PubRank

Renata Boldrini

Author PubWeight™ 52.17‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Antagomir-17-5p abolishes the growth of therapy-resistant neuroblastoma through p21 and BIM. PLoS One 2008 3.68
2 Effects of botulinum toxin type a in the bladder wall of children with neurogenic bladder dysfunction: a comparison of histological features before and after injections. J Urol 2011 1.50
3 Feasibility and diagnostic agreement in teledermatopathology using a virtual slide system. Hum Pathol 2007 1.39
4 Id2 is critical for cellular proliferation and is the oncogenic effector of N-myc in human neuroblastoma. Cancer Res 2002 1.36
5 Malignant pancreatic endocrine tumor in a child with tuberous sclerosis. Am J Surg Pathol 2003 1.21
6 The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children. Eur J Paediatr Neurol 2011 1.09
7 Unexplained neonatal respiratory distress due to congenital surfactant deficiency. J Pediatr 2007 1.09
8 Genotype-phenotype relationship in human ATP6i-dependent autosomal recessive osteopetrosis. Am J Pathol 2003 1.09
9 Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation. Neuromuscul Disord 2006 1.06
10 Chemotherapy and surgery in children with cystic echinococcosis. Pediatr Infect Dis J 2010 1.05
11 Inflammatory myofibroblastic tumors in childhood: a report from the Italian Cooperative Group studies. Cancer 2010 1.04
12 Impact of a single nucleotide polymorphism in the MDM2 gene on neuroblastoma development and aggressiveness: results of a pilot study on 239 patients. Clin Cancer Res 2008 1.03
13 Bladder augmentation using acellular collagen biomatrix: a pilot experience in exstrophic patients. Pediatr Surg Int 2012 0.96
14 Cystic dysplasia of the rete testis: report of two cases and review of the literature. Pediatr Dev Pathol 2002 0.93
15 NF-kappaB, and not MYCN, regulates MHC class I and endoplasmic reticulum aminopeptidases in human neuroblastoma cells. Cancer Res 2010 0.93
16 Expression of the lipogenic enzyme fatty acid synthase (FAS) in retinoblastoma and its correlation with tumor aggressiveness. Invest Ophthalmol Vis Sci 2003 0.93
17 A child with painful legs. Lancet 2005 0.92
18 Nephroblastoma: multidrug-resistance P-glycoprotein expression in tumor cells and intratumoral capillary endothelial cells. Am J Clin Pathol 2002 0.91
19 Sex cord-stromal tumors of the testis in children. A clinicopathologic report from the Italian TREP project. J Pediatr Surg 2010 0.91
20 Recurrent metanephric stromal tumor in an infant. Urology 2011 0.91
21 A multimodal strategy based on surgery, radiotherapy, ICE regimen and high dose chemotherapy in atypical teratoid/rhabdoid tumours: a single institution experience. J Neurooncol 2008 0.91
22 Pediatric adrenocortical tumors: morphological diagnostic criteria and immunohistochemical expression of matrix metalloproteinase type 2 and human leucocyte-associated antigen (HLA) class II antigens. Results from the Italian Pediatric Rare Tumor (TREP) Study project. Hum Pathol 2011 0.90
23 Slipped capital femoral epiphysis: an ultrastructural study before and after osteosynthesis. Acta Orthop 2010 0.90
24 Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6. Biochem Biophys Res Commun 2009 0.89
25 High histologic and overall response to dose intensification of ifosfamide, carboplatin, and etoposide with cyclophosphamide, doxorubicin, and vincristine in patients with high-risk Ewing sarcoma family tumors: the Bambino Gesù Children's Hospital experience. Cancer 2006 0.87
26 Severe liver disease in early childhood due to fibrinogen storage and de novo gamma375Arg-->Trp gene mutation. J Pediatr 2006 0.87
27 Pleuropulmonary blastoma, a distinctive neoplasm of childhood: report of three cases. Pediatr Radiol 2007 0.87
28 Pediatric extra-renal rhabdoid tumors with unusual morphology: a diagnostic pitfall for small biopsies. Pathol Res Pract 2009 0.85
29 IRF1 and NF-kB restore MHC class I-restricted tumor antigen processing and presentation to cytotoxic T cells in aggressive neuroblastoma. PLoS One 2012 0.84
30 Distribution of cystinosin-LKG in human tissues. Histochem Cell Biol 2012 0.84
31 Pharmacological inhibition of EZH2 as a promising differentiation therapy in embryonal RMS. BMC Cancer 2014 0.83
32 Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review. Ultrastruct Pathol 2013 0.83
33 Teratoma with a malignant somatic component in pediatric patients: the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) experience. Pediatr Blood Cancer 2010 0.82
34 Neoplastic disease and deletion 22q11.2: a multicentric study and report of two cases. Pediatr Pathol Mol Med 2003 0.81
35 Protein glutathionylation increases in the liver of patients with non-alcoholic fatty liver disease. J Gastroenterol Hepatol 2007 0.81
36 Comparison of two different conditioning regimens before autologous transplantation for children with high-risk neuroblastoma. Anticancer Res 2012 0.81
37 Expression of the lipogenic enzyme fatty acid synthase (FAS) as a predictor of poor outcome in nephroblastoma: an interinstitutional study. Med Pediatr Oncol 2003 0.81
38 Different pattern of matrix metalloproteinases expression in alveolar versus embryonal rhabdomyosarcoma. J Pediatr Surg 2004 0.80
39 Early immunopathological diagnosis of ichthyosis with confetti in two sporadic cases with new mutations in keratin 10. Acta Derm Venereol 2014 0.80
40 High-resolution array CGH profiling identifies Na/K transporting ATPase interacting 2 (NKAIN2) as a predisposing candidate gene in neuroblastoma. PLoS One 2013 0.80
41 Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis. Hum Mutat 2009 0.80
42 Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy. Biochem Biophys Res Commun 2011 0.78
43 Neonatal-onset nemaline myopathy mimicking congenital diaphragmatic hernia. J Pediatr Surg 2007 0.77
44 Wolman disease associated with hemophagocytic lymphohistiocytosis: attempts for an explanation. Eur J Pediatr 2014 0.77
45 ABCA3 mutation and pulmonary hypertension: a link with alveolar capillary dysplasia? J Pediatr 2008 0.77
46 Structural Defects of Laminin β3 N-terminus Underlie Junctional Epidermolysis Bullosa with Altered Granulation Tissue Response. Acta Derm Venereol 2016 0.76
47 Congenital Askin tumor with favorable outcome: case report and review of the literature. J Pediatr Surg 2012 0.76
48 'Tell me about your pain': abdominal pain and a history of bullying. BMJ Case Rep 2011 0.76
49 Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect. Respir Res 2011 0.76
50 Unusual aspects of desmoplastic small round cell tumor. Ultrastruct Pathol 2004 0.76
51 Expression of multidrug resistance-associated proteins in paediatric soft tissue sarcomas before and after chemotherapy. Int J Oncol 2012 0.76
52 Detection and clinical significance of disseminated tumour cells at diagnosis in bone marrow of children with localised rhabdomyosarcoma. Eur J Cancer 2005 0.76
53 Clinical and molecular evidence for c-kit receptor as a therapeutic target in neuroblastic tumors. Clin Cancer Res 2005 0.76
54 Peripheral medulloepithelioma: a rare tumor with a potential target therapy. J Transl Med 2014 0.75
55 GATA-4 and FOG-2 expression in pediatric ovarian sex cord-stromal tumors replicates embryonal gonadal phenotype: results from the TREP project. PLoS One 2012 0.75
56 Sicca syndrome associated with Tropheryma whipplei intestinal infection. J Clin Microbiol 2002 0.75
57 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
58 Vesiculopustular eruption in a neonate with trisomy 21 syndrome as a clue of transient myeloproliferative disorders. Cutis 2010 0.75
59 Frequent Occurrence of Aplasia Cutis Congenita in Bullous Dermolysis of the Newborn. Acta Derm Venereol 2016 0.75
60 Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations. Eur J Hum Genet 2016 0.75
61 Expression of glial cell line-derived neurotrophic factor and neurturin in mature kidney, nephrogenic rests, and nephroblastoma: possible role as differentiating factors. Pediatr Dev Pathol 2004 0.75
62 Lipoid Proteinosis: A Previously Unrecognized Mutation and Therapeutic Response to Acitretin. Acta Derm Venereol 2017 0.75
63 Cutaneous Crohn disease mimicking anal condylomata in a child. J Am Acad Dermatol 2010 0.75
64 Long-term follow-up of a spontaneously improving patient with junctional epidermolysis bullosa associated with ITGB4 c.3977-19T>A splicing mutation. Acta Derm Venereol 2013 0.75
65 Solitary fibrous tumor of the pleura in a 6-year-old boy. J Pediatr Surg 2012 0.75
66 Nephroblastoma. DNA characteristics and their modifications induced by prenephrectomy chemotherapy: a cytofluorimetric study. Pediatr Pathol Mol Med 2002 0.75
67 Microscopic neoplastic thrombosis in localised nephroblastoma: does it influence outcome? Eur J Cancer 2010 0.75
68 Bax mutation and overexpression inversely correlate with immature phenotype and prognosis of childhood germ cell tumors. Oncol Rep 2007 0.75
69 A case of neonatal linear IgA bullous dermatosis with severe eye involvement. Acta Derm Venereol 2015 0.75
70 A rare case of segmental neurofibromatosis with multiple blue-red pseudoatrophic plaques. Cutis 2014 0.75
71 Malignant pheochromocytoma in a 16-year-old patient with neurofibromatosis type 1. Pediatr Dev Pathol 2014 0.75
72 Continuing response to subsequent treatment lines with tyrosine kinase inhibitors in an adolescent with metastatic renal cell carcinoma. J Pediatr Hematol Oncol 2011 0.75
73 Epithelioid osteosarcoma of the jaw. Pediatr Blood Cancer 2009 0.75