Campagne de collecte 15 septembre 2024 – 1 octobre 2024
C'est quoi, la collecte de fonds?
recherche de livres
livres
recherche d'articles
articles
Campagne de collecte:
21.0% pourcents atteints
S'identifier
S'identifier
les utilisateurs autorisés sont disponibles :
recommandations personnelles
Telegram bot
historique de téléchargement
envoyer par courrier électronique ou Kindle
gestion des listes de livres
sauvegarder dans mes Favoris
Personnel
Requêtes de livres
Recherche
Revues
La participation
Faire un don
Litera Library
Faire un don de livres papier
Ajouter des livres papier
Ouvrir LITERA Point
Volume 18; Issue 1
Main
Hereditary Cancer in Clinical Practice
Volume 18; Issue 1
Hereditary Cancer in Clinical Practice
Volume 18; Issue 1
1
Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53
Omran, Meis
,
Blomqvist, Lennart
,
Brandberg, Yvonne
,
Pal, Niklas
,
Kogner, Per
,
Ståhlbom, Anne Kinhult
,
Tham, Emma
,
Bajalica-Lagercrantz, Svetlana
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 751 KB
Vos balises:
2020
2
Group plus âminiâ individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction
Hynes, Jaclyn
,
MacMillan, Andrée
,
Fernandez, Sara
,
Jacob, Karen
,
Carter, Shannon
,
Predham, Sarah
,
Etchegary, Holly
,
Dawson, Lesa
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Langue:
english
Fichier:
PDF, 902 KB
Vos balises:
english, 2020
3
Ubiquitous neurocognitive dysfunction in familial adenomatous polyposis: proof-of-concept of the role of APC protein in neurocognitive function
Cruz-Correa, Marcia Roxana
,
Sala, Ana Cecilia
,
Cintrón, Beatriz
,
Hernández, Jessica
,
Olivera, Myrta
,
Cora, Adrian
,
Moore, Constance M.
,
Luciano, Carlos A.
,
Soto-Salgado, Marievelisse
,
Giardiello, Fr
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 578 KB
Vos balises:
2020
4
Diet, weight management, physical activity and Ovarian & Breast Cancer Risk in women with BRCA1/2 pathogenic Germline gene variants: systematic review
Coletta, Adriana M.
,
Peterson, Susan K.
,
Gatus, Leticia A.
,
Krause, Kate J.
,
Schembre, Susan M.
,
Gilchrist, Susan C.
,
Arun, Banu
,
You, Y. Nancy
,
Rodriguez-Bigas, Miguel A.
,
Strong, Larkin L.
,
Lu, Kare
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 795 KB
Vos balises:
2020
5
The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health care
Møller, Pål
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Langue:
english
Fichier:
PDF, 578 KB
Vos balises:
english, 2020
6
An interesting case of likely BRCA2 related bilateral breast cancer with metastasis in the fimbrial part of fallopian tube
Boltežar, LuÄka
,
GaÅ¡ljeviÄ, Gorana
,
NovakoviÄ, Srdjan
,
Stegel, Vida
,
Å kof, Erik
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 1.40 MB
Vos balises:
2020
7
A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families
Djursby, Malene
,
Wadt, Karin
,
Frederiksen, Jane Hübertz
,
Madsen, Majbritt Busk
,
Berchtold, Lukas Adrian
,
Hasselby, Jane Preuss
,
Willemoe, Gro Linno
,
Hansen, Thomas v. O.
,
Gerdes, Anne-Marie
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 868 KB
Vos balises:
2020
8
Development and validation of next generation sequencing based 35-gene hereditary cancer panel
Chan, Wing
,
Lee, Mianne
,
Yeo, Zhen Xuan
,
Ying, Dingge
,
Grimaldi, Keith A.
,
Pickering, Craig
,
Yang, Michael M. S.
,
Sundaram, Senthil K.
,
Tzang, Lawrence C. H.
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 732 KB
Vos balises:
2020
9
Correction to: Expectations and psychological issues before genetic counseling: analysis of distress determinant factors
Ballatore, Zelmira
,
Bracci, Raffaella
,
Maccaroni, Elena
,
Svarca, Lucia
,
Bianchi, Francesca
,
Belvederesi, Laura
,
Brugiati, Cristiana
,
Pagliaretta, Silvia
,
Murrone, Alberto
,
Bini, Federica
,
Pistelli, Mi
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 189 KB
Vos balises:
2020
10
Adherence to National Comprehensive Cancer Network Guidelines for BRCA testing among high risk breast Cancer patients: a retrospective chart review study
Bobbili, Priyanka
,
Olufade, Temitope
,
DerSarkissian, Maral
,
Shenolikar, Rahul
,
Yu, Hong
,
Duh, Mei Sheng
,
Tung, Nadine
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 295 KB
Vos balises:
2020
11
Increased risk for uterine cancer among first-degree relatives to Swedish gastric cancer patients
Samola Winnberg, Johanna
,
Rudd, Eva
,
Keränen, Anne
,
Lagerstedt-Robinson, Kristina
,
Lindblom, Annika
,
Nilsson, Magnus
,
Lindblad, Mats
,
Sjödahl, Krister
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 526 KB
Vos balises:
2020
12
Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example
Hemminki, Kari
,
Srivastava, Aayushi
,
Rachakonda, Sivaramakrishna
,
Bandapalli, Obul
,
Nagore, Eduardo
,
Hemminki, Akseli
,
Kumar, Rajiv
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 930 KB
Vos balises:
2020
13
Polymorphisms in MMP-1, MMP-2, MMP-7, MMP-13 and MT2A do not contribute to breast, lung and colon cancer risk in polish population
BiaÅkowska, Katarzyna
,
Marciniak, Wojciech
,
MuszyÅska, Magdalena
,
Baszuk, Piotr
,
Gupta, Satish
,
Jaworska-Bieniek, Katarzyna
,
Sukiennicki, Grzegorz
,
Durda, Katarzyna
,
Gromowski, Tomasz
,
Lener, Marcin
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 563 KB
Vos balises:
2020
14
An American patient with polyposis carrying a Scandinavian AXIN2 pathogenic variant
Macklin-Mantia, Sarah K.
,
Riegert-Johnson, Douglas L.
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 526 KB
Vos balises:
2020
15
Retrospective review of outcomes in patients with DNA-damage repair related pancreatic cancer
Macklin-Mantia, Sarah K.
,
Hines, Stephanie L.
,
Kasi, Pashtoon M.
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 598 KB
Vos balises:
2020
16
Expectations and psychological issues before genetic counseling: analysis of distress determinant factors
Ballatore, Zelmira
,
Bracci, Raffaella
,
Maccaroni, Elena
,
Svarca, Lucia
,
Bianchi, Francesca
,
Belvederesi, Laura
,
Brugiati, Cristiana
,
Pagliaretta, Silvia
,
Murrone, Alberto
,
Bini, Federica
,
Pistelli, Mi
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 488 KB
Vos balises:
2020
17
Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden
Andersson, Andreas
,
Hawranek, Carolina
,
Ãfverholm, Anna
,
Ehrencrona, Hans
,
Grill, Kalle
,
Hajdarevic, Senada
,
Melin, Beatrice
,
Tham, Emma
,
Hellquist, Barbro Numan
,
Rosén, Anna
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 1.08 MB
Vos balises:
2020
18
Patients with unexplained mismatch repair deficiency are interested in updated genetic testing
Omark, Jessica
,
Vilar, Eduardo
,
You, Y Nancy
,
Dunnington, Leslie
,
Noblin, Sarah
,
Stevens, Blair
,
Mork, Maureen
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 680 KB
Vos balises:
2020
19
Preferences for breast cancer prevention among women with a BRCA1 or BRCA2 mutation
Mansfield, Carol A.
,
Metcalfe, Kelly A.
,
Snyder, Carrie
,
Lindeman, Geoffrey J.
,
Posner, Joshua
,
Friedman, Sue
,
Lynch, Henry T.
,
Narod, Steven A.
,
Evans, D. Gareth
,
Liede, Alexander
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 1.81 MB
Vos balises:
2020
20
An in-depth exploration of the post-test informational needs of BRCA1 and BRCA2 pathogenic variant carriers in Asia
Yuen, Jeanette
,
Fung, Si Ming
,
Sia, Chin Leong
,
Venkatramani, Mallika
,
Shaw, Tarryn
,
Courtney, Eliza
,
Li, Shao-Tzu
,
Chiang, Jianbang
,
Tan, Veronique Kiak-Mien
,
Tan, Benita Kiat-Tee
,
Ngeow, Joanne
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 557 KB
Vos balises:
2020
21
Biological and clinical impact of central nervous system hemangioblastomas in Chinese patients with von Hippel-Lindau disease: implications for treatment
Liu, Zhen
,
Li, Liang
,
Yi, Zhiqiang
,
Duan, Hongzhou
,
Lu, Runchun
,
Li, Chunwei
,
Li, Lei
,
Gong, Kan
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 1.09 MB
Vos balises:
2020
22
Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation
Khaddour, Karam
,
Fields, Ryan C.
,
Ansstas, Michael
,
Rosman, Ilana S.
,
Ansstas, George
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 1.30 MB
Vos balises:
2020
23
Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in Singapore
Ting, Kay Reen
,
Ong, Pei Yi
,
Wei, Samuel Ow Guan
,
Parameswaran, Rajeev
,
Khoo, Chin Meng
,
Deepak, Doddabele Srinivasa
,
Lee, Soo-Chin
Journal:
Hereditary Cancer in Clinical Practice
Année:
2020
Fichier:
PDF, 1.06 MB
Vos balises:
2020
1
Suivez
ce lien
ou recherchez le bot "@BotFather" sur Telegram
2
Envoyer la commande /newbot
3
Entrez un nom pour votre bot
4
Spécifiez le nom d'utilisateur pour le bot
5
Copier le dernier message de BotFather et le coller ici
×
×