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  1. Article: Les bonnes questions de Platon.

    Petite, Jacques

    Revue medicale suisse

    2008  Volume 4, Issue 158, Page(s) 1286–1287

    Title translation The thoughtful questions of Plato.
    MeSH term(s) Greek World/history ; History, Ancient ; Humans ; Philosophy/history
    Language French
    Publishing date 2008-05-21
    Publishing country Switzerland
    Document type Historical Article ; Journal Article
    ZDB-ID 2177010-4
    ISSN 1660-9379
    ISSN 1660-9379
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Espoirs dans le traitement des morsures de serpents et autres animaux venimeux.

    Petite, Jacques

    Revue medicale suisse

    2007  Volume 3, Issue 138, Page(s) 2919–2920

    Title translation Hope in the treatment of snake bites and other venomous animals.
    MeSH term(s) Animals ; Antivenins/therapeutic use ; Humans ; Scorpions ; Snake Bites/therapy
    Chemical Substances Antivenins
    Language French
    Publishing date 2007-12-19
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2177010-4
    ISSN 1660-9379
    ISSN 1660-9379
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: La plainte d'Andromaque. Réflexions sur l'accompagnement au mourant.

    Petite, Jacques

    Revue medicale suisse

    2006  Volume 2, Issue 88, Page(s) 2703

    Title translation The complaint of Andromache: reflections on accompanying the dying.
    MeSH term(s) Attitude ; Attitude to Death ; France ; Greece ; History, 19th Century ; History, 20th Century ; History, Ancient ; Humans ; Intuition ; Life ; Literature/history ; Love ; Philosophy, Medical/history
    Language French
    Publishing date 2006-11-22
    Publishing country Switzerland
    Document type Historical Article ; Journal Article
    ZDB-ID 2177010-4
    ISSN 1660-9379
    ISSN 1660-9379
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Viper bites: treat or ignore? Review of a series of 99 patients bitten by Vipera aspis in an alpine Swiss area.

    Petite, Jacques

    Swiss medical weekly

    2005  Volume 135, Issue 41-42, Page(s) 618–625

    Abstract: In a well defined alpine area of Switzerland (Valais, about 300000 inhabitants, tourists included) we studied retrospectively over 32 years, 99 patients bitten by vipers (Vipera aspis, the likely unique species in this area). The annual incidence was ... ...

    Abstract In a well defined alpine area of Switzerland (Valais, about 300000 inhabitants, tourists included) we studied retrospectively over 32 years, 99 patients bitten by vipers (Vipera aspis, the likely unique species in this area). The annual incidence was estimated at 3/100,000, as in other European countries. The mortality was 0% for the adults. The patients, 72 adults and 17 children (13 years and less), were classified in four groups: grade 0 no envenomation (8%), grade 1 minimal (42%), grade 2 moderate (40%), and grade 3 severe envenomation (10%). The 10 patients of grade 3 showed impressive clinical signs and blood abnormalities, as exemplified by our three most severe cases. Only patients of grade 3 must be treated with antivenom and other intensive treatments, but all patients, even grade 1, especially small children, must be observed for several hours.
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Animals ; Decision Making ; Female ; Humans ; Male ; Medical Audit ; Middle Aged ; Snake Bites/epidemiology ; Snake Bites/therapy ; Switzerland/epidemiology ; Viperidae
    Language English
    Publishing date 2005-10-15
    Publishing country Switzerland
    Document type Case Reports ; Journal Article
    ZDB-ID 2036179-8
    ISSN 1424-3997 ; 1424-7860
    ISSN (online) 1424-3997
    ISSN 1424-7860
    DOI 10.4414/smw.2005.11198
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  5. Article ; Online: Feasibility of Bioengineered Tracheal and Bronchial Reconstruction Using Stented Aortic Matrices.

    Martinod, Emmanuel / Chouahnia, Kader / Radu, Dana M / Joudiou, Pascal / Uzunhan, Yurdagul / Bensidhoum, Morad / Santos Portela, Ana M / Guiraudet, Patrice / Peretti, Marine / Destable, Marie-Dominique / Solis, Audrey / Benachi, Sabiha / Fialaire-Legendre, Anne / Rouard, Hélène / Collon, Thierry / Piquet, Jacques / Leroy, Sylvie / Vénissac, Nicolas / Santini, Joseph /
    Tresallet, Christophe / Dutau, Hervé / Sebbane, Georges / Cohen, Yves / Beloucif, Sadek / d'Audiffret, Alexandre C / Petite, Hervé / Valeyre, Dominique / Carpentier, Alain / Vicaut, Eric

    JAMA

    2018  Volume 319, Issue 21, Page(s) 2212–2222

    Abstract: Importance: Airway transplantation could be an option for patients with proximal lung tumor or with end-stage tracheobronchial disease. New methods for airway transplantation remain highly controversial.: Objective: To establish the feasibility of ... ...

    Abstract Importance: Airway transplantation could be an option for patients with proximal lung tumor or with end-stage tracheobronchial disease. New methods for airway transplantation remain highly controversial.
    Objective: To establish the feasibility of airway bioengineering using a technique based on the implantation of stented aortic matrices.
    Design, setting, and participants: Uncontrolled single-center cohort study including 20 patients with end-stage tracheal lesions or with proximal lung tumors requiring a pneumonectomy. The study was conducted in Paris, France, from October 2009 through February 2017; final follow-up for all patients occurred on November 2, 2017.
    Exposures: Radical resection of the lesions was performed using standard surgical techniques. After resection, airway reconstruction was performed using a human cryopreserved (-80°C) aortic allograft, which was not matched by the ABO and leukocyte antigen systems. To prevent airway collapse, a custom-made stent was inserted into the allograft. In patients with proximal lung tumors, the lung-sparing intervention of bronchial transplantation was used.
    Main outcomes and measures: The primary outcome was 90-day mortality. The secondary outcome was 90-day morbidity.
    Results: Twenty patients were included in the study (mean age, 54.9 years; age range, 24-79 years; 13 men [65%]). Thirteen patients underwent tracheal (n = 5), bronchial (n = 7), or carinal (n = 1) transplantation. Airway transplantation was not performed in 7 patients for the following reasons: medical contraindication (n = 1), unavoidable pneumonectomy (n = 1), exploratory thoracotomy only (n = 2), and a lobectomy or bilobectomy was possible (n = 3). Among the 20 patients initially included, the overall 90-day mortality rate was 5% (1 patient underwent a carinal transplantation and died). No mortality at 90 days was observed among patients who underwent tracheal or bronchial reconstruction. Among the 13 patients who underwent airway transplantation, major 90-day morbidity events occurred in 4 (30.8%) and included laryngeal edema, acute lung edema, acute respiratory distress syndrome, and atrial fibrillation. There was no adverse event directly related to the surgical technique. Stent removal was performed at a postoperative mean of 18.2 months. At a median follow-up of 3 years 11 months, 10 of the 13 patients (76.9%) were alive. Of these 10 patients, 8 (80%) breathed normally through newly formed airways after stent removal. Regeneration of epithelium and de novo generation of cartilage were observed within aortic matrices from recipient cells.
    Conclusions and relevance: In this uncontrolled study, airway bioengineering using stented aortic matrices demonstrated feasibility for complex tracheal and bronchial reconstruction. Further research is needed to assess efficacy and safety.
    Trial registration: clinicaltrials.gov Identifier: NCT01331863.
    MeSH term(s) Adult ; Aged ; Aorta/transplantation ; Autografts ; Bioengineering/methods ; Bronchi/surgery ; Feasibility Studies ; Female ; Follow-Up Studies ; Humans ; Lung Neoplasms/surgery ; Male ; Middle Aged ; Pneumonectomy ; Reconstructive Surgical Procedures/methods ; Stents ; Trachea/pathology ; Trachea/surgery ; Tracheal Diseases/pathology ; Tracheal Diseases/surgery ; Tracheal Stenosis/surgery
    Language English
    Publishing date 2018-05-25
    Publishing country United States
    Document type Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2018.4653
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  6. Article: Pyruvate modifies glycolytic and oxidative metabolism of rat embryonic spinal cord astrocyte cell lines and prevents their spontaneous transformation.

    Rouleau, Caroline / Rakotoarivelo, Clovis / Petite, Didier / Lambert, Karen / Fabre, Christine / Bonardet, Andrée / Mercier, Jacques / Baldet, Pierre / Privat, Alain / Langley, Keith / Mersel, Marcel

    Journal of neurochemistry

    2007  Volume 100, Issue 6, Page(s) 1589–1598

    Abstract: This study aimed to provide detailed data on mitochondrial respiration of normal astrocyte cell lines derived from rat embryonic spinal cord. Astrocytes in early passages (EP), cultured without pyruvate for more than 35 passages, defined here as late ... ...

    Abstract This study aimed to provide detailed data on mitochondrial respiration of normal astrocyte cell lines derived from rat embryonic spinal cord. Astrocytes in early passages (EP), cultured without pyruvate for more than 35 passages, defined here as late passages (LP), undergo spontaneous transformation. To study initial steps in cell transformation, EP data were compared with those of LP cells. LP cells had reduced glycolysis, fewer mitochondria and extremely low oxidative rates, resulting from a dysfunction of complexes I and II + III of the respiratory chain. Treatment of EP cells with pyruvate until they were, by definition, LP cultures prevented transformation of these cells. Pyruvate-treated EP cells had more mitochondria than normal cells but slightly lower respiratory rates. The increase of mitochondrial content thus appears to act as a compensatory effect to maintain oxidative phosphorylation in these LP 'non-transformed' cells, in which mitochondrial function is reduced. However, pyruvate treatment of transformed LP cells during additional passages did not significantly restore their oxidative metabolism. These data highlight changes accompanying spontaneous astrocyte transformation and suggest potential targets for the control of astrocyte proliferation and reaction to various insults to the central nervous system.
    MeSH term(s) Aging/drug effects ; Aging/physiology ; Animals ; Astrocytes/drug effects ; Astrocytes/ultrastructure ; Cells, Cultured ; Electron Transport Chain Complex Proteins/metabolism ; Embryo, Mammalian ; Glycolysis/drug effects ; Mitochondria/drug effects ; Oxygen Consumption/drug effects ; Pyruvic Acid/metabolism ; Pyruvic Acid/pharmacology ; Rats ; Spinal Cord/cytology
    Chemical Substances Electron Transport Chain Complex Proteins ; Pyruvic Acid (8558G7RUTR)
    Language English
    Publishing date 2007-03
    Publishing country England
    Document type Journal Article
    ZDB-ID 80158-6
    ISSN 1471-4159 ; 0022-3042 ; 1474-1644
    ISSN (online) 1471-4159
    ISSN 0022-3042 ; 1474-1644
    DOI 10.1111/j.1471-4159.2006.04318.x
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  7. Article: In vivo imaging with cellular resolution of bone marrow cells transplanted into the ischemic brain of a mouse.

    Tran-Dinh, Alexy / Dinh, Alexy Tran / Kubis, Nathalie / Tomita, Yutaka / Karaszewski, Bartosz / Calando, Yolande / Oudina, Karim / Petite, Hervé / Seylaz, Jacques / Pinard, Elisabeth

    NeuroImage

    2006  Volume 31, Issue 3, Page(s) 958–967

    Abstract: The aim of the study was to monitor in vivo and noninvasively the fate of single bone marrow cells (BMCs) transplanted into the ischemic brain of unirradiated mice. In vivo imaging was performed through a closed cranial window, throughout the 2 weeks ... ...

    Abstract The aim of the study was to monitor in vivo and noninvasively the fate of single bone marrow cells (BMCs) transplanted into the ischemic brain of unirradiated mice. In vivo imaging was performed through a closed cranial window, throughout the 2 weeks following cell transplantation, using laser-scanning confocal fluorescence microscopy. The window was chronically implanted above the left parieto-occipital cortex in C57BL/6J adult mice. BMC (3 x 10(5) nucleated cells in 0.5 microL medium) from 5-week-old transgenic mice, ubiquitously expressing green fluorescent protein (GFP), was transplanted into the ipsilateral cortex 24 h after the induction of focal ischemia by coagulation of the left middle cerebral artery (n = 15). Three nonischemic mice served as controls. Repeated in vivo imaging, up to a depth of 200 microm, revealed that BMCs survived within the ischemic and peri-ischemic cortex, migrated significantly towards the lesion, proliferated and adopted a microglia-like morphology over 2 weeks. These results were confirmed using ex vivo imaging after appropriate immunocytochemical treatments. This study indicates that confocal fluorescence microscopy is a reliable and unique tool to repeatedly assess with cellular resolution the in vivo dynamic fate of fluorescent cells transplanted into a mouse brain. These results also provide the first in vivo findings on the fate of single BMCs transplanted into the ischemic brain of unirradiated mice.
    MeSH term(s) Animals ; Bone Marrow Cells/pathology ; Bone Marrow Transplantation/pathology ; Brain Ischemia/pathology ; Cell Division/physiology ; Cell Movement/physiology ; Cell Survival/physiology ; Cerebral Cortex/blood supply ; Cerebral Cortex/pathology ; Green Fluorescent Proteins/analysis ; Image Processing, Computer-Assisted ; Infarction, Middle Cerebral Artery/pathology ; Laser Scanning Cytometry ; Mice ; Mice, Inbred C57BL ; Microglia/pathology
    Chemical Substances Green Fluorescent Proteins (147336-22-9)
    Language English
    Publishing date 2006-07-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1147767-2
    ISSN 1095-9572 ; 1053-8119
    ISSN (online) 1095-9572
    ISSN 1053-8119
    DOI 10.1016/j.neuroimage.2006.01.019
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