Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

11 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus.
Girardet A, Viart V, Plaza S, Daina G, De Rycke M, Des Georges M, Fiorentino F, Harton G, Ishmukhametova A, Navarro J, Raynal C, Renwick P, Saguet F, Schwarz M, SenGupta S, Tzetis M, Roux AF, Claustres M. Girardet A, et al. Among authors: ishmukhametova a. Eur J Hum Genet. 2016 Apr;24(4):469-78. doi: 10.1038/ejhg.2015.99. Epub 2015 May 27. Eur J Hum Genet. 2016. PMID: 26014425 Free PMC article.
Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital service.
Girardet A, Ishmukhametova A, Viart V, Plaza S, Saguet F, Verriere G, Hamamah S, Coupier I, Haquet E, Anahory T, Willems M, Claustres M. Girardet A, et al. Among authors: ishmukhametova a. Reprod Biomed Online. 2018 Feb;36(2):154-163. doi: 10.1016/j.rbmo.2017.10.113. Epub 2017 Nov 22. Reprod Biomed Online. 2018. PMID: 29203382
Germline mosaicism is a pitfall in PGD for X-linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal origin.
Viart V, Willems M, Ishmukhametova A, Dufernez F, Anahory T, Hamamah S, Schmitt S, Claustres M, Girardet A. Viart V, et al. Among authors: ishmukhametova a. Prenat Diagn. 2017 Feb;37(2):201-205. doi: 10.1002/pd.4982. Epub 2017 Jan 5. Prenat Diagn. 2017. PMID: 27943351
Molecular Characterization of a Rare Case of Monozygotic Dichorionic Diamniotic Twin Pregnancy after Single Blastocyst Transfer in Preimplantation Genetic Testing (PGT).
Brouillet S, Mereuze S, Ranisavljevic N, Chauveau C, Hamamah S, Cattin J, Verebi C, Cabrol C, Ishmukhametova A, Girardet A, Anahory T, Willems M. Brouillet S, et al. Among authors: ishmukhametova a. Int J Mol Sci. 2022 Sep 16;23(18):10835. doi: 10.3390/ijms231810835. Int J Mol Sci. 2022. PMID: 36142745 Free PMC article.
[Diabetic gastroenteropathy: modern methods of diagnosis and treatment].
Kuznetsov KO, Mikheeva AJ, Ishmukhametova AA, Tolstykh TA, Gallyametdinova AR, Botirova ZU, Zabirova AA, Sharipova AS, Shaikhlislamova AB, Abdrakhmanova DR. Kuznetsov KO, et al. Among authors: ishmukhametova aa. Probl Endokrinol (Mosk). 2022 Jul 13;68(5):67-78. doi: 10.14341/probl13082. Probl Endokrinol (Mosk). 2022. PMID: 36337020 Free PMC article. Russian.
11 results