1651-1905 < 1651-2227 < 1682-4016

Facettes : Author.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 ; P. Macarthur ; D. Hunter	A “G” DELETION SYNDROME ANTI‐MONGOLISM
000510 (1989)	J. Nielsen	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 ; J. Bultas ; A. Linhart ; J. C. Lubanda ; S. Magage ; P. Uklikova ; T. Palecek ; J. Ledvinova ; H. Poupetova ; R. Dobrovolny ; M. Hrebicek ; M. Elleder	FABRY DISEASE – CLINICAL MANIFESTATIONS AND GENETICS
000E44 (1982)		ANNUAL MEETING OF SENTAC
000E50 (2007)		MUCOPOLYSACCHARIDOSIS TYPE II
001247 (1984)	P. Vajro A. Romano ; A. Fontanella ; V. Oggero ; R. Vecchione ; D. H. Shmerling	Aagenaes's Syndrome in an Italian Child
001727 (2005)	C. Kampmann ; Fa Baehner ; C. Whybra ; M. Bajbouj ; K. Baron ; M. Knuf ; Cm Wiethoff ; H. Trübel ; M. Beck	The right ventricle in Fabry disease
001A21 (2007)		MUCOPOLYSACCHARIDE DISORDERS AND OTHER LYSOSOMAL STORAGE DISEASES
001A93 (2006)	Uma Ramaswami ; Catharina Whybra ; Rosella Parini ; Guillem Pintos-Morell ; Atul Mehta ; Gere Sunder-Plassmann ; Urs Widmer ; Michael Beck	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 ; J. Muller-Hocker ; B. Wiebecke ; B. H. Belohradsky	First Description of “Indian Childhood Cirrhosis” in a Non‐Indian Infant in Europe
002334 (2002)	Yh Lien ; L. Lai	Genotype‐phenotype correlation in Fabry disease: studies in ten unrelated families
002365 (2002)	K. Azibi ; C. Heltianu ; C. Caillaud ; J. Manicom ; Jp Puech ; A. Kahn ; L. Poenaru	Fabry disease: from clinical manifestations to molecular mechanisms
002460 (2010)	Sv Lourenço ; P. Boggio ; K. Suguyama ; Mms Nico	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 ; L. S. Taitz	TURNER'S SYNDROME IN ONE OF MONOZYGOTIC TWINS WITH MOSAICISM
002E11 (1974)	Aagen S	HEREDITARY RECURRENT CHOLESTASIS WITH LYMPHOEDEMA–TWO NEW FAMILIES
002F32 (1967)	Minna Yssing ; Herluf Jensen ; Stig Jarnum	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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