List of bibliographic references
Number of relevant bibliographic references: 47.
[0-20] [
0 - 20][
0 - 47][
20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 000053 (2013) |
M. Elise Radina [États-Unis] | Toward a Theory of Health‐Related Family Quality of Life |
| 000138 (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 |
| 000184 (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 |
| 000271 (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 |
| 000483 (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 |
| 000576 (2012) |
Filiz Hazan [Turquie] ; Pia Ostergaard [Royaume-Uni] ; Taylan Ozturk [Turquie] ; Esin Kantekin [Turquie] ; Fusun Atlihan [Turquie] ; Steve Jeffery [Royaume-Uni] ; Ferda Ozkinay [Turquie] | A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family |
| 000E52 (2009) |
M. Elise Radina [États-Unis] | Breast Cancer‐Related Lymphedema: Implications for Family Leisure Participation |
| 001533 (2007) |
S. Kumar [Arabie saoudite] ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; Peter Mortimer (dermatologue) [Royaume-Uni] ; S. Jeffery [Royaume-Uni] | A family with lymphoedema‐distichiasis where identical twins have a discordant phenotype |
| 001585 (2006) |
D. Rigopoulos [Grèce] ; H. Petropoulou [Grèce] ; M. Nikolopoulou [Grèce] ; O. Kalogirou [Grèce] ; A. Katsambas [Grèce] | Total congenital anonychia in two children of the same family |
| 001749 (2006) |
J. B. Mallinger ; J. J. Griggs ; C. G. Shields [États-Unis] | Family communication and mental health after breast cancer |
| 001C63 (2005) |
Seiji Mizuno [Japon] ; Yasukazu Yamada [Japon] ; Kenichiro Yamada [Japon] ; Noriko Nomura [Japon] ; Nobuaki Wakamatsu [Japon] | Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation |
| 001E11 (2004) |
T. Hamada [Japon] ; N. Ishii [Japon] ; Y. Kawano [Japon] ; Y. Takahashi [Japon] ; M. Inoue [Japon] ; S. Yasumoto [Japon] ; T. Hashimoto [Japon] | The P25L mutation in the KRT5 gene in a Japanese family with epidermolysis bullosa simplex with mottled pigmentation |
| 001F13 (2004) |
K. E. Loft [Royaume-Uni] ; D. Shearer [Royaume-Uni] | P‐41 Psychogenic alopecia by fur‐plucking in a family of seal‐point Siamese cats: three cases |
| 001F94 (2004) |
Bradley K. Mccoll [Australie] ; Steven A. Stacker [Australie] ; Marc G. Achen [Australie] | Molecular regulation of the VEGF family – inducers of angiogenesis and lymphangiogenesis |
| 002027 (2004) |
| Index to Journal of Family Nursing Volume 10 |
| 002028 (2004) |
Fatma Silan [Italie, Turquie] ; Ilker Aydogan [Italie] ; Ayse Kavak [Italie] ; Tiziano Bardaro [Italie] ; Michele D Rso [Italie] | Incontinentia pigmenti with NEMO mutation in a Turkish family |
| 002109 (2004) |
S. Trompezinski [France] ; O. Berthier-Vergnes [France] ; A. Denis [France] ; D. Schmitt [France] ; J. Viac [France] | Comparative expression of vascular endothelial growth factor family members, VEGF‐B, ‐C and ‐D, by normal human keratinocytes and fibroblasts |
| 002113 (2004) |
Débora Romeo Bertola [Brésil] ; Alexandre C. Pereira [Brésil] ; Paulo S. L. De Oliveira [Brésil] ; Chong A. Kim [Brésil] ; José Eduardo Krieger [Brésil] | Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation |
| 002162 (2004) |
Cagri Yildirim-Toruner [États-Unis] ; Kavitha Subramanian [États-Unis] ; Lamya El Manjra [États-Unis] ; Emily Chen [États-Unis] ; Stanley Goldstein ; Emilia Vitale [États-Unis, Italie] | A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema‐distichiasis syndrome associated with renal disease and diabetes mellitus |
| 002291 (2003) |
Philippe Debeer [Belgique] ; E. Pykels [Belgique] ; J. Lammens [Belgique] ; K. Devriendt [Belgique] ; J. Fryns [Belgique] | Melorheostosis in a family with autosomal dominant osteopoikilosis: Report of a third family |
| 002661 (2002) |
D. Concolino [Italie] ; M A Iembo [Italie] ; E. Rossi [Italie] ; S. Giglio [Italie] ; G. Coppola [Italie] ; E. Miraglia Del Giudice [Italie] ; P. Strisciuglio [Italie] | Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions |
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