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1. Full Text Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study
by Charlier, Caroline, Dr and Perrodeau, Élodie, MSc and Leclercq, Alexandre, MSc and Cazenave, Benoît, MD and Pilmis, Benoît, MD and Henry, Benoît, MD and Lopes, Amanda, MD and Maury, Mylène M, PhD and Moura, Alexandra, PhD and Goffinet, François, MD and Dieye, Hélène Bracq and Thouvenot, Pierre and Ungeheuer, Marie-Noëlle, MD and Tourdjman, Mathieu, MD and Goulet, Véronique, MD and de Valk, Henriette, MD and Lortholary, Olivier, Prof and Ravaud, Philippe, Prof and Lecuit, Marc, Prof and MONALISA Study Grp and MONALISA study group
Lancet Infectious Diseases, The, ISSN 1473-3099, 2017, Volume 17, Issue 5, pp. 510 - 519
Summary Background Listeriosis is a severe foodborne infection and a notifiable disease in France. We did a nationwide prospective study to characterise its... 
Infectious Disease | MORTALITY | MENINGITIS | INFECTIOUS DISEASES | MONOCYTOGENES | RISK-FACTORS | MANAGEMENT | GUIDELINES | SURVEILLANCE | PREGNANCY | Foodborne Diseases - microbiology | Infant, Newborn, Diseases - epidemiology | Prognosis | Prospective Studies | Humans | Listeriosis - diagnosis | Bacteremia - mortality | Male | Infant, Newborn, Diseases - microbiology | Listeriosis - epidemiology | Mandatory Reporting | Listeria monocytogenes - classification | Adult | Female | Pregnancy Complications, Infectious - microbiology | Infant, Newborn | Meningoencephalitis - epidemiology | France - epidemiology | Meningoencephalitis - mortality | Pregnancy Complications, Infectious - epidemiology | Risk Factors | Listeria monocytogenes - isolation & purification | Hospitalization | Infectious Disease Transmission, Vertical | Pregnancy | Meningoencephalitis - microbiology | Bacteremia - epidemiology | Listeriosis - microbiology | Aged | Population Surveillance | Listeriosis | Neonates | Food-borne diseases | Disease | Brain stem | Clinical trials | Infections | Genomes | Gestation | Epidemiology | Risk factors | Windows (intervals) | Listeria | Meningitis | Public health | Food | Dexamethasone | Bacterial infections | Mortality | Fetuses | Regression analysis | Clustering | Patients | Bacteremia | Meningoencephalitis | Studies | Surveillance | Medical prognosis | Health risk assessment | Cancer | Life Sciences
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2. Full Text Paraganglioma and phaeochromocytoma: From genetics to personalized medicine
by Favier, Judith and Amar, Laurence and Gimenez-Roqueplo, Anne-Paule
Nature Reviews Endocrinology, ISSN 1759-5029, 02/2015, Volume 11, Issue 2, pp. 101 - 111
Paragangliomas and phaeochromocytomas are neuroendocrine tumours whose pathogenesis and progression are very strongly influenced by genetics. A germline... 
MITOCHONDRIAL COMPLEX II | MALIGNANT PHEOCHROMOCYTOMAS | SUCCINATE-DEHYDROGENASE | POSITRON-EMISSION-TOMOGRAPHY | HIPPEL-LINDAU DISEASE | SPORADIC PHEOCHROMOCYTOMAS | ENDOCRINOLOGY & METABOLISM | TUMOR-SUPPRESSOR GENE | GERMLINE MUTATIONS | SDH MUTATIONS | METASTATIC PHEOCHROMOCYTOMAS | Neuroendocrine Tumors - pathology | Paraganglioma - pathology | Paraganglioma - genetics | Humans | Pheochromocytoma - pathology | Pheochromocytoma - genetics | Adrenal Gland Neoplasms - genetics | Adrenal Gland Neoplasms - pathology | Precision Medicine - methods | Neuroendocrine Tumors - genetics | Oncology, Experimental | Research | Cancer
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3. Full Text Genetic Testing in Pheochromocytoma or Functional Paraganglioma
by Laurence Amar and Jérôme Bertherat and Eric Baudin and Christiane Ajzenberg and Brigitte Bressac-de Paillerets and Olivier Chabre and Bernard Chamontin and Brigitte Delemer and Sophie Giraud and Arnaud Murat and Patricia Niccoli-Sire and Stéphane Richard and Vincent Rohmer and Jean-Louis Sadoul and Laurence Strompf and Martin Schlumberger and Xavier Bertagna and Pierre-François Plouin and Xavier Jeunemaitre and Anne-Paule Gimenez-Roqueplo
Journal of Clinical Oncology, ISSN 0732-183X, 12/2005, Volume 23, Issue 34, pp. 8812 - 8818
Purpose To assess the yield and the clinical value of systematic screening of susceptibility genes for patients with pheochromocytoma (pheo) or functional... 
DIAGNOSIS | COMPLEX-II | ONCOLOGY | SDHD GENE | MUTATION | FEATURES | Humans | Middle Aged | Iron-Sulfur Proteins - genetics | Male | Paraganglioma - diagnosis | Germ-Line Mutation - genetics | Genetic Testing - methods | Adrenal Gland Neoplasms - diagnosis | Aged, 80 and over | Adult | Female | Von Hippel-Lindau Tumor Suppressor Protein - genetics | Neurofibromatosis 1 - genetics | France | Child | Protein Subunits - genetics | Genetic Predisposition to Disease - genetics | Membrane Proteins - genetics | Paraganglioma - genetics | Pheochromocytoma - diagnosis | Gene Frequency | Genotype | Neurofibromatosis 1 - diagnosis | Phenotype | Succinate Dehydrogenase - genetics | Algorithms | Adolescent | Pheochromocytoma - genetics | Aged | Adrenal Gland Neoplasms - genetics | Proto-Oncogene Proteins c-ret - genetics
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4. Full Text Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma
by Ben Aim, Laurène and Pigny, Pascal and Castro-Vega, Luis Jaime and Buffet, Alexandre and Amar, Laurence and Bertherat, Jérôme and Drui, Delphine and Guilhem, Isabelle and Baudin, Eric and Lussey-Lepoutre, Charlotte and Corsini, Carole and Chabrier, Gérard and Briet, Claire and Faivre, Laurence and Cardot-Bauters, Catherine and Favier, Judith and Gimenez-Roqueplo, Anne-Paule and Burnichon, Nelly
Journal of Medical Genetics, ISSN 0022-2593, 2019, Volume 56, Issue 8, pp. 513 - 520
Knowing the genetic status of patients affected by paragangliomas and pheochromocytomas (PPGL) is important for the guidance of their management and their... 
somatic mutations | pheochromocytoma | next generation sequencing | mosaicism | paraganglioma | DIAGNOSIS | CONFER | ADRENAL-TUMORS | RECOMMENDATIONS | PREDISPOSITION | GENETICS & HEREDITY | GERMLINE MUTATIONS | SDH MUTATIONS | IMMUNOHISTOCHEMISTRY | Pheochromocytoma | Genes | Paraganglioma | Genomes | Mutation rates | Leukocytes | Paraffin | Patients | Genetic screening | Next-generation sequencing | Mosaicism | Software | Mutation | Deoxyribonucleic acid--DNA | Cancer | Tumors
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5. Full Text Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
by Waszak, Sebastian M and Northcott, Paul A and Buchhalter, Ivo and Robinson, Giles W and Sutter, Christian and Groebner, Susanne and Grund, Kerstin B and Brugières, Laurence and Jones, David T W and Pajtler, Kristian W and Morrissy, A Sorana and Kool, Marcel and Sturm, Dominik and Chavez, Lukas and Ernst, Aurelie and Brabetz, Sebastian and Hain, Michael and Zichner, Thomas and Segura-Wang, Maia and Weischenfeldt, Joachim and Rausch, Tobias and Mardin, Balca R and Zhou, Xin and Baciu, Cristina and Lawerenz, Christian and Chan, Jennifer A and Varlet, Pascale and Guerrini-Rousseau, Lea and Fults, Daniel W and Grajkowska, Wiesława and Hauser, Peter and Jabado, Nada and Ra, Young-Shin and Zitterbart, Karel and Shringarpure, Suyash S and De La Vega, Francisco M and Bustamante, Carlos D and Ng, Ho-Keung and Perry, Arie and MacDonald, Tobey J and Hernáiz Driever, Pablo and Bendel, Anne E and Bowers, Daniel C and McCowage, Geoffrey and Chintagumpala, Murali M and Cohn, Richard and Hassall, Timothy and Fleischhack, Gudrun and Eggen, Tone and Wesenberg, Finn and Feychting, Maria and Lannering, Birgitta and Schüz, Joachim and Johansen, Christoffer and Andersen, Tina V and Röösli, Martin and Kuehni, Claudia E and Grotzer, Michael and Kjaerheim, Kristina and Monoranu, Camelia M and Archer, Tenley C and Duke, Elizabeth and Pomeroy, Scott L and Shelagh, Redmond and Frank, Stephan and Sumerauer, David and Scheurlen, Wolfram and Ryzhova, Marina V and Milde, Till and Kratz, Christian P and Samuel, David and Zhang, Jinghui and Solomon, David A and Marra, Marco and Eils, Roland and Bartram, Claus R and von Hoff, Katja and Rutkowski, Stefan and Ramaswamy, Vijay and Gilbertson, Richard J and Korshunov, Andrey and Taylor, Michael D and Lichter, Peter and Malkin, David and Gajjar, Amar and Korbel, Jan O and Pfister, Stefan M and Sahlgrenska akademin and Institute of Clinical Sciences, Department of Pediatrics and Göteborgs universitet and Gothenburg University and Institutionen för kliniska vetenskaper, Avdelningen för pediatrik and Sahlgrenska Academy
The Lancet Oncology, ISSN 1470-2045, 06/2018, Volume 19, Issue 6, pp. 785 - 798
Medulloblastoma is associated with rare hereditary cancer predisposition syndromes; however, consensus medulloblastoma predisposition genes have not been... 
BREAST-CANCER | CHILDHOOD-CANCER | ONCOLOGY | LANDSCAPE | TP53 MUTATION | SUBGROUPS | FANCONI-ANEMIA | PALB2 | SOMATIC MUTATIONS | BRAIN-TUMORS | CHILDREN | Medicine, Experimental | Genetic research | Clinical trials | Medical research | Medulloblastoma | fanconi-anemia | Oncology | breast-cancer | tp53 | somatic mutations | mutation | subgroups | palb2 | brain-tumors | children | childhood-cancer | Cancer and Oncology | landscape | Cancer och onkologi
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6. Hyperaldostéronisme primaire
by Amar, Laurence
La Revue du praticien, ISSN 0035-2640, 06/2015, Volume 65, Issue 6, pp. 817 - 821
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7. Primary aldosteronism
by Amar, Laurence
La Revue du praticien, ISSN 0035-2640, 06/2015, Volume 65, Issue 6, p. 817
Primary aldosteronism affects 6% of hypertensive patients. The diagnosis should be suspected in any patient with severe or resistant hypertension or... 
Adrenocortical Adenoma - surgery | Adrenocortical Adenoma - diagnosis | Humans | Adrenal Cortex Neoplasms - surgery | Calcium Channel Blockers - therapeutic use | Renin - analysis | Aldosterone - analysis | Antihypertensive Agents - therapeutic use | Hypertension - etiology | Hypokalemia - diagnosis | Adrenalectomy | Hyperaldosteronism - diagnosis | Adrenal Cortex Neoplasms - diagnosis | Algorithms | Hyperaldosteronism - etiology | Hypertension - therapy | Hyperaldosteronism - therapy
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8. Full Text Proceedings of Réanimation 2017, the French Intensive Care Society International Congress
by Bougouin, Wulfran and Marijon, Eloi and Planquette, Benjamin and Karam, Nicole and Dumas, Florence and Celermajer, David and Jost, Daniel and Lamhaut, Lionel and Beganton, Frankie and Cariou, Alain and Meyer, Guy and Jouven, Xavier and Bureau, Côme and Charpentier, Julien and Salem, Omar Ben Hadj and Guillemet, Lucie and Arnaout, Michel and Ferre, Alexis and Geri, Guillaume and Mongardon, Nicolas and Pène, Frédéric and Chiche, Jean-Daniel and Mira, Jean-Paul and Labro, Guylaine and Belon, François and Luu, Vinh-Phuc and Chenet, Julien and Besch, Guillaume and Puyraveau, Marc and Piton, Gaël and Capellier, Gilles and Martin, Maëlle and Lascarrou, Jean-Baptiste and Le Thuaut, Aurélie and Lacherade, Jean-Claude and Martin-Lefèvre, Laurent and Fiancette, Maud and Vinatier, Isabelle and Lebert, Christine and Bachoumas, Konstantinos and Yehia, Aihem and Henry-Laguarrigue, Matthieu and Colin, Gwenhaël and Reignier, Jean and Privat, Elodie and Escutnaire, Joséphine and Dumont, Cyrielle and