|
1
|
Fibrinogen storage disease caused by Aguadilla mutation presenting with hypobeta-lipoproteinemia and considerable liver disease.
|
J Pediatr Gastroenterol Nutr
|
2009
|
1.50
|
|
2
|
Double-blind comparison of hepatitis C histological recurrence Rate in HCV+ Liver transplant recipients given basiliximab + steroids or basiliximab + placebo, in addition to cyclosporine and azathioprine.
|
Transplantation
|
2004
|
1.49
|
|
3
|
CD44-v6 expression in smooth muscle cells in the postnatal remodeling process of ductus arteriosus.
|
Am J Cardiol
|
2006
|
1.38
|
|
4
|
Severe hepatotoxicity during combination antiretroviral treatment: incidence, liver histology, and outcome.
|
J Acquir Immune Defic Syndr
|
2003
|
1.28
|
|
5
|
Unresectable multifocal omental and peritoneal inflammatory myofibroblastic tumor in a child: revisiting the role of adjuvant therapy.
|
J Pediatr Surg
|
2011
|
1.14
|
|
6
|
Production of profibrotic cytokines by invariant NKT cells characterizes cirrhosis progression in chronic viral hepatitis.
|
J Immunol
|
2004
|
1.12
|
|
7
|
Co-expression and modulation of neuronal and endothelial nitric oxide synthase in human endothelial cells.
|
J Mol Cell Cardiol
|
2004
|
1.05
|
|
8
|
Differential detection of PAS-positive inclusions formed by the Z, Siiyama, and Mmalton variants of alpha1-antitrypsin.
|
Hepatology
|
2004
|
1.01
|
|
9
|
Treatment of Wilson's disease with zinc from the time of diagnosis in pediatric patients: a single-hospital, 10-year follow-up study.
|
J Lab Clin Med
|
2005
|
1.00
|
|
10
|
Peliosis hepatis as an early histological finding in idiopathic portal hypertension: A case report.
|
World J Gastroenterol
|
2006
|
0.92
|
|
11
|
Clinical significance of CXC chemokine receptor-4 and c-Met in childhood rhabdomyosarcoma.
|
Clin Cancer Res
|
2008
|
0.92
|
|
12
|
Sensenbrenner syndrome: a new member of the hepatorenal fibrocystic family.
|
Am J Med Genet A
|
2006
|
0.90
|
|
13
|
Mechanisms of interleukin-6 protection against ischemia-reperfusion injury in rat liver.
|
Cytokine
|
2006
|
0.89
|
|
14
|
A new ABCB11 mutation in two Italian children with familial intrahepatic cholestasis.
|
J Gastroenterol
|
2006
|
0.88
|
|
15
|
Severe liver disease in early childhood due to fibrinogen storage and de novo gamma375Arg-->Trp gene mutation.
|
J Pediatr
|
2006
|
0.87
|
|
16
|
Severe steatohepatitis in a patient with a rare neutral lipid storage disorder due to ABHD5 mutation.
|
J Hepatol
|
2008
|
0.86
|
|
17
|
Pulmonary blastomas of childhood: histologic, immunohistochemical, ultrastructural aspects and therapeutic considerations.
|
Ultrastruct Pathol
|
2005
|
0.86
|
|
18
|
Melanoma in a 5-year-old child with a giant congenital melanocytic naevus.
|
Acta Derm Venereol
|
2012
|
0.84
|
|
19
|
Buschke-Ollendorff syndrome: sparing unnecessary investigations.
|
Cutis
|
2014
|
0.84
|
|
20
|
Pathology of the liver sinusoids.
|
Histopathology
|
2014
|
0.83
|
|
21
|
Preliminary evidences on mitochondrial injury and impaired oxidative metabolism in breast cancer.
|
Mitochondrion
|
2012
|
0.81
|
|
22
|
Atorvastatin-induced prolonged cholestasis with bile duct damage.
|
Clin Drug Investig
|
2010
|
0.81
|
|
23
|
Protein gene product 9.5 and ubiquitin are expressed in metabolically active epithelial cells of normal and pathologic human kidney.
|
Nephrol Dial Transplant
|
2005
|
0.81
|
|
24
|
Necrosis of the tongue as first symptom of Polyarteritis Nodosa (PAN): unusual presentation of a rare disease in children.
|
Rheumatol Int
|
2010
|
0.81
|
|
25
|
Bile salt export pump deficiency: A de novo mutation in a child compound heterozygous for ABCB11. Laboratory investigation to study pathogenic role and transmission of two novel ABCB11 mutations.
|
Hepatol Res
|
2013
|
0.80
|
|
26
|
Different pattern of matrix metalloproteinases expression in alveolar versus embryonal rhabdomyosarcoma.
|
J Pediatr Surg
|
2004
|
0.80
|
|
27
|
Detection of neuroblastoma cells in bone marrow and peripheral blood by different techniques: accuracy and relationship with clinical features of patients.
|
Clin Cancer Res
|
2004
|
0.80
|
|
28
|
Primary yolk sac tumor of the liver: incidental finding in a patient transplanted for hepatocellular carcinoma.
|
Transpl Int
|
2008
|
0.79
|
|
29
|
Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy.
|
Biochem Biophys Res Commun
|
2011
|
0.78
|
|
30
|
Hepatic fibrinogen storage disease due to the fibrinogen γ375 Arg → Trp mutation "fibrinogen Aguadilla" is present in Arabs.
|
Saudi J Gastroenterol
|
2014
|
0.78
|
|
31
|
Sterile abscesses complicating monoclonal gammopathy of undetermined significance.
|
Eur J Haematol
|
2008
|
0.78
|
|
32
|
Adam's rib and the origin of stem cells.
|
Am J Hematol
|
2011
|
0.78
|
|
33
|
Two novel mutations in African and Asian children with progressive familial intrahepatic cholestasis type 3.
|
Dig Liver Dis
|
2011
|
0.77
|
|
34
|
Glycogenotic hepatocellular carcinoma with glycogen-ground-glass hepatocytes: histological, histochemical and microbiochemical characterization of the novel variant.
|
Histopathology
|
2012
|
0.77
|
|
35
|
Intestinal Wegener's granulomatosis in a patient with severe alpha-1-antitrypsin deficiency resulting from a unique combination of two deficiency alleles (PiZ and PiMProcida).
|
Eur J Gastroenterol Hepatol
|
2002
|
0.77
|
|
36
|
Z and Mmalton-1-antitrypsin deficiency-associated hepatocellular carcinoma: a genetic study.
|
Liver Int
|
2009
|
0.76
|
|
37
|
Eosinophilic esophagitis and Barrett's esophagus: an occasional association or an overlap disease? Esophageal 'double trouble' in two children.
|
Digestion
|
2008
|
0.76
|
|
38
|
A waterborn zoonotic helminthiase in an Italian diver: a case report of a cutaneous Sparganum infection and a review of European cases.
|
Pathog Glob Health
|
2016
|
0.75
|
|
39
|
Quantitative recovery of proviral HIV-1 DNA from leukocytes by the Dried Buffy Coat Spot method for real-time PCR determination.
|
J Virol Methods
|
2010
|
0.75
|
|
40
|
Usefulness of 18F-FDG PET/CT in an unusual case of solid-pseudopapillary pancreatic tumor in childhood with aggressive behavior.
|
Clin Nucl Med
|
2013
|
0.75
|
|
41
|
Naevoid basal cell carcinoma syndrome in a 22-month-old child presenting with multiple basal cell carcinomas and a fetal rhabdomyoma.
|
Acta Derm Venereol
|
2015
|
0.75
|
|
42
|
Alpha-1-antitrypsin deficiency: from genoma to liver disease. PiZ mouse as model for the development of liver pathology in human.
|
Liver Int
|
2014
|
0.75
|
|
43
|
A novel form of non-X-linked hyperigm associated with growth and pubertal disturbances and with lymphoma development.
|
J Pediatr
|
2006
|
0.75
|
|
44
|
Tyrosinemia type 1: metastatic hepatoblastoma with a favorable outcome.
|
Pediatrics
|
2010
|
0.75
|
|
45
|
Malignant pheochromocytoma in a 16-year-old patient with neurofibromatosis type 1.
|
Pediatr Dev Pathol
|
2014
|
0.75
|
|
46
|
Frequent detection of antiretroviral drug resistance in HIV-1-infected orphaned children followed at a donor-funded rural pediatric clinic in Dodoma, Tanzania.
|
AIDS Res Hum Retroviruses
|
2014
|
0.75
|
|
47
|
Impressive pseudotumoral proliferative nodules in a giant congenital nevus of a newborn.
|
Pediatr Dermatol
|
2012
|
0.75
|
|
48
|
Congenital myxoid and pigmented dermatofibrosarcoma protuberans: a case report.
|
Pediatr Dermatol
|
2013
|
0.75
|
|
49
|
X chromosome monosomy restricted to the left ventricle is not a major cause of isolated hypoplastic left heart.
|
Am J Med Genet A
|
2010
|
0.75
|
|
50
|
A rare case of segmental neurofibromatosis with multiple blue-red pseudoatrophic plaques.
|
Cutis
|
2014
|
0.75
|
|
51
|
Heart transplant and 2-year follow up in a child with generalized arterial calcification of infancy.
|
Eur J Pediatr
|
2014
|
0.75
|