List of bibliographic references
Number of relevant bibliographic references: 209.
[0-20] [
0 - 20][
0 - 50][
20-40]
Ident. | Authors (with country if any) | Title |
---|
000217 (1994) |
G. Borroni [Italie] ; D. Larizza [Italie] ; G. Vignati [Italie] ; C. Zaccone [Italie] ; R. Zanetta [Italie] ; G. P. Vignoli [Italie] ; V. Brazzelli [Italie] ; C. Bobba [Italie] ; G. Rabbiosi [Italie] | The dermatological spectrum of Turner syndrome |
000369 (2006) |
Charles S. Carver [États-Unis] ; Roselyn G. Smith [États-Unis] ; Vida M. Petronis [États-Unis] ; Michael H. Antoni [États-Unis] | Quality of life among long‐term survivors of breast cancer: different types of antecedents predict different classes of outcomes |
000395 (1998) |
Luis Requena ; Omar P. Sangueza | Cutaneous vascular proliferations. Part III. Malignant neoplasms, other cutaneous neoplasms with significant vascular component, and disorders erroneously considered as vascular neoplasms |
000426 (1998) |
P. Dalton [Royaume-Uni] ; B. Coppin [Royaume-Uni] ; R. James [Royaume-Uni] ; D. Skuse [Royaume-Uni] ; P. Jacobs [Royaume-Uni] | Three patients with a 45,X/46,X,psu dic(Xp) karyotype. |
000458 (2005) |
Ae Wilkerson [États-Unis] ; Ma Glasgow [États-Unis] ; Km Hiatt [États-Unis] | CD99 Immunoreactivity in Metastatic Malignant Melanoma |
000577 (1969) |
F. Kaindl | 7. Pathophysiologie der Lymphgefäße |
000603 (1999) |
A. Tsezou ; Ch Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; Em Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani [Chypre (pays)] ; Ch Theodoridis ; Pc Patsalis [Chypre (pays)] ; N. Moschonas ; S. Kitsiou | Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy |
000624 (1997) |
Hiroyuki Hashimoto ; Hiroaki Maruyama ; Rie Koshida ; Norihiko Okuda ; Kazuo Murayama ; Tetsuro Katsumi ; Kishichiro Watanabe ; Tamotsu Sato | Presence of Turner stigmata in a case of dysgenetic male pseudohermaphroditism with 45,X/46,X+mar karyotype |
000644 (1998) |
Wilfried Schmeller ; Yvonne Gaber ; Hans-Björn Gehl | Shave therapy is a simple, effective treatment of persistent venous leg ulcers |
000745 (2008) |
Marsha L. Davenport [États-Unis] | Moving Toward an Understanding of Hormone Replacement Therapy in Adolescent Girls |
000801 (1984) |
J. Craig Merrell ; Elvin G. Zook ; Robert C. Russell | Cuffing techniques in microarterial surgery |
000828 (2005) |
P. Emanuel [États-Unis] ; J. Tan [États-Unis] ; D. Rudikoff [États-Unis] ; R. Phelps [États-Unis] | Aggressive Squamous Cell Carcinoma in Kindler Syndrome: An Unusual Case |
000889 (1992) |
Brenda Finucane [États-Unis] ; Michael B. Kurtz [États-Unis] ; Charles I. Scott Jr. [États-Unis] | New mental retardation syndrome with hearing impairment, distinct facial appearance, and skeletal anomalies |
000892 (1971) |
Margarete S. Mattevi [Brésil] ; Henry Wolff [Brésil] ; F. M. Salzano [Brésil] ; Maria C. Mallmann [Brésil] | Cytogenetic, clinical and genealogical analyses in a series of gonadal dysgenesis patients and their families |
000923 (1993) |
Wei-Sean Winter [Royaume-Uni] | Distinctive autosomal or X‐linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face |
000977 (1999) |
Elizabeth M. Murray [Afrique du Sud] ; Dudley Werner [Afrique du Sud] ; Elizabeth A. Greeff [Afrique du Sud] ; Deryck A. Taylor [Afrique du Sud] | Postradiation sarcomas: 20 cases and a literature review |
000A35 (2010) |
Adrian Ling ; Rosie Dawkins ; Michael Bailey ; Michael Leung [Australie] ; Heather Cleland [Australie] ; Jonathan Serpell [Australie] ; John Kelly [Australie] | Short‐term morbidity associated with sentinel lymph node biopsy in cutaneous malignant melanoma |
000B24 (1988) |
John Royle Casley-Smith [Australie] | A Double-Blind Trial of Calcium Dobesilate in Chronic Venous Insufficiency |
000B65 (1999) |
Anita Rauch [Allemagne, États-Unis] ; Karla A. Feindt [États-Unis] ; Claire O. Leonard [États-Unis] ; Joel A. Thompson [États-Unis] ; Robert O. Hoffman [États-Unis] ; Donnell J. Creel [États-Unis] ; John M. Opitz [États-Unis] | Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: The M syndrome |
000C92 (1944) |
Kurt Glaser [États-Unis] | Congenital hereditary lymphedema (Milroy's disease) |
000D41 (1996) |
C. L. Von Ballestrem [Allemagne] ; M. G. Boavida [Portugal] ; C. Zuther [Allemagne] ; M. H. Carreiro [Portugal] ; D. David [Portugal] ; A. Gal [Allemagne] ; E. Schwinger [Allemagne] | Jumping translocation in a phenotypically normal female |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Istex/Curation
HfdIndexSelect -h $EXPLOR_AREA/Data/Istex/Curation/AbsEn.i -k "short"
HfdIndexSelect -h $EXPLOR_AREA/Data/Istex/Curation/AbsEn.i \
-Sk "short" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Istex/Curation/biblio.hfd
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Istex
|étape= Curation
|type= indexItem
|index= AbsEn.i
|clé= short
}}
| This area was generated with Dilib version V0.6.31. Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024 | |