De Michele G - Search Results

1

Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations.

Fasano D, Parisi S, Pierantoni GM, De Rosa A, Picillo M, Amodio G, Pellecchia MT, Barone P, Moltedo O, Bonifati V, De Michele G, Nitsch L, Remondelli P, Criscuolo C, Paladino S. Fasano D, et al. Among authors: de rosa a, de michele g. Cell Death Dis. 2018 Mar 7;9(3):385. doi: 10.1038/s41419-018-0410-7. Cell Death Dis. 2018. PMID: 29515184 Free PMC article.

2

Determinants of onset age in Friedreich's ataxia.

De Michele G, Filla A, Criscuolo C, Scarano V, Cavalcanti F, Pianese L, Monticelli A, Cocozza S. De Michele G, et al. J Neurol. 1998 Mar;245(3):166-8. doi: 10.1007/s004150050198. J Neurol. 1998. PMID: 9553847

3

Sexual behaviour in untreated and treated coeliac patients.

Ciacci C, De Rosa A, de Michele G, Savino G, Squillante A, Iovino P, Sabbatini F, Mazzacca G. Ciacci C, et al. Among authors: de rosa a, de michele g. Eur J Gastroenterol Hepatol. 1998 Aug;10(8):649-51. Eur J Gastroenterol Hepatol. 1998. PMID: 9744692

4

Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.

De Michele G, Cavalcanti F, Criscuolo C, Pianese L, Monticelli A, Filla A, Cocozza S. De Michele G, et al. Hum Mol Genet. 1998 Nov;7(12):1901-6. doi: 10.1093/hmg/7.12.1901. Hum Mol Genet. 1998. PMID: 9811933

5

Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features.

Pellecchia MT, Scala R, Filla A, De Michele G, Ciacci C, Barone P. Pellecchia MT, et al. Among authors: de michele g. J Neurol Neurosurg Psychiatry. 1999 Jan;66(1):32-5. doi: 10.1136/jnnp.66.1.32. J Neurol Neurosurg Psychiatry. 1999. PMID: 9886447 Free PMC article.

6

Cerebellar ataxia associated with subclinical celiac disease responding to gluten-free diet.

Pellecchia MT, Scala R, Perretti A, De Michele G, Santoro L, Filla A, Ciacci C, Barone P. Pellecchia MT, et al. Among authors: de michele g. Neurology. 1999 Oct 22;53(7):1606-8. doi: 10.1212/wnl.53.7.1606-a. Neurology. 1999. PMID: 10534283 No abstract available.

7

Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy.

Barbieri F, Pellecchia MT, Esposito E, Di Stasio E, Castaldo I, Santorelli F, Perretti A, Santoro L, De Michele G. Barbieri F, et al. Among authors: de michele g. Neurology. 2001 May 22;56(10):1412-4. doi: 10.1212/wnl.56.10.1412. Neurology. 2001. PMID: 11376202

8

Stimulation of growth hormone release in multiple system atrophy, Parkinson's disease and idiopathic cerebellar ataxia.

Pellecchia MT, Salvatore E, Pivonello R, Faggiano A, Barone P, De Michele G, Colao AM, Filla A. Pellecchia MT, et al. Among authors: de michele g. Neurol Sci. 2001 Feb;22(1):79-80. doi: 10.1007/s100720170056. Neurol Sci. 2001. PMID: 11487211

9

PARK6-linked parkinsonism occurs in several European families.

Valente EM, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Wassilowsky D, Harhangi BS, Rawal N, Caputo V, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease. Valente EM, et al. Among authors: de michele g. Ann Neurol. 2002 Jan;51(1):14-8. Ann Neurol. 2002. PMID: 11782979

10

Paradoxical response to apomorphine in a case of atypical parkinsonism.

Cicarelli G, Pellecchia MT, De Michele G, Pizzolato G, Barone P. Cicarelli G, et al. Among authors: de michele g. Mov Disord. 2002 May;17(3):604-6. doi: 10.1002/mds.10113. Mov Disord. 2002. PMID: 12112216

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