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Mark P. Johnson

Researcher at Children's Hospital of Philadelphia

Publications -  271
Citations -  13920

Mark P. Johnson is an academic researcher from Children's Hospital of Philadelphia. The author has contributed to research in topics: Fetal surgery & Prenatal diagnosis. The author has an hindex of 59, co-authored 270 publications receiving 12701 citations. Previous affiliations of Mark P. Johnson include University of Pennsylvania.

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Effect of Maternal Betamethasone Administration on Prenatal Congenital Cystic Adenomatoid Malformation Growth and Fetal Survival

TL;DR: In the fetus with a CCAM, the presence of hydrops fetalis or a CVR >1.6 is indicative of poor fetal outcome without prenatal intervention, and its potential to improve survival in high-risk groups is encouraging and warrants further controlled evaluations.
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Percutaneous fetal cystoscopy and endoscopic fulguration of posterior urethral valves

TL;DR: While it is believed that fetal cystoscopy may improve the diagnostic, prognostic, and therapeutic capabilities in the management of fetuses with lower obstructive uropathy, studies are needed to establish the actual value, risks, and limitations of this new approach in fetal medicine.
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Right congenital diaphragmatic hernia: Prenatal assessment and outcome.

TL;DR: The high incidence of preterm complications, frequent need for ECMO, and high prevalence of comorbidities are indicative of the severity of this CDH population and warrant close prenatal surveillance and delivery at a tertiary care center with ECMO capability.
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The ex utero intrapartum therapy procedure for high-risk fetal lung lesions

TL;DR: The EXIT procedure allows for controlled resection of large fetal lung lesions at delivery, avoiding acute respiratory decompensation related to mediastinal shift, air trapping, and compression of normal lung.
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Thoracoamniotic shunts: fetal treatment of pleural effusions and congenital cystic adenomatoid malformations.

TL;DR: Thoracoamniotic shunts should be considered as a treatment option for selected PE or macrocystic CCAM fetuses with hydrops or a significant risk for pulmonary hypoplasia and the neonatal survival with shunting was improved as compared with literature reports.