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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Neuroendocrine Tumors and NF1[original query]
Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience.
Annals of the New York Academy of Sciences 2006 Aug 1073 (): 138-48.
Korpershoek E, Van Nederveen F H, Dannenberg H, Petri B J, Komminoth P, Perren A, Lenders J W, Verhofstad A A, De Herder W W, De Krijger R R, Dinjens W N
Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.
The Journal of surgical research 2009 Nov 157 (1): 55-62.
Meyer-Rochow Goswin Y, Smith Janine M, Richardson Anne-Louise, Marsh Deborah J, Sidhu Stan B, Robinson Bruce G, Benn Diana
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.
Annals of surgical oncology 2013 May 20 (5): 1444-50.
Fishbein Lauren, Merrill Shana, Fraker Douglas L, Cohen Debbie L, Nathanson Katherine
Activating FGFR1 Mutations in Sporadic Pheochromocytomas.
World journal of surgery 2017 11 42 (2): 482-489.
Welander Jenny, ?ysiak Ma?gorzata, Brauckhoff Michael, Brunaud Laurent, Söderkvist Peter, Gimm Oliv
Blood-based next-generation sequencing analysis of neuroendocrine neoplasms.
Oncotarget 2020 6 11 (19): 1749-1757.
Zakka Katerina, Nagy Rebecca, Drusbosky Leylah, Akce Mehmet, Wu Christina, Alese Olatunji B, El-Rayes Bassel F, Kasi Pashtoon Murtaza, Mody Kabir, Starr Jason, Shaib Walid
Pseudohypoxic pheochromocytomas and paragangliomas dominate in children.
Pediatric blood & cancer 2021 3 68 (7): e28981.
Redlich Antje, Pamporaki Christina, Lessel Lienhard, Frühwald Michael C, Vorwerk Peter, Kuhlen Michae
Mutation Frequency in Main Susceptibility Genes Among Patients With Head and Neck Paragangliomas.
Frontiers in genetics 2020 11 614908.
Snezhkina Anastasiya V, Fedorova Maria S, Pavlov Vladislav S, Kalinin Dmitry V, Golovyuk Alexander L, Pudova Elena A, Guvatova Zulfiya G, Melnikova Nataliya V, Dmitriev Alexey A, Razmakhaev George S, Poloznikov Andrey A, Alekseeva Galina S, Kaprin Andrey D, Krasnov George S, Kudryavtseva Anna
Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma.
Gene 2023 4 147432.
Tabebi Mouna, Frikha Fakher, Volpe Massimiliano, Gimm Oliver, Söderkvist Pet
Clinical exome next?generation sequencing panel for hereditary pheochromocytoma and paraganglioma diagnosis.
Experimental and therapeutic medicine 2025 1 29 (2): 34.
Beatrice Melli, Vincenza Ylenia Cusenza, Sandra Martinelli, Federica Castiglione, Loretta Fornaciari, Andrea Palicelli, Luca Braglia, Enrico Farnetti, Aurelio Negro, Simonetta Rosato, Andrea Frasoldati, Maicol Baldini, Chiara Grasselli, Davide Nico
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