Results
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6401.
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6402.
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MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. [electronic resource] by
- Burnichon, Nelly
- Cascón, Alberto
- Schiavi, Francesca
- Morales, Nicole Paes
- Comino-Méndez, Iñaki
- Abermil, Nasséra
- Inglada-Pérez, Lucía
- de Cubas, Aguirre A
- Amar, Laurence
- Barontini, Marta
- de Quirós, Sandra Bernaldo
- Bertherat, Jérôme
- Bignon, Yves-Jean
- Blok, Marinus J
- Bobisse, Sara
- Borrego, Salud
- Castellano, Maurizio
- Chanson, Philippe
- Chiara, María-Dolores
- Corssmit, Eleonora P M
- Giacchè, Mara
- de Krijger, Ronald R
- Ercolino, Tonino
- Girerd, Xavier
- Gómez-García, Encarna B
- Gómez-Graña, Alvaro
- Guilhem, Isabelle
- Hes, Frederik J
- Honrado, Emiliano
- Korpershoek, Esther
- Lenders, Jacques W M
- Letón, Rocío
- Mensenkamp, Arjen R
- Merlo, Anna
- Mori, Luigi
- Murat, Arnaud
- Pierre, Peggy
- Plouin, Pierre-François
- Prodanov, Tamara
- Quesada-Charneco, Miguel
- Qin, Nan
- Rapizzi, Elena
- Raymond, Victoria
- Reisch, Nicole
- Roncador, Giovanna
- Ruiz-Ferrer, Macarena
- Schillo, Frank
- Stegmann, Alexander P A
- Suarez, Carlos
- Taschin, Elisa
- Timmers, Henri J L M
- Tops, Carli M J
- Urioste, Miguel
- Beuschlein, Felix
- Pacak, Karel
- Mannelli, Massimo
- Dahia, Patricia L M
- Opocher, Giuseppe
- Eisenhofer, Graeme
- Gimenez-Roqueplo, Anne-Paule
- Robledo, Mercedes
Producer: 20121105
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 18
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6403.
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Phenotypic variability and risk of malignancy in SDHC-linked paragangliomas: lessons from three unrelated cases with an identical germline mutation (p.Arg133*). [electronic resource] by
- Bickmann, Julia K
- Sollfrank, Stefanie
- Schad, Arno
- Musholt, Thomas J
- Springer, Erik
- Miederer, Matthias
- Bartsch, Oliver
- Papaspyrou, Konstantinos
- Koutsimpelas, Dimitrios
- Mann, Wolf J
- Weber, Matthias M
- Lackner, Karl J
- Rossmann, Heidi
- Fottner, Christian
Producer: 20140714
In:
The Journal of clinical endocrinology and metabolism vol. 99
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6404.
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6405.
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Paragangliomas arise through an autonomous vasculo-angio-neurogenic program inhibited by imatinib. [electronic resource] by
- Verginelli, Fabio
- Perconti, Silvia
- Vespa, Simone
- Schiavi, Francesca
- Prasad, Sampath Chandra
- Lanuti, Paola
- Cama, Alessandro
- Tramontana, Lorenzo
- Esposito, Diana Liberata
- Guarnieri, Simone
- Sheu, Artenca
- Pantalone, Mattia Russel
- Florio, Rosalba
- Morgano, Annalisa
- Rossi, Cosmo
- Bologna, Giuseppina
- Marchisio, Marco
- D'Argenio, Andrea
- Taschin, Elisa
- Visone, Rosa
- Opocher, Giuseppe
- Veronese, Angelo
- Paties, Carlo T
- Rajasekhar, Vinagolu K
- Söderberg-Nauclér, Cecilia
- Sanna, Mario
- Lotti, Lavinia Vittoria
- Mariani-Costantini, Renato
Producer: 20190701
In:
Acta neuropathologica vol. 135
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6406.
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6407.
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6408.
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Clinical significance and peculiarities of succinate dehydrogenase B and hypoxia inducible factor 1α expression in parasympathetic versus sympathetic paragangliomas. [electronic resource] by
- Bernardo-Castiñeira, Cristóbal
- Sáenz-de-Santa-María, Inés
- Valdés, Nuria
- Astudillo, Aurora
- Balbín, Milagros
- Pitiot, Ana S
- Jiménez-Fonseca, Paula
- Scola, Bartolomé
- Tena, Isabel
- Molina-Garrido, María-José
- Sevilla, María-Agustina
- Beristein, Elena
- Forga, Lluís
- Villabona, Carles
- Oriola, Josep
- Halperin, Irene
- Suarez, Carlos
- Chiara, María-Dolores
Producer: 20200527
In:
Head & neck vol. 41
Availability: No items available.
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6409.
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6410.
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6411.
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6412.
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6413.
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6414.
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6415.
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6416.
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6417.
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6418.
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6419.
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Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients. [electronic resource] by
- Castellano, M
- Mori, L
- Giacchè, M
- Agliozzo, E
- Tosini, R
- Panarotto, A
- Cappelli, C
- Mulatero, P
- Cumetti, D
- Veglio, F
- Agabiti-Rosei, E
Producer: 20061212
In:
Annals of the New York Academy of Sciences vol. 1073
Availability: No items available.
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6420.
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