2025
Leveraging Artificial Intelligence in the Diagnosis and Management of Pulmonary Embolism
Mojibian H, Khosla A. Leveraging Artificial Intelligence in the Diagnosis and Management of Pulmonary Embolism. 2025, 1-15. DOI: 10.1007/978-3-030-70904-4_72-1.Peer-Reviewed Original Research
2022
What Every Provider Should Know About the 2020–2021 Updated AUA/ASRM Guidelines on Male Factor Infertility
Choksi A, Harnisch B, Honig S. What Every Provider Should Know About the 2020–2021 Updated AUA/ASRM Guidelines on Male Factor Infertility. Current Sexual Health Reports 2022, 14: 31-38. DOI: 10.1007/s11930-022-00325-y.Peer-Reviewed Original ResearchMale factor infertilityFactor infertilityASRM guidelinesCo-morbid conditionsCases of infertilityPossible co-morbid conditionsCorrectable etiologyMale patientsSurgical treatmentSpecific etiologyMedical conditionsInfertile malesInfertilityRecent FindingsThePractice statementsFactor assessmentEtiologyGenetic anomaliesTherapeutic capabilitiesGuidelinesOverall improvementPatientsAdditional attentionImproved understandingReproductive potential
2021
Imaging evaluation of uterine perforation and rupture
Aboughalia H, Basavalingu D, Revzin MV, Sienas LE, Katz DS, Moshiri M. Imaging evaluation of uterine perforation and rupture. Abdominal Radiology 2021, 46: 4946-4966. PMID: 34129055, DOI: 10.1007/s00261-021-03171-z.Peer-Reviewed Original ResearchConceptsUterine perforationUterine wall injuryWall injuryMulti-modality imaging featuresSite of perforationInitial imaging modalityImaging modalitiesNon-gravid uterusMagnetic resonance imagingImportant problem-solving toolBowel injurySubstantial morbidityFertility preservationCatheter angiographyImaging featuresUS findingsSecondary signsComputed tomographyResonance imagingTime mortalityInjuryPerforationUltrasoundTherapeutic capabilitiesRupture
1999
Inherited metabolic disease
Schilsky M. Inherited metabolic disease. Current Opinion In Gastroenterology 1999, 15: 200-207. PMID: 17023946, DOI: 10.1097/00001574-199905000-00004.Peer-Reviewed Original ResearchMetabolic diseasesCrigler-Najjar syndromeDonor hepatocytesMetabolic disordersGenetic hemochromatosisNew treatmentsHuman recipientsWilson's diseaseDiseaseBilirubin glucuronidationGene mutationsFunctional effectsTherapeutic capabilitiesTreatmentDisordersRespective gene productsPast yearTransplantationPathophysiologyMetal metabolismSyndromePathogenesisGlucuronidationHemochromatosisLiver
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