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Luigi Maione, M.D.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Nettore IC, Maione L, Palatucci G, Dolce P, Franchini F, Ungaro P, Belfiore A, Colao A, Macchia PE. Flavor identification inversely correlates with body mass index (BMI). Nutr Metab Cardiovasc Dis. 2020 Jul 24; 30(8):1299-1305. PMID: 32513578.
    Citations:    
  2. Nettore IC, Maione L, Desiderio S, De Nisco E, Franchini F, Palatucci G, Ungaro P, Cantone E, Macchia PE, Colao A. Influences of Age, Sex and Smoking Habit on Flavor Recognition in Healthy Population. Int J Environ Res Public Health. 2020 02 04; 17(3). PMID: 32033174.
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  3. Maione L, Pala G, Bouvattier C, Trabado S, Papadakis G, Chanson P, Bouligand J, Pitteloud N, Dwyer AA, Maghnie M, Young J. Congenital hypogonadotropic hypogonadism/Kallmann syndrome is associated with statural gain in both men and women: a monocentric study. Eur J Endocrinol. 2020 Feb; 182(2):185. PMID: 31770102.
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  4. Young J, Xu C, Papadakis GE, Acierno JS, Maione L, Hietamäki J, Raivio T, Pitteloud N. Clinical Management of Congenital Hypogonadotropic Hypogonadism. Endocr Rev. 2019 04 01; 40(2):669-710. PMID: 30698671.
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  5. De Rosa A, Nettore IC, Cantone E, Maione L, Desiderio S, Peluso S, Saccà F, Manganelli F, Bruzzese D, Colao A, De Michele G, Macchia PE. The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease. Neurol Sci. 2019 Jul; 40(7):1351-1356. PMID: 30895397.
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  6. Maione L, Chanson P. National acromegaly registries. Best Pract Res Clin Endocrinol Metab. 2019 04; 33(2):101264. PMID: 30894298.
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  7. Maione L, Fèvre A, Nettore IC, Manilall A, Francou B, Trabado S, Bouligand J, Guiochon-Mantel A, Delemer B, Flanagan CA, Macchia PE, Millar RP, Young J. Similarities and differences in the reproductive phenotypes of women with congenital hypogonadotrophic hypogonadism caused by GNRHR mutations and women with polycystic ovary syndrome. Hum Reprod. 2019 Jan 01; 34(1):137-147. PMID: 30476149.
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  8. Briet C, Ilie MD, Kuhn E, Maione L, Brailly-Tabard S, Salenave S, Cariou B, Chanson P. Changes in metabolic parameters and cardiovascular risk factors after therapeutic control of acromegaly vary with the treatment modality. Data from the Bicêtre cohort, and review of the literature. Endocrine. 2019 02; 63(2):348-360. PMID: 30397873.
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  9. Maione L, Dwyer AA, Francou B, Guiochon-Mantel A, Binart N, Bouligand J, Young J. GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing. Eur J Endocrinol. 2018 Mar; 178(3):R55-R80. PMID: 29330225.
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  10. Millar RP, Sonigo C, Anderson RA, George J, Maione L, Brailly-Tabard S, Chanson P, Binart N, Young J. Hypothalamic-Pituitary-Ovarian Axis Reactivation by Kisspeptin-10 in Hyperprolactinemic Women With Chronic Amenorrhea. J Endocr Soc. 2017 Nov 01; 1(11):1362-1371. PMID: 29264460.
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  11. Petrossians P, Daly AF, Natchev E, Maione L, Blijdorp K, Sahnoun-Fathallah M, Auriemma R, Diallo AM, Hulting AL, Ferone D, Hana V, Filipponi S, Sievers C, Nogueira C, Fajardo-Montañana C, Carvalho D, Hana V, Stalla GK, Jaffrain-Réa ML, Delemer B, Colao A, Brue T, Neggers SJCMM, Zacharieva S, Chanson P, Beckers A. Acromegaly at diagnosis in 3173 patients from the Liège Acromegaly Survey (LAS) Database. Endocr Relat Cancer. 2017 10; 24(10):505-518. PMID: 28733467.
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  12. Maione L, Colao A, Young J. Bone mineral density in older patients with never-treated congenital hypogonadotropic hypogonadism. Endocrine. 2018 01; 59(1):231-233. PMID: 28577250.
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  13. Bry-Gauillard H, Larrat-Ledoux F, Levaillant JM, Massin N, Maione L, Beau I, Binart N, Chanson P, Brailly-Tabard S, Hall JE, Young J. Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH. J Clin Endocrinol Metab. 2017 Apr 01; 102(4):1102-1111. PMID: 28324034.
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  14. Nettore IC, De Nisco E, Desiderio S, Passaro C, Maione L, Negri M, Albano L, Pivonello R, Pivonello C, Portella G, Ungaro P, Colao A, Macchia PE. Selenium supplementation modulates apoptotic processes in thyroid follicular cells. Biofactors. 2017 May 06; 43(3):415-423. PMID: 28251705.
    Citations: 1     Fields:    Translation:AnimalsCells
  15. Maione L, Brue T, Beckers A, Delemer B, Petrossians P, Borson-Chazot F, Chabre O, François P, Bertherat J, Cortet-Rudelli C, Chanson P. Changes in the management and comorbidities of acromegaly over three decades: the French Acromegaly Registry. Eur J Endocrinol. 2017 May; 176(5):645-655. PMID: 28246150.
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  16. Paepegaey AC, Salenave S, Kamenicky P, Maione L, Brailly-Tabard S, Young J, Chanson P. Cabergoline Tapering Is Almost Always Successful in Patients With Macroprolactinomas. J Endocr Soc. 2017 Mar 01; 1(3):221-230. PMID: 29264479.
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  17. Maione L, Brailly-Tabard S, Nevoux J, Bouligand J, Young J. Reversal of congenital hypogonadotropic hypogonadism in a man with Kallmann syndrome due to SOX10 mutation. Clin Endocrinol (Oxf). 2016 12; 85(6):988-989. PMID: 27616149.
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  18. Kuhn E, Maione L, Bouchachi A, Rozière M, Salenave S, Brailly-Tabard S, Young J, Kamenicky P, Assayag P, Chanson P. Long-term effects of pegvisomant on comorbidities in patients with acromegaly: a retrospective single-center study. Eur J Endocrinol. 2015 Nov; 173(5):693-702. PMID: 26429918.
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  19. Maione L, Cantone E, Nettore IC, Cerbone G, De Brasi D, Maione N, Young J, Di Somma C, Sinisi AA, Iengo M, Macchia PE, Pivonello R, Colao A. Flavor perception test: evaluation in patients with Kallmann syndrome. Endocrine. 2016 May; 52(2):236-43. PMID: 26209039.
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  20. Maione L, Tortora F, Modica R, Ramundo V, Riccio E, Daniele A, Belfiore MP, Colao A, Pisani A, Faggiano A. Pituitary function and morphology in Fabry disease. Endocrine. 2015 Nov; 50(2):483-8. PMID: 25896551.
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  21. Giton F, Trabado S, Maione L, Sarfati J, Le Bouc Y, Brailly-Tabard S, Fiet J, Young J. Sex steroids, precursors, and metabolite deficiencies in men with isolated hypogonadotropic hypogonadism and panhypopituitarism: a GCMS-based comparative study. J Clin Endocrinol Metab. 2015 Feb; 100(2):E292-6. PMID: 25393641.
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  22. Trabado S, Lamothe S, Maione L, Bouvattier C, Sarfati J, Brailly-Tabard S, Young J. Congenital hypogonadotropic hypogonadism and Kallmann syndrome as models for studying hormonal regulation of human testicular endocrine functions. Ann Endocrinol (Paris). 2014 May; 75(2):79-87. PMID: 24815726.
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  23. Chemla D, Attal P, Maione L, Veyer AS, Mroue G, Baud D, Salenave S, Kamenicky P, Bobin S, Chanson P. Impact of successful treatment of acromegaly on overnight heart rate variability and sleep apnea. J Clin Endocrinol Metab. 2014 Aug; 99(8):2925-31. PMID: 24780045.
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  24. Trabado S, Maione L, Bry-Gauillard H, Affres H, Salenave S, Sarfati J, Bouvattier C, Delemer B, Chanson P, Le Bouc Y, Brailly-Tabard S, Young J. Insulin-like peptide 3 (INSL3) in men with congenital hypogonadotropic hypogonadism/Kallmann syndrome and effects of different modalities of hormonal treatment: a single-center study of 281 patients. J Clin Endocrinol Metab. 2014 Feb; 99(2):E268-75. PMID: 24243640.
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  25. Maione L, Albarel F, Bouchard P, Gallant M, Flanagan CA, Bobe R, Cohen-Tannoudji J, Pivonello R, Colao A, Brue T, Millar RP, Lombes M, Young J, Guiochon-Mantel A, Bouligand J. R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism. PLoS One. 2013; 8(7):e69616. PMID: 23936060.
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  26. Maione L, Benadjaoud S, Eloit C, Sinisi AA, Colao A, Chanson P, Ducreux D, Benoudiba F, Young J. Computed tomography of the anterior skull base in Kallmann syndrome reveals specific ethmoid bone abnormalities associated with olfactory bulb defects. J Clin Endocrinol Metab. 2013 Mar; 98(3):E537-46. PMID: 23348397.
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  27. Massin N, Bry H, Vija L, Maione L, Constancis E, Haddad B, Morel Y, Claessens F, Young J. Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation. Clin Endocrinol (Oxf). 2012 Oct; 77(4):593-8. PMID: 22469007.
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  28. Maione L, Garcia C, Bouchachi A, Kallel N, Maison P, Salenave S, Young J, Assayag P, Chanson P. No evidence of a detrimental effect of cabergoline therapy on cardiac valves in patients with acromegaly. J Clin Endocrinol Metab. 2012 Sep; 97(9):E1714-9. PMID: 22723314.
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  29. Salenave S, Trabado S, Maione L, Brailly-Tabard S, Young J. Male acquired hypogonadotropic hypogonadism: diagnosis and treatment. Ann Endocrinol (Paris). 2012 Apr; 73(2):141-6. PMID: 22541999.
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  30. Young J, Metay C, Bouligand J, Tou B, Francou B, Maione L, Tosca L, Sarfati J, Brioude F, Esteva B, Briand-Suleau A, Brisset S, Goossens M, Tachdjian G, Guiochon-Mantel A. SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development. Hum Reprod. 2012 May; 27(5):1460-5. PMID: 22416012.
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  31. Bouvattier C, Maione L, Bouligand J, Dodé C, Guiochon-Mantel A, Young J. Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism. Nat Rev Endocrinol. 2011 Oct 18; 8(3):172-82. PMID: 22009162.
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  32. Trabado S, Maione L, Salenave S, Baron S, Galland F, Bry-Gauillard H, Guiochon-Mantel A, Chanson P, Pitteloud N, Sinisi AA, Brailly-Tabard S, Young J. Estradiol levels in men with congenital hypogonadotropic hypogonadism and the effects of different modalities of hormonal treatment. Fertil Steril. 2011 Jun; 95(7):2324-9, 2329.e1-3. PMID: 21536274.
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  33. Sinisi AA, Asci R, Bellastella G, Maione L, Esposito D, Elefante A, De Bellis A, Bellastella A, Iolascon A. Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: case report. Hum Reprod. 2008 Oct; 23(10):2380-4. PMID: 18596028.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.