166 related articles for article (PubMed ID: 21385172)
1. Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis.
Giambona A; Makrydimas G; Leto F; Damiani G; Jakil MC; Picciotto F; Renda D; Fiorino R; Renda MC; Schillaci G; Gueli-Alletti D; Nicolaides KH; Maggio A
Br J Haematol; 2011 Apr; 153(2):268-72. PubMed ID: 21385172
[TBL] [Abstract][Full Text] [Related]
2. Fetal aneuploidy diagnosed at celocentesis for early prenatal diagnosis of congenital hemoglobinopathies.
Giambona A; Leto F; Passarello C; Vinciguerra M; Cigna V; Schillaci G; Picciotto F; Lauricella S; Nicolaides KH; Makrydimas G; Damiani G; Maggio A
Acta Obstet Gynecol Scand; 2018 Mar; 97(3):312-321. PubMed ID: 29292496
[TBL] [Abstract][Full Text] [Related]
3. Short-term safety of celocentesis for the mother and the fetus.
Makrydimas G; Kaponis A; Skentou C; Lolis D
Ultrasound Obstet Gynecol; 2002 Mar; 19(3):243-5. PubMed ID: 11896943
[TBL] [Abstract][Full Text] [Related]
4. Celocentesis for early prenatal diagnosis of hemoglobinopathy.
Makrydimas G; Damiani G; Jakil C; Cigna V; Orlandi M; Picciotto F; Schillaci G; Cassarà F; Vinciguerra M; Leto F; Giambona A; Maggio A; Nicolaides KH
Ultrasound Obstet Gynecol; 2020 Nov; 56(5):672-677. PubMed ID: 32339311
[TBL] [Abstract][Full Text] [Related]
5. [Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters].
Ferrari M; Cantù Rajnoldi A; Cremonesi L; Donzelli C; Pietri S; Tedeschi S; Travi M; Nicolini U; Brambati B
Pediatr Med Chir; 1984; 6(6):769-73. PubMed ID: 6545587
[TBL] [Abstract][Full Text] [Related]
6. Early prenatal diagnosis by celocentesis.
Makrydimas G; Georgiou I; Bouba I; Lolis D; Nicolaides KH
Ultrasound Obstet Gynecol; 2004 May; 23(5):482-5. PubMed ID: 15133800
[TBL] [Abstract][Full Text] [Related]
7. First-trimester diagnosis of congenital cytomegalovirus infection after maternal primary infection in early pregnancy: feasibility study of viral genome amplification by PCR on chorionic villi obtained by CVS.
Faure-Bardon V; Fourgeaud J; Guilleminot T; Magny JF; Salomon LJ; Bernard JP; Leruez-Ville M; Ville Y
Ultrasound Obstet Gynecol; 2021 Apr; 57(4):568-572. PubMed ID: 33533526
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experience.
Chadefaux-Vekemans B; Rabier D; Cadoudal N; Lescoat A; Chabli A; Aupetit J; Dumez Y; Oury JF
Prenat Diagn; 2006 Sep; 26(9):814-8. PubMed ID: 16821251
[TBL] [Abstract][Full Text] [Related]
9. First-trimester fetal diagnosis for haemoglobinopathies: report on 200 cases.
Old JM; Fitches A; Heath C; Thein SL; Weatherall DJ; Warren R; McKenzie C; Rodeck CH; Modell B; Petrou M
Lancet; 1986 Oct; 2(8510):763-7. PubMed ID: 2876231
[TBL] [Abstract][Full Text] [Related]
10. Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies.
Williamson R; Eskdale J; Coleman DV; Niazi M; Loeffler FE; Modell BM
Lancet; 1981 Nov; 2(8256):1125-7. PubMed ID: 6118574
[No Abstract] [Full Text] [Related]
11. Prenatal cytogenetic diagnosis. Amniotic cell culture versus chorionic villus sampling.
Bell JA; Pearn JH; Smith A
Med J Aust; 1987 Jan; 146(1):27-9. PubMed ID: 3796391
[TBL] [Abstract][Full Text] [Related]
12. [Prenatal diagnosis].
Miny P; Tercanli S; Gänshirt D; Holzgreve W
Ther Umsch; 1995 Dec; 52(12):792-800. PubMed ID: 8539649
[TBL] [Abstract][Full Text] [Related]
13. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities.
Rhoads GG; Jackson LG; Schlesselman SE; de la Cruz FF; Desnick RJ; Golbus MS; Ledbetter DH; Lubs HA; Mahoney MJ; Pergament E
N Engl J Med; 1989 Mar; 320(10):609-17. PubMed ID: 2645520
[TBL] [Abstract][Full Text] [Related]
14. Outcome of first-trimester chorionic villus sampling for genetic investigation in multiple pregnancy.
Brambati B; Tului L; Guercilena S; Alberti E
Ultrasound Obstet Gynecol; 2001 Mar; 17(3):209-16. PubMed ID: 11309169
[TBL] [Abstract][Full Text] [Related]
15. Amniocentesis and chorionic villus sampling.
Stone JL; Lockwood CJ
Curr Opin Obstet Gynecol; 1993 Apr; 5(2):211-7. PubMed ID: 8490091
[TBL] [Abstract][Full Text] [Related]
16. Embryo-fetal erythroid cell selection from celomic fluid allows earlier prenatal diagnosis of hemoglobinopathies.
Giambona A; Damiani G; Leto F; Jakil C; Renda D; Cigna V; Schillaci G; Picciotto F; Nicolaides KH; Passarello C; Makrydimas G; Maggio A
Prenat Diagn; 2016 Apr; 36(4):375-81. PubMed ID: 26891446
[TBL] [Abstract][Full Text] [Related]
17. First-trimester fetal reduction to a singleton infant or twins: outcome in relation to the final number and karyotyping before reduction by transabdominal chorionic villus sampling.
Brambati B; Tului L; Camurri L; Guercilena S
Am J Obstet Gynecol; 2004 Dec; 191(6):2035-40. PubMed ID: 15592288
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of ataxia-telangiectasia and Nijmegen Breakage syndrome by the assay of radioresistant DNA synthesis.
Kleijer WJ; van der Kraan M; Los FJ; Jaspers NG
Int J Radiat Biol; 1994 Dec; 66(6 Suppl):S167-74. PubMed ID: 7836844
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of beta-thalassaemia and other haemoglobinopathies in India.
Thakur (Mahadik) C; Vaz F; Banerjee M; Kapadia C; Natrajan PG; Yagnik H; Gangal S
Prenat Diagn; 2000 Mar; 20(3):194-201. PubMed ID: 10719320
[TBL] [Abstract][Full Text] [Related]
20. Chorionic villus sampling for early prenatal diagnosis at Bhumibol Adulyadej Hospital.
Rueangchainikhom W; Sarapak S; Orungrote N
J Med Assoc Thai; 2008 Jan; 91(1):1-6. PubMed ID: 18386536
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]