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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
1996 | 3 |
1997 | 3 |
1998 | 1 |
2024 | 0 |
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8 results
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Page 1
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Science. 1996 Mar 8;271(5254):1423-7. doi: 10.1126/science.271.5254.1423.
Science. 1996.
PMID: 8596916
Frataxin fracas.
Cossée M, Campuzano V, Koutnikova H, Fischbeck K, Mandel JL, Koenig M, Bidichandani SI, Patel PI, Moltè MD, Cañizares J, De Frutos R, Pianese L, Cavalcanti F, Monticelli A, Cocozza S, Montermini L, Pandolfo M.
Cossée M, et al.
Nat Genet. 1997 Apr;15(4):337-8. doi: 10.1038/ng0497-337.
Nat Genet. 1997.
PMID: 9090376
No abstract available.
Item in Clipboard
Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 cases.
De Michele G, Di Maio L, Filla A, Majello M, Cocozza S, Cavalcanti F, Mirante E, Campanella G.
De Michele G, et al.
Neuropediatrics. 1996 Feb;27(1):3-7. doi: 10.1055/s-2007-973740.
Neuropediatrics. 1996.
PMID: 8677022
Item in Clipboard
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13.
Montermini L, Rodius F, Pianese L, Moltò MD, Cossée M, Campuzano V, Cavalcanti F, Monticelli A, Palau F, Gyapay G, et al.
Montermini L, et al.
Am J Hum Genet. 1995 Nov;57(5):1061-7.
Am J Hum Genet. 1995.
PMID: 7485155
Free PMC article.
Item in Clipboard
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.
Filla A, De Michele G, Cavalcanti F, Pianese L, Monticelli A, Campanella G, Cocozza S.
Filla A, et al.
Am J Hum Genet. 1996 Sep;59(3):554-60.
Am J Hum Genet. 1996.
PMID: 8751856
Free PMC article.
Item in Clipboard
The effect of parental gender on the GAA dynamic mutation in the FRDA gene.
Pianese L, Cavalcanti F, De Michele G, Filla A, Campanella G, Calabrese O, Castaldo I, Monticelli A, Cocozza S.
Pianese L, et al.
Am J Hum Genet. 1997 Feb;60(2):460-3.
Am J Hum Genet. 1997.
PMID: 9012421
Free PMC article.
No abstract available.
Item in Clipboard
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.
Montermini L, Andermann E, Labuda M, Richter A, Pandolfo M, Cavalcanti F, Pianese L, Iodice L, Farina G, Monticelli A, Turano M, Filla A, De Michele G, Cocozza S.
Montermini L, et al.
Hum Mol Genet. 1997 Aug;6(8):1261-6. doi: 10.1093/hmg/6.8.1261.
Hum Mol Genet. 1997.
PMID: 9259271
Item in Clipboard
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family.
Rizzi R, Carelli V, Monari L, Mochi M, Liguori R, Sensi M, Cocozza S, Filla A, Montagna P.
Rizzi R, et al.
Ital J Neurol Sci. 1998 Feb;19(1):41-4. doi: 10.1007/BF03028811.
Ital J Neurol Sci. 1998.
PMID: 10935859
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