadine Magy, Sophie Valleix, Gilles Grateau, Marie-Paule Algros, Romain Guillemain, Bernadette Kantelip, Marc Delpech, Jean-Louis Dupond,

A French family in which three individuals had familial amyloid polyneuropathy (FAP) was investigated. The proband presented cardiomyopathy with atrial arrhythmia and then developed axonal polyneuropathy, carpal tunnel syndrome, and sclerodactyly. Nucleotide sequencing of exons 2, 3 and 4 of the transthyretin (TTR) gene revealed heterozygosity for a single base ... Read more >>

Amyloid (Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis)
[2002, 9(4):272-275]

Cited: 2 times

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