European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma
Plouin, P F, Amar, L, Dekkers, O M, Fassnacht, M, Gimenez-Roqueplo, A P, Lenders, J W M, Lussey-Lepoutre, C, Steichen, O
Published in European journal of endocrinology (01.05.2016)
Published in European journal of endocrinology (01.05.2016)
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Journal Article
Metastatic pheochromocytoma and paraganglioma: focus on therapeutics
Plouin, P-F, Fitzgerald, P, Rich, T, Ayala-Ramirez, M, Perrier, N D, Baudin, E, Jimenez, C
Published in Hormone and metabolic research (01.05.2012)
Published in Hormone and metabolic research (01.05.2012)
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Journal Article
Outcomes of adrenalectomy in patients with unilateral primary aldosteronism: a review
Steichen, O, Zinzindohoué, F, Plouin, P-F, Amar, L
Published in Hormone and metabolic research (01.03.2012)
Published in Hormone and metabolic research (01.03.2012)
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Journal Article
Catheter-based Radiofrequency Renal-nerve Ablation in Patients with Resistant Hypertension
Azizi, M, Steichen, O, Frank, M, Bobrie, G, Plouin, P.-F, Sapoval, M
Published in European journal of vascular and endovascular surgery (01.03.2012)
Published in European journal of vascular and endovascular surgery (01.03.2012)
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Journal Article
Electroencephalography in premature and full-term infants. Developmental features and glossary
André, M, Lamblin, M.-D, d’Allest, A.M, Curzi-Dascalova, L, Moussalli-Salefranque, F, Nguyen The Tich, S, Vecchierini-Blineau, M.-F, Wallois, F, Walls-Esquivel, E, Plouin, P
Published in Neurophysiologie clinique (01.05.2010)
Published in Neurophysiologie clinique (01.05.2010)
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The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathway
Gimenez-Roqueplo, Anne-Paule, Favier, Judith, Rustin, Pierre, Mourad, Jean-Jacques, Plouin, Pierre-François, Corvol, Pierre, Rötig, Agnès, Jeunemaitre, Xavier
Published in American journal of human genetics (01.12.2001)
Published in American journal of human genetics (01.12.2001)
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Journal Article
Normal EEG in childhood: From neonates to adolescents
Eisermann, M, Kaminska, A, Moutard, M.-L, Soufflet, C, Plouin, P
Published in Neurophysiologie clinique (01.01.2013)
Published in Neurophysiologie clinique (01.01.2013)
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Journal Article
Devastating epileptic encephalopathy in school-aged children (DESC): A pseudo encephalitis
Mikaeloff, Y., Jambaqué, I., Hertz-Pannier, L., Zamfirescu, A., Adamsbaum, C., Plouin, P., Dulac, O., Chiron, C.
Published in Epilepsy research (01.04.2006)
Published in Epilepsy research (01.04.2006)
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Journal Article
Treatment of malignant pheochromocytoma
Adjallé, R, Plouin, P F, Pacak, K, Lehnert, H
Published in Hormone and metabolic research (01.09.2009)
Published in Hormone and metabolic research (01.09.2009)
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Journal Article
Inheritance of arterial lesions in renal fibromuscular dysplasia
PERDU, J, BOUTOUYRIE, P, GIMENEZ -ROQUEPLO, A.-P, JEUNEMAITRE, X, BOURGAM, C, STEM, N, LALOUX, B, BOZEC, E, AZIZI, M, BONAITI-PELLIE, C, PLOUIN, P.-F, LAURENT, S
Published in Journal of human hypertension (01.05.2007)
Published in Journal of human hypertension (01.05.2007)
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Journal Article
ESC Guidelines on the diagnosis and treatment of peripheral artery diseases: Document covering atherosclerotic disease of extracranial carotid and vertebral, mesenteric, renal, upper and lower extremity arteries: the Task Force on the Diagnosis and Treatment of Peripheral Artery Diseases of the European Society of Cardiology (ESC)
Tendera, Michal, Aboyans, Victor, Bartelink, Marie-Louise, Baumgartner, Iris, Clément, Denis, Collet, Jean-Philippe, Cremonesi, Alberto, De Carlo, Marco, Erbel, Raimund, Fowkes, F Gerry R, Heras, Magda, Kownator, Serge, Minar, Erich, Ostergren, Jan, Poldermans, Don, Riambau, Vincent, Roffi, Marco, Röther, Joachim, Sievert, Horst, van Sambeek, Marc, Zeller, Thomas
Published in European heart journal (01.11.2011)
Published in European heart journal (01.11.2011)
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Web Resource
Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts
Molinari, F, Kaminska, A, Fiermonte, G, Boddaert, N, Raas‐Rothschild, A, Plouin, P, Palmieri, L, Brunelle, F, Palmieri, F, Dulac, O, Munnich, A, Colleaux, L
Published in Clinical genetics (01.08.2009)
Published in Clinical genetics (01.08.2009)
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Journal Article
Factors associated with perioperative morbidity and mortality in patients with pheochromocytoma : Analysis of 165 operations at a single center
PLOUIN, Pierre-Francois, DUCLOS, Jean-Marc, SOPPELSA, Frederique, BOUBLIL, Gaetan, CHATELLIER, Gilles
Published in The journal of clinical endocrinology and metabolism (01.04.2001)
Published in The journal of clinical endocrinology and metabolism (01.04.2001)
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Journal Article
Salivary aldosterone as a diagnostic aid in primary aldosteronism
Manolopoulou, J, Gerum, S, Mulatero, P, Rossignol, P, Plouin, P-F, Reincke, M, Bidlingmaier, M
Published in Hormone and metabolic research (01.06.2010)
Published in Hormone and metabolic research (01.06.2010)
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Journal Article
Saliva as a medium for aldosterone measurement in repeated sampling studies
Manolopoulou, J., Mulatero, P., Maser-Gluth, C., Rossignol, P., Spyroglou, A., Vakrilova, Y., Petersenn, S., Zwermann, O., Plouin, P.F., Reincke, M., Bidlingmaier, M.
Published in Steroids (10.10.2009)
Published in Steroids (10.10.2009)
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