Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Pheochromocytoma and MAX[original query] |
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| A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. The Journal of clinical endocrinology and metabolism 2013 Jul 98 (7): E1248-56. Rattenberry Eleanor, Vialard Lindsey, Yeung Anna, Bair Hayley, McKay Kirsten, Jafri Mariam, Canham Natalie, Cole Trevor R, Denes Judit, Hodgson Shirley V, Irving Richard, Izatt Louise, Korbonits Márta, Kumar Ajith V, Lalloo Fiona, Morrison Patrick J, Woodward Emma R, Macdonald Fiona, Wallis Yvonne, Maher Eamonn |
| Long-term prognosis of patients with pediatric pheochromocytoma. Endocrine-related cancer 2014 Feb 21 (1): 17-25. Bausch Birke, Wellner Ulrich, Bausch Dirk, Schiavi Francesca, Barontini Marta, Sanso Gabriela, Walz Martin K, Peczkowska Mariola, Weryha Georges, Dall'igna Patrizia, Cecchetto Giovanni, Bisogno Gianni, Moeller Lars C, Bockenhauer Detlef, Patocs Attila, Rácz Karoly, Zabolotnyi Dmitry, Yaremchuk Svetlana, Dzivite-Krisane Iveta, Castinetti Frederic, Taieb David, Malinoc Angelica, von Dobschuetz Ernst, Roessler Jochen, Schmid Kurt W, Opocher Giuseppe, Eng Charis, Neumann Hartmut P |
| Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma. The Journal of clinical endocrinology and metabolism 2014 Jul 99 (7): E1352-60. Welander Jenny, Andreasson Adam, Juhlin C Christofer, Wiseman Roger W, Bäckdahl Martin, Höög Anders, Larsson Catharina, Gimm Oliver, Söderkvist Pet |
| Universal genetic screening uncovers a novel presentation of an SDHAF2 mutation. The Journal of clinical endocrinology and metabolism 2014 Jul 99 (7): E1392-6. Casey Ruth, Garrahy Aoife, Tuthill Antoinette, O'Halloran Domhnall, Joyce Caroline, Casey Mary B, O'Shea Paula, Bell Marc |
| Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2015 Aug . Lee C H, Cheung C Y Y, Chow W S, Woo Y C, Yeung C Y, Lang B H H, Fong C H Y, Kwok K H M, Chen S P L, Mak C M, Tan K C B, Lam K S |
| Genotype-Dependent Brown Adipose Tissue Activation in Patients With Pheochromocytoma and Paraganglioma. The Journal of clinical endocrinology and metabolism 2015 Nov jc20153205. Puar Troy, van Berkel Anouk, Gotthardt Martin, Havekes Bas, Hermus Ad R M M, Lenders Jacques W M, van Marken Lichtenbelt Wouter D, Xu Ying, Brans Boudewijn, Timmers Henri J L |
| [Hereditary pheochromocytoma-associated syndromes. Part 2]. Terapevticheskii arkhiv 2017 6 87 (10): 115-119. Yukina M Yu, Troshina E A, Beltsevich D |
| 18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma. The Journal of clinical endocrinology and metabolism 2018 3 103 (4): 1574-1582. Taïeb David, Jha Abhishek, Guerin Carole, Pang Ying, Adams Karen T, Chen Clara C, Romanet Pauline, Roche Philippe, Essamet Wassim, Ling Alexander, Quezado Martha M, Castinetti Frédéric, Sebag Fréderic, Pacak Kar |
| Loss of BAP1 in Pheochromocytomas and Paragangliomas Seems Unrelated to Genetic Mutations. Endocrine pathology 2019 11 30 (4): 276-284. Maffeis Valeria, Cappellesso Rocco, Nicolè Lorenzo, Guzzardo Vincenza, Menin Chiara, Elefanti Lisa, Schiavi Francesca, Guido Maria, Fassina Ambrog |
| Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma. Oncotarget 2019 11 10 (57): 5919-5931. Albattal Shatha, Alswailem Meshael, Moria Yosra, Al-Hindi Hindi, Dasouki Majed, Abouelhoda Mohamed, Alkhail Hala Aba, Alsuhaibani Entissar, Alzahrani Ali |
| Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX Deletion. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2020 6 52 (11): 784-787. Petignot Sandrine, Daly Adrian F, Castermans Emilie, Korpershoek Esther, Scagnol Irène, Beckers Pablo, Dideberg Vinciane, Rohmer Vincent, Bours Vincent, Beckers Albe |
| Genetic and Clinical Profiles of Pheochromocytoma and Paraganglioma: A Single Center Study. Frontiers in endocrinology 2020 12 11 574662. Ma Xiaosen, Li Ming, Tong Anli, Wang Fen, Cui Yunying, Zhang Xuebin, Zhang Yushi, Chen Shi, Li Yux |
| Genetic predisposition to neural crest-derived tumors: revisiting the role of KIF1B. Endocrine connections 2020 10 9 (10): 1042-1050. Cardot Bauters Catherine, Leteurtre Emmanuelle, Carnaille Bruno, Do Cao Christine, Espiard Stéphanie, Penven Malo, Destailleur Evelyne, Szuster Isabelle, Lovecchio Tonio, Leclerc Julie, Frénois Fredéric, Esquivel Emmanuel, Dahia Patricia L M, Ait-Yahya Emilie, Crépin Michel, Pigny Pasc |
| Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia. Medicina (Kaunas, Lithuania) 2022 Aug 58 (8): . Provenzano Aldesia, Chetta Massimiliano, De Filpo Giuseppina, Cantini Giulia, La Barbera Andrea, Nesi Gabriella, Santi Raffaella, Martinelli Serena, Rapizzi Elena, Luconi Michaela, Maggi Mario, Mannelli Massimo, Ercolino Tonino, Canu Letiz |
| A case of juvenile-onset pheochromocytoma with KIF1B p.V1529M germline mutation. Endocrine journal 2022 1 69 (6): 705-716. Nezu Masahiro, Hirotsu Yosuke, Amemiya Kenji, Katsumata Miho, Watanabe Tomomi, Takizawa Soichi, Inoue Masaharu, Mochizuki Hitoshi, Hosaka Kyoko, Oyama Toshio, Omata Mas |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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