Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Stanley S. Grant"'
Publikováno v:
Fetal Diagnosis and Therapy. 19:127-130
Objective: The role of the human fibroblast growth factor receptor (FGFR) gene family in current prenatal diagnosis and management of craniosynostosis syndromes and skeletal dysplasias is discussed. Method: We present the antenatal ultrasound finding
Autor:
W. Vollert, Peter G. Pryde, S. Sadullah, Darko Plecas, Mordechai Hallak, Rosalinde J. M. Snijders, Mark P. Johnson, A. Abbas, Janet Vaughan, Katharine D. Wenstrom, H.K. Dhillon, B. Arabin, Roger A. Williamson, Stanley M. Berry, Hans K. Weitzel, Stanley S. Grant, Spasoje Petkovic, Karel Kithier, Mark I. Evans, Carl P. Werner, Masahiko Ando, Bojan V. Stimec, Nicholas M. Fisk, P.G. Ransley, Rolf Becker, P.G. Duffy, Nelson B. Isada, Milan Terzic, Merlene L. Benner, Mary Phyllis Whitcomb, M.Y. Hammadeh, Jan Cejka, D.G. Talbert, A. Mohnhaupt, Glenda M. Mueller, K. H. Nicolaides, Susan L. Sipes, Kazuo Momma, Patricia Lange
Publikováno v:
Fetal Diagnosis and Therapy. 9:65-72
Autor:
Roger A. Williamson, Stanley S. Grant, John A. Widness, Louise C. Estle, Carl P. Weiner, Susan L. Sipes, Katharine D. Wenstrom
Publikováno v:
American Journal of Obstetrics and Gynecology. 165:1302-1307
Forty-eight of 128 pregnancies complicated by maternal red blood cell alloimmunization (49%) received a total of 142 intravascular transfusions (range, 1 to 7) for treatment of severe anemia (hematocrit, ⪯30%). Thirteen fetuses (27%) had hydrops wh
Autor:
Susan L. Sipes, Stanley S. Grant, John A. Widness, Roger A. Williamson, Carl P. Weiner, Katharine D. Wenstrom
Publikováno v:
American Journal of Obstetrics and Gynecology. 165:546-553
Between January 1985 and November 1990, 128 pregnancies complicated by maternal red blood cell alloimmunization were referred to our Fetal Diagnosis and Treatment Unit. We examined the premise that an evaluation of fetal blood would accurately identi
Publikováno v:
American Journal of Perinatology. 8:263-268
One explanation for an abnormal maternal serum alpha-fetoprotein (MSAFP) may be an abnormal placenta. A specimen for MSAFP and a series of umbilical artery waveforms were obtained prior to amniocentesis from 144 consecutive women referred for either
Publikováno v:
American journal of obstetrics and gynecology. 178(3)
Our goal was to evaluate the performance of prenatal serum screening for trisomy 18.All 40,762 samples for maternal serum testing (August 1991 to June 1994) with a trisomy 18-positive screen (n = 175, alpha-fetoproteinor =0.75 multiples of the median
Publikováno v:
American journal of obstetrics and gynecology. 170(2)
OBJECTIVE: Our purpose was to examine the ability of the multiple-marker screening test (maternal serum A-fetoprotein, human chorionic gonadotropin, unconjugated estriol, and maternal age) to detect fetal Turner syndrome. STUDY DESIGN: We reviewed 27
Autor:
Stanley S. Grant, Roger A. Williamson, Katharine D. Wenstrom, Carl P. Weiner, Susan L. Sipes, Glenda M. Mueller
Publikováno v:
Fetal diagnosis and therapy. 9(1)
Though echogenic fetal bowel has been associated with meconium ileus and/or peritonitis, it may be a normal finding in the second trimester. The purpose of this study is to determine which characteristics might distinguish fetuses ultimately having a
Autor:
Stanley S. Grant, Jerry D. Hudson, Jane P. Getchell, Katharine D. Wenstrom, Roger A. Williamson
Publikováno v:
American journal of obstetrics and gynecology. 169(4)
OBJECTIVE: Our purpose was to evaluate our experience with a statewide, multiple-marker Down syndrome screening program. STUDY DESIGN: The results of 18,712 screening tests performed from July 1, 1991, to Oct. 31, 1992, were reviewed. Amniocentesis a
Autor:
Roger A. Williamson, Katharine D. Wenstrom, Stanley S. Grant, Louise C. Estle, Susan L. Sipes, David C. Trawick
Publikováno v:
American journal of obstetrics and gynecology. 167(6)
OBJECTIVE: The purpose of our study was to determine whether the trend of three maternal serum α-fetoprotein samples was more predictive of pregnancy outcome than the initial sample in the evaluation of patients with unexplained α-fetoprotein eleva