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Effects of renal care coordinator case management on outcomes in incident dialysis patients.
Clin Nephrol. 2016 Mar;85(3):152-8. doi: 10.5414/CN108713.
Clin Nephrol. 2016.
PMID: 26833299
Type I sialidosis: a clinical, biochemical and neuroradiological study.
Palmeri S, Villanova M, Malandrini A, van Diggelen OP, Huijmans JG, Ceuterick C, Rufa A, DeFalco D, Ciacci G, Martin JJ, Guazzi G.
Palmeri S, et al. Among authors: defalco d.
Eur Neurol. 2000;43(2):88-94. doi: 10.1159/000008141.
Eur Neurol. 2000.
PMID: 10686466
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CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic study.
Malandrini A, Galli L, Villanova M, Palmeri S, Parrotta E, DeFalco D, Cappelli M, Grieco GS, Renieri A, Guazzi G.
Malandrini A, et al. Among authors: defalco d.
Eur Neurol. 1998 Oct;40(3):164-8. doi: 10.1159/000007974.
Eur Neurol. 1998.
PMID: 9748675
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A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers.
Malandrini A, Palmeri S, Villanova M, Parrotta E, Sicurelli F, Amato D, DeFalco D, Guazzi GC.
Malandrini A, et al. Among authors: defalco d.
Brain Dev. 1997 Apr;19(3):209-11. doi: 10.1016/s0387-7604(96)00563-3.
Brain Dev. 1997.
PMID: 9134193
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Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions.
Malandrini A, Scarpini C, Villanova M, Sicurelli F, Parrotta E, DeFalco D, Guazzi GC.
Malandrini A, et al. Among authors: defalco d.
Acta Neurol Scand. 1996 Jul;94(1):60-2. doi: 10.1111/j.1600-0404.1996.tb00040.x.
Acta Neurol Scand. 1996.
PMID: 8874595
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Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy.
Malandrini A, Scarpini C, Palmeri S, Villanova M, Parrotta E, Tripodi S, Giani S, DeFalco D, Guazzi GC.
Malandrini A, et al. Among authors: defalco d.
Brain Dev. 1996 Jan-Feb;18(1):59-63. doi: 10.1016/0387-7604(95)00098-4.
Brain Dev. 1996.
PMID: 8907345
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