يعرض 1 - 10 نتائج من 233,632 نتيجة بحث عن '"HEREDITARY"', وقت الاستعلام: 1.39s تنقيح النتائج
  1. 1
    رسالة جامعية
    Directed hereditary species and Decomposition spaces of intervals

    المؤلفون: Forero Baquero, Wilson Javier

    مرشدي الرسالة: Kock, Joachim Christian

    المصدر: TDX (Tesis Doctorals en Xarxa)

    مصطلحات موضوعية: Espai de descomposició, Espacios de descomposición, Decomposition spaces, Espècie hereditària dirigida, Especie hereditaria dirigida, Directed hereditary species, Topos, Ciències Experimentals

    الوقت: 515.1

    وصف الملف: application/pdf

    الوصول الحر: http://hdl.handle.net/10803/689774Test

    استعراض التسجيلة في TDX

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  2. 2
    دورية أكاديمية
    Population-Level Identification of Patients With Lynch Syndrome for Clinical Care, Quality Improvement, and Research.

    المؤلفون: Sharaf, Ravi N.1,2 (AUTHOR) Ras9030@med.cornell.edu, Udaltsova, Natalia3 (AUTHOR), Li, Dan3,4 (AUTHOR), Pai, Rish K.5 (AUTHOR), Sinha, Soham2 (AUTHOR), Li, Zixuan2 (AUTHOR), Corley, Douglas A.3 (AUTHOR)

    المصدر: JCO Clinical Cancer Informatics. 6/5/2024, Vol. 8, p1-14. 14p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *HEREDITARY cancer syndromes, *CLINICAL medicine, *IDENTIFICATION, *GENETIC testing, *MEDICAL screening

    مصطلحات جغرافية: CALIFORNIA

    الشركة/الكيان: KAISER Permanente (Company)


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  3. 3
    دورية أكاديمية
    Frameshift mutations in peripheral blood as a biomarker for surveillance of Lynch syndrome.

    المؤلفون: Song, Yurong1 (AUTHOR) songy3@mail.nih.gov, Loomans-Kropp, Holli2,3 (AUTHOR), Baugher, Ryan N4 (AUTHOR), Somerville, Brandon1 (AUTHOR), Baxter, Shaneen S1 (AUTHOR), Kerr, Travis D1 (AUTHOR), Plona, Teri M4 (AUTHOR), Mellott, Stephanie D4 (AUTHOR), Young, Todd B4 (AUTHOR), Lawhorn, Heidi E4 (AUTHOR), Wei, Lei5 (AUTHOR), Hu, Qiang5 (AUTHOR), Liu, Song5 (AUTHOR), Hutson, Alan5 (AUTHOR), Pinto, Ligia1 (AUTHOR), Potter, John D6,7,8 (AUTHOR), Sei, Shizuko2 (AUTHOR), Gelincik, Ozkan9 (AUTHOR), Lipkin, Steven M9 (AUTHOR), Gebert, Johannes10 (AUTHOR)

    المصدر: JNCI: Journal of the National Cancer Institute. Jun2024, Vol. 116 Issue 6, p957-965. 9p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *FRAMESHIFT mutation, *DNA mismatch repair, *RECEIVER operating characteristic curves, *HEREDITARY cancer syndromes, *BIOMARKERS


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  4. 4
    دورية أكاديمية
    Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia.

    المؤلفون: Beslow, Lauren A.1 (AUTHOR) beslow@chop.edu, Vossough, Arastoo2 (AUTHOR), Kim, Helen3 (AUTHOR), Nelson, Jeffrey3 (AUTHOR), Lawton, Michael T.4 (AUTHOR), Pollak, Jeffrey5 (AUTHOR), Lin, Doris D. M.6 (AUTHOR), Ratjen, Felix7 (AUTHOR), Hammill, Adrienne M.8 (AUTHOR), Hetts, Steven W.9 (AUTHOR), Gossage, James R.10 (AUTHOR), Whitehead, Kevin J.11 (AUTHOR), Faughnan, Marie E.12 (AUTHOR), Krings, Timo13 (AUTHOR), Brain Vascular Malformation Consortium HHT Investigator Group (AUTHOR), Atherton, Mary E. (AUTHOR), Chakinala, Murali M. (AUTHOR), Clancy, Marianne S. (AUTHOR), Henderson, Katharine (AUTHOR), Hetts, Steven (AUTHOR)

    المصدر: Child's Nervous System. Jul2024, Vol. 40 Issue 7, p2101-2108. 8p.

    مصطلحات موضوعية: *HEREDITARY hemorrhagic telangiectasia, *CEREBRAL arteriovenous malformations, *INTRACRANIAL hemorrhage, *ANGIOGRAPHY, *SURGICAL excision


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  5. 5
    دورية أكاديمية
    Clinicopathological characteristics of Lynch-like syndrome.

    المؤلفون: Nakamori, Sakiko1 (AUTHOR), Takao, Misato1 (AUTHOR), Takao, Akinari2 (AUTHOR), Natsume, Soichiro1 (AUTHOR), Iijima, Takeru3,4 (AUTHOR), Kojika, Ekumi3,4 (AUTHOR), Nakano, Daisuke1 (AUTHOR), Kawai, Kazushige1 (AUTHOR), Inokuchi, Takuhiko3 (AUTHOR), Fujimoto, Ai3 (AUTHOR), Urushibara, Makiko3 (AUTHOR), Horiguchi, Shin-ichiro5 (AUTHOR), Ishida, Hideyuki6 (AUTHOR), Yamaguchi, Tatsuro2,6 (AUTHOR) tatsuro@yamaguchi.email.ne.jp

    المصدر: International Journal of Clinical Oncology. Jul2024, Vol. 29 Issue 7, p944-952. 9p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *GENETIC testing, *COLORECTAL cancer, *CLINICAL pathology, *SYNDROMES, *MEDICAL screening


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  6. 6
    دورية أكاديمية
    Incidence and molecular characteristics of deficient mismatch repair conditions across nine different tumors and identification of germline variants involved in Lynch-like syndrome.

    المؤلفون: Ito, Tetsuya1 (AUTHOR) tez1028@saitama-med.ac.jp, Yamaguchi, Tatsuro2 (AUTHOR), Kumamoto, Kensuke3 (AUTHOR), Suzuki, Okihide1,4 (AUTHOR), Chika, Noriyasu1 (AUTHOR), Kawakami, Satoru5 (AUTHOR), Nagai, Tomonori6 (AUTHOR), Igawa, Tsukasa7 (AUTHOR), Fujiyoshi, Kenji8 (AUTHOR), Akagi, Yoshito8 (AUTHOR), Arai, Tomio9 (AUTHOR), Akagi, Kiwamu10 (AUTHOR), Eguchi, Hidetaka11 (AUTHOR), Okazaki, Yasushi11 (AUTHOR), Ishida, Hideyuki1,4 (AUTHOR)

    المصدر: International Journal of Clinical Oncology. Jul2024, Vol. 29 Issue 7, p953-963. 11p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *DNA mismatch repair, *GENETIC counseling, *GERM cells, *BLADDER, *TUMORS


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  7. 7
    دورية أكاديمية
    Modifiable risk factors for cancer among people with lynch syndrome: an international, cross-sectional survey.

    المؤلفون: Power, Robert F.1,2 (AUTHOR), Doherty, Damien E.3 (AUTHOR), Horgan, Roberta4 (AUTHOR), Fahey, Pat4 (AUTHOR), Gallagher, David J.1,2,5 (AUTHOR), Lowery, Maeve A.1,5 (AUTHOR), Cadoo, Karen A.1,2,5 (AUTHOR) KCadoo@stjames.ie

    المصدر: Hereditary Cancer in Clinical Practice. 6/14/2024, Vol. 22 Issue 1, p1-10. 10p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *BEHAVIOR modification, *PATIENT advocacy, *CANCER patients, *DISEASE risk factors, *HEALTH behavior

    النص الكامل

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  8. 8
    دورية أكاديمية
    Functional analysis of MMR gene VUS from potential Lynch syndrome patients.

    المؤلفون: Mahdouani, Marwa1,2 (AUTHOR) marwamahdouani95@gmail.com, Zhuri, Drenushe3 (AUTHOR), Sezginer Guler, Hazal3 (AUTHOR), Hmida, Dorra1,4 (AUTHOR), Sana, Mokni4,5 (AUTHOR), Azaza, Mohamed6 (AUTHOR), Ben Said, Mariem7 (AUTHOR), Masmoudi, Saber7 (AUTHOR), Hmila, Fahmi4,8 (AUTHOR), Youssef, Sabri9 (AUTHOR), Ben Sghaier, Rihab1,2 (AUTHOR), Brieger, Angela10 (AUTHOR), Zeuzem, Stefan10 (AUTHOR), Saad, Ali1,4 (AUTHOR), Gurkan, Hakan3 (AUTHOR), Yalcintepe, Sinem3 (AUTHOR), Gribaa, Moez1,4 (AUTHOR), Plotz, Guido10 (AUTHOR) marwamahdouani95@gmail.com

    المصدر: PLoS ONE. 6/6/2024, Vol. 19 Issue 6, p1-18. 18p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *FUNCTIONAL analysis, *DNA mismatch repair, *GENETIC variation, *MISSENSE mutation, *COLORECTAL cancer

    النص الكامل

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  9. 9
    دورية أكاديمية
    Leveraging Electronic Health Record Data to Understand Gaps Underlying the Underdiagnosis of Lynch Syndrome.

    المؤلفون: Maoz, Asaf1,2,3 (AUTHOR), Yurgelun, Matthew B.1,2,3 (AUTHOR) matthew_yurgelun@dfci.harvard.edu

    المصدر: JCO Clinical Cancer Informatics. 6/5/2024, Vol. 8, p1-4. 4p.

    مصطلحات موضوعية: *HEREDITARY nonpolyposis colorectal cancer, *ELECTRONIC health records, *DATA recorders & recording


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  10. 10
    دورية أكاديمية
    De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia.

    المؤلفون: Beslow, Lauren A.1 (AUTHOR) beslow@chop.edu, Krings, Timo2 (AUTHOR), Kim, Helen3 (AUTHOR), Hetts, Steven W.4 (AUTHOR), Lawton, Michael T.5 (AUTHOR), Ratjen, Felix6 (AUTHOR), Whitehead, Kevin J.7 (AUTHOR), Gossage, James R.8 (AUTHOR), McCulloch, Charles E.9 (AUTHOR), Clancy, Marianne10 (AUTHOR), Bagheri, Negar11 (AUTHOR), Faughnan, Marie E.11 (AUTHOR)

    المصدر: Pediatric Neurology. Jun2024, Vol. 155, p120-125. 6p.

    مصطلحات موضوعية: *HEREDITARY hemorrhagic telangiectasia, *CEREBRAL arteriovenous malformations, *HUMAN abnormalities, *SIZE of brain, *INTRACRANIAL hemorrhage


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