1651-1905 < 1651-2227 < 1682-4016

Facettes : Author.f AffPays.f AffOrg.f AffRegion.f AffVille.f

List of bibliographic references

Number of relevant bibliographic references: 43.
[0-20] [0 - 20][0 - 43][20-40]

Ident.	Authors (with country if any)	Title
000314 (1973)	H. G. Richmond [Royaume-Uni] ; P. Macarthur [Royaume-Uni] ; D. Hunter [Royaume-Uni]	A “G” DELETION SYNDROME ANTI‐MONGOLISM
000510 (1989)	J. Nielsen [Danemark]	What More Can Be Done for Girls and Women with Turner's Syndrome and Their Parents?
000768 (2007)		FABRY DISEASE: SAFETY
000B27 (2006)	D. Karetova [République tchèque] ; J. Bultas [République tchèque] ; A. Linhart [République tchèque] ; J. C. Lubanda [République tchèque] ; S. Magage [République tchèque] ; P. Uklikova [République tchèque] ; T. Palecek [République tchèque] ; J. Ledvinova [République tchèque] ; H. Poupetova [République tchèque] ; R. Dobrovolny [République tchèque] ; M. Hrebicek [République tchèque] ; M. Elleder [République tchèque]	FABRY DISEASE – CLINICAL MANIFESTATIONS AND GENETICS
000E44 (1982)		ANNUAL MEETING OF SENTAC
000E50 (2007)		MUCOPOLYSACCHARIDOSIS TYPE II
001247 (1984)	P. Vajro A. Romano [Suisse] ; A. Fontanella [Suisse] ; V. Oggero [Suisse] ; R. Vecchione [Suisse] ; D. H. Shmerling [Suisse]	Aagenaes's Syndrome in an Italian Child
001727 (2005)	C. Kampmann [Allemagne] ; Fa Baehner [Allemagne] ; C. Whybra [Allemagne] ; M. Bajbouj [Allemagne] ; K. Baron [Allemagne] ; M. Knuf [Allemagne] ; Cm Wiethoff [Allemagne] ; H. Trübel [Allemagne] ; M. Beck [Allemagne]	The right ventricle in Fabry disease
001A21 (2007)		MUCOPOLYSACCHARIDE DISORDERS AND OTHER LYSOSOMAL STORAGE DISEASES
001A93 (2006)	Uma Ramaswami [Royaume-Uni] ; Catharina Whybra [Allemagne] ; Rosella Parini [Italie] ; Guillem Pintos-Morell [Espagne] ; Atul Mehta [Royaume-Uni] ; Gere Sunder-Plassmann [Autriche] ; Urs Widmer [Suisse] ; Michael Beck [Allemagne]	Clinical manifestations of Fabry disease in children: Data from the Fabry Outcome Survey
001D09 (2003)		Doppler ultrasound examination of patients affected by Fabry disease
001E29 (1989)	M. Weiss [Allemagne] ; J. Muller-Hocker [Allemagne] ; B. Wiebecke [Allemagne] ; B. H. Belohradsky	First Description of “Indian Childhood Cirrhosis” in a Non‐Indian Infant in Europe
002334 (2002)	Yh Lien [États-Unis] ; L. Lai [États-Unis]	Genotype‐phenotype correlation in Fabry disease: studies in ten unrelated families
002365 (2002)	K. Azibi [France] ; C. Heltianu ; C. Caillaud [France] ; J. Manicom [France] ; Jp Puech [France] ; A. Kahn [France] ; L. Poenaru [France]	Fabry disease: from clinical manifestations to molecular mechanisms
002460 (2010)	Sv Lourenço [Brésil] ; P. Boggio [Brésil] ; K. Suguyama [Brésil] ; Mms Nico [Brésil]	Severe and relapsing upper lip enlargement in a 10‐year‐old boy (Discussion and Diagnosis)
002872 (1973)		NORWEGIAN PAEDIATRIC SOCIETY
002D89 (1972)	A. M. Potter [Royaume-Uni] ; L. S. Taitz [Royaume-Uni]	TURNER'S SYNDROME IN ONE OF MONOZYGOTIC TWINS WITH MOSAICISM
002E11 (1974)	Aagen S [Norvège]	HEREDITARY RECURRENT CHOLESTASIS WITH LYMPHOEDEMA–TWO NEW FAMILIES
002F32 (1967)	Minna Yssing [Danemark] ; Herluf Jensen [Danemark] ; Stig Jarnum [Danemark]	Dietary Treatment of Protein‐Losing Enteropathy
002F49 (2007)		FABRY DISEASE: GENOTYPE‐PHENOTYPE STUDIES; EPIDEMIOLOGY; SCREENING AND MANAGEMENT
003109 (2007)		FABRY DISEASE: EFFICACY OF ENZYME REPLACEMENT THERAPY

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