List of bibliographic references
Number of relevant bibliographic references: 19.
| Ident. | Authors (with country if any) | Title |
|---|
| 000001 (2014) |
P. Dessart [France] ; X. Deries [France] ; M. Guerin-Moreau [France] ; F. Troussier [France] ; L. Martin [France] | Syndrome des ongles jaunes: deux cas pédiatriques |
| 000018 (2013) |
S. Elguazzar [Maroc] ; T. Benouachane [Maroc] ; A. Nasri [Maroc] ; A. Malihy [Maroc] ; H. Tligui [Maroc] ; A. Bentahila [Maroc] | Mucormycose cutanée ilio-fémorale avec extension endo-pelvienne chez un enfant immunocompétent |
| 000060 (2012) |
Stéphane Vignes [France] | LYMPHŒDÈMES |
| 000096 (2012) |
Gwendolyn De Bruyn [Belgique] ; Alexandra Casaer [Belgique] ; Katrien Devolder [Belgique] ; Geert Van Acker [Belgique] ; Hilde Logghe [Belgique] ; Koen Devriendt [Belgique] ; Luc Cornette [Belgique] | Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression |
| 000099 (2012) |
Hiroyuki Ishida [Japon] ; Kosuke Imai [Japon] ; Kenichi Honma [Japon] ; Shin-Ichi Tamura [Japon] ; Toshihiko Imamura [Japon] ; Masafumi Ito [Japon] ; Shigeaki Nonoyama [Japon] | GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia |
| 000178 (2011) |
Kazuyo Ichimori [Suisse] ; Eric A. Ottesen [États-Unis] | Eliminating lymphatic filariasis |
| 000190 (2011) |
Michael Lucas [États-Unis] ; Yohanna Andrade [États-Unis] | CONGENITAL LYMPHEDEMA WITH TUBEROUS SCLEROSIS AND CLINICAL HIRSCHSPRUNG DISEASE |
| 000248 (2010) |
Mahtab Samimi [France] ; Annabel Maruani [France] ; Marie-Christine Machet [France] ; Françoise Baulieu [France] ; Laurent Machet [France] ; Gérard Lorette [France] | Lymphatic Compression by Sclerotic Patches of Morphea: An Original Mechanism of Lymphedema in a Child |
| 000272 (2010) |
Catherine M. L. Roberts [Royaume-Uni] ; Janet E. Angus [Royaume-Uni] ; Ian H. Leach [Royaume-Uni] ; Elizabeth M. Mcdermott [Royaume-Uni] ; David A. Walker [Royaume-Uni] ; Jane C. Ravenscroft [Royaume-Uni] | A novel NEMO gene mutation causing osteopetrosis, lymphoedema, hypohidrotic ectodermal dysplasia and immunodeficiency (OL-HED-ID) |
| 000320 (2009) |
Smadar Eventov-Friedman [Israël] ; Amihood Singer [Israël] ; Eric S. Shinwell [Israël] | Microcephaly, lymphedema, chorioretinopathy and atrial septal defect : a case report and review of the literature |
| 000494 (2006) |
S. Bahloul [Tunisie] ; Th. Kammoun [Tunisie] ; N. Zroud [Tunisie] ; H. Aloulou [Tunisie] ; M. Ellouze [Tunisie] ; A. Mahfoudh [Tunisie] ; M. Hachicha [Tunisie] | Les lymphoedèmes primitifs de l'enfant : A propos de 4 observations |
| 000590 (2005) |
Melissa L. Loscalzo [États-Unis] ; Phillip L. Van [États-Unis] ; Vincent B. Ho [États-Unis] ; Vladimir K. Bakalov [États-Unis] ; Douglas R. Rosing [États-Unis] ; Carol A. Malone [États-Unis] ; Harry C. Dietz [États-Unis] ; Carolyn A. Bondy [États-Unis] | Association between fetal lymphedema and congenital cardiovascular defects in turner syndrome |
| 000655 (2003) |
Elena Chiappini [Italie] ; Luisa Galli [Italie] ; Maria Grazia Giudizi [Italie] ; Chiara Azzari [Italie] ; Augusto Antonio Niccoli [Italie] ; Sergio Romagnani [Italie] ; Maurizio De Martino [Italie] | Selective deficiency of na CD4+ T-lymphocytes in a child with congenital lymphoedema |
| 000F65 (1987) |
M. Magid ; N. B. Esterly ; J. Prendiville ; C. Fujisaki | The yellow nail syndrome in a 8-year-old girl |
| 001012 (1986) |
D. M. Smeltzer ; G. B. Stickler ; R. E. Fleming | Primary lymphatic dysplasia in children: chylothorax, chylopus ascites, and generalized lymphatic dysplasia |
| 001030 (1986) |
C. A. Crowe ; L. H. Dickerman | Brief clinical report: a genetic association between microcephaly and lymphedema |
| 001058 (1985) |
D. M. Smeltzer ; G. B. Stickler ; A. Schirger | Primary lymphedema in children and adolescents: a follow-up study and review |
| 001078 (1985) |
A. K. C. Leung | Dominantly inherited syndrome of microcephaly and congenital lymphedema |
| 001102 (1984) |
G. Accarpio ; G. C. Larghero ; S. Vigna ; C. Roccatagliata ; G. Rocca ; R. Nati | Unusual chylolymphedema of congenital origin |
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