2022
Isolated Terminal Ileitis in Children
Alper A, Bennett A, Rottmann D, Morotti R, Escalera S, Phatak U, Pashankar D. Isolated Terminal Ileitis in Children. Journal Of Pediatric Gastroenterology And Nutrition 2022, 76: 338-342. PMID: 36729703, DOI: 10.1097/mpg.0000000000003679.Peer-Reviewed Original ResearchConceptsCrohn's diseaseTerminal ileitisAbnormal C-reactive protein levelsC-reactive protein levelsBowel wall thickeningLong-term outcomesRadiological evidenceRadiological featuresSevere inflammationPediatric literatureHigh prevalenceIleitisWall thickeningProtein levelsChildrenPrevalenceAdultsColonoscopyInflammationEndoscopicHistologicDiseaseMonths
2020
Motility Disorders of the Gastrointestinal Tract
Morotti R, Jain D. Motility Disorders of the Gastrointestinal Tract. Practical Anatomic Pathology 2020, 313-337. DOI: 10.1007/978-3-030-51268-2_13.Peer-Reviewed Original ResearchMotility disordersGastrointestinal tractRole of immunohistochemistryVisceral myopathyVisceral neuropathyClinical correlatesHirschsprung's diseaseHistologic characteristicsCommon disorderAdverse effectsDisordersHistochemical stainsMotility functionTractNeuropathyMedicationsImmunohistochemistryWorkupMyopathyDiseaseDiagnosis
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
2009
Chronic Rejection Preceded by Central Perivenulitis, Rapidly Ensuing After Liver Transplantation in a Pediatric Patient
Miloh T, Magid M, Iyer K, Kerkar N, Morotti R. Chronic Rejection Preceded by Central Perivenulitis, Rapidly Ensuing After Liver Transplantation in a Pediatric Patient. Seminars In Liver Disease 2009, 29: 134-138. PMID: 19235665, DOI: 10.1055/s-0029-1202551.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAlanine TransaminaseAntiviral AgentsAspartate AminotransferasesBiopsyChronic DiseaseEpstein-Barr Virus InfectionsGraft RejectionHepatolenticular DegenerationHumansImmunosuppressive AgentsLiverLiver TransplantationMaleReoperationTreatment OutcomeUp-RegulationVasculitisVenulesViral LoadConceptsCentral perivenulitisChronic rejectionLiver transplantationPolymerase chain reactionModerate acute cellular rejectionAcute cellular rejectionFulminant Wilson's diseaseAcute rejectionCellular rejectionEBV seroconversionImmunosuppressive treatmentLiver transaminasesLiver biopsyPediatric patientsAntiviral therapyCase reportNaive statusWilson's diseaseChain reactionTransplantationDiseaseWeeksSubsequent increaseRejectionImmunosuppression
1999
Demonstration of Communication between Alveolus and Interstitium in Persistent Interstitial Pulmonary Emphysema: Case Report
Yao J, Fasano M, Morotti R, Caprio M, Greco M. Demonstration of Communication between Alveolus and Interstitium in Persistent Interstitial Pulmonary Emphysema: Case Report. Pediatric And Developmental Pathology 1999, 2: 484-487. PMID: 10441627, DOI: 10.1007/s100249900153.Peer-Reviewed Original ResearchConceptsPersistent interstitial pulmonary emphysemaInterstitial pulmonary emphysemaPulmonary emphysemaHyaline membrane diseaseAirway ruptureUncommon complicationPremature infantsMechanical ventilationMembrane diseaseCase reportImmunohistochemical stainsAlveolar levelPresumed mechanismDiseaseAirway systemInterstitiumEmphysema
1990
Fetal hemolytic disease in a patient immunized by six antibodies: diagnosis and treatment.
Tantalo V, Rossi E, Gianotti G, Morotti R, Zuliani G, Buscaglia M, Galligani M. Fetal hemolytic disease in a patient immunized by six antibodies: diagnosis and treatment. Annali Di Ostetricia, Ginecologia, Medicina Perinatale 1990, 111: 321-5. PMID: 2092607.Peer-Reviewed Original ResearchConceptsFetal hemolytic diseaseSevere fetal anemiaSevere haemolytic diseaseFetal blood samplesFetal blood groupRare alloantibodyIntrauterine transfusionFetal anemiaMaternal antibodiesWeeks' gestationPregnant womenHaemolytic diseaseHemolytic diseaseCompatible donorsBlood samplesIndirect CoombsBlood groupAntibodiesDiseasePositive outcomesTransfusionAlloantibodiesPatientsPregnancyAnemia
1983
Hemolytic disease of the newborn due to rare alloantibodies
Zuliani G, Moroni G, Buscaglia M, Morotti R, Pardi G. Hemolytic disease of the newborn due to rare alloantibodies. International Journal Of Clinical And Laboratory Research 1983, 13: 449-457. PMID: 6419339, DOI: 10.1007/bf02906926.Peer-Reviewed Original Research