Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Reiner, Veitia"'
Autor:
Hager barakizou, Gannouni Souha, Thouraya Kamoun, Muhammed Mehdi, Fernanda Amary, Zilla Huma, Anne-laure Todeschini, Reiner Veitia, Malcolm Donaldson
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 107-113 (2022)
Ovarian causes of precocious pseudo-puberty (PPP) include McCune-Albright syndrome (MAS) and juvenile granulosa cell tumour (JGCT). We describe a case of PPP in which bilateral ovarian enlargement with multiple cysts progressed to unilateral JGCT. A
Externí odkaz:
https://doaj.org/article/4316d518cba84646ad07adaa5729732a
Autor:
Hager Barakizou, Gannouni Souha, Thouraya Kamoun, Muhammed Mehdi, Fernanda Amary, Zilla Huma, Anne-laure Todeschini, Reiner Veitia, Malcolm Donaldson
Publikováno v:
Journal of clinical research in pediatric endocrinology. 14(1)
Ovarian causes of precocious pseudo-puberty (PPP) include McCune-Albright syndrome (MAS) and juvenile granulosa cell tumour (JGCT). We describe a case of PPP in which bilateral ovarian enlargement with multiple cysts progressed to unilateral JGCT. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df6cf2cabaadd43af146f3c2013502db
https://pubmed.ncbi.nlm.nih.gov/33849266
https://pubmed.ncbi.nlm.nih.gov/33849266
Autor:
Souha Gannouni, Fernanda Amary, Reiner Veitia, Muhammed Mehdi, Hager Barakizou, Malcolm Donaldson, Zilla Huma, Anne-Laure Todeschini, Thouraya Kamoun
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Ovarian causes of precocious pseudo-puberty (PPP) include McCune-Albright syndrome (MAS) and juvenile granulosa cell tumour (JGCT). We describe a case of PPP in which bilateral ovarian enlargement with multiple cysts progressed to unilateral JGCT. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff625537a0ea164bc279baa080621ccb
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0039
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0039
Gene dosage is important is an important issue both in cell and evolutionary biology. Most genes are present in two copies in eukaryotic cells. The first outstanding exception is monoallelic gene expression (MA) that concerns genes localized on the X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99197ae1703acde8b1e6c3f417eee109
https://doi.org/10.1101/2021.01.12.426466
https://doi.org/10.1101/2021.01.12.426466
Autor:
Johnny S. Younis, Anne-Laure Todeschini, Montserrat Milà, Stavit Shalev, Reiner Veitia, Sandrine Caburet, Lilach Peled Perets, Maria Isabel Alvarez-Mora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87e77a74209e72bc9367a3d239f6fce6
https://doi.org/10.1111/cge.13803/v2/response1
https://doi.org/10.1111/cge.13803/v2/response1
Autor:
Reiner Veitia
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fde56139f8cdd35cc4426e8a71b70165
https://doi.org/10.1530/endoabs.41.s22.2
https://doi.org/10.1530/endoabs.41.s22.2
Autor:
Reiner Veitia
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad8b9b7ce4423a91dc1fce43cc123577
https://doi.org/10.1530/endoabs.32.s3.1
https://doi.org/10.1530/endoabs.32.s3.1
Publikováno v:
Biologie aujourd'hui. 205(4)
Early ovarian development has long been thought of as a default pathway switched on passively by the absence of SRY gene. Recent genetic and transcriptomic studies challenge this view and show that two master pathways simultaneously repress male-spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7eedfb93f31d121fc5b45050fad321e1
https://pubmed.ncbi.nlm.nih.gov/22251856
https://pubmed.ncbi.nlm.nih.gov/22251856
Autor:
Reiner Veitia
Publikováno v:
AfCS-Nature Molecule Pages.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91a545e7bf07d35bb57eb7424ba0508e
https://doi.org/10.1038/mp.a003959.01
https://doi.org/10.1038/mp.a003959.01
Autor:
Elfride, De Baere, Silvia, Copelli, Sandrine, Caburet, Paul, Laissue, Diane, Beysen, Sophie, Christin-Maitre, Philippe, Bouchard, Reiner, Veitia, Marc, Fellous
Publikováno v:
Pediatric endocrinology reviews : PER. 2(4)
Recently the molecular basis of the blepharophimosis-ptosis-epicanthus inversus-syndrome (BPES), an autosomal dominant developmental disorder of the eyelids and ovary, was elucidated. This syndromic form of premature ovarian failure (POF) is caused b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::869ad423b92d34073ebcd39bb91455f8
https://pubmed.ncbi.nlm.nih.gov/16208278
https://pubmed.ncbi.nlm.nih.gov/16208278