Guía Práctica en Diagnóstico Prenatal, Revisión Bibliográfica

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28. Dunne MG, Johnson ML. The ultrasonic demostration of fetal anormalities in utero. Reprod Med 1979;23/4:195-206.
29. Hobbins JC, Grannum PA,Berkowitz BC y cols. Ultrasound in the diagnosis of congenital anomalies. Am J Obstet Gynecol 1979;134:331-345.
30. Bonilla F. Diagnóstico prenatal de las malformaciones fetales.Barcelona: Jims,1983.
31. Carrera JM. Ecografía obstétrica, 2 edición. Barcelona Salvat Editores, 1985.
32. Carrera JM. Control ecográfico sistemático para el diagnóstico de malformaciones fetales: 24 años de experiencia. Prog Diag Prenat 1994;6:379-389.
33. Westin B. Hysteroscipy in early pregnancy. Lancet 1954;2:872.
34. Hobbins JG, Mahoney MJ. In utero diagnosis of hemoglobinopathies technic for obtainig fetal blood. N Engl J Med 1973;290:1065-1067.
35. Hobbins JC,Mahoney MJ,Goldstein LA. New method of intrauterine evluation by thecombined use of fetoscopy and ultasound. Aqm J Obstet Gynecol 1973;118:1069-1072.
36. Phillips JM. Fetoscopy. An overview . J Reprod Md 1975;15:69-72
37. Rocker I,Lawrence KM. Intrauterine fetal visualitation and blood sampling. En: Marken JD, Stenge-Rutkkkowski S, Schiwinder E, eds. Prenatal diagnosis Stuttgart: Ferdinand Enke, 1978.
38. Rodeck CH. Fetoscopy guided by real time ultrasound for pure fetal blood samples, fetal skin samples and examination of the fetus in utero. Br J Obstet Gynaecol 1980;87:449-456.
39. Rodeck CH. Value of fetoscopy in prenatal diagnosis. J Roy Soc Med 1980;75:29-33.
40, Rodeck CH, Eadi RAJ, Gosden CM. Prenatal diagnosis of epydermolysis bullosa letalis. Lancet 1980; 1:949-952.
41. Valenti C. Endoamnioscopio and fetal biopsy: A new technique. Am J Obstet Gynecol 1972:1:949952
42. Rodeck CH, Patrick AD, Pembrey ME y cols. Fetal liver biopsy for prenatal diagnosis of ornithine carbamyltransferace deficiency. Lancet 1982;1:189-194.
43. Valenti C. Antenatal detection of hemoglobinopathies. AM J Obstet Gynecol 1973;115:851
44. Rodeck CH, Campbell S. Sampling pure fetal blood by fetoscopy in second trimester of pregnacy. BR Med J 1978;11:728-730.
45. Rodeck CH, Campbell S. Umbilical cord insertion as a source of pure fetal blood for prenatal diagnosis. Lancet 1979;1:1244-1245.
46. Nicolaides KH,Rodeck CH. The use of fetoscopy in the management of severe Rhesus isoinmunisation. Nápoles: Intrnational Symposium on Inmuniphysiology of reproduction, 1982.
47. Kullander S, Sandahl B. Fetal chromosome analysis after transcevical placental biopsies during early pregnancy. Acta Obstet Gynecol Scand 1973;52:355-359.
48. Kazy Z, Rozovsky IS, Bakarev VA. Chorion biopsy in early pregnancy: a new method of early prenatal diagnosis for inherited disorders. Prenatal diagnosis 1982;2:39-45.
49. Ward RHT, Modell B, Petrou M y cols. Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound. Br Med J 1983;286:1542-1544.
50. Rodeck CH, Morsman JM, Gosden CM. The development of an improve technique for first trimester microsampling of chorion. Br Med J 1983;90:1113-1118.
51. Daffos F, Capella-Pavlovsky M, Forestier F. A new procedure for pure fetal bloodmsampling in utero. Prenat Diag 1983;3
52. Bennett P, Moore G. Biología molecular para perinatólogos. Barcelona Masson , 1994.
53. Arbert W, Smith H, Mathaus D. Citados de biología molecular. Barcelona: Masson 1.994.
54. Berg P (1972). Citado por Bennett. Biología molecular para perinatólogos.
55. Southern EM (1975). Citado por Bennett. Biología molecular para perinatólogos. Barcelona Masson.1994
56. Saiki RK, Scharf S, Faloona F y cols. Enzymatic amplification of B-globin genomic sequences an restriction  site analysis for of sickle cell anemia. Science 1985;239:1350-1354.
57. Levi S, Hyjazi Y, Shaaps Jp. Sensivity and especifity of routine antenatal screening for congenital anomalies by ultrasound: tha Belgian multicentry study. Ulta Obstet Gynecol 1991;1:102-110
58. Eik-Nes SA, Okland O,Aure JC. Ultrasound screening in pregnancy. Lancet 1984;1:1347.
59. Cuckle HS, Wald NJ, Lindembaumn Rh. Maternal serum alpha fetoprotein measuremnet: a screening test for Down Syndrome. Lancet 1984;1:926-929.
60. Merkatz IR, Nitowsky HM,Macri JM, Johnson WT, An association between low maternal serum AFP and fetal chromosome abnormalities. Am J Obstet Gynecol 1984;148:885.894.
61. Bogart MH,Pandian MR, Jones OW. Abnormal materialserum chorionic gonadotropin levels in normalities pregnancies with fetal chromosomal abnormalities. Prenat Diag 1987;7:623-630.
62. Canick JA, Knight Gjk, Palomaki GE y cols. Lowsecond trimester maternal serum unconjugated oestriol in pregnancies with Down´s syndrome. Br J Obstet Gynecol 1988;95:330-333.
63. Benacerraf BR, Gelman R, Frigoletto FDJ. A sonographic sign for the detection in the second trimester fetuses with Down´s syndrome. Am J Obstet Gynecol 1985;151:1078.
64. Benacerraf BR, Gelman R, Frogoleto FDJ. Sonographic identification of second trimester fetuses with Down´s syndrome. N Engl J Med 1987;317:1371.
65. Veiga A, Santaló J, Vidal F, Calderón G, Gimenez C, Boada M, Egozcue J, Barri PN. Twin pregnancy after preimplantation diagnosis for sex selection. Hum Reprod 1994;9:2156-2159.
66. Handyside AN, Pattinson Jk, Penketh RJ,Decanthy JD, Winston RM. Biopsy of human preimplantation embryos and sexing by DNA amplification. Lancet 1989;i:347-349.
67. Handyside AH, Kontagianni EH, Winston RM. Pregnancies from biopsied human preimplantation sexed by Y- specific DNA amplifications. Nature 1990; 344:768-770.
68. Dokars A, Sargent IL, Barlow DH. Blastocyst biopsy following IVE. Prenat Diag 1992;12
69. Pergament E. Preimplantation diagnosis: a patient perspective. Prenat Diag. 1991,11:493-500
70. Bianchi DW, Flint AF,Pizzimenti MF, Knon JHM, Latt SA. Isolation of fetal DNA from nucleated eritrocytes in maternal blood. Proc Natl Acad Sci USA 1990;87:3279-3283.
71. De la Riva AM, Marqués Gubern A. Prevención y diagnóstico prenatal de los defectos del tubo neural. Cir Pediatr 1990;3:35-36.
72. Martinez Frias ML. Defectos congénitos en España. Diez años de vigilancia epidemiológica. Estudios sanitarios. Dirección general de planificación sanitaria. Ministerio de sanidad y consumo. Madrid, 1989.
73. Hibbard BM. The role of folic acid in pregnancy: with particular reference to anaemia, abruption and abortion. J Obstet Gynaecol Br Commomv 71:529-42,1964
74. Hibbard DE, Smithells RW. Folic acid metabolism and human embryophaty. Lancet 1:1254, 1965.
75. Nelson MM, Forfar JO. Associations between drugs administered during pregnancy and congenital abnormalities of the fetus. Br J Med 1:523-527,1971.
76. Smithells RW, Shepard S, Schorah CJ, et al. Possible prevention of neural-tube defects by periconceptional vitamin supplemntation. Lancet 1: 339.340, 1980
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