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Inflammatory fibroid polyp of the anus in a 12‐month‐old girl: Case report and review of the literature

Journal of paediatrics and child health, 2022-08, Vol.58 (8), p.1313-1316

2022

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Changes in Shear Wave Elastography after Lumacaftor/Ivacaftor Treatment in Children with Cystic Fibrosis

Current drug safety, 2023-01, Vol.18 (1), p.93-96

2023

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PlGF and sFlt‐1 levels in patients with non‐transfusion‐dependent thalassemia: Correlations with markers of iron burden and endothelial dysfunction

European journal of haematology, 2018-06, Vol.100 (6), p.630-635

2018

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Improvement in Intestinal-Failure-Associated Liver Disease by Using Parenteral Fish Oil as Monotherapy: Case-Based Review of the Literature

Reports (MDPI), 2023-06, Vol.6 (2), p.28

2023

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Seroprevalence of Hepatitis C in Children Without Identifiable Risk-Factors: A Systematic Review and Meta-Analysis

Journal of pediatric gastroenterology and nutrition, 2021-06, Vol.72 (6), p.e140-e148

2021

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Seroprevalence of Hepatitis C in Children Without Identifiable Risk‐Factors

Journal of pediatric gastroenterology and nutrition, 2021-06, Vol.72 (6), p.e140-e148

2021

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Renal manifestations in a cohort of pediatric patients with inflammatory bowel disease

Arab journal of gastroenterology, 2024-08, Vol.25 (3), p.284-287

2024

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Use of Therapeutic Surfactant Lavage in a Preterm Infant with Massive Pulmonary Hemorrhage

Clinics and practice, 2012-08, Vol.2 (3), p.e74

2012

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Genetic landscape of pediatric acute liver failure of indeterminate origin

Hepatology (Baltimore, Md.), 2024-05, Vol.79 (5), p.1075-1087

2024

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Pl GF and sF lt‐1 levels in patients with non‐transfusion‐dependent thalassemia: Correlations with markers of iron burden and endothelial dysfunction

European journal of haematology, 2018-06, Vol.100 (6), p.630-635

2018

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Assessment of oxidative stress in patients with sickle cell disease: The glutathione system and the oxidant–antioxidant status

Blood cells, molecules, & diseases, 2011-03, Vol.46 (3), p.220-225

2011

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Plasma neutrophil gelatinase-associated lipocalin levels are markedly increased in patients with non-transfusion-dependent thalassemia: Lack of association with markers of erythropoiesis, iron metabolism and renal function

Clinical biochemistry, 2014-08, Vol.47 (12), p.1060-1064

2014

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FRI-436-Congenital porto-systemic shunts in children: Preliminary results from the IRCPSS

Journal of hepatology, 2019-04, Vol.70 (1), p.e586-e586

2019

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FRI312 - Clinical features and natural history of 1154 Alagille syndrome patients: results from the international multicenter GALA study group

Journal of hepatology, 2020-08, Vol.73, p.S554-S555

2020

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Adhesion molecules and high-sensitivity C-reactive protein levels in patients with sickle cell beta-thalassaemia

European journal of clinical investigation, 2012-01, Vol.42 (1), p.27-33

2012

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Clinical features and natural history of 1154 Alagille syndrome patients: results from the international multicenter GALA study group

JOURNAL OF HEPATOLOGY, 2020, Vol.73, p.S554-S555

2020

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The Role of Liver Transplantation in Undifferentiated Embryonal Sarcoma of the Liver in Children

Journal of pediatric hematology/oncology, 2016-08, Vol.38 (6), p.495-496

2016

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Soluble endothelial adhesion molecules and inflammation markers in patients with β-thalassemia intermedia

Blood cells, molecules, & diseases, 2009-11, Vol.43 (3), p.230-234

2009

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Association of Endothelial Dysfunction and Angiogenesis in Patients with Thalassemia Intermedia

Blood, 2011-11, Vol.118 (21), p.1084-1084

2011

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Soluble Endoglin and Its Interaction with Adhesion Molecules in Patients with Thalassemia Intermedia

Blood, 2008-11, Vol.112 (11), p.5408-5408

2008

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Lipids, Lipoproteins, Apolipoproteins, Selected Trace Elements and Minerals in the Serum of Children on Valproic Acid Monotherapy

Basic & clinical pharmacology & toxicology, 2006-06, Vol.98 (6), p.599-603

2006

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Observation of a Rare Hemoglobin Variant [Hb Lulu Island, 107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a +-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family

Hemoglobin, 2006, Vol.30 (4), p.409-418

2006

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Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a β+-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family

Hemoglobin, 2006, Vol.30 (4), p.409-418

2006

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Congenital Hepatic Fibrosis, Caroli’s Disease, and Other Fibrocystic Liver Diseases

Textbook of Pediatric Gastroenterology, Hepatology and Nutrition, 2016, p.647-661

2016

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Inflammatory fibroid polyp of the anus in a 12‐month‐old girl: Case report and review of the literature

Changes in Shear Wave Elastography after Lumacaftor/Ivacaftor Treatment in Children with Cystic Fibrosis

PlGF and sFlt‐1 levels in patients with non‐transfusion‐dependent thalassemia: Correlations with markers of iron burden and endothelial dysfunction

Improvement in Intestinal-Failure-Associated Liver Disease by Using Parenteral Fish Oil as Monotherapy: Case-Based Review of the Literature

Seroprevalence of Hepatitis C in Children Without Identifiable Risk-Factors: A Systematic Review and Meta-Analysis

Seroprevalence of Hepatitis C in Children Without Identifiable Risk‐Factors

Renal manifestations in a cohort of pediatric patients with inflammatory bowel disease

Use of Therapeutic Surfactant Lavage in a Preterm Infant with Massive Pulmonary Hemorrhage

Genetic landscape of pediatric acute liver failure of indeterminate origin

Pl GF and sF lt‐1 levels in patients with non‐transfusion‐dependent thalassemia: Correlations with markers of iron burden and endothelial dysfunction

Assessment of oxidative stress in patients with sickle cell disease: The glutathione system and the oxidant–antioxidant status

Plasma neutrophil gelatinase-associated lipocalin levels are markedly increased in patients with non-transfusion-dependent thalassemia: Lack of association with markers of erythropoiesis, iron metabolism and renal function

FRI-436-Congenital porto-systemic shunts in children: Preliminary results from the IRCPSS

FRI312 - Clinical features and natural history of 1154 Alagille syndrome patients: results from the international multicenter GALA study group

Adhesion molecules and high-sensitivity C-reactive protein levels in patients with sickle cell beta-thalassaemia

Clinical features and natural history of 1154 Alagille syndrome patients: results from the international multicenter GALA study group

The Role of Liver Transplantation in Undifferentiated Embryonal Sarcoma of the Liver in Children

Soluble endothelial adhesion molecules and inflammation markers in patients with β-thalassemia intermedia

Association of Endothelial Dysfunction and Angiogenesis in Patients with Thalassemia Intermedia

Soluble Endoglin and Its Interaction with Adhesion Molecules in Patients with Thalassemia Intermedia

Lipids, Lipoproteins, Apolipoproteins, Selected Trace Elements and Minerals in the Serum of Children on Valproic Acid Monotherapy

Observation of a Rare Hemoglobin Variant [Hb Lulu Island, 107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a +-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family

Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a β+-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family

Congenital Hepatic Fibrosis, Caroli’s Disease, and Other Fibrocystic Liver Diseases

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