Search Results - "Castinetti, Frederic"

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    Radiation techniques in aggressive pituitary tumours and carcinomas by Castinetti, Frederic

    Published in Reviews in endocrine & metabolic disorders (01-06-2020)
    “…Defining the role of radiation techniques in treatment of aggressive pituitary tumours and carcinomas is a difficult task: indeed, studies reported in the…”
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    Aggressive pituitary tumours and pituitary carcinomas by Raverot, Gérald, Ilie, Mirela Diana, Lasolle, Hélène, Amodru, Vincent, Trouillas, Jacqueline, Castinetti, Frédéric, Brue, Thierry

    Published in Nature reviews. Endocrinology (01-11-2021)
    “…Although usually benign, anterior pituitary tumours occasionally exhibit aggressive behaviour, with invasion of surrounding tissues, rapid growth, resistance…”
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    Long-term follow-up of ipilimumab-induced hypophysitis, a common adverse event of the anti-CTLA-4 antibody in melanoma by Albarel, Frédérique, Gaudy, Caroline, Castinetti, Frédéric, Carré, Tiphaine, Morange, Isabelle, Conte-Devolx, Bernard, Grob, Jean-Jacques, Brue, Thierry

    Published in European journal of endocrinology (01-02-2015)
    “…ObjectiveFew data are published on the long-term follow-up of ipilimumab-induced hypophysitis, a cytotoxic T-lymphocyte antigen 4 antibody. We characterized…”
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    Challenges in molecular diagnosis of multiple endocrine neoplasia by Romanet, Pauline, Charnay, Théo, Sahakian, Nicolas, Cuny, Thomas, Castinetti, Frédéric, Barlier, Anne

    Published in Frontiers in endocrinology (Lausanne) (27-09-2024)
    “…Multiple endocrine neoplasia (MEN) is a group of rare genetic diseases characterized by the occurrence of multiple tumors of the endocrine system in the same…”
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    A comprehensive review on MEN2B by Castinetti, Frederic, Moley, Jeffrey, Mulligan, Lois, Waguespack, Steven G

    Published in Endocrine-related cancer (01-02-2018)
    “…MEN2B is a very rare autosomal dominant hereditary tumor syndrome associated with medullary thyroid carcinoma (MTC) in 100% cases, pheochromocytoma in 50%…”
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    Real-life clinical impact of a five-tiered classification of pituitary tumors by Sahakian, Nicolas, Appay, Romain, Resseguier, Noémie, Graillon, Thomas, Piazzola, Cécilia, Laure, Cécilia, Figarella-Branger, Dominique, Régis, Jean, Castinetti, Frédéric, Brue, Thierry, Dufour, Henry, Cuny, Thomas

    Published in European journal of endocrinology (01-12-2022)
    “…Introduction Usually benign, pituitary tumors (PT) can be invasive and aggressive with a propensity to progress and/or recur. Trouillas’s clinicopathological…”
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    Management of clinically non-functioning pituitary adenoma by Chanson, Philippe, Raverot, Gerald, Castinetti, Frédéric, Cortet-Rudelli, Christine, Galland, Françoise, Salenave, Sylvie

    Published in Annales d'endocrinologie (01-07-2015)
    “…Abstract Clinically NFPA is currently the preferred term for designing all the pituitary adenomas which are not hormonally active (in other words, not…”
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    Outcome of non-functioning ACTH pituitary tumors: silent does not mean indolent by Sahakian, Nicolas, Goetz, Lise, Appay, Romain, Graillon, Thomas, Raingeard, Isabelle, Piazzola, Cécilia, Regis, Jean, Castinetti, Frédéric, Brue, Thierry, Dufour, Henry, Cuny, Thomas

    Published in Pituitary (01-10-2024)
    “…Introduction Silent corticotroph tumors (siACTH) represent a rare entity of pituitary tumors (PT), usually more aggressive than other PT. Few predictor factors…”
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    Surgical indications for pituitary tumors during pregnancy: a literature review by Graillon, Thomas, Cuny, Thomas, Castinetti, Frédéric, Courbière, Blandine, Cousin, Marie, Albarel, Frédérique, Morange, Isabelle, Bruder, Nicolas, Brue, Thierry, Dufour, Henry

    Published in Pituitary (01-04-2020)
    “…Purpose Surgical indications for pituitary tumors during pregnancy are rare, and are derived from a balance between expected benefits, particularly for…”
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    MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectives by Amodru, Vincent, Taieb, David, Guerin, Carole, Romanet, Pauline, Paladino, Nunzia, Brue, Thierry, Cuny, Thomas, Barlier, Anne, Sebag, Frederic, Castinetti, Frederic

    Published in Endocrine (01-09-2020)
    “…Multiple endocrine neoplasia type 2 (MEN2) is a rare hereditary syndrome due to mutations of the proto-oncogene REarranged during Transfection (RET), defined…”
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    HCG-responsive aldosteronoma with transient secretion during pregnancy confirmed through HCG-stimulated adrenal venous sampling by Castinetti, Frederic, Guerin, Carole, Louiset, Estelle, Lacroix, André

    Published in Frontiers in endocrinology (Lausanne) (28-02-2023)
    “…Primary aldosteronism can be regulated by the ectopic expression of G-protein coupled receptors in aldosteronomas or bilateral hyperplasias. We report a rare…”
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    Germinal defects of SDHx genes in patients with isolated pituitary adenoma by Mougel, Grégory, Lagarde, Arnaud, Albarel, Frédérique, Essamet, Wassim, Luigi, Perrine, Mouly, Céline, Vialon, Magaly, Cuny, Thomas, Castinetti, Frédéric, Saveanu, Alexandru, Brue, Thierry, Barlier, Anne, Romanet, Pauline

    Published in European journal of endocrinology (01-10-2020)
    “…Background: The ‘3PAs’ syndrome, associating pituitary adenoma (PA) and pheochromocytoma/paraganglioma (PPGL), is sometimes associated with mutations in…”
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    Pheochromocytoma surgery without systematic preoperative pharmacological preparation: insights from a referral tertiary center experience by Buisset, Cyrille, Guerin, Carole, Cungi, Pierre-Julien, Gardette, Mickael, Paladino, Nunzia-Cinzia, Taïeb, David, Cuny, Thomas, Castinetti, Frederic, Sebag, Frederic

    Published in Surgical endoscopy (01-02-2021)
    “…Background Despite significant advances in imaging and genetics, as well as surgical and anesthetic innovations, morbidity in pheochromocytoma surgery remains…”
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    Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man by Bando, Hironori, Brinkmeier, Michelle L, Castinetti, Frederic, Fang, Qing, Lee, Mi-Sun, Saveanu, Alexandru, Albarel, Frédérique, Dupuis, Clémentine, Brue, Thierry, Camper, Sally A

    Published in Human molecular genetics (13-01-2023)
    “…Congenital hypopituitarism is a genetically heterogeneous condition that is part of a spectrum disorder that can include holoprosencephaly. Heterozygous…”
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