Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anne K. Lawrence"'
Autor:
Jamie L. Fraser, Matthew T. Whitehead, Adre J. du Plessis, Pranoot Tanpaiboon, Laura Sanapo, Paul Kruszka, Anne K. Lawrence, Sho Yano, Maximilian Muenke
Publikováno v:
Prenatal Diagnosis. 41:778-790
Objective Report a single-center 12-year experience in the fetal diagnosis of diencephalic-mesencephalic junction dysplasia (DMJD) to expand the phenotype with Magnetic resonance imaging (MRI)-based classification, evaluate genetic etiologies, and as
Publikováno v:
Pediatric Radiology. 50:1801-1809
With the demand for fetal imaging and fetal care programs on the rise, the authors of this manuscript review the components of building a successful fetal imaging center. Creating an environment that engages a multidisciplinary team, utilizing a cent
Publikováno v:
Pediatric Radiology. 48:979-991
Chondrodysplasia punctata is a skeletal dysplasia caused by a diverse spectrum of etiologies, with outcomes ranging from antenatal demise to a normal life span. Prenatal detection can be challenging. To review a series of cases of chondrodysplasia pu
Publikováno v:
Pediatric radiology. 50(13)
With the demand for fetal imaging and fetal care programs on the rise, the authors of this manuscript review the components of building a successful fetal imaging center. Creating an environment that engages a multidisciplinary team, utilizing a cent
Publikováno v:
Pediatric radiology. 48(4)
Fetal medicine programs within children’s hospitals have been developed to ensure access to pediatric specialists across multiple disciplines. The cases that present to these programs are usually complex and require involvement of a multidisciplina
Publikováno v:
Pediatric radiology. 46(2)
Fetal abnormalities are present in 3-5% of all pregnancies, leading to increased anxiety and the need for important discussions between patients and their care providers. Regardless of the severity of the anomaly, receiving the information can be tra
Publikováno v:
Pediatric radiology. 46(1)
Atelencephaly is a rare lethal congenital brain malformation characterized by underdevelopment of the prosencephalon and is often accompanied by the facial features seen in some cases of holoprosencephaly, such as cyclopia. We report a case of atelen