Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Marian B. Macken"'
1
Abnormal Antenatal Sonogram: An Indicator of Disease Severity in Children with Posterior Urethral Valves
Autor: Marian B. Macken, Lynne McLeod, Mohamed Abdolell, Eilish Walsh, Philip Acott, Sarah Harvie
Publikováno v: Canadian Association of Radiologists Journal. 60:185-189
Purpose To review the association of an abnormal prenatal sonogram with most recent serum creatinine in patients with proven posterior urethral valves (PUV). Methods Since 1992, all live-born patients between 1992–2004 with clinically proven PUV, w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd069672b3f0f0747215d6e146f12b2
https://doi.org/10.1016/j.carj.2009.06.003
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2
Prenatal sonographic detection of congenital hepatic cyst in third trimester after normal second-trimester sonographic examination
Autor: Edward B. Grantmyre, M. Kathleen O'Brien, James R. Wright, Marian B. Macken, Moira C. Cooper, Deborah Thompson, Henry Lau
Publikováno v: Journal of Clinical Ultrasound. 28:307-310
A solitary unilocular hepatic cyst (SUHC) is a rare prenatal or neonatal finding. There are few reports of the prenatal detection of SUHC, and the progression of SUHC in utero is unknown. We present a proven case of SUHC in a fetus detected on a 34-w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0df1715869b6e1bd6fce27e45fe71289
https://doi.org/10.1002/1097-0096(200007/08)28:6<307::aid-jcu8>3.0.co
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3
Staphylococcal pericarditis, and liver and paratracheal abscesses as presentations in two new cases of interleukin-1 receptor associated kinase 4 deficiency
Autor: Andrew C. Issekutz, Marian B. Macken, Jean-Laurent Casanova, Horst von Bernuth, Cheng-Lung Ku, Bo Li, Tong-Jun Lin, Jeannette Comeau
Publikováno v: The Pediatric infectious disease journal. 27(2)
BACKGROUND A deficiency in the interleukin-1 receptor activated kinase 4 (IRAK-4) has recently been associated with severe recurrent, predominantly Gram-positive bacterial infections. CLINICAL PRESENTATION Two unrelated Canadian children with unique
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::070fbd3b0db05239cdee3e1170215d05
https://pubmed.ncbi.nlm.nih.gov/18174872
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4
A child with chromosome 22q11.2 deletion syndrome and a bilobed gallbladder
Autor: Charlotte Morley, Elizabeth A. Cummings, Matthias H. Schmidt, Marian B. Macken, James R. Clarke
Publikováno v: Pediatric radiology. 37(2)
We present an 11-year-old girl with a chromosome 22q11.2 microdeletion, velocardiofacial syndrome (VCFS), and a bilobed gallbladder as an incidental finding on abdominal sonography. The finding was confirmed by magnetic resonance cholangiopancreatogr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17ca9239f5fd696623bd7b717727b8c
https://pubmed.ncbi.nlm.nih.gov/17131146
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5
Prenatal infantile cortical hyperostosis (Caffey's disease): a 'hepatic myeloid hyperplasia-pulmonary hypoplasia sequence' can explain the lethality of early onset cases
Autor: Michiel C. Van den Hof, James R. Wright, Marian B. Macken
Publikováno v: Prenatal diagnosis. 25(10)
Background Infantile cortical hyperostosis (ICH) is benign and self-limiting when it presents near or after birth but is usually lethal when it presents earlier. Methods We present the clinical, ultrasonic, radiographic and pathologic findings in an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::174f3d12c370aa4622b252cb21ebab35
https://pubmed.ncbi.nlm.nih.gov/16193456
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