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Wyszukujesz frazę ""Potjer, Thomas P."" wg kryterium: Autor

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    Wyświetlanie 1-8 z 8
    Tytuł:
    SDHAF2 -Linked Metastatic Paraganglioma: A Case Report with Implications for Counseling and Follow-Up of Pathogenic SDHAF2 Variant Carriers.
    Autorzy:
    de Jong MAM; Department of Otorhinolaryngology and Head and Neck Surgery, Leiden University Medical Center, Leiden, Netherlands.
    Corssmit EPM; Department of Endocrinology and Metabolic Diseases, Leiden University Medical Center, Leiden, Netherlands.
    Jansen JC; Department of Otorhinolaryngology and Head and Neck Surgery, Leiden University Medical Center, Leiden, Netherlands.
    Potjer TP; Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands.
    Bayley JL; Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
    Hensen EF; Department of Otorhinolaryngology and Head and Neck Surgery, Leiden University Medical Center, Leiden, Netherlands.
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    Źródło:
    Case reports in otolaryngology [Case Rep Otolaryngol] 2024 Mar 20; Vol. 2024, pp. 2111531. Date of Electronic Publication: 2024 Mar 20 (Print Publication: 2024).
    Typ publikacji:
    Case Reports
    Raport
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines.
    Autorzy:
    Chau C; Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    van Doorn R; Department of Dermatology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    van Poppelen NM; Department of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.; Department of Ophthalmology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
    van der Stoep N; Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    Mensenkamp AR; Department of Clinical Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
    Sijmons RH; Department of Genetics, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
    van Paassen BW; Department of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
    van den Ouweland AMW; Department of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
    Naus NC; Department of Ophthalmology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
    van der Hout AH; Department of Genetics, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
    Potjer TP; Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    Bleeker FE; Department of Clinical Genetics, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
    Wevers MR; Department of Clinical Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
    van Hest LP; Department of Clinical Genetics, Amsterdam University Medical Centers, 1081 HV Amsterdam, The Netherlands.
    Jongmans MCJ; Department of Clinical Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.; Department of Clinical Genetics, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
    Marinkovic M; Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    Bleeker JC; Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    Jager MJ; Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    Luyten GPM; Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands. .
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    Źródło:
    Cancers [Cancers (Basel)] 2019 Aug 04; Vol. 11 (8). Date of Electronic Publication: 2019 Aug 04.
    Typ publikacji:
    Journal Article
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.
    Autorzy:
    Potjer TP; Department of Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands. t.p.potjer@lumc.nl.
    van der Stoep N; Department of Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands. n.van_der_.
    Houwing-Duistermaat JJ; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands. .
    Konings IC; Department of Gastroenterology and Hepatology,Erasmus MC, University Medical Center, Rotterdam, The Netherlands. .
    Aalfs CM; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands. .
    van den Akker PC; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands. p..
    Ausems MG; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands. .
    Dommering CJ; Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The Netherlands. .
    van der Kolk LE; Department of Clinical Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands. .
    Maiburg MC; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands. .
    Spruijt L; Department of Clinical Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands. .
    Wagner A; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, The Netherlands. .
    Vasen HF; The Netherlands Foundation for the Detection of Hereditary Tumours, Leiden, The Netherlands. .
    Hes FJ; Department of Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands. .
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    Źródło:
    BMC research notes [BMC Res Notes] 2015 Jun 26; Vol. 8, pp. 264. Date of Electronic Publication: 2015 Jun 26.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Germ-Line Mutation*
    Polymorphism, Single Nucleotide*
    Cyclin-Dependent Kinase Inhibitor p16/*genetics
    Dysplastic Nevus Syndrome/*genetics
    Melanoma/*genetics
    Skin Neoplasms/*genetics
    Adult ; Aged ; Aged, 80 and over ; Alleles ; Case-Control Studies ; Dysplastic Nevus Syndrome/complications ; Dysplastic Nevus Syndrome/pathology ; Female ; Heterozygote ; Humans ; Male ; Melanoma/complications ; Melanoma/pathology ; Middle Aged ; Netherlands ; Odds Ratio ; Pancreatic Neoplasms/complications ; Pancreatic Neoplasms/genetics ; Pancreatic Neoplasms/pathology ; Pedigree ; Risk Factors ; Skin Neoplasms/complications ; Skin Neoplasms/pathology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Prospective risk of cancer and the influence of tobacco use in carriers of the p16-Leiden germline variant.
    Autorzy:
    Potjer TP; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
    Kranenburg HE; Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
    Bergman W; Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.
    de Vos tot Nederveen Cappel WH; Department of Gastroenterology and Hepatology, Isala Clinics, Zwolle, The Netherlands.
    van Monsjou HS; Deparment of Otorhinolaryngology, Leiden University Medical Center, Leiden, The Netherlands.
    Barge-Schaapveld DQ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
    Vasen HF; Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
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    Źródło:
    European journal of human genetics : EJHG [Eur J Hum Genet] 2015 May; Vol. 23 (5), pp. 711-4. Date of Electronic Publication: 2014 Sep 17.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Germ-Line Mutation*
    Heterozygote*
    Cyclin-Dependent Kinase Inhibitor p16/*genetics
    Neoplasms/*etiology
    Tobacco Use/*adverse effects
    Adult ; Aged ; Cohort Studies ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Neoplasms/diagnosis ; Neoplasms/epidemiology ; Odds Ratio
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-8 z 8

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