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1. 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
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | 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 | Index Medicus
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2. 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
Life Sciences & Biomedicine | Oncology | Science & Technology | Medicine, Experimental | Genetic research | Clinical trials | Medical research | Medulloblastoma | Index Medicus | fanconi-anemia | breast-cancer | tp53 | somatic mutations | mutation | subgroups | palb2 | brain-tumors | children | childhood-cancer | Cancer and Oncology | landscape | Cancer och onkologi
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3. 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
somatic mutations | pheochromocytoma | next generation sequencing | mosaicism | paraganglioma | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Pheochromocytoma | Genes | Paraganglioma | Genomes | Mutation rates | Leukocytes | Paraffin | Patients | Genetic screening | Next-generation sequencing | Mosaicism | Software | Mutation | Deoxyribonucleic acid--DNA | Cancer | Tumors | Index Medicus
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4. 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
Life Sciences & Biomedicine | Oncology | Science & Technology | Adrenals. Adrenal axis. Renin-angiotensin system (diseases) | Biological and medical sciences | Endocrinopathies | Non tumoral diseases. Target tissue resistance. Benign neoplasms | Medical sciences | Tumors | 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 | Index Medicus
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5. Full Text Diagnosing phaeochromocytoma/paraganglioma in a patient presenting with critical illness: biochemistry versus imaging
by Amar, Laurence and Eisenhofer, Graeme
Clinical endocrinology (Oxford), ISSN 0300-0664, 09/2015, Volume 83, Issue 3, pp. 298 - 302
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Reproducibility of Results | Pheochromocytoma - diagnosis | Humans | Paraganglioma - urine | Adrenal Gland Neoplasms - blood | Metanephrine - urine | Critical Illness | Paraganglioma - diagnosis | Pheochromocytoma - urine | Adrenal Gland Neoplasms - urine | Paraganglioma - blood | Metanephrine - blood | Adrenal Gland Neoplasms - diagnosis | Diagnostic Imaging - methods | Pheochromocytoma - blood | Time Factors | Sensitivity and Specificity | Biochemistry | Urine | Illnesses | Mortality | Index Medicus
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6. Full Text Primary aldosteronism and pregnancy
by Landau, Ester and Amar, Laurence
Annales d'endocrinologie, ISSN 0003-4266, 2016, Volume 77, Issue 2, pp. 148 - 160
Internal Medicine | Endocrinology & Metabolism | Pregnancy | Hyperaldostéronisme primaire | Grossesse | Primary aldosteronism preeclampsia | Spironolactone | Préclampsie | Life Sciences & Biomedicine | Science & Technology | Prenatal Care - methods | Humans | Pregnancy Complications - surgery | Hyperaldosteronism - complications | Antihypertensive Agents - administration & dosage | Hypertension - drug therapy | Hypertension - surgery | Pregnancy Complications - diagnosis | Antihypertensive Agents - adverse effects | Hypertension - etiology | Adrenalectomy | Hyperaldosteronism - diagnosis | Female | Hyperaldosteronism - surgery | Index Medicus
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7. Full Text Editorial: miRNA Regulatory Pathways in Metazoans. Advances From in vivo and ex vivo Studies
by Amar, Laurence and Seitz, Hervé
Frontiers in genetics, ISSN 1664-8021, 2019, Volume 10, pp. 147 - 147
Genetic aspects | Cellular signal transduction | MicroRNA | Research | Metazoa | Life Sciences | Animal genetics | Genetics | Biochemistry, Molecular Biology | Genomics | antiviral and proviral microRNAs | small molecule screen | target RNA-directed microRNA degradation | intracytoplasmic localization | metazoan microRNAs | imprinted microRNA genes
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8. Full Text Diagnostic criteria for adrenal venous sampling
by Steichen, Olivier and Amar, Laurence
Current opinion in endocrinology, diabetes, and obesity, ISSN 1752-296X, 06/2016, Volume 23, Issue 3, pp. 218 - 224
blood specimen collection | hyperaldosteronism | catheterization | adrenal glands/blood supply | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Catheterization - standards | Hyperaldosteronism - diagnosis | Adrenal Glands - blood supply | Veins | Humans | Index Medicus | Life Sciences | Human health and pathology
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9. Full Text An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC , or SDHD gene mutations: a retrospective and prospective analysis
by van Nederveen, Francien H, MD and Gaal, José, MD and Favier, Judith, PhD and Korpershoek, Esther, BSc and Oldenburg, Rogier A, MD and de Bruyn, Elly MCA, BSc and Sleddens, Hein FBM, BSc and Derkx, Pieter, BSc and Rivière, Julie, BSc and Dannenberg, Hilde, MD and Petri, Bart-Jeroen, MD and Komminoth, Paul, Prof and Pacak, Karel, Prof and Hop, Wim CJ, PhD and Pollard, Patrick J, MD and Mannelli, Massimo, Prof and Bayley, Jean-Pierre, PhD and Perren, Aurel, MD and Niemann, Stephan, PhD and Verhofstad, Albert A, MD and de Bruïne, Adriaan P, Prof and Maher, Eamonn R, Prof and Tissier, Frédérique, MD and Méatchi, Tchao, MD and Badoual, Cécile, MD and Bertherat, Jérôme, Prof and Amar, Laurence, MD and Alataki, Despoina, MD and Van Marck, Eric, Prof and Ferrau, Francesco, MD and François, Jerney, BSc and de Herder, Wouter W, MD and Peeters, Mark-Paul FM Vrancken, MD and van Linge, Anne, MD and Lenders, Jacques WM, Prof and Gimenez-Roqueplo, Anne-Paule, Prof and de Krijger, Ronald R, MD and Dinjens, Winand NM, Dr
The lancet oncology, ISSN 1470-2045, 2009, Volume 10, Issue 8, pp. 764 - 771
Hematology, Oncology and Palliative Medicine | Life Sciences & Biomedicine | Oncology | Science & Technology | Membrane Proteins - genetics | Paraganglioma - genetics | Pheochromocytoma - diagnosis | Humans | Middle Aged | Male | Paraganglioma - diagnosis | Blotting, Western | Syndrome | Adrenal Gland Neoplasms - diagnosis | Immunohistochemistry - methods | Young Adult | Succinate Dehydrogenase - genetics | DNA Mutational Analysis | Adolescent | Germ-Line Mutation | Adult | Female | Pheochromocytoma - genetics | Aged | Adrenal Gland Neoplasms - genetics | Child | Immunohistochemistry | Hypertension | Molecular genetics | Gene mutations | Developmental biology | Genetic research | Genetic aspects | Universities and colleges | Human genetics | Tumors | Index Medicus
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