Zobrazeno 1 - 10
of 126
pro vyhledávání: '"C. Livieri"'
Publikováno v:
Metabolism. 47:1490-1493
In obese children, both spontaneous and stimulated growth hormone (GH) secretion are impaired but a normal or increased height velocity is usually observed. This study was undertaken to explain the discrepancy between impaired GH secretion and normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23e2357b7f4ffd1699d7d159e9483310
https://doi.org/10.1016/s0026-0495(98)90075-0
https://doi.org/10.1016/s0026-0495(98)90075-0
Autor:
Alberto Fois, Kirk Kittikamron, David H. Ledbetter, Paolo Simi, Elena Rossi, Lucia Pucci, Romeo Carrozzo, Andrea Corrias, Orsetta Zuffardi, Luciano Beccaria, Susan L. Christian, C. Livieri, L. Bosio
Publikováno v:
The American Journal of Human Genetics. 61(1):228-231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77c90cff16ce543062337488e0383563
Publikováno v:
Rivista di Neuroradiologia. 16:435-437
We describe the results of a study on 21 patients with adrenogenital syndrome without neurological symptoms who underwent neurological examination, neurophysiological tests and MR scan. Only five patients (23.8%) had a negative neuroradiological exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5ba1276d8b59c6f5f4bd3c302801d8e
https://doi.org/10.1177/197140090301600317
https://doi.org/10.1177/197140090301600317
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 4:310-315
As several studies have reported that 35% of patients with polycystic ovary syndrome are obese and that this syndrome seems to originate during the early phase of sexual maturation, we undertook a study of such subjects. We studied ultrasound and hor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::436706103597f9670e8a995f15f2c0f7
https://doi.org/10.1046/j.1469-0705.1994.04040310.x
https://doi.org/10.1046/j.1469-0705.1994.04040310.x
Autor:
L. Bosio, C. Livieri, G. Caselli, Patrizia Bruzzi, Lorenzo Iughetti, Luigi Gargantini, L. Ragusa, Andrea Corrias, Barbara Predieri, Graziano Grugni
Publikováno v:
European journal of pediatrics. 167(6)
Prader-Willi syndrome (PWS), a genetic disorder due to an alteration in the paternally derived long arm of chromosome 15, is characterized by a complex clinical picture (short stature, obesity, hypogonadism) that seems to be referable to as a central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e0c13bcd0fcb55dfe3b847ca859e3e3
https://pubmed.ncbi.nlm.nih.gov/17805568
https://pubmed.ncbi.nlm.nih.gov/17805568
Autor:
Carla Uggetti, Vittorio Cosi, C. Livieri, Elisa Candeloro, Stefano Bastianello, Anna Pichiecchio, Maria Grazia Egitto, Roberto Bergamaschi
Publikováno v:
Archives of neurology. 63(3)
Background Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis. Past reports suggested that brain white matter could be involved in CAH. Objective To detect the presence, and possible changes over time,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73a619f23ad8c7afe00125c8c2ba4720
https://pubmed.ncbi.nlm.nih.gov/16540460
https://pubmed.ncbi.nlm.nih.gov/16540460
Autor:
Elisa Candeloro, C. Livieri, Vittorio Cosi, Carla Uggetti, Diego Franciotta, Roberto Bergamaschi
Publikováno v:
Archives of neurology. 61(12)
Background Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis, generally caused by a total or partial deficiency in 21-hydroxylase, due to a deletion of or mutations in the CYP21 gene (the gene that cod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31659eaaccce7660780ea82bdcfb2f42
https://pubmed.ncbi.nlm.nih.gov/15596619
https://pubmed.ncbi.nlm.nih.gov/15596619
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 92(9)
During the neonatal period the diagnosis of the Prader-Willi syndrome (PWS) is difficult because the syndrome is expressed mainly by severe hypotonia at this age and the typical clinical features of later life are not yet present.To identify all the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35bf50439352da924c361372961b50b3
https://pubmed.ncbi.nlm.nih.gov/14599075
https://pubmed.ncbi.nlm.nih.gov/14599075
Autor:
V L, Brunelli, G, Russo, S, Bertelloni, L, Gargantini, R, Balducci, L, Chiesa, C, Livieri, C, De Sanctis, S, Einaudi, R, Virdis, G, Saggese, G, Chiumello
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 16
To investigate the influence of target height (TH), gender, phenotype, glucocorticoid formulation and age at onset of treatment on final height (FH) in patients with 21-hydroxylase deficiency (21OHD).Clinical data of 93 patients--46 simple virilizing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2e2f5d382b82222edc945d8b4c5b634
https://pubmed.ncbi.nlm.nih.gov/12729404
https://pubmed.ncbi.nlm.nih.gov/12729404
Autor:
Laura Maccarini, Sergio Comizzoli, C. Livieri, Marianna Guarcello, Anna Maria Castellazzi, Amedeo Pietri, Giovanna Maria Clelia Turconi, Carla Roggi, Gianfranco Piva
Publikováno v:
European journal of nutrition. 43(4)
Many human milk benefits have been well documented; nevertheless the newborn potential risk to the xenobiotic exposition may be relevant and it requires a biological monitoring in general prevention. Concerning this problem, attention should be paid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0a1473664ebaa45a00d89ac579d6a1
https://pubmed.ncbi.nlm.nih.gov/15309437
https://pubmed.ncbi.nlm.nih.gov/15309437