List of bibliographic references
Number of relevant bibliographic references: 100.
[0-20] [
0 - 20][
0 - 50][
20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 000081 (1999) |
D. Mowat [Australie] ; A. Jauch ; L. Robson ; A. Smith | Duplication within chromosome 5q characterized by fluorescence in situ hybridization. |
| 000242 (2000) |
P. Huppke [Allemagne] ; H J Christen ; B. Sattler ; F. Hanefeld | Two brothers with Hennekam syndrome and cerebral abnormalities. |
| 000415 (2000) |
D J Amor [Australie] ; R J Leventer ; S. Hayllar ; A. Bankier | Polymicrogyria associated with scalp and limb defects: variant of Adams-Oliver syndrome. |
| 000471 (2000) |
K. Morooka | [Distichiasis-lymphedema syndrome]. |
| 000615 (2001) |
I. Casteels ; K. Devriendt ; A. Leys ; H. Van Cleynenbreuge. ; P. Demaerel ; F. De Tavernier ; J. Fryns | Autosomal dominant microcephaly—lymphoedema-chorioretinal dysplasia syndrome |
| 000689 (2001) |
B. Granel [France] ; J. Serratrice ; V. Juhan ; P. Champsaur ; C. Weiller-Merli ; X. Pache ; L. Swiader ; P. Disdier ; P J Weiller | Severe lower limbs lymphedema of late onset revealing polysplenia syndrome--a case report. |
| 000833 (2001) |
M M Van Haelst [Pays-Bas] ; J. Hoogeboom ; R J Galjaard ; W J Kleijer ; N S Den Hollander ; R R De Krijger ; R C Hennekam ; M F Niermeijer | Lymphangiectasia with persistent Müllerian derivatives: confirmation of autosomal recessive Urioste syndrome. |
| 000936 (2002) |
Carlo Bellini [Italie] ; Cesare Arioni ; Massimo Mazzella ; Corradino Campisi ; Gioconda Taddei ; Francesco Boccardo ; Giovanni Serra | Lymphoscintigraphic evaluation of congenital lymphedema of the newborn. |
| 000961 (????) |
Curt P. Samlaska [États-Unis] | Congenital lymphedema and distichiasis. |
| 000980 (2002) |
Sophie Dupuis-Girod [France] ; Nadège Corradini ; Smail Hadj-Rabia ; Jean-Christophe Fournet ; Laurence Faivre ; Françoise Le Deist ; Philippe Durand ; Rainer Döffinger ; Asma Smahi ; Alain Israel ; Gilles Courtois ; Nicole Brousse ; Stéphane Blanche ; Arnold Munnich ; Alain Fischer ; Jean-Laurent Casanova ; Christine Bodemer | Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother. |
| 000A31 (2002) |
G. Brice ; S. Mansour ; R. Bell ; J. Collin ; A. Child ; A. Brady ; M. Sarfarazi ; K. Burnand ; S. Jeffery ; Peter Mortimer (dermatologue) [Royaume-Uni] ; V. Murday | Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24 |
| 000A34 (2002) |
F. Forzano [Italie] ; F. Faravelli ; A. Loy ; M. Di Rocco | Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype. |
| 000B29 (2002) |
Inge D C. Van Balkom ; Mariel Alders ; Judith Allanson ; Carlo Bellini ; Ulrich Frank ; Greetje De Jong ; Ingeborg Kolbe ; Didier Lacombe ; Stan Rockson ; Peter Rowe ; Frits Wijburg ; Raoul C M. Hennekam | Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review. |
| 000B81 (2002) |
M. Bahuau [France] ; C. Houdayer ; M. Tredano ; V. Soupre ; R. Couderc ; M-P Vazquez | FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate. |
| 000B96 (2003) |
Brad Angle [États-Unis] ; Frank Yen ; Joseph H. Hersh ; Gordon Gowans | Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome. |
| 000C23 (????) |
Glen Brice | Diagnostic difficulties in lymphedema distichiasis. |
| 000D73 (2003) |
Carlo Bellini [Italie] ; Massimo Mazzella ; Cesare Arioni ; Corradino Campisi ; Gioconda Taddei ; Paolo Tomà ; Francesco Boccardo ; Raoul C. Hennekam ; Giovanni Serra | Hennekam syndrome presenting as nonimmune hydrops fetalis, congenital chylothorax, and congenital pulmonary lymphangiectasia. |
| 000D76 (2003) |
Luitgard M. Neumann [Allemagne] ; Ianina Scheer ; Jürgen Kunze ; Brigitte Stöver | Cerebral manifestations, hemihypertrophy and lymphoedema of one leg in a child with epidermal nevus syndrome (Schimmelpenning-Feuerstein-Mims). |
| 000D88 (2003) |
M. Ameen [Royaume-Uni] ; G. Brice ; Peter Mortimer (dermatologue) [Royaume-Uni] | Clinicopathological case 2: lymphoedema-distichiasis syndrome. |
| 001572 (1964) |
Harold F. Falls [États-Unis] ; Elsa D. Kertesz [États-Unis] | A New Syndrome Combining Pterygium Colli with Developmental Anomalies of the Eyelids and Lymphatics of the Lower Extremities* |
| 001723 (2003) |
L I Al-Gazali ; J. Hertecant ; R. Ahmed ; N A Khan ; R. Padmanabhan | Further delineation of Hennekam syndrome. |
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