F H Menko
Overview
Explore the profile of F H Menko including associated specialties, affiliations and a list of published articles.
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Articles
81
Citations
1857
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Recent Articles
1.
van Riel L, Kets C, van Hest L, Menko F, Boerrigter B, Franken S, et al.
Fam Cancer
. 2024 Jun;
23(4):579-582.
PMID: 38900222
No abstract available.
2.
Johannesma P, van de Beek I, van der Wel J, Paul M, Houweling A, Jonker M, et al.
Springerplus
. 2016 Sep;
5(1):1506.
PMID: 27652079
Background And Objectives: Birt-Hogg-Dubé syndrome is an autosomal dominant disorder characterized by skin fibrofolliculomas, lung cysts, spontaneous pneumothorax and renal cell cancer due to germline folliculin (FLCN) mutations (Menko et...
3.
Ghorbanoghli Z, Nieuwenhuis M, Houwing-Duistermaat J, Jagmohan-Changur S, Hes F, Tops C, et al.
Fam Cancer
. 2016 Feb;
15(4):563-70.
PMID: 26880076
Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by germline mutations in the APC gene and characterized by the development of multiple colorectal adenomas and a high risk...
4.
Rijken J, Niemeijer N, Corssmit E, Jonker M, Leemans C, Menko F, et al.
Clin Genet
. 2015 Apr;
89(1):128-32.
PMID: 25827221
In the Netherlands, the majority of hereditary paragangliomas (PGL) is caused by SDHD, SDHB and SDHAF2 mutations. Founder mutations in SDHD are particularly prevalent, but several SDHB founder mutations have...
5.
Johannesma P, van Moorselaar R, Horenblas S, van der Kolk L, Thunnissen E, van Waesberghe J, et al.
Case Rep Med
. 2014 Apr;
2014:618675.
PMID: 24772173
Birt-Hogg-Dubé (BHD) syndrome is a cancer disorder caused by a pathogenic FLCN mutation characterized by fibrofolliculomas, lung cysts, pneumothorax, benign renal cyst, and renal cell carcinoma (RCC). In this case...
6.
Vasen H, Ghorbanoghli Z, Bourdeaut F, Cabaret O, Caron O, Duval A, et al.
J Med Genet
. 2014 Feb;
51(5):283-93.
PMID: 24556086
Lynch syndrome (LS) is an autosomal dominant disorder caused by a defect in one of the DNA mismatch repair genes: MLH1, MSH2, MSH6 and PMS2. In the last 15 years,...
7.
Mutsaers P, van de Loosdrecht A, Tawana K, Bodor C, Fitzgibbon J, Menko F
Leukemia
. 2013 Apr;
27(11):2247-8.
PMID: 23563236
No abstract available.
8.
Houweling A, Gijezen L, Jonker M, van Doorn M, Oldenburg R, van Spaendonck-Zwarts K, et al.
Br J Cancer
. 2011 Dec;
105(12):1912-9.
PMID: 22146830
Background: Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant condition caused by germline FLCN mutations, and characterised by fibrofolliculomas, pneumothorax and renal cancer. The renal cancer risk, cancer phenotype and pneumothorax...
9.
Johannesma P, van der Klift H, van Grieken N, Troost D, Te Riele H, Jacobs M, et al.
Clin Genet
. 2011 Jan;
80(3):243-55.
PMID: 21261604
Childhood brain tumours may be due to germline bi-allelic mismatch repair (MMR) gene mutations in MLH1, MSH2, MSH6 or PMS2. These mutations can also lead to colorectal neoplasia and haematological...
10.
Vos J, Oosterwijk J, Gomez-Garcia E, Menko F, Jansen A, Stoel R, et al.
Clin Genet
. 2010 Dec;
79(3):207-18.
PMID: 21114486
Previous studies on the counsellees' perception of DNA test results did not clarify whether counsellees were asked about their recollections or interpretations, and focused only on patients' own risks and...