families < family < fantasy

Facettes : Author.f AffPays.f AffRegion.f AffVille.f AffOrg.f KwdFr.f Mesh.f MeshFr.f

List of bibliographic references indexed by family

Number of relevant bibliographic references: 93.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000083 (2017)	J. Easley ; B. Miedema ; M. A. O Rien [Canada] ; J. Carroll [Canada] ; D. Manca ; F. Webster [Canada] ; E. Grunfeld [Canada]	The role of family physicians in cancer care: perspectives of primary and specialty care providers
000537 (2017)	Aniel Jessica Leticia Brambila-Tapia [Mexique] ; José Elías García-Ortiz [Mexique] ; Pascal Brouillard [Belgique] ; Ha-Long Nguyen [Belgique] ; Miikka Vikkula [Belgique] ; Blanca Estela Ríos-González [Mexique] ; Roberto De Jesús Sandoval-Mu Iz [Mexique] ; Ana Karen Sandoval-Talamantes [Mexique] ; Lucina Bobadilla-Morales [Mexique] ; Jorge Román Corona-Rivera [Mexique] ; Lisette Arnaud-Lopez [Mexique]	GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome.
000633 (2017)	Hong-Yan Liu [République populaire de Chine] ; Ji-Fang Xiao [République populaire de Chine] ; Jia Huang [République populaire de Chine] ; Yue Wang [République populaire de Chine] ; Dong Wu [République populaire de Chine] ; Tao Li [République populaire de Chine] ; Hong-Dan Wang [République populaire de Chine] ; Liang-Jie Guo [République populaire de Chine] ; Qian-Nan Guo [République populaire de Chine] ; Hai Xiao [République populaire de Chine] ; Xue Lyu [République populaire de Chine] ; Zheng-Hong Yu [République populaire de Chine]	Diagnosis with Multiple Epiphyseal Dysplasia Using Whole-exome Sequencing in a Chinese Family
000B83 (2016)	Fiona Y. Y. Ng ; Marianne E. Bourke ; Brin F. S. Grenyer	Recovery from Borderline Personality Disorder: A Systematic Review of the Perspectives of Consumers, Clinicians, Family and Carers
000D69 (2016)	Ling-Wen Ding [Singapour] ; Takayuki Ikezoe [Japon] ; Kar-Tong Tan [Singapour] ; Masakazu Mori [Japon] ; Anand Mayakonda [Singapour] ; Wenwen Chien [Singapour] ; De-Chen Lin [Singapour, États-Unis] ; Yan-Yi Jiang [Singapour] ; Michael Lill [États-Unis] ; Henry Yang [Singapour] ; Qiao-Yang Sun [Singapour] ; H. Phillip Koeffler [Singapour, États-Unis]	Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency
000F83 (2016)	Chia-Fang Chung ; Sean A. Munson ; Matthew J. Thompson ; Laura-Mae Baldwin ; Jeffrey Kaplan ; Randall Cline ; Beverly B. Green	Implementation of a New Kiosk Technology for Blood Pressure Management in a Family Medicine Clinic: from the WWAMI Region Practice and Research Network
001499 (2016)	Gianluca Caridi [Italie] ; Elif Yilmaz Gulec [Turquie] ; Monica Campagnoli [Italie] ; Francesca Lugani [Italie] ; Hasan Onal [Turquie] ; Duzgun Kilic [Turquie] ; Monica Galliano [Italie] ; Lorenzo Minchiotti [Italie]	A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family
001D57 (2015)	Juehua Gao [États-Unis] ; Yi-Hua Chen [États-Unis] ; Loann C. Peterson [États-Unis]	GATA family transcriptional factors: emerging suspects in hematologic disorders
001E04 (2015)	Ashwin Dalal [Inde] ; Aneek D. Bhowmik [Inde] ; Divya Agarwal [Inde] ; Shubha R. Phadke [Inde]	Exome sequencing & homozygosity mapping for identification of genetic aetiology for spastic ataxia in a consanguineous family
002251 (2015)	N F Liu ; Z. Yu ; Y. Luo ; D. Sun ; Z. Yan	A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.
002708 (2014)	H. Partsch [Autriche] ; Bb Lee [États-Unis]	Phlebology and lymphology--a family affair.
002E64 (2014)	Carole Sargent [Royaume-Uni] ; Julien Bauer [Royaume-Uni] ; Muhamed Khalil [États-Unis] ; Parker Filmore [États-Unis] ; Michael Bernas [États-Unis] ; Marlys Witte [États-Unis] ; M. Peggy Pearson [États-Unis] ; Robert P. Erickson [États-Unis]	A Five Generation Family with a Novel Mutation in FOXC2 and Lymphedema Worsening to Hydrops in the Youngest Generation
003566 (2013)	Imran Rafi [Royaume-Uni] ; Susmita Chowdhury [Royaume-Uni] ; Tom Chan [Royaume-Uni] ; Ibrahim Jubber [Royaume-Uni] ; Mohammad Tahir [Royaume-Uni] ; Simon De Lusignan [Royaume-Uni]	Improving the management of people with a family history of breast cancer in primary care: before and after study of audit-based education
003A25 (2013)	M. Elise Radina [États-Unis]	Toward a Theory of Health‐Related Family Quality of Life
003B10 (2013)	Susan A. Oliveria [États-Unis] ; Elyse Shuk [États-Unis] ; Jennifer L. Hay [États-Unis] ; Maureen Heneghan [États-Unis] ; Jacqueline M. Goulart [États-Unis] ; Katherine Panageas [États-Unis] ; Alan C. Geller [États-Unis] ; Allan C. Halpern [États-Unis]	Melanoma survivors: health behaviors, surveillance, psychosocial factors, and family concerns
003B56 (2013)	B. Berisha [Allemagne] ; S. Schilffarth [Allemagne] ; R. Kenngott [Allemagne] ; F. Sinowatz [Allemagne] ; H. H. D. Meyer [Allemagne] ; D. Schams [Allemagne]	Expression of Lymphangiogenic Vascular Endothelial Growth Factor Family Members in Bovine Corpus Luteum
003C43 (2013)	G. Brice [Royaume-Uni] ; P. Ostergaard ; S. Jeffery ; K. Gordon [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. Mansour	A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family
003E39 (2012)	Alfonso Colombatti [Italie] ; Paola Spessotto [Italie] ; Roberto Doliana [Italie] ; Maurizio Mongiat [Italie] ; Giorgio Maria Bressan [Italie] ; Gennaro Esposito [Italie]	The EMILIN/Multimerin Family
004075 (2012)	Edyta Sutkowska [Pologne] ; Justyna Gil ; Agnieszka Stembalska ; Aneta Hill-Bator ; Andrzej Szuba	Novel mutation in the FOXC2 gene in three generations of a family with lymphoedema-distichiasis syndrome.
004208 (2012)	Jung-Won Lim ; Kimlin T. Ashing-Giwa	Is family functioning and communication associated with health-related quality of life for Chinese- and Korean-American breast cancer survivors?
004786 (2012)	B. Zöller [Suède] ; J. Ji [Suède] ; J. Sundquist [Suède, États-Unis] ; K. Sundquist [Suède]	Family history and risk of hospital treatment for varicose veins in Sweden

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