132 related articles for article (PubMed ID: 21932595)
1. Preimplantation genetic diagnosis (PGD)--prevention of the birth of children affected with endocrine diseases.
Altarescu G; Barenholz O; Renbaum P; Beeri R; Levy-Lahad E; Margalioth EJ; Brooks B; Varshaver I; Eldar-Geva T
J Pediatr Endocrinol Metab; 2011; 24(7-8):543-8. PubMed ID: 21932595
[TBL] [Abstract][Full Text] [Related]
2. First successful application of preimplantation genetic diagnosis and haplotyping for congenital hyperinsulinism.
Qubbaj W; Al-Swaid A; Al-Hassan S; Awartani K; Deek H; Coskun S
Reprod Biomed Online; 2011 Jan; 22(1):72-9. PubMed ID: 21115269
[TBL] [Abstract][Full Text] [Related]
3. Can preimplantation genetic diagnosis be used for monogenic endocrine diseases?
Yeager S; Mehta S; Sodhi M; Shah B
J Pediatr Endocrinol Metab; 2019 Dec; 32(12):1305-1310. PubMed ID: 31490775
[TBL] [Abstract][Full Text] [Related]
4. Preimplantation Genetic Diagnosis of Multiple Endocrine Neoplasia Type 2A Using Informative Markers Identified by Targeted Sequencing.
Chen S; Li S; Zhang J; Zhang L; Chen Y; Wang L; Jin L; Hu Y; Qi X; Huang H; Xu C
Thyroid; 2018 Mar; 28(3):281-287. PubMed ID: 29378479
[TBL] [Abstract][Full Text] [Related]
5. Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line.
Altarescu G; Renbaum P; Eldar-Geva T; Brooks B; Varshaver I; Avitzour M; Margalioth EJ; Levy-Lahad E; Elstein D; Epsztejn-Litman S; Eiges R
Prenat Diagn; 2011 Sep; 31(9):853-60. PubMed ID: 21706504
[TBL] [Abstract][Full Text] [Related]
6. Birth of a healthy boy following preimplantation genetic diagnosis for congenital adrenal hyperplasia.
Reihani-Sabet F; Eftekhari-Yazdi P; Boroujeni PB; Saffari JR; Almadani N; Boloori S; Zamanian MR
JBRA Assist Reprod; 2020 May; 24(2):227-230. PubMed ID: 32072793
[TBL] [Abstract][Full Text] [Related]
7. Pregnancy after preimplantation genetic diagnosis for Sanjad-Sakati syndrome.
Hellani A; Aqueel A; Jaroudi K; Ozand P; Coskun S
Prenat Diagn; 2004 Apr; 24(4):302-6. PubMed ID: 15065107
[TBL] [Abstract][Full Text] [Related]
8. Preimplantation genetic diagnosis for hereditary endocrine disease.
Lietman SA
Endocr Pract; 2011; 17 Suppl 3():28-32. PubMed ID: 21550946
[TBL] [Abstract][Full Text] [Related]
9. Sanjad-Sakati syndrome in a Tunisian child.
Kerkeni E; Sakka R; Sfar S; Bouaziz S; Ghedira N; Ben Ameur K; Ben Hmida H; Chioukh FZ; Ghédira ES; Gribaa M; Monastiri K
Arch Pediatr; 2015 Sep; 22(9):951-5. PubMed ID: 26231322
[TBL] [Abstract][Full Text] [Related]
10. [Clinical analysis of preimplantation genetic diagnosis with HLA matching for beta-thalassemia].
Liu XY; Wang J; Zeng YH; Ding CH; Shen XT; Zhou W; Li R; Zhou CQ; Xu YW
Zhonghua Fu Chan Ke Za Zhi; 2016 Jul; 51(7):491-7. PubMed ID: 27465867
[TBL] [Abstract][Full Text] [Related]
11. The Bedouin mutation c.155-166del of the TBCE gene in a patient with Sanjad-Sakati syndrome of Moroccan origin.
Ratbi I; Lyahyai J; Kabiri M; Banouar M; Zerkaoui M; Barkat A; Sefiania A
Ann Saudi Med; 2015; 35(2):170-2. PubMed ID: 26336027
[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. Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.
Altarescu G; Eldar-Geva T; Varshower I; Brooks B; Haran EZ; Margalioth EJ; Levy-Lahad E; Renbaum P
Hum Reprod; 2009 Dec; 24(12):3225-9. PubMed ID: 19687056
[TBL] [Abstract][Full Text] [Related]
14. [Analysis of clinical outcomes of different embryo stage biopsy in array comparative genomic hybridization based preimplantation genetic diagnosis and screening].
Shen JD; Wu W; Shu L; Cai LL; Xie JZ; Ma L; Sun XP; Cui YG; Liu JY
Zhonghua Fu Chan Ke Za Zhi; 2017 Dec; 52(12):828-834. PubMed ID: 29325267
[No Abstract] [Full Text] [Related]
15. The mutation-free embryo for in vitro fertilization selected by MALBAC-PGD resulted in a healthy live birth from a family carrying PKD 1 mutation.
Li W; Ma Y; Yu S; Sun N; Wang L; Chen D; Yang G; Lu S; Li Y; Yang B; Mei C
J Assist Reprod Genet; 2017 Dec; 34(12):1653-1658. PubMed ID: 28825164
[TBL] [Abstract][Full Text] [Related]
16. Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers.
Tan YQ; Tan K; Zhang SP; Gong F; Cheng DH; Xiong B; Lu CF; Tang XC; Luo KL; Lin G; Lu GX
Hum Reprod; 2013 Sep; 28(9):2581-92. PubMed ID: 23847111
[TBL] [Abstract][Full Text] [Related]
17. Three hundred and thirty cycles of preimplantation genetic diagnosis for serious genetic disease: clinical considerations affecting outcome.
Grace J; El-Toukhy T; Scriven P; Ogilvie C; Pickering S; Lashwood A; Flinter F; Khalaf Y; Braude P
BJOG; 2006 Dec; 113(12):1393-401. PubMed ID: 17176278
[TBL] [Abstract][Full Text] [Related]
18. [Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].
de Die-Smulders CE; Land JA; Dreesen JC; Coonen E; Evers JL; Geraedts JP
Ned Tijdschr Geneeskd; 2004 Dec; 148(50):2491-6. PubMed ID: 15638197
[TBL] [Abstract][Full Text] [Related]
19. Preimplantation genetic diagnosis of single-gene disorders: experience with more than 200 cycles conducted by a reference laboratory in the United States.
Gutiérrez-Mateo C; Sánchez-García JF; Fischer J; Tormasi S; Cohen J; Munné S; Wells D
Fertil Steril; 2009 Nov; 92(5):1544-56. PubMed ID: 18937943
[TBL] [Abstract][Full Text] [Related]
20. Genetic diseases and aneuploidies can be detected with a single blastocyst biopsy: a successful clinical approach.
Minasi MG; Fiorentino F; Ruberti A; Biricik A; Cursio E; Cotroneo E; Varricchio MT; Surdo M; Spinella F; Greco E
Hum Reprod; 2017 Aug; 32(8):1770-1777. PubMed ID: 28633287
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
