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THERAPEUTICS AND CLINICAL RISK MANAGEMENT, ISSN 1178-203X, 2010, Volume 6, Issue default, pp. 367 - 381
Osteogenesis imperfecta (OI) is the most common bone genetic disorder and it is characterized by bone brittleness and various degrees of growth disorder.... 
dentinogenesis imperfecta | adult onset deafness | connective tissue malfunction | bone brittleness | "brittle bone disease" | blue sclerae | HEALTH CARE SCIENCES & SERVICES | joint laxity | short stature | osteogenesis imperfecta | progressive skeletal deformities | bone genetic disorder
Journal Article
Journal of Bone and Mineral Metabolism, ISSN 0914-8779, 7/2012, Volume 30, Issue 4, pp. 434 - 438
Journal Article
Pediatric Annals, ISSN 0090-4481, 04/2016, Volume 45, Issue 4, pp. e116 - e119
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 2018
Gonadotropin-releasing hormone agonists (GnRH-a) are common treatment options for central precocious puberty (CPP) in childhood. GnRH-a treatment is useful and... 
arterial hypertension | GnRH-a | precocious puberty
Journal Article
European Journal of Nutrition, ISSN 1436-6207, 3/2019, Volume 58, Issue 2, pp. 731 - 742
Journal Article
Journal Article
NUTRIENTS, ISSN 2072-6643, 05/2019, Volume 11, Issue 5, p. 1070
Journal Article
by Bonomi, Marco and Vezzoli, Valeria and Krausz, Csilla and Guizzardi, Fabiana and Vezzani, Silvia and Simoni, Manuela and Bassi, Ivan and Duminuco, Paolo and Di Iorgi, Natascia and Giavoli, Claudia and Pizzocaro, Alessandro and Russo, Gianni and Moro, Mirella and Fatti, Letizia and Ferlin, Alberto and Mazzanti, Laura and Zatelli, Maria Chiara and Cannavò, Salvo and Isidori, Andrea M and Pincelli, Angela Ida and Prodam, Flavia and Mancini, Antonio and Limone, Paolo and Tanda, Maria Laura and Gaudino, Rossella and Salerno, Mariacarolina and Francesca, Pregnolato and Maghnie, Mohamad and Maggi, Mario and Persani, Luca and Aimaretti, G and Altobell, M and Ambrosio, M.R and Andrioli, M and Angelett, G and Arecco, F and Arnald, G and Arosio, M and Balsamo, A and Baldassarr, M and Bartalena, L and Bazzon, N and Beccari, L and Beck-Peccoz, P and Bellastella, G and Bellizz, M and Benedicent, F and Bernasconi, S and Bizzarri, C and Bona, G and Bonadonna, S and Borrett, G and Boschetti, M and Brunani, A and Brunelli, V and Buz, F and Cacciatore, C and Cangiano, B and Cappa, M and Casalone, R and Cassio, A and Cavarzere, P and Cherubini, V and Ciampani, T and Cicognan, D and Cignarell, A and Cisternin, M and Colombo, P and Corbetta, S and Corciul, N and Corona, G and Cozzi, R and Crivellaro, C and Dalle Mule, I and Danesi, L and Eli, A.V.D and Degli Uberti, E and De Leo, S and Della Valle, E and De Marchi, M and Di Iorgi, N and Di Mambr, A and Fabbri, A and Foresta, C and Forti, G and Franceschi, A.R and Garolla, A and Ghezzi, M and Giacomozzi, C and Giusti, M and Grosso, E and Guabello, G and Guarneri, M.P and Grugni, G and Lanfranco, F and Lania, A and Lanzi, R and Larizza, L and Lenzi, A and Loche, S and ... and Italian Network Cent Hypogonadism and Italian Network on Central Hypogonadism
European Journal of Endocrinology, ISSN 0804-4643, 01/2018, Volume 178, Issue 1, pp. 23 - 32
Journal Article
Journal Article
Italian Journal of Pediatrics, ISSN 1720-8424, 01/2018, Volume 44, Issue 1, pp. 10 - 6
Background: Neonatal screening for 21 hydroxylase deficiency is designed to detect classical form of congenital adrenal hyperplasia (CAH). It is still unclear... 
Newborn screening | 17-Ohp | Congenital adrenal hyperplasia | Premature pubarche | HYPERANDROGENISM | METABOLIC SYNDROME | CONGENITAL ADRENAL-HYPERPLASIA | BIRTH-WEIGHT | PRETERM INFANTS | PRECOCIOUS PUBARCHE | 17-ALPHA-HYDROXYPROGESTERONE | GESTATIONAL-AGE | 17-HYDROXYPROGESTERONE LEVELS | STEROID 21-HYDROXYLASE DEFICIENCY | PEDIATRICS
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 11/2016, Volume 174, Issue 11, p. 395
Objective To evaluate the incidence of congenital hypothyroidism (CH) with delayed TSH elevation among low-birth-weight (LBW) newborns in North-Eastern Italy... 
Neonates | Congenital diseases | Low-birth-weight | Infants | Thyroid gland | Hypothyroidism | Medical screening | Thyroid-stimulating hormone | Newborn babies | Thyroxine | Birth weight | Diagnosis | Thyroid
Journal Article