Malawi < Malformation < Malformation complexe

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List of bibliographic references

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

Ident.	Authors (with country if any)	Title
000271 (2010)	Mary C. O'Driscoll [Royaume-Uni] ; Kim Jenny [États-Unis] ; Sulagna Saitta [États-Unis] ; William B. Dobyns [États-Unis] ; Karen W. Gripp [États-Unis]	Agenesis of the Corpus Callosum and Congenital Lymphedema: A Novel Recognizable Syndrome?
000279 (2009)	Ewa Tuleja [France] ; Maria Arrault [France] ; Stéphane Vignes [France]	Un clin d'œil héréditaire...
000725 (2002)	I. Lazareth [France]	Classification des lymphoedèmes
000899 (2000)	D. J. Amor [Australie] ; R. J. Leventer [Australie] ; S. Hayllar [Australie] ; A. Bankier [Australie]	Polymicrogyria associated with scalp and limb defects : Variant of Adams-Oliver syndrome
000A94 (1998)	R. J. Bolt [Pays-Bas] ; W. Peelen [Pays-Bas] ; P. G. J. Nikkels [Pays-Bas] ; T. P. V. M. De Jong [Pays-Bas]	Congenital lymphoedema of the genitalia
000A96 (1998)	R. Avrahami [Israël] ; M. Haddad [Israël] ; A. Zelikovski [Israël]	Combined surgical correction of bilateral congenital lower limb lymphedema with associated anomalies
000C56 (1995)	C. A. Harwood [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]	Causes and clinical manifestations of lymphatic failure
000D50 (1993)	J. O'B. Hourihane [Royaume-Uni] ; C. P. Bennett ; R. Chaudhuri ; S. A. Robb ; N. D. T. Martin [Royaume-Uni]	A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema
000E32 (1991)	A. B. Jamjoom [Arabie saoudite] ; B. G. Mathew ; H. B. Coakham	A variant of the syndrome of spinal arachnoid cysts with multiple congential defects
000E56 (1990)	B. M. O'Brien	The role of microsurgery in modern surgery
000E95 (1989)	E. Foldi ; M. Foldi ; L. Clodius	The lymphedema chaos: a lancet
000E99 (1989)	C. Levine	Primary disorders of the lymphatic vessels ― a unified concept
000F04 (1989)	J. M. Opitz ; J. F. Reynolds ; J. M. Fitzgerald	Mandibulofacial dysostosis or bilateral hemifacial microsomia with hearing loss, telecanthus, tetramelic postaxial hexadactyly, congenital hypotonia and lymphedema with joint hypermobility, and pigmentary dysplasia: a new syndrome?
000F17 (1989)	R. C. M. Hennekam ; R. A. Geerdink ; B. C. J. Hamel ; F. A. M. Hennekam ; P. Kraus ; J. A. Rammeloo ; A. A. W. Tillemans	Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation
000F28 (1988)	J.-N. Fiessinger ; G. Franco	Lymphœdème primitif des membres inférieurs
000F32 (1988)	R. Cluzan	Les lymphœdèmes primaires
000F34 (1988)	V. S. Krylov ; N. O. Milanov ; K. G. Abalmassov	L'efficacité des anastomoses lympho-veineuses
000F45 (1988)	P. Gloviczki ; J. Fisher ; L. H. Hollier ; P. C. Pairolero ; A. Schirger ; H. W. Wahner	Microsurgical lymphovenous anastomosis for treatment of lymphedema: a critical review
000F71 (1987)	R. F. Dale	Primary lymphoedema when found with distichiasis is of the type defined as bilateral hyperplasia by lymphography
000F76 (1987)	H. Gajraj ; S. G. E. Barker ; K. G. Burnand ; N. L. Browse	Lymphangiosarcoma complicating chronic primary lymphoedema
000F78 (1987)	A. Koren ; A. Zelikovski ; M. Melloul ; M. Haddad ; R. Reiss	Isotopic lymphangiography to evaluate lymphedema before and after operative treatment

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