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2020

Central hypogonadism in Klinefelter syndrome: report of two cases and review of the literature

Cangiano, B., Indirli, R., Profka, E., Castellano, E., Goggi, G., Vezzoli, V., Mantovani, G., Arosio, M., Persani, L., Borretta, G., Ferrante, E. & Bonomi, M., Jan 1 2020, (Accepted/In press) In : Journal of Endocrinological Investigation.

Research output: Contribution to journalArticle

2019

45,X/46,X,i(Yp): Importance of Assessment and Support during Puberty and Adolescence

Gaudino, R., Maines, E., Guizzardi, F., Vezzoli, V., Krausz, C., Cavarzere, P., Piacentini, G., Antoniazzi, F. & Bonomi, M., Oct 1 2019, In : Sexual Development. 13, 3, p. 118-124 7 p.

Research output: Contribution to journalArticle

Addressing gaps in care of people with conditions affecting sex development and maturation

on behalf of COST Actions DSDnet and GnRH Network as well as the European Reference Network for Rare Endocrine Conditions (Endo–ERN), Oct 1 2019, In : Nature Reviews Endocrinology. 15, 10, p. 615-622 8 p.

Research output: Contribution to journalArticle

A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism

Indirli, R., Cangiano, B., Profka, E., Mantovani, G., Persani, L., Arosio, M., Bonomi, M. & Ferrante, E., Nov 12 2019, In : Frontiers in Endocrinology. 10, 781.

Research output: Contribution to journalArticle

Open Access

Genetics of ncHH: from a peculiar inheritance of a novel GNRHR mutation to a comprehensive review of the literature

Cioppi, F., Riera-Escamilla, A., Manilall, A., Guarducci, E., Todisco, T., Corona, G., Colombo, F., Bonomi, M., Flanagan, C. A. & Krausz, C., Jan 2019, In : Andrology. 7, 1, p. 88-101 14 p.

Research output: Contribution to journalArticle

GnRH antagonist treatment of malignant adrenocortical tumors

Doroszko, M., Chrusciel, M., Stelmaszewska, J., Slezak, T., Anisimowicz, S., Plöckinger, U., Quinkler, M., Bonomi, M., Wolczynski, S., Huhtaniemi, I., Toppari, J. & Rahman, N. A., Jan 1 2019, In : Endocrine-Related Cancer. 26, 1, p. 103-117 15 p.

Research output: Contribution to journalArticle

High-Density Lipoprotein Function Is Reduced in Patients Affected by Genetic or Idiopathic Hypogonadism

Adorni, M. P., Zimetti, F., Cangiano, B., Vezzoli, V., Bernini, F., Caruso, D., Corsini, A., Sirtori, C. R., Cariboni, A., Bonomi, M. & Ruscica, M., Jun 19 2019, In : Journal of Clinical Endocrinology and Metabolism. 104, 8, p. 3097-3107 11 p.

Research output: Contribution to journalArticle

Selenium supplementation in the management of thyroid autoimmunity during pregnancy: results of the “SERENA study”, a randomized, double-blind, placebo-controlled trial

Mantovani, G., Isidori, A. M., Moretti, C., Di Dato, C., Greco, E., Ciolli, P., Bonomi, M., Petrone, L., Fumarola, A., Campagna, G., Vannucchi, G., Di Sante, S., Pozza, C., Faggiano, A., Lenzi, A. & Giannetta, E., Jan 1 2019, In : Endocrine. 66, 3, p. 542-550

Research output: Contribution to journalArticle

Selenium supplementation in the management of thyroid autoimmunity during pregnancy: results of the “SERENA study”, a randomized, double-blind, placebo-controlled trial

Mantovani, G., Isidori, A. M., Moretti, C., Di Dato, C., Greco, E., Ciolli, P., Bonomi, M., Petrone, L., Fumarola, A., Campagna, G., Vannucchi, G., Di Sante, S., Pozza, C., Faggiano, A., Lenzi, A. & Giannetta, E., 2019, In : Endocrine. 66, 3, p. 542-550 9 p.

Research output: Contribution to journalArticle

Thyroid function in Klinefelter syndrome: a multicentre study from KING group

KING group, Oct 1 2019, In : Journal of Endocrinological Investigation. 42, 10, p. 1199-1204 6 p.

Research output: Contribution to journalArticle

2018

A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome

Roche, E. F., McGowan, A., Koulouri, O., Turgeon, M. O., Nicholas, A. K., Heffernan, E., El-Khairi, R., Abid, N., Lyons, G., Halsall, D., Bonomi, M., Persani, L., Dattani, M. T., Gurnell, M., Bernard, D. J. & Schoenmakers, N., Dec 1 2018, In : Clinical Endocrinology. 89, 6, p. 813-823 11 p.

Research output: Contribution to journalArticle

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)

Bonomi, M., Vezzoli, V., Krausz, C., Guizzardi, F., Vezzani, S., Simoni, M., Bassi, I., Duminuco, P., Di Iorgi, N., Giavoli, C., Pizzocaro, A., Russo, G., Moro, M., Fatti, L., Ferlin, A., Mazzanti, L., Zatelli, M. C., Cannavò, S., Isidori, A. M., Pincelli, A. I. & 11 others, Prodam, F., Mancini, A., Limone, P., Tanda, M. L., Gaudino, R., Salerno, M., Francesca, P., Maghnie, M., Maggi, M., Persani, L. & Hypogonadism, I. N. O. C., Jan 2018, In : European Journal of Endocrinology. 178, 1, p. 23-32 10 p.

Research output: Contribution to journalArticle

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)

Bonomi, M., Vezzoli, V., Krausz, C., Guizzardi, F., Vezzani, S., Simoni, M., Bassi, I., Duminuco, P., Di Iorgi, N., Giavoli, C., Pizzocaro, A., Russo, G., Moro, M., Fatti, L., Ferlin, A., Mazzanti, L., Zatelli, M. C., Cannavò, S., Isidori, A. M., Pincelli, A. I. & 11 others, Prodam, F., Mancini, A., Limone, P., Tanda, M. L., Gaudino, R., Salerno, M., Francesca, P., Maghnie, M., Maggi, M., Persani, L. & Italian Network on Central Hypogonadism, Jan 2018, In : European Journal of Endocrinology. 178, 1, p. 23-32 10 p.

Research output: Contribution to journalArticle

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)

Bonomi, M., Vezzoli, V., Krausz, C., Guizzardi, F., Vezzani, S., Simoni, M., Bassi, I., Duminuco, P., Di Iorgi, N., Giavoli, C., Pizzocaro, A., Russo, G., Moro, M., Fatti, L., Ferlin, A., Mazzanti, L., Zatelli, M. C., Cannavò, S., Isidori, A. M., Pincelli, A. I. & 31 others, Prodam, F., Mancini, A., Maghnie, M., Persani, L., Arosio, M., Balsamo, A., Beck-Peccoz, P., Bizzarri, C., Boschetti, M., Brunani, A., Brunelli, V., Cappa, M., Colombo, P., Corbetta, S., Corona, G., Di Iorgi, N., Fabbri, A., Ghezzi, M., Grosso, E., Grugni, G., Lania, A., Larizza, L., Lombardi, V., Mantovani, G., Mencarelli, M. A., Porcelli, P., Rossi, G., Sala, E., Spada, A., Weber, G. & on behalf of the Italian Network on Central Hypogonadism (NICe group), Jan 1 2018, In : European Journal of Endocrinology. 178, 1, p. 23-32 10 p.

Research output: Contribution to journalArticle

Clinical and genetic characterisation of a series of patients with triple A syndrome

Kurnaz, E., Duminuco, P., Aycan, Z., Savaş-Erdeve, Ş., Muratoğlu Şahin, N., Keskin, M., Bayramoğlu, E., Bonomi, M. & Çetinkaya, S., Mar 2018, In : European Journal of Pediatrics. p. 1-7 7 p.

Research output: Contribution to journalArticle

Hypogonadotropic hypogonadism and pituitary hypoplasia as recurrent features in Ulnar-Mammary syndrome

Galazzi, E., Duminuco, P., Moro, M., Guizzardi, F., Marazzi, N., Sartorio, A., Avignone, S., Bonomi, M., Persani, L. & Bonati, M. T., Dec 1 2018, In : Endocrine Connections. 7, 12, p. 1432-1441 10 p.

Research output: Contribution to journalArticle

Hypogonadotropic hypogonadism and pituitary hypoplasia as recurrent features in Ulnar-Mammary syndrome

Galazzi, E., Duminuco, P., Moro, M., Guizzardi, F., Marazzi, N., Sartorio, A., Avignone, S., Bonomi, M., Persani, L. & Bonati, M. T., Dec 1 2018, In : Endocrine Connections. 7, 12, p. 1432-1441 10 p.

Research output: Contribution to journalArticle

2017

A frequent oligogenic involvement in congenital hypothyroidism

de Filippis, T., Gelmini, G., Paraboschi, E., Vigone, M. C., Di Frenna, M., Marelli, F., Bonomi, M., Cassio, A., Larizza, D., Moro, M., Radetti, G., Salerno, M., Ardissino, D., Weber, G., Gentilini, D., Guizzardi, F., Duga, S. & Persani, L., Jul 1 2017, In : Human Molecular Genetics. 26, 13, p. 2507-2514 8 p.

Research output: Contribution to journalArticle

A frequent oligogenic involvement in congenital hypothyroidism

de Filippis, T., Gelmini, G., Paraboschi, E., Vigone, M. C., Di Frenna, M., Marelli, F., Bonomi, M., Cassio, A., Larizza, D., Moro, M., Radetti, G., Salerno, M., Ardissino, D., Weber, G., Gentilini, D., Guizzardi, F., Duga, S. & Persani, L., 2017, In : Human Molecular Genetics. 26, 13, p. 2507-2514 8 p.

Research output: Contribution to journalArticle

A frequent oligogenic involvement in congenital hypothyroidism

de Filippis, T., Gelmini, G., Paraboschi, E., Vigone, M. C., Di Frenna, M., Marelli, F., Bonomi, M., Cassio, A., Larizza, D., Moro, M., Radetti, G., Salerno, M., Ardissino, D., Weber, G., Gentilini, D., Guizzardi, F., Duga, S. & Persani, L., Jul 1 2017, In : Human Molecular Genetics. 26, 13, p. 2507-2514 8 p.

Research output: Contribution to journalArticle

A frequent oligogenic involvement in congenital hypothyroidism

de Filippis, T., Gelmini, G., Paraboschi, E., Vigone, MC., Di Frenna, M., Marelli, F., Bonomi, M., Cassio, A., Larizza, D., Moro, M., Radetti, G., Salerno, M., Ardissino, D., Weber, G., Gentilini, D., Guizzardi, F., Duga, S. & Persani, L., 2017, In : Human Molecular Genetics. 26, 13, p. 2507-2514 8 p.

Research output: Contribution to journalArticle

Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism

Badiu, C., Bonomi, M., Borshchevsky, I., Cools, M., Craen, M., Ghervan, C., Hauschild, M., Hershkovitz, E., Hrabovszky, E., Juul, A., Kim, S. H., Kumanov, P., Lecumberri, B., Lemos, M. C., Neocleous, V., Niedziela, M., Djurdjevic, S. P., Persani, L., Phan-Hug, F., Pignatelli, D. & 9 others, Pitteloud, N., Popovic, V., Quinton, R., Skordis, N., Smith, N., Stefanija, M. A., Xu, C., Young, J. & Dwyer, A. A., Mar 20 2017, In : Orphanet Journal of Rare Diseases. 12, 1, 57.

Research output: Contribution to journalArticle

Mild TSH resistance: Clinical and hormonal features in childhood and adulthood

Vigone, M. C., Di Frenna, M., Guizzardi, F., Gelmini, G., de Filippis, T., Mora, S., Caiulo, S., Sonnino, M., Bonomi, M., Persani, L. & Weber, G., Nov 1 2017, In : Clinical Endocrinology. 87, 5, p. 587-596 10 p.

Research output: Contribution to journalArticle

Mild TSH resistance: clinical and hormonal features in childhood and adulthood

Vigone, MC., Di Frenna, M., Guizzardi, F., Gelmini, G., de Filippis, T., Mora, S., Caiulo, S., Sonnino, M., Bonomi, M., Persani, L. & Weber, G., 2017, In : Clinical Endocrinology. 87, 5, p. 587-596 10 p.

Research output: Contribution to journalArticle

Sperm recovery and ICSI outcomes in Klinefelter syndrome: A systematic review and meta-analysis

Corona, G., Pizzocaro, A., Lanfranco, F., Garolla, A., Pelliccione, F., Vignozzi, L., Ferlin, A., Foresta, C., Jannini, E. A., Maggi, M., Lenzi, A., Pasquali, D., Francavilla, S., Balercia, G., Bonomi, M., Calogero, A., Fabbri, A., Francavilla, F., Giagullì, V., Pivonello, R. & 25 others, Radicioni, A., Rochira, V., Accardo, G., Cangiano, B., Condorelli, R. A., Cordeschi, G., D'Andrea, S., Di Mambro, A., Esposito, D., Galdiero, M., Giovannini, L., Granata, A. R. M., La Vignera, S., Motta, G., Negri, L., Persani, L., Salzano, C., Santi, D., Selice, R., Simoni, M., Tatone, C., Tirabassi, G., Tresoldi, A. S., Vicari, E. & On behalf of the Klinefelter ItaliaN Group (KING), May 1 2017, In : Human Reproduction Update. 23, 3, p. 265-275 11 p., dmx008.

Research output: Contribution to journalArticle

2016

IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management

Joustra, S. D., Heinen, C. A., Schoenmakers, N., Bonomi, M., Ballieux, B. E. P. B., Turgeon, M-O., Bernard, D. J., Fliers, E., Van Trotsenburg, A. S. P., Losekoot, M., Persani, L., Wit, J. M., Biermasz, N. R., Pereira, A. M., Oostdijk, W. & IGSF1 Clinical Care Group, Apr 2016, In : Journal of Clinical Endocrinology and Metabolism. 101, 4, p. 1627-36 10 p.

Research output: Contribution to journalArticle

2015

A newvariant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia

Vezzoli, V., Duminuco, P., Vottero, A., Kleinau, G., Schülein, R., Minari, R., Bassi, I., Bernasconi, S., Persani, L. & Bonomi, M., 2015, In : Human Molecular Genetics. 24, 21, p. 6003-6012 10 p.

Research output: Contribution to journalArticle

2014

Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways

Libri, D. V., Kleinau, G., Vezzoli, V., Busnelli, M., Guizzardi, F., Sinisi, A. A., Pincelli, A. I., Mancini, A., Russo, G., Beck-Peccoz, P., Loche, S., Crivellaro, C., Maghnie, M., Krausz, C., Persani, L. & Bonomi, M., 2014, In : Journal of Clinical Endocrinology and Metabolism. 99, 3

Research output: Contribution to journalArticle

Kallmann's syndrome and normosmic isolated hypogonadotropic hypogonadism: Two largely overlapping manifestations of one rare disorder

Bonomi, M., Cappa, M., Cariboni, A., Di Schiavi, E., Fabbri, A., Ferlin, A., Foresta, C., Ghizzoni, L., Jannini, E., Krausz, C., Loche, S., Lombardo, F., Maggi, M., Maggi, R., Maghnie, M., Mancini, A., Merlo, G., Panzica, G., Radetti, G., Russo, G. & 3 others, Simoni, M., Sinisi, A. A. & Persani, L., 2014, In : Journal of Endocrinological Investigation. 37, 5, p. 499-500 2 p.

Research output: Contribution to journalArticle

2013

The IGSF1 deficiency syndrome: Characteristics of male and female patients

Joustra, S. D., Schoenmakers, N., Persani, L., Campi, I., Bonomi, M., Radetti, G., Beck-Peccoz, P., Zhu, H., Davis, T. M. E., Sun, Y., Corssmit, E. P., Appelman-Dijkstra, N. M., Heinen, C. A., Pereira, A. M., Varewijck, A. J., Janssen, J. A. M. J. L., Endert, E., Hennekam, R. C., Lombardi, M. P., Mannens, M. M. A. M. & 9 others, Bak, B., Bernard, D. J., Breuning, M. H., Chatterjee, K., Dattani, M. T., Oostdijk, W., Biermasz, N. R., Wit, J. M. & Van Trotsenburg, A. S. P., Dec 2013, In : Journal of Clinical Endocrinology and Metabolism. 98, 12, p. 4942-4952 11 p.

Research output: Contribution to journalArticle

The unusual adequate development of a child with severe central hypothyroidsmnegative at neonatal thyrotropin screening

Libri, D. V., Trettene, A., Bonomi, M., Beck-Peccoz, P., Persani, L. & Salvatoni, A., Oct 2013, In : Journal of Endocrinological Investigation. 36, 9, p. 788-789 2 p.

Research output: Contribution to journalArticle

2012

Blood cell mitochondrial DNA content and premature ovarian aging

Bonomi, M., Somigliana, E., Cacciatore, C., Busnelli, M., Rossetti, R., Bonetti, S., Paffoni, A., Mari, D., Ragni, G., Persani, L., Arosio, M., Beck-Peccoz, P., Biondi, M., Bione, S., Bruni, V., Brigante, C., Cannavò, S., Cavallo, L., Cisternino, M., Colombo, I. & 46 others, Corbetta, S., Crosignani, P. G., D'Avanzo, M. G., Dalprà, L., Danesino, C., Di Battista, E., Di Prospero, F., Donti, E., Einaudi, S., Falorni, A., Foresta, C., Fusi, F., Garofalo, N., Giotti, I., Lanzi, R., Larizza, D., Locatelli, N., Loli, P., Madaschi, S., Maghnie, M., Maiore, S., Mantero, F., Marozzi, A., Marzotti, S., Migone, N., Nappi, R., Palli, D., Patricelli, M. G., Pisani, C., Prontera, P., Petraglia, F., Radetti, G., Renieri, A., Ricca, I., Ripamonti, A., Rossetti, R., Russo, G., Russo, S., Tonacchera, M., Toniolo, D., Torricelli, F., Vegetti, W., Villa, N., Vineis, P., Wasniewsk, M. & Zuffardi, O., Aug 3 2012, In : PLoS One. 7, 8, e42423.

Research output: Contribution to journalArticle

Diagnostic and therapeutic challenges of acquired thyrotropic deficiency

Persani, L., Bonomi, M., Radin, R. & Beck-Peccoz, P., Apr 2012, In : Annales d'Endocrinologie. 73, 2, p. 138-140 3 p.

Research output: Contribution to journalArticle

Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemia

Calebiro, D., Gelmini, G., Cordella, D., Bonomi, M., Winkler, F., Biebermann, H., De Marco, A., Marelli, F., Libri, D. V., Antonica, F., Vigone, M. C., Cappa, M., Mian, C., Sartorio, A., Beck-Peccoz, P., Radetti, G., Weber, G. & Persani, L., Jan 2012, In : Journal of Clinical Endocrinology and Metabolism. 97, 1

Research output: Contribution to journalArticle

Increased loss of the Y chromosome in peripheral blood cells in male patients with autoimmune thyroiditis

Persani, L., Bonomi, M., Lleo, A., Pasini, S., Civardi, F., Bianchi, I., Campi, I., Finelli, P., Miozzo, M., Castronovo, C., Sirchia, S., Gershwin, M. E. & Invernizzi, P., May 2012, In : Journal of Autoimmunity. 38, 2-3

Research output: Contribution to journalArticle

Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement

Sun, Y., Bak, B., Schoenmakers, N., Van Trotsenburg, A. S. P., Oostdijk, W., Voshol, P., Cambridge, E., White, J. K., Le Tissier, P., Gharavy, S. N. M., Martinez-Barbera, J. P., Stokvis-Brantsma, W. H., Vulsma, T., Kempers, M. J., Persani, L., Campi, I., Bonomi, M., Beck-Peccoz, P., Zhu, H., Davis, T. M. E. & 21 others, Hokken-Koelega, A. C. S., Del Blanco, D. G., Rangasami, J. J., Ruivenkamp, C. A. L., Laros, J. F. J., Kriek, M., Kant, S. G., Bosch, C. A. J., Biermasz, N. R., Appelman-Dijkstra, N. M., Corssmit, E. P., Hovens, G. C. J., Pereira, A. M., Den Dunnen, J. T. D., Wade, M. G., Breuning, M. H., Hennekam, R. C., Chatterjee, K., Dattani, M. T., Wit, J. M. & Bernard, D. J., Dec 2012, In : Nature Genetics. 44, 12, p. 1375-1381 7 p.

Research output: Contribution to journalArticle

New understandings of the genetic basis of isolated idiopathic central hypogonadism

Bonomi, M., Libri, D. V., Guizzardi, F., Guarducci, E., Maiolo, E., Pignatti, E., Asci, R. & Persani, L., Jan 2012, In : Asian Journal of Andrology. 14, 1, p. 49-56 8 p.

Research output: Contribution to journalArticle

2011

Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet

Calebiro, D., Porazzi, P., Bonomi, M., Lisi, S., Grindati, A., De Nittis, D., Fugazzola, L., Marinò, M., Bottà, G. & Persani, L., Sep 2011, In : Journal of Endocrinological Investigation. 34, 8, p. 593-598 6 p.

Research output: Contribution to journalArticle

Syndromes de résistance à TSH

Translated title of the contribution: Syndromes of resistance to TSHPersani, L., Gelmini, G., Marelli, F., Beck-Peccoz, P. & Bonomi, M., Apr 2011, In : Annales d'Endocrinologie. 72, 2, p. 60-63 4 p.

Research output: Contribution to journalArticle

2010

Genetics and phenomics of hypothyroidism due to TSH resistance

Persani, L., Calebiro, D., Cordella, D., Weber, G., Gelmini, G., Libri, D., De Filippis, T. & Bonomi, M., Jun 2010, In : Molecular and Cellular Endocrinology. 322, 1-2, p. 72-82 11 p.

Research output: Contribution to journalArticle

Rituximab treatment in patients with active Graves' orbitopathy: Effects on proinflammatory and humoral immune reactions

Vannucchi, G., Campi, I., Bonomi, M., Covelli, D., Dazzi, D., Currò, N., Simonetta, S., Bonara, P., Persani, L., Guastella, C., Wall, J., Beck-Peccoz, P. & Salvi, M., Sep 2010, In : Clinical and Experimental Immunology. 161, 3, p. 436-443 8 p.

Research output: Contribution to journalArticle

2009

A family with complete resistance to thyrotropin-releasing hormone

Bonomi, M., Busnelli, M., Beck-Peccoz, P., Costanzo, D., Antonica, F., Dolci, C., Pilotta, A., Buzi, F. & Persani, L., Feb 12 2009, In : New England Journal of Medicine. 360, 7, p. 731-734 4 p.

Research output: Contribution to journalArticle

Primary ovarian insufficiency: X chromosome defects and autoimmunity

Persani, L., Rossetti, R., Cacciatore, C. & Bonomi, M., Aug 2009, In : Journal of Autoimmunity. 33, 1, p. 35-41 7 p.

Research output: Contribution to journalArticle

2008

Activator protein-1 and smad proteins synergistically regulate human follicle-stimulating hormone β-promoter activity

Wang, Y., Fortin, J., Lamba, P., Bonomi, M., Persani, L., Roberson, M. S. & Bernard, D. J., Nov 2008, In : Endocrinology. 149, 11, p. 5577-5591 15 p.

Research output: Contribution to journalArticle

2007
2006

Structural differences in the hinge region of the glycoprotein hormone receptors: Evidence from the sulfated tyrosine residues

Bonomi, M., Busnelli, M., Persani, L., Vassart, G. & Costagliola, S., Dec 2006, In : Molecular Endocrinology. 20, 12, p. 3351-3363 13 p.

Research output: Contribution to journalArticle