Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Antonio Balsamo"'
Autor:
Federico Baronio, Alice Marzatico, Rosaria De Iasio, Rita Ortolano, Antonio Fanolla, Giorgio Radetti, Antonio Balsamo, Andrea Pession, Alessandra Cassio
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 6, p 2187 (2023)
Premature pubarche (PP) could represent the first manifestation of non-classic congenital adrenal hyperplasia caused by 21 hydroxylase deficiency (NC21OHD) (10–30% of cases). In the last 20 years, the necessity of performing an ACTH test to diagnos
Externí odkaz:
https://doaj.org/article/13295b992d6643728d336b072bb9049c
Autor:
Carla Bizzarri, Rita Ortolano, Silvia Einaudi, Mariangela Chiarito, Tommaso Aversa, Mariacarolina Salerno, Federico Baronio, Laura Guazzarotti, Angela Alibrandi, Maria Felicia Faienza, Domenico Corica, Donatella Capalbo, Barbara Baldini Ferroli, Enrica Abrigo, Malgorzata Wasniewska, Anna Grandone, Antonio Balsamo, Antonietta Spinuzza, Gianni Russo, Letteria Morabito
Background: Children with nonclassical congenital adrenal hyperplasia (NCCAH) often present increased growth velocity secondary to elevation of adrenal androgens that accelerates bone maturation and might compromise adult height (AH). Objective: The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757b4b6d64728e5d253ec60d3fd3a87d
http://hdl.handle.net/11588/828454
http://hdl.handle.net/11588/828454
Autor:
Stefano Gualandi, E Cacciari, Antonio Balsamo, Eveline Barbieri, Davide Tassinari, Stefano Zucchini, Alessandro Cicognani
Publikováno v:
Archives of Disease in Childhood. 84:340-343
AIM—To compare final height in two groups of low birth weight children examined for short stature: the first group untreated because of normal growth hormone (GH) secretion, the second treated with human growth hormone (hGH) because of abnormal sec
Autor:
Stefano Gualandi, Stefano Zucchini, Antonio Balsamo, Alessandra Cassio, Alessandro Cicognani, Andrea Pasini, E Cacciari, Silvana Salardi, Piero Pirazzoli
Publikováno v:
Clinical Endocrinology. 51:733-739
OBJECTIVE Birth weight influences both postnatal growth and the initial response to GH therapy in GH-deficient subjects, but its relationship to final height is uncertain. Therefore, we examined final height results in a group of subjects treated for
Autor:
Piero Pirazzoli, Davide Tassinari, Antonio Balsamo, Emanuele Cacciari, Stefano Gualandi, Alessandro Cicognani, Alessandra Cassio, Stefano Zucchini, Silvana Salardi, Andrea Pasini, Gabriella Carla
Publikováno v:
European Journal of Endocrinology. :53-60
The aim of the present study was to evaluate retrospectively the influence of various auxological and laboratory parameters on final height in a group of GH-deficient children after replacement therapy and to compare their final height with that of a
Autor:
Emmanuel Mignot, Uberto Pagotto, Oliviero Bruni, Piero Pirazzoli, Elena Finotti, Filippo Bernardi, Shahrad Taheri, Alessandro Cicognani, Antonio Balsamo, Giuseppe Plazzi, Fabio Pizza, Francesca Poli, Raffaele Ferri, Lino Nobili
Publikováno v:
Sleep. 36(2)
Address correspondence to: Giuseppe Plazzi, MD, PhD, Department of Neurological Sciences,Via Ugo Foscolo 7, 40123 Bologna, Italy; Tel: +39 051 209 29 26; Fax: +39 051 209 29 63; E-mail: giuseppe.plazzi@unibo.itStudy Objectives: We analyzed the potent
Autor:
C Colli, Paola Tassoni, Antonio Balsamo, Davide Tassinari, Emanuele Cacciari, Alessandro Cicognani, Alessandra Cassio
Publikováno v:
The Journal of Pediatrics. 126:474-477
To determine long-term growth response to growth hormone (GH) therapy in patients with isolated GH deficiency who had been small for gestational age and in those who had been appropriate in size for gestational age.Longitudinal, case-control study.Pe
Autor:
Dina Lazareva, Lilia Baldazzi, Antonio Balsamo, Alessandra Cassio, Federico Baronio, Alessandra Antelli, Alessandro Cicognani
We report on a DAX1 gene investigation in a patient with X-linked adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism (HH) in order to identify mutations causing this disorder and to confirm the clinical diagnosis. The description of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26889a499172149859b19f72144b7cf7
http://hdl.handle.net/11585/21797
http://hdl.handle.net/11585/21797
Autor:
G. Parisi, Paola Tassoni, E Cacciari, Piero Pirazzoli, Antonio Balsamo, Stefano Zucchini, Alessandro Cicognani, M Mandini
Publikováno v:
The Journal of clinical endocrinology and metabolism. 74(6)
Possible causes of error in the diagnosis of isolated GH deficiency are the variability of GH response to repeated tests, the existence of transient GH deficiencies, and the low GH levels found in short statured children with delayed puberty. Sixty-t
Gonadal and adrenal secretion of dehydroepiandrosterone sulfate in prepubertal and pubertal subjects
Autor:
G. Bolelli, E Cacciari, E Frejaville, Alessandra Cassio, Antonio Balsamo, Maurizio Capelli, Franco Zappulla, Ventura D
Publikováno v:
Scopus-Elsevier
The Authors have evaluated the relationship between the secretion of dehydroepiandrosterone sulfate (DHA-S) by the adrenal glands and by the gonads in a group of prepubertal and pubertal subjects ("short normal"), both males and females. In the male