Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Emanuele Cacciari"'
Autor:
Silvana Salardi, G. Parenti Castelli, M. Tesei, Carla Bovina, Luca Ragni, Stefano Zucchini, Emanuele Cacciari, Marilena D'Aurelio, Gianluca Sgarbi, Graziella Biagini, Pugnaloni A, Giorgio Lenaz
Publikováno v:
European Journal of Histochemistry, Vol 45, Iss 1 (2009)
We have investigated by immuno-electron microscopy the presence of phosphotyrosine in cells as a whole and in different cell districts (nucleus, cytoplasm, plasma membrane, and mitochondria) in peripheral blood lymphocytes of IDDM (insulindependent d
Autor:
Anna Wedell, Lorella Barp, Svetlana Lajic, Antonio Balsamo, Lilia Baldazzi, Emanuele Cacciari, Alessandro Cicognani, Michela Barbaro, Piero Pirazzoli, Tiina Robins
Publikováno v:
Journal of Molecular Medicine. 84:521-528
Congenital adrenal hyperplasia (CAH) is most commonly due to 21-hydroxylase deficiency and presents with a wide spectrum of clinical manifestations, from prenatal virilization and salt-wasting in the neonatal period to precocious pubarche and late-on
Autor:
Michela Barbaro, Lilia Baldazzi, Federico Baronio, Antonio Balsamo, Milva Orquidea Bal, Emanuele Cacciari, Alessandra Cassio, Alessandro Cicognani, Krissi Kontaxaki, Monia Gennari
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 88:5680-5688
In a retrospective study we evaluated long-term growth, pubertal developmental patterns to final height (FH), and medication in 55 patients (35 females) affected by 21-hydroxylase deficiency. The patients were classified into 3 groups according to pr
Autor:
Alessandro Borghesi, Carl Joachim Partsch, Martin Chalumeau, Wilma Oostdijk, Gérard Bréart, Sze May Ng, Charalambos G Hadjiathanasiou, Emanuele Cacciari, Raja Brauner, Mariangela Cisternino, Mohammed Didi, Alessandra Cassio, Charalambos Theodoridis, Wolfgang G. Sippell, Dick Mul
Publikováno v:
The Journal of Pediatrics. 143:445-450
To test the sensitivities of recently published American recommendations predicting occult intracranial lesion (OICL) in girls with central precocious puberty (CPP), and to validate a previously derived diagnosis rule predicting OICL based on age at
Autor:
Giuliana Missiroli, Elena Corbelli, Emanuele Cacciari, Antonio Balsamo, Alessandro Cicognani, Milva Orquidea Bal, Grazia Damiani, Alessandra Cassio, Stefano Gualandi
Publikováno v:
Pediatrics. 111:1055-1060
Objective. To compare the effects of therapy with thyroxine (T4) plus triiodothyronine (T3) versus T4 alone from the first days of life in screened congenital hypothyroid (CH) infants.Methods. We examined 14 CH infants diagnosed by neonatal screening
Autor:
Roberta Santoni, Stefano Zucchini, Silvana Salardi, Emanuele Cacciari, Alessandro Cicognani, Luca Ragni, Elena Corbelli, Daniela Elleri
Publikováno v:
Pediatric Diabetes. 4:4-9
Aim: The purpose of the present study was to compare relationships between the clinical presentation of type 1 diabetes in children and residual β-cell secretion and long-term metabolic control. Methods: This retrospective study was conducted in 66
Autor:
Davide Tassinari, Ilaria Corsini, Emanuele Cacciari, Salvatore Cazzato, Alessandro Cicognani, Filippo Bernardi, Silvana Salardi, Luca Ragni
Publikováno v:
Pediatric Pulmonology. 37:17-23
A cross-sectional study design was undertaken to assess pulmonary function in children with insulin-dependent diabetes mellitus (IDDM), and to establish if there is any relationship with diabetic factors and complications. Thirty-eight children (10 +
Publikováno v:
Scopus-Elsevier
OBJECTIVE To study the effectiveness of luteinising hormone releasing hormone (LHRH) analogues in improving final height in girls affected by early puberty. PATIENTS Forty six consecutive girls with onset of puberty aged 7.5–8.5 years randomly divi
Autor:
Emanuele Cacciari, Laura Mazzanti
Publikováno v:
The Journal of Pediatrics. 133:688-692
Objective: There is a high prevalence of congenital heart defects in patients with Turner's syndrome. Few studies have reported echocardiographic data in unselected patients according to the different chromosomal patterns. The aim of our study was to
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