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Journal of Immunology (Baltimore, Md. : 1950)|March 22, 2000
Induction of functional IL-8 receptors by IL-4 and IL-13 in human monocytesR Bonecchi, F Facchetti, S Dusi, et al.
European Cytokine Network|September 8, 1999
A small synthetic molecule capable of preferentially inhibiting the production of the CC chemokine monocyte chemotactic protein-1M Sironi, A Guglielmotti, N Polentarutti, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 1996
Effects of phenylalanine, histidine, and leucine on basal and GHRH-stimulated GH secretion and on PRL, insulin, and glucose levels in short children. Comparison with the effects of arginineJ Bellone, M R Valetto, G Aimaretti, et al.
Hormone Research|May 15, 2002
Induction of puberty in the hypogonadal girl--practices and attitudes of pediatric endocrinologists in EuropeW Kiess, G Conway, M Ritzen, et al.
The New England Journal of Medicine|October 6, 2000
Central diabetes insipidus in children and young adultsM Maghnie, G Cosi, E Genovese, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|June 27, 2001
[A case of female pseudohermaphroditism caused by maternal androluteoma]C Gallo, M Pancaldi, G Gargano, et al.
The Journal of Pathology|July 1, 1996
Expression of ICAM-1 and VCAM-1 in human malignant mesotheliomaL P Ruco, P A de Laat, C Matteucci, et al.
European Cytokine Network|November 27, 1998
Interleukin-1beta and interferon-gamma differentially regulate release of monocyte chemotactic protein-1 and interleukin-8 by human bronchial epithelial cellsV H van der Velden, M M Verheggen, S Bernasconi, et al.
Hormone Research|May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and reviewL Garavelli, P Cerruti-Mainardi, R Virdis, et al.
Italian Journal of Pediatrics|March 11, 2018
Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomaliesI Maini, I Ivanovski, O Djuric, et al.
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