Uziel G - Search Results

1

Classification of childhood white matter disorders using proton MR spectroscopic imaging.

Bizzi A, Castelli G, Bugiani M, Barker PB, Herskovits EH, Danesi U, Erbetta A, Moroni I, Farina L, Uziel G. Bizzi A, et al. Among authors: uziel g. AJNR Am J Neuroradiol. 2008 Aug;29(7):1270-5. doi: 10.3174/ajnr.A1106. Epub 2008 May 15. AJNR Am J Neuroradiol. 2008. PMID: 18483189 Free PMC article.

2

MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.

Farina L, Chiapparini L, Uziel G, Bugiani M, Zeviani M, Savoiardo M. Farina L, et al. Among authors: uziel g. AJNR Am J Neuroradiol. 2002 Aug;23(7):1095-100. AJNR Am J Neuroradiol. 2002. PMID: 12169463 Free PMC article.

3

L-2-Hydroxyglutaric aciduria: MRI in seven cases.

D'Incerti L, Farina L, Moroni I, Uziel G, Savoiardo M. D'Incerti L, et al. Among authors: uziel g. Neuroradiology. 1998 Nov;40(11):727-33. doi: 10.1007/s002340050673. Neuroradiology. 1998. PMID: 9860123

4

Cerebral white matter involvement in children with mitochondrial encephalopathies.

Moroni I, Bugiani M, Bizzi A, Castelli G, Lamantea E, Uziel G. Moroni I, et al. Among authors: uziel g. Neuropediatrics. 2002 Apr;33(2):79-85. doi: 10.1055/s-2002-32372. Neuropediatrics. 2002. PMID: 12075488

5

X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8.

Bizzi A, Bugiani M, Salomons GS, Hunneman DH, Moroni I, Estienne M, Danesi U, Jakobs C, Uziel G. Bizzi A, et al. Among authors: uziel g. Ann Neurol. 2002 Aug;52(2):227-31. doi: 10.1002/ana.10246. Ann Neurol. 2002. PMID: 12210795

6

Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduria.

Moroni I, D'Incerti L, Farina L, Rimoldi M, Uziel G. Moroni I, et al. Among authors: uziel g. Neurol Sci. 2000 Apr;21(2):103-8. doi: 10.1007/s100720070104. Neurol Sci. 2000. PMID: 10938189

7

Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cysts.

Bugiani M, Moroni I, Bizzi A, Nardocci N, Bettecken T, Gärtner J, Uziel G. Bugiani M, et al. Among authors: uziel g. Neuropediatrics. 2003 Aug;34(4):211-4. doi: 10.1055/s-2003-42209. Neuropediatrics. 2003. PMID: 12973663

8

GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy.

Bugiani M, Al Shahwan S, Lamantea E, Bizzi A, Bakhsh E, Moroni I, Balestrini MR, Uziel G, Zeviani M. Bugiani M, et al. Among authors: uziel g. Neurology. 2006 Jul 25;67(2):273-9. doi: 10.1212/01.wnl.0000223832.66286.e4. Epub 2006 May 17. Neurology. 2006. PMID: 16707726 Clinical Trial.

9

Effects of riboflavin in children with complex II deficiency.

Bugiani M, Lamantea E, Invernizzi F, Moroni I, Bizzi A, Zeviani M, Uziel G. Bugiani M, et al. Among authors: uziel g. Brain Dev. 2006 Oct;28(9):576-81. doi: 10.1016/j.braindev.2006.04.001. Epub 2006 Jun 5. Brain Dev. 2006. PMID: 16737791 Clinical Trial.

10

Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities.

Mora M, Moroni I, Uziel G, di Blasi C, Barresi R, Farina L, Morandi L. Mora M, et al. Among authors: uziel g. Neuromuscul Disord. 1996 Oct;6(5):377-81. doi: 10.1016/0960-8966(96)00359-8. Neuromuscul Disord. 1996. PMID: 8938702

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

146 results

Search Page

Filters