Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alan J. Sacks"'
Publikováno v:
North Carolina Medical Journal. 84
The coronavirus pandemic brought challenges to rural maternal health. A patient-centered collaborative health care model using telehealth and health technologies was developed by professionals at ECU and implemented in Carteret, Duplin, Chowan, and D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a553a408376d95924600f94c66f0e766
https://doi.org/10.18043/001c.67809
https://doi.org/10.18043/001c.67809
Autor:
Eric P. Hoffman, Mark P. Johnson, Alan J. Sacks, Anne Greb, Mark I. Evans, Louis M. Kunkel, Haig H. Kazazian, C. D. Boehm
Publikováno v:
American Journal of Obstetrics and Gynecology. 165:728-732
Deoxyribonucleic acid techniques can be used to diagnose Duchenne muscular dystrophy prenatally in male fetuses that are at risk. Deoxyribonucleic acid-based prenatal diagnosis can be impossible when there is only one prior affected male and there is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64545f49c4144f1179c4b21aff9ca903
https://doi.org/10.1016/0002-9378(91)90318-l
https://doi.org/10.1016/0002-9378(91)90318-l
Autor:
Brian K. Iriye, K. T. Kip, Donald Roberts, Robert C. Rollins, Alan J. Sacks, Joseph Adasheck, William N. Evans, C. F. Luna, Humberto Restrepo, Juan C. Collazos, Ruben J. Acherman
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 26(12)
Objective. Congenital cardiac malformations are common developmental anomalies. In the United States, congenital heart disease is the number one cause of infant mortality from congenital malformations. Prenatal diagnosis of congenital heart defects a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abed665e42c4358d1bc584697173c85e
https://pubmed.ncbi.nlm.nih.gov/18029914
https://pubmed.ncbi.nlm.nih.gov/18029914
Autor:
Gregory L. Goyert, Faisal Qureshi, Anne Greb, Arie Drugan, Alan J. Sacks, Mark I. Evans, Mark P. Johnson
Publikováno v:
American Journal of Medical Genetics. 36:94-96
We present the first reported case of prenatally diagnosed dup(22q) syndrome in a 20-year-old woman referred for genetic counseling because of a low maternal serum alpha-fetoprotein value. An ultrasound study at 22 weeks demonstrated oligohydramnios,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ad22f8bdba16dd166a26f89bfb5e05f
https://doi.org/10.1002/ajmg.1320360118
https://doi.org/10.1002/ajmg.1320360118
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 68:645-649
The earliest diagnosis and treatment of obstructed fetal bladder is reported. Placement of vesico-amniotic shunt at 14.5 weeks of gestation enabled preservation of bilateral renal function and maintenance of normal amniotic fluid volume with normal p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::214c7f4993a3c84aced955c3e828524c
https://doi.org/10.3109/00016348909013286
https://doi.org/10.3109/00016348909013286
Publikováno v:
JAMA: The Journal of the American Medical Association. 261:1785
Intrauterine treatment of fetal cerebral ventriculomegaly has been largely abandoned, as the results have been disappointing compared with those of standard neonatal treatment. However, we suggest that the natural history of ventriculomegaly diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e5eeb32dd62bb3e5e335779c63fb7d
https://doi.org/10.1001/jama.1989.03420120123038
https://doi.org/10.1001/jama.1989.03420120123038
Publikováno v:
Obstetrics & Gynecology; May1996, Vol. 87 Issue 5 part 2, p838-840, 3p
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