Professor, Pathology and Laboratory Medicine, Perelman School of Medicine
Pathology
Dr. Pierre A. Russo, MD
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Pierre Russo practices Pathology. Dr. Pierre A. Russo is also published. He has 59 publications published. The lastest publication: "Autoimmune enteropathy.'
Publications
- The inflammatory phenotype of the fibrous plate is distinct from the liver and correlates with clinical outcome in biliary atresia.
- A challenging Case of Focal Extrahepatic Duct Obstruction/Hypoplasia in Alagille Syndrome.
- Streptococcal infection as possible trigger for dense deposit disease (C3 glomerulopathy).
- Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.
- Bilateral pheochromocytomas, hemihyperplasia, and subtle somatic mosaicism: the importance of detecting low-level uniparental disomy.
- Extra-Hepatic Cholangiocyte Cilia are Abnormal in Biliary Atresia.
- Portal and sinusoidal fibrosis are common on liver biopsy after Fontan surgery.
- Secondary Syphilitic Hepatitis in a 17-year-old Girl.
- The precarious state of the liver after a Fontan operation: summary of a multidisciplinary symposium.
- Lymphocytic gastritis in pediatric celiac disease.
- Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence.
- Design and validation of the biliary atresia research consortium histologic assessment system for cholestasis in infancy.
- DNA hypomethylation causes bile duct defects in zebrafish and is a distinguishing feature of infantile biliary atresia.
- Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development.
- Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3.
- Anthropometric, serologic, and laboratory correlation with villous blunting in pediatric celiac disease: diabetics are different.
- CD68 expression is markedly different in Crohn's disease and the colitis associated with chronic granulomatous disease.
- SMARCB1/INI1 alterations and hepatoblastoma: another extrarenal rhabdoid tumor revealed?
- Loss of INI1 expression defines a unique subset of pediatric undifferentiated soft tissue sarcomas.
- Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype.
- Use of sirolimus in IPEX and IPEX-like children.
- Frequency and clinical correlations of granulomas in children with Crohn disease.
- RNA-containing cytoplasmic inclusion bodies in ciliated bronchial epithelium months to years after acute Kawasaki disease.
- Evidence for the epithelial to mesenchymal transition in biliary atresia fibrosis.
- Kawasaki disease: four case reports of cardiopathy with an institutional and literature review.
- Adult autoimmune enteropathy: Mayo Clinic Rochester experience.
- Interlobular bile duct loss in pediatric cholestatic disease is associated with aberrant cytokeratin 7 expression by hepatocytes.
- Hamartomatous tongue lesions in children.
- Differentiating ulcerative colitis from Crohn disease in children and young adults: report of a working group of the North American Society for Pediatric Gastroenterol...
- Bile duct proliferation in liver-specific Jag1 conditional knockout mice: effects of gene dosage.
- A 10-year-old boy with a 6-month history of gingival bleeding and epistaxis.
- Fetal pulmonary malformations: defining histopathology.
- A 2-year-old girl with chronic and recurrent emesis.
- A 2-year-old boy with emesis and facial edema.
- Does "cystic" biliary atresia represent a distinct clinical and etiological subgroup? A series of three cases.
- Primary sclerosing cholangitis in children: a histologic follow-up study.
- Non-invasive fluorescence imaging of cell death in fresh human colon epithelia treated with 5-Fluorouracil, CPT-11 and/or TRAIL.
- Hepatosplenic T-cell lymphoma in an adolescent patient after immunomodulator and biologic therapy for Crohn disease.
- A 2-year-old girl with persistent ascites.
- Immunohistochemical analysis of hSNF5/INI1 distinguishes renal and extra-renal malignant rhabdoid tumors from other pediatric soft tissue tumors.
- The zebrafish onecut gene hnf-6 functions in an evolutionarily conserved genetic pathway that regulates vertebrate biliary development.
- Allelic loss but absence of mutations in the polyspecific transporter gene BWR1A on 11p15.5 in hepatoblastoma.
- Knee pain in a 12-year-old girl.
- Cases in pediatric gastroenterology from the Children's Hospital of Philadelphia: a 14-year-old boy with jaundice and pruritus.
- Frequent mutation reversion inversely correlates with clinical severity in a genetic liver disease, hereditary tyrosinemia.
- Enlarging thigh mass in a 13-month-old boy.
- Biliary atresia.
- Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors.
- Biliary atresia associated with a fatty acid oxidation defect.
- Centrilobular fibrosis in long-term follow-up of pediatric liver transplant recipients.
- Inflammatory bowel disease in children 5 years of age and younger.
- Pathological case of the month. Type IV sacrococcygeal teratoma with yolk sac (endodermal sinus) tumor presenting with failure to thrive and perianal pain.
- Tyrosinemia: a review.
- Autoimmune enteropathy.
- Wheat starch intolerance in patients with celiac disease.
- Function of GATA Factors in the Adult Mouse Liver.
- Enteropathies of infancy and childhood.
- Immunohistochemical expression of glypican-3 in pediatric tumors: an analysis of 414 cases.
Doctors Specialties
- Pediatric Pathology
- Pathology
Accepted Insurances
Education
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University of Pittsburgh Medical Center -
McGill University Faculty of Medicine
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