Zobrazeno 1 - 10
of 78
pro vyhledávání: '"F. Colabucci"'
Autor:
Letizia Ragusa, R. M. Cento, Antonino Alberti, Caterina Proto, Gaetano Fiore, Antonio Lanzone, F. Colabucci
Publikováno v:
Human Reproduction. 12:1709-1713
Ovarian sensitivity to follicle stimulating hormone (FSH) during the early follicular phase of the human menstrual cycle was studied in six post-menarchal patients with Down's syndrome and 12 normo-ovulatory women. Pure FSH (75 IU) was given i.v. to
Publikováno v:
American Journal of Medical Genetics. 66:269-272
We describe a patient with primordial microcephalic dwarfism with severe intrauterine growth retardation and severe and progressive postnatal deficit in length, weight and head circumference. The patient was extroverted and sociable but mildly mental
Autor:
Antonio Lanzone, F. Colabucci, Corrado Romano, G. Boemi, Caterina Proto, Letizia Ragusa, R. M. Cento, Antonino Alberti
Publikováno v:
Scopus-Elsevier
We examined the basal body temperature curves and the endocrine pattern of 20 cycles from women with Down syndrome with regular menstrual cycles. Data were compared with those obtained from an age-matched population of healthy women with regular mens
Publikováno v:
Minerva anestesiologica. 65(7-8)
Poor or no clinical signs of psychological distress are usually observed in patients affected by severe or profound mental retardation (MR). The aim of this study was to use clinical and hormonal parameters in order to compare the amount of stress in
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 10(4)
We report two cases of structural variations of chromosome 9 associated with hypogonadotropic hypogonadism and azoospermia in adolescent boys. One patient also had a partially imperforated urethral meatus. Histological examination revealed that both
Publikováno v:
American journal of medical genetics. 66(3)
We describe a patient with primordial microcephalic dwarfism with severe intrauterine growth retardation and severe and progressive postnatal deficit in length, weight and head circumference. The patient was extroverted and sociable but mildly mental
Publikováno v:
Minerva anestesiologica. 62(10)
The case of a woman of 27 affected by the Prader-Willi syndrome who underwent general anaesthesia for dental surgery is reported. The patient presented severe mental retardation, small stature, moderate muscular hypotonia, hyperphagia, obesity, and d
Publikováno v:
Minerva pediatrica. 48(10)
The aim of this analysis is to evaluate the gonadal function in children with true undescended testes and in those with retractile testes, in order to verify a possible impairment of the testicular steroidogenesis due to the permanent or transitory a
Autor:
A. Rossodivita, F. Colabucci
Publikováno v:
American journal of medical genetics. 49(2)
We report on a child with Klinefelter syndrome and short stature due to idiopathic growth hormone deficiency (IGHD). His height was below the mid-parental height, with a significant delay in bone age. Height velocity increased from 4.5 to 8.2 cm/year
Autor:
F, Colabucci, M, Catorina, R, Fresu, P, Giordano, C, Rendeli, M F, Valentino, T, Mazzone, R, Ricci
Publikováno v:
Hormone and metabolic research. Supplement series. 26
Serum levels of C4 complement factor are lower in diabetic patients: it is supposed that this finding is related to genetic inheritance factors of diabetes. The purpose is to compare C4 levels in newborns of diabetic mothers with maternal metabolic c