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BACHNER L
BRULS T
BELDJORD C
BILLUART P
SOUFIR N
BIENVENU T
VINET MC
MALASPINA E
MARCHIANI V
BERTINI E
KAHN A
FRANZONI E
CHELLY J
Citation: V. Desportes et al., X-LINKED NEURODEGENERATIVE SYNDROME WITH CONGENITAL ATAXIA, LATE-ONSET PROGRESSIVE MYOCLONIC ENCEPHALOPATHY AND SELECTIVE MACULAR DEGENERATION, LINKED TO XP22.33-PTER, American journal of medical genetics, 64(1), 1996, pp. 69-72
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HAUSER E
STEINBOCK H
SZYPER M
HOLSTEEN V
OSTERGAARD J
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BERQUIN P
BOULLOCHE J
BOURGEOIS M
CARRIERE JP
CHABROL B
CHIRON C
CLARIS O
ECHENNE B
GAUTHIERMOREL D
LIVET MO
LOPEZ N
MANCINI J
NETTER JC
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RICHELME CH
ROUSSELLE C
DESTMARTIN A
DESWARTE M
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BRANDL U
KURLEMANN G
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SPOHR HL
AARTS WFM
BEGEER JH
HEERSMA DJ
LAAN LAEM
PETERS ACB
CAVAZZUTTI GB
CURATOLO P
FOIS A
FRANZONI E
GOBBI G
INCORPORA G
VIGEVANO F
CAMPISTOL J
CAMPOS J
CASAS C
HERRANZ JL
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PRATS JM
AMARK P
BLENNOW G
THEORELL K
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BRANDT W
BUTI D
DULAC O
FARRELL K
MOSHE S
MOTTE J
PLOUIN P
SHIELDS WD
MUMFORD JP
DUMAS C
WOOD S
Citation: J. Aicardi et al., VIGABATRIN AS INITIAL THERAPY FOR INFANTILE SPASMS - A EUROPEAN RETROSPECTIVE SURVEY, Epilepsia, 37(7), 1996, pp. 638-642
Authors:
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AMBROSETTO P
CARLA G
TANI G
FRANZONI E
CACCIARI E
Citation: S. Zucchini et al., PRIMARY EMPTY SELLA - DIFFERENCES AND SIMILARITIES BETWEEN CHILDREN AND ADULTS, Acta paediatrica, 84(12), 1995, pp. 1382-1385
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AVINO G
BANCHINI G
BANIN P
BARONI M
BASSANETTI F
BENSO L
BERGAMASCHI R
BIASINI G
BOSCHERINI B
BUSTI G
CASADEI GP
CECCHI MT
CIATTO C
COMELLINI L
DEFANTI CA
DAPELO A
DIGILIO MC
FERA F
FRANZONI E
GABRIELLI O
GARAVELLI L
GALASSO C
GENNARI G
GIANNOTTI A
GITTI F
IWANEJKO G
LAMA G
LANZI G
LORENZETTI ME
MARGARI L
MARTINI C
MASTROIACOVO PP
MICHELI R
MIGLIORE MR
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PASQUINELLI A
PALLOTTA R
PANIZON F
PAVONE L
PELLEGRINI C
PERNIOLA T
RABUSIN M
ROMANO C
ROSSI LN
RUGGIERI M
SEGRE A
SIMONATI A
SAVASTA S
SCORZA P
TOZZOLA A
VANNELLI S
VULLO C
ZAMBRINO CA
ZAMPINO G
ZANOLINI C
ZELANTE L
Citation: P. Balestrazzi et al., TAKE-CARE PROTOCOL FOR NFI SYMPTOMS-FREE PATIENTS, Rivista italiana di pediatria, 21(2), 1995, pp. 253-257
Authors:
ROBINSON WP
WAGSTAFF J
BERNASCONI F
BACCICHETTI C
ARTIFONI L
FRANZONI E
SUSLAK L
SHIH LY
AVIV H
SCHINZEL AA
Citation: Wp. Robinson et al., UNIPARENTAL DISOMY EXPLAINS THE OCCURRENCE OF THE ANGELMAN OR PRADER-WILLI-SYNDROME IN PATIENTS WITH AN ADDITIONAL SMALL INV DUP(15) CHROMOSOME, Journal of Medical Genetics, 30(9), 1993, pp. 756-760