2011
Progressive Familial Intrahepatic Cholestasis (PFIC) Type 1, 2, and 3: A Review of the Liver Pathology Findings
Morotti R, Suchy F, Magid M. Progressive Familial Intrahepatic Cholestasis (PFIC) Type 1, 2, and 3: A Review of the Liver Pathology Findings. Seminars In Liver Disease 2011, 31: 003-010. PMID: 21344347, DOI: 10.1055/s-0031-1272831.Peer-Reviewed Original ResearchMeSH KeywordsAdenosine TriphosphatasesATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 11ATP-Binding Cassette TransportersCholestasis, IntrahepaticDisease ProgressionGenetic Predisposition to DiseaseHeredityHumansLiverPhenotypePrognosisTerminology as TopicConceptsProgressive familial intrahepatic cholestasis type 1Intrahepatic cholestatic diseasesLiver pathology findingsCharacteristic pathologic featuresAutosomal recessive hereditary diseaseBile acid formationRecessive hereditary diseaseLiver histologyPathologic featuresHepatocellular originPathology findingsCholestatic diseaseDisease progressionFIC1 deficiencyMDR3 deficiencyBSEP deficiencyType 1DiseaseHereditary diseaseFirst descriptionDeficiencySpecific genotypesMolecular studiesCholestasisComplications
1994
Hyperechoic fetal bowel: The perinatal consequences
Bahado‐Singh R, Morotti R, Copel I, Mahoney M. Hyperechoic fetal bowel: The perinatal consequences. Prenatal Diagnosis 1994, 14: 981-987. PMID: 7899272, DOI: 10.1002/pd.1970141014.Peer-Reviewed Original ResearchConceptsCystic fibrosisFetal populationHyperechoic fetal bowelRate of complicationsIntrauterine growth retardationPerinatal consequencesFetal bowelFetal demiseAdverse outcomesBowel echogenicityHigh prevalencePrenatal sonogramsPriori riskGrowth retardationFibrosisWarrants investigationComplicationsChromosome abnormalitiesHigh rateFetusesRiskRisk figuresAneuploidyPopulationPrematurity