about
Functional and prognostic relevance of the -173 polymorphism of the macrophage migration inhibitory factor gene in systemic-onset juvenile idiopathic arthritis.The shortness of Pygmies is associated with severe under-expression of the growth hormone receptor.The prevalence of growth hormone deficiency and celiac disease in short children.A 5.8 Mb interstitial deletion on chromosome Xq21.1 in a boy with intellectual disability, cleft palate, hearing impairment and combined growth hormone deficiency.Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency.Effect of growth hormone (GH) on the immune system.Failure to thrive as presentation in a patient with 22q11.2 microdeletion.Growth hormone and disease severity in early stage of multiple sclerosis.Late diagnosis of celiac disease in an asymptomatic infant with growth failure.Short stature in children with coeliac disease.An intragenic deletion within CTNNA2 intron 7 in a boy with short stature and speech delay: A case report.The pygmy short stature enigma.Breastfeeding and its gamut of benefits.Identification of Autophagy-Related Genes and Their Regulatory miRNAs Associated with Celiac Disease in Children.Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome.Is BaF3 bioassay useful to identify patients with bioinactive growth hormone?Omitting duodenal biopsy in children with suspected celiac disease and extra-intestinal symptoms.Long-term growth hormone therapy in mitochondrial cytopathy.A functional promoter haplotype of macrophage migration inhibitory factor is linked and associated with juvenile idiopathic arthritis.Is retesting in growth hormone deficient children really useful?Mutation screening of the macrophage migration inhibitory factor gene: positive association of a functional polymorphism of macrophage migration inhibitory factor with juvenile idiopathic arthritis.Severe growth hormone deficiency and pituitary malformation in a patient with chromosome 2p25 duplication and 2q37 deletion.Tall stature: a difficult diagnosis?A 18p11.23-p11.31 microduplication in a boy with psychomotor delay, cerebellar vermis hypoplasia, chorioretinal coloboma, deafness and GH deficiency.Metabolic parameters and adipokine profile in growth hormone deficient (GHD) children before and after 12-month GH treatment.Effect of human recombinant growth hormone therapy on circulating levels of erythropoietin and granulocyte-colony stimulating factor in short children.Serum cytokine levels in GH-deficient children during substitutive GH therapy.Changes in growth hormone receptor gene expression during therapy in children with juvenile idiopathic arthritis.Hyperimmunoglobulinaemia in Babinga Pygmies is present from infancy.Development of antibodies against growth hormone (GH) during rhGH therapy in a girl with idiopathic GH deficiency: a case report.Secular trends in growth of African Pygmies and Bantu.[Fluticasone in the therapy of asthmatic children: short-term effects on growth]Unreliability of classic provocative tests for the diagnosis of growth hormone deficiency.Coeliac children treated for growth hormone deficiency reach normal final height.Granulocyte colony-stimulating factor and antibiotics in the prophylaxis of a murine model of polymicrobial peritonitis and sepsis.Protective effect of ciliary neurotrophic factor (CNTF) in a model of endotoxic shock: action mechanisms and role of CNTF receptor alpha.Different long-term response to growth hormone therapy in small- versus appropriate-for-gestational-age children with growth hormone deficiency.Analysis of growth hormone receptor gene expression in tall and short stature children.Efficacy of long-term growth hormone therapy in short non-growth hormone-deficient children.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Cristina Meazza
@ast
Cristina Meazza
@en
Cristina Meazza
@es
Cristina Meazza
@nl
type
label
Cristina Meazza
@ast
Cristina Meazza
@en
Cristina Meazza
@es
Cristina Meazza
@nl
prefLabel
Cristina Meazza
@ast
Cristina Meazza
@en
Cristina Meazza
@es
Cristina Meazza
@nl
P108
P106
P108
P21
P31
P496
0000-0002-1152-3793