323 related articles for article (PubMed ID: 27815806)
1. First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration.
Trachoo O; Satirapod C; Panthan B; Sukprasert M; Charoenyingwattana A; Chantratita W; Choktanasiri W; Hongeng S
J Assist Reprod Genet; 2017 Jan; 34(1):109-116. PubMed ID: 27815806
[TBL] [Abstract][Full Text] [Related]
2. Birth of a healthy child after preimplantation genetic screening of embryos from sperm of a man with non-mosaic Down syndrome.
Aghajanova L; Popwell JM; Chetkowski RJ; Herndon CN
J Assist Reprod Genet; 2015 Sep; 32(9):1409-13. PubMed ID: 26139158
[TBL] [Abstract][Full Text] [Related]
3. Delayed intracytoplasmic sperm injection (ICSI) with trophectoderm biopsy and preimplantation genetic screening (PGS) show increased aneuploidy rates but can lead to live births with single thawed euploid embryo transfer (STEET).
Sachdev NM; Grifo JA; Licciardi F
J Assist Reprod Genet; 2016 Nov; 33(11):1501-1505. PubMed ID: 27255569
[TBL] [Abstract][Full Text] [Related]
4. Preimplantation genetic diagnosis: state of the art.
Basille C; Frydman R; El Aly A; Hesters L; Fanchin R; Tachdjian G; Steffann J; LeLorc'h M; Achour-Frydman N
Eur J Obstet Gynecol Reprod Biol; 2009 Jul; 145(1):9-13. PubMed ID: 19411132
[TBL] [Abstract][Full Text] [Related]
5. Birth of healthy children after preimplantation diagnosis of beta-thalassemia.
Jiao ZX; Zhuang GL; Zhou CQ; Shu YM; Li J; Liang XY
Chin Med J (Engl); 2004 Apr; 117(4):483-7. PubMed ID: 15109434
[TBL] [Abstract][Full Text] [Related]
6. [Preimplantation genetic diagnosis for beta-thalassemia using whole genome amplification].
Jiao ZX; Zhuang GL; Zhou CQ; Shu YM; Li J; Zhang MF; Deng MF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):447-8. PubMed ID: 14556205
[TBL] [Abstract][Full Text] [Related]
7. Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene.
Cangül H; Ozdemir O; Yakut T; Okan M; Morgan NV; Baytan B; Kurian MA; Spiegel R; Maher ER
Turk J Pediatr; 2009; 51(2):161-5. PubMed ID: 19480328
[TBL] [Abstract][Full Text] [Related]
8. Reduction of the multiple pregnancy rate in a preimplantation genetic diagnosis programme after introduction of single blastocyst transfer and cryopreservation of blastocysts biopsied on day 3.
El-Toukhy T; Kamal A; Wharf E; Grace J; Bolton V; Khalaf Y; Braude P
Hum Reprod; 2009 Oct; 24(10):2642-8. PubMed ID: 19567414
[TBL] [Abstract][Full Text] [Related]
9. Dilemmas encountered with preimplantation diagnosis of aneuploidy in human embryos.
Allan J; Edirisinghe R; Anderson J; Jemmott R; Nandini AV; Gattas M
Aust N Z J Obstet Gynaecol; 2004 Apr; 44(2):117-23. PubMed ID: 15089834
[TBL] [Abstract][Full Text] [Related]
10. Novel homozygous PANK2 mutation causing atypical pantothenate kinase-associated neurodegeneration (PKAN) in a Cypriot family.
Tanteles GA; Spanou-Aristidou E; Antoniou C; Christophidou-Anastasiadou V; Kleopa KA
J Neurol Sci; 2014 May; 340(1-2):233-6. PubMed ID: 24655737
[TBL] [Abstract][Full Text] [Related]
11. First unaffected pregnancy using preimplantation genetic diagnosis for sickle cell anemia.
Xu K; Shi ZM; Veeck LL; Hughes MR; Rosenwaks Z
JAMA; 1999 May; 281(18):1701-6. PubMed ID: 10328069
[TBL] [Abstract][Full Text] [Related]
12. Preferential selection and transfer of euploid noncarrier embryos in preimplantation genetic diagnosis cycles for reciprocal translocations.
Wang L; Shen J; Cram DS; Ma M; Wang H; Zhang W; Fan J; Gao Z; Zhang L; Li Z; Xu M; Leigh DA; Trounson AO; Liu J; Yao Y
Fertil Steril; 2017 Oct; 108(4):620-627.e4. PubMed ID: 28863935
[TBL] [Abstract][Full Text] [Related]
13. First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening.
Daina G; Ramos L; Obradors A; Rius M; Martinez-Pasarell O; Polo A; Del Rey J; Obradors J; Benet J; Navarro J
Clin Genet; 2013 Jul; 84(1):70-3. PubMed ID: 22998423
[TBL] [Abstract][Full Text] [Related]
14. Successful application of preimplantation genetic diagnosis for Leigh syndrome.
Unsal E; Aktaş Y; Uner O; BaltacI A; Ozcan S; Turhan F; Baltaci V
Fertil Steril; 2008 Nov; 90(5):2017.e11-3. PubMed ID: 18778816
[TBL] [Abstract][Full Text] [Related]
15. Rescue intracytoplasmic sperm injection and preimplantation genetic diagnosis in combination can result in pregnancy.
DeUgarte CM; Li M; Jordan B; Hill D; DeCherney A; Surrey M
Fertil Steril; 2006 Jul; 86(1):200-2. PubMed ID: 16818034
[TBL] [Abstract][Full Text] [Related]
16. Genotyping single-sperm cells by universal MARSALA enables the acquisition of linkage information for combined pre-implantation genetic diagnosis and genome screening.
Wu H; Shen X; Huang L; Zeng Y; Gao Y; Shao L; Lu B; Zhong Y; Miao B; Xu Y; Wang Y; Li Y; Xiong L; Lu S; Xie XS; Zhou C
J Assist Reprod Genet; 2018 Jun; 35(6):1071-1078. PubMed ID: 29790070
[TBL] [Abstract][Full Text] [Related]
17. Pregnancy outcomes following 24-chromosome preimplantation genetic diagnosis in couples with balanced reciprocal or Robertsonian translocations.
Idowu D; Merrion K; Wemmer N; Mash JG; Pettersen B; Kijacic D; Lathi RB
Fertil Steril; 2015 Apr; 103(4):1037-42. PubMed ID: 25712573
[TBL] [Abstract][Full Text] [Related]
18. Siblings with the adult-onset slowly progressive type of pantothenate kinase-associated neurodegeneration and a novel mutation, Ile346Ser, in PANK2: clinical features and (99m)Tc-ECD brain perfusion SPECT findings.
Doi H; Koyano S; Miyatake S; Matsumoto N; Kameda T; Tomita A; Miyaji Y; Suzuki Y; Sawaishi Y; Kuroiwa Y
J Neurol Sci; 2010 Mar; 290(1-2):172-6. PubMed ID: 20006850
[TBL] [Abstract][Full Text] [Related]
19. Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses.
Yan L; Huang L; Xu L; Huang J; Ma F; Zhu X; Tang Y; Liu M; Lian Y; Liu P; Li R; Lu S; Tang F; Qiao J; Xie XS
Proc Natl Acad Sci U S A; 2015 Dec; 112(52):15964-9. PubMed ID: 26712022
[TBL] [Abstract][Full Text] [Related]
20. Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV.
De Vos A; Sermon K; Van de Velde H; Joris H; Vandervorst M; Lissens W; De Paepe A; Liebaers I; Van Steirteghem A
Hum Genet; 2000 Jun; 106(6):605-13. PubMed ID: 10942108
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
