Zobrazeno 1 - 10
of 94
pro vyhledávání: '"C A Stratakis"'
Autor:
Amanda Swain, Ag Lopez, A. Levasseur, Amandine Septier, Igor Tauveron, Ingrid Plotton, D. Dufour, Florian Guillou, Am Lefrançois-Martinez, A. Martinez, Isabelle Sahut-Barnola, Hervé Lefebvre, Cyril Djari, Fr Faucz, J. Wilmouth, Jc Pointud, Pierre Val, Nathanaëlle Montanier, C. A. Stratakis, Seppo Vainio, Crystal Kamilaris
Large Cell Calcifying Sertoli Cell Tumors (LCCSCTs) are among the most frequent lesions occurring in Carney complex (CNC) male patients. Although they constitute a key diagnostic criterion for this rare multiple neoplasia syndrome resulting from inac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92cb7dc70408f768888ab6a5b3c3adc8
https://hal.archives-ouvertes.fr/hal-03100406
https://hal.archives-ouvertes.fr/hal-03100406
Autor:
P Giannakopoulou, D.A. Kazis, S Chatzikonstantinou, C A Stratakis, C Lyssikatos, O Pikou, T Geroukis, Sevasti Bostanjopoulou, P Poulios
Publikováno v:
The International journal of neuroscience. 132(7)
"Carney Complex (CNC) is a familial lentiginosis syndrome, caused byWe describe a Greek family diagnosed with CNC after recurrent embolic strokes, secondary to left-sided atrial myxomas. There are limited cases in the literature describing this type
Autor:
C. Ribes, Eric Pasmant, Maria Candida Barisson Villares Fragoso, Herve Lefebvre, Lucas Bouys, Igor Tauveron, Isadora Pontes Cavalcante, Karine Perlemoine, P. Vaduva, F. Bonnet, Marie-Odile North, M. Barat, G. Giannone, Mathilde Sibony, Eric Letouzé, Anna Vaczlavik, Roberta Armignacco, Martin Reincke, Jérôme Bertherat, F. Violon, A. Berthon, C. A. Stratakis, Guillaume Assié, L. Groussin, Anne Jouinot, R. Libe, Bertrand Dousset, Philippe Emy, Bruno Ragazzon, L. Guignat, Magalie Haissaguerre, Stéphanie Espiard
Publikováno v:
Annales d'Endocrinologie. 82:239
Publikováno v:
Hormone and Metabolic Research. 48:764-770
Chronic exposure to supraphysiologic levels of glucocorticoids (GCs) is associated with impaired bone mineral density, an increase in fracture rates, and, in growing children, compromised linear growth. GCs inhibit bone formation in part by decreasin
Publikováno v:
Hormone and metabolic research = Hormon-und Stoffwechselforschung = Hormones et metabolisme, vol 48, iss 4
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare type of bilateral adrenal hyperplasia leading to hypercortisolemia. Adrenal nodularity is often appreciable with computed tomography (CT); however, accurate radiologic characterizatio
Autor:
Paula Pezzuto, Jousilene de Sales Tavares, Amilcar Tanuri, Fabio R. Faucz, G S de Azevedo, Renato S. Aguiar, Áurea Nogueira de Melo, Átila Duque Rossi, Bruno Luiz Fonseca Schamber-Reis, Cynthia Chester Cardoso, J J Mattapallil, C. A. Stratakis
Rossi ÁD, Faucz FR, Melo A, Pezzuto P, de Azevedo GS, Schamber-Reis BLF, Tavares JS, Mattapallil JJ, Tanuri A, Aguiar RS, Cardoso CC, Stratakis CA (Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; National Institutes of Health, Bethes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47ebfee19d305232061b4d6f10fd283
https://europepmc.org/articles/PMC6338508/
https://europepmc.org/articles/PMC6338508/
Autor:
Meg Keil, Mary Walter, C. Lyssikatos, Shanna Bernstein, S. Ten, C. A. Stratakis, Adrian S. Dobs, Robert D. Shamburek, Evgenia Gourgari, D. Khurana, Alan T. Remaley, Maya Lodish, R. Wesley, Maureen Sampson
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 100:4291-4298
Adult women with polycystic ovarian syndrome (PCOS) have an increased risk for cardiovascular disease, but the evidence for this is controversial in adolescents and young women with PCOS. Measurement of low-density lipoprotein (LDL) particle number,
Autor:
Jérôme Bertherat, Stéphanie Espiard, Fabio R. Faucz, Ludivine Drougat, C. A. Stratakis, Annabel Berthon
Publikováno v:
Human molecular genetics. 26(18)
Inactivating mutations in the Armadillo repeat-containing 5 (ARMC5) gene have recently been discovered in primary macronodular adrenal hyperplasia (PMAH), a cause of Cushing syndrome. Biallelic ARMC5 inactivation in PMAH suggested that ARMC5 may have
Autor:
Bruno Ragazzon, F. Cormier, Jérôme Bertherat, F. Rocchetti, F. Basso, Marthe Rizk-Rabin, S. Rodriguez, C. A. Stratakis, Maria Nesterova
Publikováno v:
Hormone and Metabolic Research
Hormone and Metabolic Research, Thieme Publishing, 2014, 46 (12), pp.883-888. ⟨10.1055/s-0034-1389951⟩
Hormone and Metabolic Research, Thieme Publishing, 2014, 46 (12), pp.883-888. ⟨10.1055/s-0034-1389951⟩
The cyclic AMP/protein kinase A signaling cascade is one of the main pathways involved in the pathogenesis of adrenocortical tumors. The PKA R1A and R2B proteins are the most abundant regulatory subunits in endocrine tissues. Inactivating mutations o
Autor:
Jérôme Bertherat, Denise M. Kay, Laura C. Hernández-Ramírez, Maya Lodish, F. Chasseloup, Nathan Pankratz, Fabio R. Faucz, C. A. Stratakis, T. Giampaolo, Prashant Chittiboina, James L. Mills
Publikováno v:
Annales d'Endocrinologie. 79:239-240
Introduction La neoplasie endocrienne multiple de type 4 (NEM4) est liee a des mutations germinales inactivatrices du gene CDKN1B. Un seul cas de maladie de Cushing a ete decrit dans ce contexte. Cependant, l’expression de CDKN1B est souvent diminu