K Keymolen
Overview
Explore the profile of K Keymolen including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
30
Citations
236
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Van Der Kelen A, Santos-Ribeiro S, de Vos A, Verdyck P, De Rycke M, Berckmoes V, et al.
Hum Reprod
. 2021 Jun;
36(9):2558-2566.
PMID: 34142115
Study Question: What is the likelihood of success of a single cycle of preimplantation genetic testing for monogenic disorders (PGT-M), measured as the cumulative live birth rate (CLBR) and based...
2.
Belva F, Bonduelle M, Buysse A, Van den Bogaert A, Hes F, Roelants M, et al.
Hum Reprod
. 2020 Aug;
35(9):2149-2162.
PMID: 32772109
Study Question: Is there a relationship between karyotype abnormalities in fetuses and children conceived by ICSI and their father's semen parameters? Summary Answer: The de novo chromosomal abnormality rate in...
3.
De Rycke M, de Vos A, Belva F, Berckmoes V, Bonduelle M, Buysse A, et al.
J Hum Genet
. 2020 Feb;
65(5):445-454.
PMID: 32103123
Preimplantation genetic testing-human leukocyte antigen '(PGT-HLA) only' refers to the HLA typing of single or few cells biopsied from in vitro fertilized preimplantation embryos. The aim of the procedure is...
4.
Leemans G, De Raeve L, Keymolen K
J Eur Acad Dermatol Venereol
. 2019 Dec;
34(4):876-879.
PMID: 31803976
Background: Trichothiodystrophy (TTD) describes a group of rare genetic disorders of DNA repair, characterized by sulphur-deficient hair, skin anomalies and systemic complications like preterm delivery, neurological impairment, haematological and ophthalmological...
5.
Berckmoes V, Verdyck P, De Becker P, de Vos A, Verheyen G, Van der Niepen P, et al.
Hum Reprod
. 2019 Mar;
34(5):949-958.
PMID: 30927425
Study Question: What are the factors influencing the success rate for couples undergoing preimplantation genetic testing (PGT) for polycystic kidney disease (PKD)? Summary Answer: In our study cohort, the live...
6.
Stouffs K, Stergachis A, Vanderhasselt T, Dica A, Janssens S, Vandervore L, et al.
Clin Genet
. 2018 Apr;
94(2):246-251.
PMID: 29652087
ZNF335 plays an essential role in neurogenesis and biallelic variants in ZNF335 have been identified as the cause of severe primary autosomal recessive microcephaly in 2 unrelated families. We describe,...
7.
Pintens S, Pierret L, Keymolen K, Gutermuth J, De Raeve L
J Eur Acad Dermatol Venereol
. 2015 Oct;
30(10):e42-e43.
PMID: 26446056
No abstract available.
8.
Jansen A, Oostra A, Desprechins B, De Vlaeminck Y, Verhelst H, Regal L, et al.
Neurology
. 2011 Mar;
76(11):988-92.
PMID: 21403111
Background: Mutations in the TUBA1A gene have been reported in patients with lissencephaly and perisylvian pachygyria. Methods: Twenty-five patients with malformations of cortical development ranging from lissencephaly to polymicrogyria were...
9.
Gheyle L, Keymolen K, Halewijck S, Gordts F
B-ENT
. 2008 May;
4(1):1-6.
PMID: 18500015
Objective: To investigate indications, features and outcome of pediatric tracheotomy in our ENT department. Methods: A retrospective chart review of all pediatric patients who underwent tracheotomy between 1992 and 2006...
10.
Mathys R, Deconinck H, Keymolen K, Jansen A, Van Esch H
Bull Soc Belge Ophtalmol
. 2007 Nov;
(305):49-53.
PMID: 18018428
We present the ophthalmologic findings in a boy with a deletion of Xp22 comprising the gene for Nance-Horan syndrome. Different mechanisms underlying the visual impairment in Nance-Horan syndrome are discussed.