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Author
Filla A
Filla A
References (2)
1. Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia - Rinaldi_2015_JAMA.Neurol_72_561
Title :
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia -
Rinaldi_2015_JAMA.Neurol_72_561
Author(s) :
Rinaldi C
,
Schmidt T
,
Situ AJ
,
Johnson JO
,
Lee PR
,
Chen KL
,
Bott LC
,
Fado R
,
Harmison GH
,
Parodi S
,
Grunseich C
,
Renvoise B
,
Biesecker LG
,
De Michele G
,
Santorelli FM
,
Filla A
,
Stevanin G
,
Durr A
,
Brice A
,
Casals N
,
Traynor BJ
,
Blackstone C
,
Ulmer TS
,
Fischbeck KH
Ref :
JAMA Neurol ,
72
:561 , 2015
Abstract :
View Abstract
PubMedSearch :
Rinaldi_2015_JAMA.Neurol_72_561
PubMedID
:
25751282
2. Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataracts (PHARC) screening in an Italian population - Criscuolo_2013_Eur.J.Neurol_20_e60
Title :
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataracts (PHARC) screening in an Italian population -
Criscuolo_2013_Eur.J.Neurol_20_e60
Author(s) :
Criscuolo C
,
Guacci A
,
Carbone R
,
Lieto M
,
Salsano E
,
Nanetti L
,
Michele GD
,
Filla A
Ref :
Eur Journal of Neurology ,
20
:e60 , 2013
Abstract :
View Abstract
PubMedSearch :
Criscuolo_2013_Eur.J.Neurol_20_e60
PubMedID
:
23490117