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Current Awareness

  • 1. Books, reviews & symposia
  • Hormones, cytokines and fetal anomalies in habitual abortion (Review). Carp H, Torchinsky A, Fein A, Toder V. Gynecol Endocrinol (2001) 15 472-483
  • Preimplantation genetics: An explanation for poor human fertility?. Delhanty JDA. Ann Hum Genet (2001) 65 331-338
  • In utero transplantation of haemopoietic stem cells. Flake AW. Best Pract Res Clin Haematol (2001) 14 671-683
  • Methodological limitations of economic evaluations of antenatal screening. Petrou S. Health Econ (2001) 10 775-778
  • Prenatal screening for neural tube defects (Review). Rajesh R, Thomas SV. Natl Med J India (2001) 14 343-346
  • 2. General interest
  • 4D, or not 4D: That is the question (Editorial). Campbell S. Ultrasound Obstet Gynecol (2002) 19 1-4
  • Diploid sperm and the origin of triploidy (Editorial). Egozcue S, Blanco J, Vidal F, Egozcue J. Hum Reprod (2002) 17 5-7
  • Preimplantation sex selection for family balancing in India (Editorial). Malpani A, Malpani A, Modi D. Hum Reprod (2002) 17 11-12
  • Prenatal testing: Towards realistic expectations of patients, providers and policy makers (Opinion). Marteau TM. Ultrasound Obstet Gynecol (2002) 19 5-6
  • Obstetric cholestasis - may have serious consequences for the fetus, and needs to be taken seriously (Editorial). Milkiewicz P, Elias E, Williamson C, Weaver J. Br Med J (2002) 324 123-124
  • Screening for Down's syndrome: Antenatal screening has human costs (Letter). Venn-Treloar J. Br Med J (2002) 324 110
  • Screening for Down's syndrome: Costings are crucial to model (Letter). Whittle M. Br Med J (2002) 324 111
  • Screening for Down's syndrome: Conclusions do not reflect reality (Letter). Reynolds T. Br Med J (2002) 324 111
  • Screening for Down's syndrome: Modelling does not predict reality accurately (Letter). Howe D. Br Med J (2002) 324 111-112
  • Screening for Down's syndrome (Reply). Gilbert RE, Augood C, Gupta R, Logan S, Ades AE, Sculpher M, Van den Meulen JHP. Br Med J (2002) 324 112
  • Screening for Down's syndrome: Ratio of femoral length to tibial length needs to be evaluated extensively (Letter). Sachdev P, Bahl S, Puliyel JM. Br Med J (2002) 324 112
  • Screening for Down's syndrome: Nuchal translucency screening may help detect congenital heart disease (Letter). Simpson JM. Br Med J (2002) 324 112
  • 3. Normal fetal development
  • The human ductus venosus between 13 and 17 weeks of gestation: Histological and morphometric studies. Mavrides E, Moscoso G, Carvalho JS, Campbell S, Thilaganathan B. Ultrasound Obstet Gynecol (2002) 19 39-46
  • 4. Gametogenesis and pre-implantation diagnosis
  • Biopsied testis cells of four 47,XXY patients: Fluorescence in situ hybridization and ICSI results. Bergere M, Wainer R, Nataf V, Gombault M, Ville Y, Selva J. Hum Reprod (2002) 17 32-37
  • Deletion of RBM and DAZ in azoospermia: Evaluation by PRINS. Kadandale JS, Wachtel SS, Tunca Y, Martens PR, Wilroy RS, Tharapel AT. Am J Med Genet (2002) 107 105-108
  • Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS). Loeys B, Nuytinck L, Van Acker P, Walraedt S, Bonduelle M, Sermon K, Hamel B, Sanchez A, Messiaen L, De Paepe A. Prenat Diagn (2002) 22 22-28
  • Rapid chromosome detection by PRINS in human sperm. Pellestor F, Imbert I, Andreo B. Am J Med Genet (2002) 107 109-114
  • Screening for Y chromosome microdeletions in 226 Slovenian subfertile men. Peterlin B, Kunej T, Sinkovec J, Gligorievska N, Zorn B. Hum Reprod (2002) 17 17-24
  • The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility. Quintana-Murci L, Krausz C, Heyer E, Gromoll J, Seifer I, Barton DE, Barrett T, Skakkebaek NE, Rajpert de Meyts E, Mitchell M, Lee AC, Jobling MA, McElreavey K. Hum Genet (2001) 108 55-58
  • ESHRE preimplantation genetic diagnosis consortium: Data collection III (May 2001). Sermon K, Harper J, Geraedts J, De Die-Smulders C, Handyside A, Hussey N, Magli MC, Munne S, Ray P, Santalo J, Staessen C, Thornhill A, Viville S, Wilton L. Hum Reprod (2002) 17 233-246
  • Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo- or azoospermia. Yao GM, Chen G, Pan TM. J Assist Reprod Genet (2001) 18 612-616
  • 5. First trimester diagnosi
  • Prenatal diagnosis of haemoglobinopathies. Arora S, Kabra M, Maheshwari M, Shastri S, Kaur D, Deka D, Kriplani A, Menon PSN. Natl Med J India (2001) 14 340-342
  • Rapid prenatal diagnosis of haemophilia (Letter). Belvini D, Salviato R, Are A, Radossi P, Tagariello G. Haemophilia (2001) 7 603-604
  • Detection of fetal cells in intrauterine lavage samples collected in the first trimester of pregnancy. Cioni R, Bussani C, Scarselli B, Barciulli F, Bucciantini S, Simi P, Fogli A, Scarselli G. Prenat Diagn (2002) 22 52-55
  • Prenatal diagnosis in Coffin-Lowry syndrome demonstrates germinal mosaicism confirmed by mutation analysis. Horn D, Delaunoy J-P, Kunze J. Prenat Diagn (2001) 21 881-884
  • Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis. Kalkanoglu HS, Romstad A, Coskun T, Guttler F. Prenat Diagn (2001) 21 868-870
  • First application of denaturing high-performance liquid chromatography (DHPLC) for prenatal diagnosis of genetic disease (Letter). Lam CW. Prenat Diagn (2002) 22 79-80
  • The diagnostic performance of cytogenetic investigation in amniotic fluid cells and chorionic villi. Los FJ, Van den Berg C, Wildschut HIJ, Brandenburg H, Den Hollander NS, Schoonderwaldt EM, Pijpers L, Galjaard RJH, Opstal DV. Prenat Diagn (2001) 211150-1158
  • Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiency. Niers LEM, Smeitink JAM, Trijbels JMF, Sengers RCA, Janssen AJM, Van den Heuvel LP. Prenat Diagn (2001) 21 871-880
  • FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy. Schuring-Blom GH, Hoovers JMN, Van Lith JMM, Knegt AC, Leschot NJ. Prenat Diagn (2001) 21 864-867
  • Carrier detection and prenatal diagnosis of hemophilia A. Wang XF, Liu YF, Li ZG, Chu HY, Sang XJ, Fan YS, Wang HL. Clin Chem Lab Med (2001) 39 1204-1208
  • Prenatal diagnosis of trisomy 20 by chorionic villus sampling (CVS): A case report with long-term outcome. Warren NS, Soukup S, King JL, Dignan PSJ. Prenat Diagn (2001) 21 1111-1113
  • Four years experience of first-trimester nuchal translucency screening for fetal aneuploides with increasing regional availability. Wayda K, Kereszturi A, Orvos H, Horvath E, Pal A, Kovacs L, Szabo J. Acta Obstet Gynecol Scand (2001) 80 1104-1109
  • First-trimester ductus venosus velocimetry in relation to nuchal translucency thickness and fetal karyotype. Zoppi MA, Putzolu M, Ibba RM, Floris M, Monni G. Fetal Diagn Ther (2002) 17 52-57
  • Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH) (Letter). Zur-Stadt U, Pruggmayer M, Jung H, Henter JI, Schneider M, Kabisch H, Janka G. Prenat Diagn (2002) 22 80-81
  • 6. Second trimester diagnosi
  • Correlation between rare chromosomal abnormalities and prenatal ultrasound findings. Al-Kouatly HB, Chasen ST, Gilbert F, Ahner R, Alonso LM, Chervenak FA. Am J Med Genet (2002) 107 197-200
  • Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: Association with elevated α-fetoprotein and cystic renal changes. Chisholm CA, Vavelidis F, Lovell MA, Sweetman L, Roe CR, Roe DS, Frerman FE, Wilson WG. Prenat Diagn (2001) 21 856-859
  • A randomised trial of progesterone prophylaxis after midtrimester amniocentesis. Corrado F, Dugo C, Cannata ML, Di Bartolo M, Scilipoti A, Stella NC. Eur J Obstet Gynecol Reprod Biol (2002) 100 196-198
  • Prenatal diagnosis of glutaric acidemias. Invited commentary: Current issues in obstetrics and genetics. Goodman SI. Prenat Diagn (2001) 21 1167-1168
  • Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts (Letter). Hengstschlager M, Bettelheim D, Rosner M, Repa C, Deutinger J, Bernaschek G. Prenat Diagn (2001) 21 897-899
  • Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus-Merzbacher disease. Inoue K, Kanai M, Tanabe Y, Kubota T, Kashork CD, Wakui K, Fukushima Y, Lupski JR, Shaffer LG. Prenat Diagn (2001) 21 1133-1136
  • A female infant with a 46,XX/48,XY,+8,+10 karyotype in prenatal diagnosis: A ‘vanishing twin’ phenomenon? (Letter). Lloveras E, Lecumberri JM, Perez C, Melero C, Zamora L, Sanchez MA, Sole F, Plaja A. Prenat Diagn (2001) 21 896-897
  • Molecular analysis of genomic DNA allows rapid, and accurate, prenatal diagnosis of peroxisomal D-bifunctional protein deficiency. Paton BC, Solly PB, Nelson PV, Pollard AN, Sharp PC, Fietz MJ. Prenat Diagn (2002) 22 38-41
  • Diagnosis of triploidy in metaphases from uncultured amniocytes (Letter). Pecile V, Demori E, Benussi DG, Dolce S, Amoroso A. Prenat Diagn (2002) 22 78-79
  • Rapid detection of chromosome aneuploidies by prenatal interphase FISH (fluorescence in situ hybridization) and its clinical utility in Japan. Sawa R, Hayashi Z, Tanaka T, Onda T, Hoshi K, Fukada Y, Takai Y, Taketani Y, Kubo T, Hamada H, Yoshida K, Nakamura Y, Okai T, Sakai M, Kaneoka T, Makino Y, Aono T, Maeda K, Honda R, Okamura H, Sago H, Kitagawa M, Minoura S, Inaba J, Terakawa N, Nagata N, Shimomura K, Sapeta MJ, Estabrooks LL. J Obstet Gynaecol Res (2001) 27 41-47
  • Prenatal diagnosis of cri du chat (5p-) syndrome in association with isolated moderate bilateral ventriculomegaly. Stefanou EGG, Hanna G, Foakes A, Crocker M, Fitchett M. Prenat Diagn (2002) 22 64-66
  • Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies. Tanemura M, Suzumori K, Nishikawa N, Ishihara Y. Prenat Diagn (2001) 21 1123-1128
  • Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH. Tsuchiya K, Schueler MG, Dev VG. Prenat Diagn (2001) 21 852-855
  • Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis. Villa N, Riva P, Colombo D, Sala E, Mariani S, Zorloni C, Crosti F, Dalpra L. Prenat Diagn (2001) 21 801-805
  • Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH). Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns J-P. Prenat Diagn (2002) 2229-33
  • Fluorescence in situ hybridization of uncultured lymphocytes from cystic hygroma fluid: A potential approach for rapid prenatal diagnosis (Letter). Xu J, Freeman V, Smith PA, Huggins M. Prenat Diagn (2002) 22 81-82
  • Association between congenital foot anomalies and gestational age at amniocentesis. Yoon G, Chernos J, Sibbald B, Lowry RB, Connors G, Simrose R, Bernier FP. Prenat Diagn (2001) 21 1137-1141
  • Significance of prenatally diagnosed del(10)(q23). Zaslav AL, Fox JE, Jacob J, Kazi R, Allan S, Shklooskaya T, Sohal D, Kleyman SM, Verma RS. Am J Med Genet (2002) 107 174-176
  • 7. Fetal diagnosis by ultrasound and other imaging
  • Split notochord syndrome: Prenatal ultrasonographic diagnosis. Almog B, Leibovitch L, Achiron R. Prenat Diagn (2001) 21 1159-1162
  • Mitochondrial DNA depletion presenting prenatally with skin edema and multisystem disease immediately after birth. Arnon S, Aviram R, Dolfin T, Regev R, Litmanovits I, Tepper R, Elpeleg ON. Prenat Diagn (2002) 22 34-37
  • Prenatal diagnosis of Joubert syndrome: A case report. Aslan H, Ulker V, Gulcan EM, Numanoglu C, Gul A, Agar M, Ark HC. Prenat Diagn (2002) 22 13-16
  • Prenatal and perinatal aspects of a giant fetal cervicothoracal lymphangioma. Axt-Fliedner R, Hendrik HJ, Schwaiger C, Ertan AK, Friedrich M, Schmidt W. Fetal Diagn Ther (2002) 17 3-7
  • A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney. Belk RA, Thomas DFM, Mueller RF, Godbole P, Markham AF, Weston MJ. J Urol (2002) 167 666-669
  • Normal cardiac flow velocities at 14-16 weeks of gestation measured by transvaginal ultrasound. Ben-Ami M, Peleg D, Haddad S, Perlitz Y. Ultrasound Obstet Gynecol (2002) 19 47-50
  • Nuchal fold thickness at 14-16 weeks' gestation as measured by transvaginal sonography. Ben-Ami M, Perlitz Y, Mukary M, Peleg D. Ultrasound Obstet Gynecol (2002) 19 60-61
  • Brains and faces in holoprosencephaly: Pre- and postnatal description of 30 cases. Blaas HGK, Eriksson AG, Salvesen KA, Isaksen CV, Christensen B, Mollerlokken G, Eik-Nes SH. Ultrasound Obstet Gynecol (2002) 19 24-38
  • Detection of fetal structural abnormalities at the 11-14 week ultrasound scan. Carvalho MHB, Brizot ML, Lopes LM, Chiba CH, Miyadahira S, Zugaib M. Prenat Diagn (2002) 22 1-4
  • Three-dimensional ultrasonography of osteogenesis imperfecta at early pregnancy (Letter). Chang LW, Chang CH, Yu CH, Chang FM. Prenat Diagn (2002) 22 77-78
  • Molecular diagnosis of a novel heterozygous 268C[RIGHTWARDS ARROW]T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis. Chen CP, Chern SR, Du SH, Wang W. Prenat Diagn (2002) 22 5-7
  • Three-dimensional ultrasound in the evaluation of complex anomalies associated with fetal ventral midline defects (Letter). Chen CP, Shih JC, Tzen CY, Wang W. Ultrasound Obstet Gynecol (2002) 19 102-104
  • Myomectomy during the first trimester associated with fetal limb anomalies and hydrocephalus in a twin pregnancy. Danzer E, Holzgreve W, Batukan C, Miny P, Tercanli S, Hoesli I. Prenat Diagn (2001) 21 848-851
  • Diagnostic and therapeutic dilemma with large prenatally detected cystic adrenal masses. De Luca JL, Rousseau T, Durand C, Sagot P, Sapin E. Fetal Diagn Ther (2002) 17 11-16
  • Prenatal diagnosis of suprasellar arachnoid cyst and postnatal endoscopic treatment (Case Report). Golash A, Mitchell G, Mallucci C, May P, Pilling D. Child Nerv Syst (2001) 17 739-742
  • Dehydrated hereditary stomatocytosis: A cause of prenatal ascites. Grootenboer S, Barro C, Cynober T, Schischmanoff PO, Ayoubi JM, Tchernia G, Delaunay J, Pons JC. Prenat Diagn (2001) 21 1114-1118
  • Prenatal diagnosis of kyphomelic dysplasia. Guala A, Biroli E, Bassini P, Botta G, Licata D, Di Cara G, Franceschini D, Franceschini P. Prenat Diagn (2001) 21 1146-1149
  • Early transvaginal biometry of fetal orbits: A cross-sectional study. Guariglia L, Rosati P. Fetal Diagn Ther (2002) 17 42-47
  • Uterine artery Doppler velocimetry in patients with idiopathic hydramnios. Hershkovitz R, Sheiner E, Furman B, Smolin A, Hallak M, Mazor M. Fetal Diagn Ther (2002) 17 48-51
  • Prenatal diagnosis of lissencephaly (type II) by ultrasound and fast magnetic resonance Imaging. Kojima K, Suzuki Y, Seki K, Yamamoto T, Sato T, Tanaka T, Suzumori K. Fetal Diagn Ther (2002) 17 34-36
  • Diagnosis of skeletal dysplasia by multidisciplinary assessment: A report of two cases of thanatophoric dysplasia. Kolble N, Sobetzko D, Ersch J, Stallmach T, Eich G, Huch R, Huch A, Superti-Furga A, Wisser J. Ultrasound Obstet Gynecol (2002) 19 92-98
  • Middle cerebral artery Doppler study in fetuses with homozygous α-thalassaemia-1 at 12-13 weeks of gestation. Lam YH, Yin Tang MH. Prenat Diagn (2002) 22 56-58
  • Serial sonographic findings of four fetuses with homozygous α-thalassemia-1 from 21 weeks onwards. Leung WC, Oepkes D, Seaward G, Ryan G. Ultrasound Obstet Gynecol (2002) 19 56-59
  • Outcome of prenatally diagnosed fetal hydronephrosis. Liang CC, Cheng PJ, Lin CJ, Chen HW, Chao AS, Chang SD. J Reprod Med (2002) 47 27-32
  • Prenatal diagnosis of arthrogryposis multiplex congenita with increased nuchal translucency but without any underlying fetal neurogenic or myogenic pathology. Madazli R, Tuysuz B, Aksoy F, Barbaros M, Uludag S, Ocak V. Fetal Diagn Ther (2002) 17 29-33
  • Duplication of chromosome 2 in association with ventriculomegaly: A case report. Martin WL, Pretlove S, Mercer A, Platt CC, Roberts E, Davison V, Kilby MD. Prenat Diagn (2001) 21 1169-1170
  • Poor prenatal detection rate of cardiac anomalies in Noonan syndrome. Menashe M, Arbel R, Raveh D, Achiron R, Yagel S. Ultrasound Obstet Gynecol (2002) 19 51-55
  • Fetal heart-rate monitoring (Letter). Mol BW. Lancet (2002) 359 261
  • Fetal heart-rate monitoring (Reply). Amer-Wahlin I, Herbst A, Marsal K. Lancet (2002) 359 261-262
  • Cerebro-costo-mandibular syndrome in a father and a female fetus: Early prenatal ultrasonographic diagnosis and autosomal dominant transmission. Morin G, Gekas J, Naepels P, Gondry J, Devauchelle B, Testelin S, Sevestre H, Thepot F, Mathieu M. Prenat Diagn (2001) 21 890-893
  • Neural tube defects in missed abortions embryoscopic and cytogenetic findings. Philipp T, Kalousek DK. Am J Med Genet (2002) 107 52-57
  • Amnion rupture sequence in a first trimester missed abortion. Philipp T, Kalousek DK. Prenat Diagn (2001) 21 835-838
  • Wiedemann-Beckwith Syndrome: Further prenatal characterization of the condition. Reish O, Lerer I, Amiel A, Heyman E, Herman A, Dolfin T, Abeliovich D. Am J Med Genet (2002) 107 209-213
  • Fetal magnetic encephalography: A new tool for intrauterine fetal monitoring? (German, English Abstract). Schauf B, Lowery C, Wilson JD, Eswaran H, Birbaumer N, Aydeniz B, Wallweiner D, Preissl H. Geburtshilfliche Frauenheilk (2001) 61 880-887
  • Prenatal diagnosis of hydrocephalus-stenosis of the aqueduct of Sylvius by ultrasound in the first trimester of pregnancy. Report of two cases. Senat MV, Bernard JP, Delezoide A, Saugier-Veber P, Hillion Y, Roume J, Ville Y. Prenat Diagn (2001) 21 1129-1132
  • Antenatal diagnosis of spinal lipomas. Thorne JA, Pierre-Kahn A, Sonigo P. Child Nerv Syst (2001) 17 697-703
  • Prenatal diagnosis of isolated anorectal atresia with colonic perforation. Tongsong T, Chanprapaph P. J Obstet Gynaecol Res (2001) 27 241-244
  • Sonographic fetal weight estimation in a south-east Asian population. Venkat A, Chinnaiya A, Gopal M, Mongelli JM. J Obstet Gynaecol Res (2001) 27 275-279
  • Minor sonographic signs of trisomy 21 at 15-20 weeks' gestation in fetuses born without malformations: A prospective study. Viora E, Errante G, Bastonero S, Sciarrone A, Campogrande M. Prenat Diagn (2001) 21 1163-1166
  • Three-dimensional ultrasound evaluation of short-rib polydactyly syndrome type II in the second trimester: A case report. Viora E, Sciarrone A, Bastonero S, Errante G, Botta G, Campogrande M. Ultrasound Obstet Gynecol (2002) 19 88-91
  • Improvement of mesenteric superior artery Doppler velocimetry by amnioinfusion in fetal gastroschisis. Volumenie JL, De Lagausie P, Guibourdenche J, Oury JF, Vuillard E, Saizou C, Luton D. Prenat Diagn (2001) 21 1171-1174
  • Prenatal diagnosis of cloacal anomalies. Warne S, Chitty LS, Wilcox DT. BJU Int (2002) 89 78-81
  • MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and mullerian duct anomalies. Witters I, Devriendt K, Spinnewijn D, Moerman PH, Van Assche FA, Fryns JP. Am J Med Genet (2002) 107 233-236
  • Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: Further evidence for autosomal recessive inheritance of hydranencephaly, Fowler type. Witters I, Moerman PH, Devriendt K, Braet P, Van Schoubroeck D, Van Assche FA, Fryns JP. Am J Med Genet (2002) 108 41-44
  • Semilobar holoprosencephaly in a 46,XY female fetus. Witters I, Moerman P, Muenke M, Van Assche FA, Devriendt K, Legius E, Van Schoubroeck D, Fryns JP. Prenat Diagn (2001) 21 839-841
  • Split-hand/split-foot malformation with paternal mutation in the p63 gene. Witters I, Van Bokhoven H, Goossens A, Van Assche FA, Fryns JP. Prenat Diagn (2001) 21 1119-1122
  • Antenatal diagnosis of prune belly syndrome at 11 weeks of gestation. Yamamoto H, Nishikawa S, Hayashi T, Sagae S, Kudo R. J Obstet Gynaecol Res (2001) 27 37-40
  • Heterogeneity in fetal akinesia deformation sequence (FADS): Autopsy confirmation in three 20-21-week fetuses. Yfantis H, Nonaka D, Castellani R, Harman C, Sun CC. Prenat Diagn (2002) 22 42-47
  • Sonographic determination of fetal size from 20 weeks of gestation onward correlates with birth weight. Yoshida S, Unno N, Kagawa H, Shinozuka N, Kozuma S, Taketani Y. J Obstet Gynaecol Res (2001) 27 205-211
  • 8. Maternal screening
  • Singleton versus duplicate assays in maternal serum screening (Letter). Benn PA. Prenat Diagn (2001) 21 894-895
  • Singleton versus duplicate assays in maternal serum screening (Reply). Hackshaw AK, Wald NJ, George LM. Prenat Diagn (2001) 21 895-896
  • Antenatal screening for HIV (Letter). Bramley D, Graves N. N Z Med J (2002) 115 24
  • Accuracy of single measurements of pregnancy-associated plasma protein-A, human chorionic gonadotropin and progesterone in the diagnosis of early pregnancy failure. Dumps P, Meisser A, Pons D, Morales MA, Anguenot JL, Campana A, Bischof P. Eur J Obstet Gynecol Reprod Biol (2002) 100 174-180
  • Maternal serum screening marker levels in consanguineous couples (Letter). Khan NR, Saeed M, Cuckle HS. Prenat Diagn (2001) 21 1177-1179
  • Sequential first and second trimester screening tests: Correlation of the markers' levels in normal versus Down syndrome affected pregnancies (Letter). Maymon R, Bergman M, Segal S, Dreazen E, Weinraub Z, Herman A. Prenat Diagn (2001) 21 1175-1177
  • α-Fetoprotein values in amniotic fluid obtained during early amniocentesis (11-13 weeks). Nwebube NI, Lockitch G, Halstead C, Johnson J, Wilson RD. Fetal Diagn Ther (2002) 17 25-28
  • A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60percent. Rosen DJD, Kedar I, Amiel A, Ben-Tovim T, Petel Y, Kaneti H, Tohar M, Fejgin MD. Prenat Diagn (2002) 22 59-63
  • Raised maternal serum placenta growth factor concentration during the second trimester is associated with Down syndrome. Su YN, Hsu JJ, Lee CN, Cheng WF, Kung CCS, Hsieh FJ. Prenat Diagn (2002) 22 8-12
  • The influence of smoking and parity on serum markers for Down's syndrome screening. Tislaric D, Brajenovic-Milic B, Ristic S, Latin V, Zuvic-Butorac M, Bacic J, Petek M, Kapovic M. Fetal Diagn Ther (2002) 17 17-21
  • Basal FSH, estradiol and inhibin B concentrations in women with a previous Down's syndrome affected pregnancy. Van Montfrans JM, Van Hooff MHA, Martens F, Lambalk CB. Hum Reprod (2002) 17 44-47
  • Maternal uniparental heterodisomy for chromosome 2: Detection through ‘atypical’ maternal AFP/hCG levels, with update on a previous case. Wolstenholme J, White I, Sturgiss S, Carter J, Plant N, Goodship JA. Prenat Diagn (2001) 21 813-817
  • 9. Screening for carriers of genetic abnormality
  • Neonatal screening for cystic fibrosis (German). Eichler I, Stockler-Ipsiroglu S. Monatsschr Kinderheilk (2001) 149 1311-1318
  • Novel mutations in the human CYP21 gene. Levo A, Partanen J. Prenat Diagn (2001) 21 885-889
  • Neonatal screening for congenital malformations. Results and perspectives of the birth registry Mainz Model (German). Queisser-Luft A, Wiesel A, Stolz G, Borck G, Schlaefer K, Zabel B, Spranger J. Monatsschr Kinderheilk (2001) 149 1319-1325
  • 10. Technological developments
  • Expanded newborn screening using tandem mass spectrometry (German). Roscher AA, Fingerhut R, Liebl B, Olgemoller B. Monatsschr Kinderheilk (2001) 149 1297-1303
  • Simple vibroacoustic foetal stimulator (Technical note). Stojanovic D, Frkovic A, Filiplic-Stojanovic H, Kirincic N. J Med Engn Tech (2001) 25 269-272
  • Microarray-biochip-technology (German). Zabel B. Monatsschr Kinderheilk (2001) 149 1304-1310
  • 11. Confined placental mosaicism and uniparental disomy
  • Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20. Salafsky IS, MacGregor SN, Claussen U, Von Eggeling F. Prenat Diagn (2001) 21 860-863
  • 13. Fetal cells in maternal circulation
  • Kinetics of fetal cellular and cell-free DNA in the maternal circulation during and after pregnancy: Implications for noninvasive prenatal diagnosis. Ariga H, Ohto H, Busch MP, Imamura S, Watson R, Reed W, Lee TH. Transfusion (2001) 41 1524-1530
  • Fetal and maternal progenitor cells in co-culture respond equally to erythropoietin. Bohmer RM, Johnson KL, Bianchi DW. Prenat Diagn (2001) 21 818-823
  • Novel feto-specific mRNA species suitable for identification of fetal cells from the maternal circulation. Boye K, Hougaard DM, Ebbesen P, Vuust J, Christiansen M. Prenat Diagn (2001) 21 806-812
  • New technique using galactose-specific lectin for isolation of fetal cells from maternal blood. Kitagawa M, Sugiura K, Omi H, Akiyama Y, Kanayama K, Shinya M, Tanaka T, Yura H, Sago H. Prenat Diagn (2002) 22 17-21
  • Identification of triploid trophoblast cells in peripheral blood of a woman with a partial hydatidiform molar pregnancy. Van Wijk IJ, De Hoon AC, Griffioen S, Mulders MAM, Tjoa ML, Van Vugt JMG, Oudejans CBM. Prenat Diagn (2001) 21 1142-1145
  • Enrichment, immunomorphological, and genetic characterization of fetal cells circulating in maternal blood. Vona G, Beroud C, Benachi A, Quenette A, Bonnefont JP, Romana S, Munnich A, Verkemans M, Dumez Y, Lacour B, Paterlini-Brechot P. Am J Pathol (2002) 160 51-58
  • Fetal nucleated red blood cells from CVS washings: An aid to development of first trimester non-invasive prenatal diagnosis. Voullaire L, Ioannou P, Nouri S, Williamson R. Prenat Diagn (2001) 21 827-834
  • 14. Fetal therapy
  • The multiple pregnancy: Reduction and selective feticide: Indication, management and ethical aspects (German). Hackeloer BJ, Hansmann M. Geburtshilfliche Frauenheilk (2001) 61 1007-1011
  • Atypical ectopic pregnancy and culdocentesis: Still a valuable emergency medicine procedure (Case Report). Herd AM, Sokal J. Can Fam Physician (2001) 47 2057-2058
  • Successful intrauterine shunting of a sacrococcygeal teratoma (SCT) causing fetal bladder obstruction. Jouannic JM, Dommergues M, Auber F, Bessis R, Nihoul-Fekete C, Dumez Y. Prenat Diagn (2001) 21 824-826
  • Complications in pregnancy: Diagnosis and treatment of habitual abortions. Steck T. Geburtshilfliche Frauenheilk (2001) 61 906-908
  • Ultrasound-guided umbilical cord occlusion using bipolar diathermy for stage III/IV twin-twin transfusion syndrome. Taylor MJO, Shalev E, Tanawattanacharoen S, Jolly M, Kumar S, Weiner E, Cox PM, Fisk NM. Prenat Diagn (2002) 22 70-76
  • Treatment of fetal congenital complete heart block with maternal administration of β-sympathomimetics (terbutaline): A case report. Yoshida H, Iwamoto M, Sakakibara H, Shigeta H, Hirahara F, Sato K. Gynecol Obstet Invest (2001) 52 142-144
  • 15. Psychosocial aspects
  • Preimplantation diagnosis - Point: Not against the child, but for the mother (German). Diedrich K, Ludwig M. Geburtshilfliche Frauenheilk (2001) 61 902-903
  • Preimplantation diagnosis: Counterpoint - Selection goes against the duty to heal (German). Schmid-Tannwald I. Geburtshilfliche Frauenheilk (2001) 61 904-905
  • Variation in uptake of serum screening: The role of service delivery. Dormandy E, Michie S, Weinman J, Marteau TM. Prenat Diagn (2002) 22 67-69
  • Folic acid awareness, knowledge and consumption among women of childbearing age in Utah 1998-2000. Feldkamp M, Friedrichs M, Marti K. Am J Med Genet (2002) 107 67-69
  • Maternal pain and anxiety in genetic amniocentesis: Expectation versus reality. Ferber A, Onyeije CI, Zelop CM, O'Reilly-Green C, Divon MY. Ultrasound Obstet Gynecol (2002) 19 13-17
  • Prenatal diagnosis for women aged 37 years and over: To have or not to have. Halliday JL, Warren R, McDonald G, Rice PL, Bell RJ, Watson LF. Prenat Diagn (2001) 21 842-847
  • Depressive reactions and stress related to prenatal medicine procedures. Kowalcek I, Muhlhoff A, Bachmann S, Gembruch U. Ultrasound Obstet Gynecol (2002) 19 18-23
  • Ethical and legal aspects in newborn screening (German). Liebl B, Von Kries R, Nennstiel-Ratzel U, Muntau AC, Roschinger W, Olgemoller B, Zapf A, Roscher AA. Monatsschr Kinderheilk (2001) 149 1326-1335
  • Receipt of information and women's attitudes towards ultrasound scanning during pregnancy. Whynes DK. Ultrasound Obstet Gynecol (2002) 19 7-12
  • Is nondirectiveness possible within the context of antenatal screening and testing?. Williams C, Alderson P, Farsides B. Soc Sci Med (2002) 54 339-347
  • Foetal images: The power of visual technology in antenatal care and the implications for women's reproductive freedom. Zechmeister I. Health Care Anal (2001) 9 387-400
  • 16. Epidemiology and environmental factors
  • Air pollution and birth weight in northern Nevada, 1991-1999. Chen L, Yang W, Jennison BL, Goodrich A, Omaye ST. Inhal Toxicol (2002) 14 141-151
  • Evaluation of data quality from the Information System on Live Births in 1997-1998 (Portuguese, English Abstract). Da Silva AAM, Ribeiro VS, Borba AF, Coimbra LC, Da Silva RA. Rev Saude Publica (2001) 35 508-514
  • Association of prenatal phenobarbital and phenytoin exposure with genital anomalies and menstrual disorders. Dessens AB, Cohen-Kettenis PT, Mellenbergh GJ, Koppe JG, Poll NEVD, Boer K. Teratology (2001) 64 181-188
  • Births, gestation and birthweights in South Tees 1990-1996 (Letter). Hall DMB, Rigby AS, Browns IR, Williams TS, Crofts D. J Public Health Med (2001) 23 253-254
  • A nomogram to predict the probability of live birth after clomiphene citrate induction of ovulation in normogonadotropic oligoamenorrheic infertility. Imani B, Eijkemans MJC, Velde ERT, Habbema IDF, Fauser BCJM. Fertil Steril (2002) 77 91-97
  • Phenobarbital following phototherapy for Crigler-Najjar syndrome type II with good fetal outcome: A case report. Ito T, Katagiri C, Ikeno S, Takahashi H, Nagata N, Terakawa N. J Obstet Gynaecol Res (2001) 27 33-35
  • Pregnancy outcomes among US Gulf War veterans: A population-based survey of 30,000 veterans. Kang H, Magee C, Mahan C, Lee K, Murphy F, Jackson L, Matanoski G. Ann Epidemiol (2001) 11 504-511
  • Prevalence of oral clefts from 1975 to 1994, Brazil (Portuguese, English Abstract). Loffredo LDM, Freitas JAD, Grigolli AAG. Rev Saude Publica (2001) 35 571-580
  • Olanzapine and pregnancy. Two case reports (German). Neumann NU, Frasch K. Nervenarzt (2001) 72 876-878
  • Outcome of pregnancies after non-amniocentesis-induced premature rupture of membranes at 14 to 23 weeks' gestation (German, English Abstract). Scholz HS, Arikan MG, Benedicic C, Petru E, Haas J, Weiss PAM. Wien Klin Wochenschr (2002) 114 50-53
  • Prepregnancy body mass index and risk of multiple congenital anomalies (Letter). Shaw GM, Nelson V, Moore CA. Am J Med Genet (2002) 107 253
  • Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida. Shaw GM, Lammer EJ, Zhu H, Baker MW, Neri E, Finnell H. Am J Med Genet (2002) 108 1-6
  • Maternal folate supplementation in pregnancy and protection against acute lymphoblastic leukaemia in childhood: A case-control study. Thompson JR, Gerald PF, Willoughby MLN, Armstrong BK. Lancet (2001) 358 1935-1940
  • Chromosomal congenital anomalies and residence near hazardous waste landfill sites. Vrijheid M, Dolk H, Armstrong B, Abramsky L, Bianchi F, Fazarinc I, Garne E, Ide R, Nelen V, Robert E, Scott JE, Stone D, Teconi R. Lancet (2002) 359 320-322
  • A case-control study of maternal alcohol consumption and intrauterine growth retardation. Yang QH, Witkiewicz BB, Olney RS, Liu YC, Davis M, Khoury MJ, Correa A, Erickson JD. Ann Epidemiol (2001) 11 497-503
  • 17. Developmental pathology
  • OEIS complex, VATER and the ongoing difficulties in terminology and delineation. Bohring A. Am J Med Genet (2002) 107 72-76
  • Reply to the research letter by Bohring: “OEIS complex, VATER and the ongoing difficulties in terminology and delineation”. Martinez-Frias ML, Bermejo E, Rodriguez-Pinilla E, Frias JL. Am J Med Genet (2002) 107 77
  • Severe perinatal liver disease associated with fetal thrombotic vasculopathy (Case Report). Dahms BB, Boyd T, Redline RW. Pediatr Dev Pathol (2002) 5 80-85
  • Demonstration of placental vascular anatomy in monochorionic twin gestations. De Paepe ME, Burke S, Luks FI, Pinar H, Singer DB. Pediatr Dev Pathol (2002) 5 37-44
  • Placental pathology in fetal Bartter syndrome (Case Report). Ernst LM, Parkash V. Pediatr Dev Pathol (2002) 5 76-79
  • Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotyping. Fan JB, Surti U, Taillon-Miller P, Hsie L, Kennedy GC, Hoffner L, Ryder T, Mutch DG, Kwok PY. Genomics (2002) 79 58-62
  • Pneumocephalus in a newborn with an open myelomeningocele (Images on pediatric neurosurgery). Garonzik IM, Samdani AF, Carson BS, Avellino AM. Pediatr Neurosurg (2001) 35 334
  • MR autopsy in fetuses. Huisman TAGM, Wisser J, Stallmach T, Krestin GP, Huch R, Kubik-Huch RA. Fetal Diagn Ther (2002) 17 58-64
  • The effect of a systemic arteriovenous fistula on the pulmonary arterial blood pressure in the fetal sheep. Jouannic JM, Martinovic J, Roussin R, Laborde F, Dumez Y, Dinh-Xuan AT. Prenat Diagn (2002) 22 48-51
  • Recurrent molar pregnancy: Report of a case with seven consecutive hydatidiform moles (Case Reports). Ozalp S, Yalcin OT, Tanir HM, Etiz E. Gynecol Obstet Invest (2001) 52 215-216
  • Combination of diaphragmatic eventration and microphthalmia/anophthalmia is probably nonrandom. Steiner RD, Dignan PSJ, Hopkin RJ, Kozielski R, Bove KE. Am J Med Genet (2002) 108 45
  • Dispermic chimerism with two abnormal cell lines, 47,XY, +21 and 47, XX, +12. Wiley JE, Madigan M, Christie JD, Smith AW. Am J Med Genet (2002) 107 64-66