Donti E - Search Results

1

Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis.

Di Filippo M, Luchetti E, Prontera P, Donti E, Floridi P, Di Gregorio M, Tambasco N, Sarchielli P, Calabresi P. Di Filippo M, et al. Among authors: donti e. J Neurol. 2011 Feb;258(2):323-4. doi: 10.1007/s00415-010-5726-x. Epub 2010 Aug 31. J Neurol. 2011. PMID: 20803344 No abstract available.

2

Myostatin depletion: a therapy for Ehlers-Danlos syndrome?

Prontera P, Belcastro V, Calabresi P, Donti E. Prontera P, et al. Among authors: donti e. Ann Neurol. 2010 Jan;67(1):147-8. doi: 10.1002/ana.21828. Ann Neurol. 2010. PMID: 20186851 No abstract available.

3

Shapiro's syndrome: Defining the clinical spectrum of the spontaneous paroxysmal hypothermia syndrome.

Tambasco N, Belcastro V, Prontera P, Nigro P, Donti E, Rossi A, Calabresi P. Tambasco N, et al. Among authors: donti e. Eur J Paediatr Neurol. 2014 Jul;18(4):453-7. doi: 10.1016/j.ejpn.2014.02.001. Epub 2014 Feb 15. Eur J Paediatr Neurol. 2014. PMID: 24594427 Review.

4

A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline.

Castrioto A, Prontera P, Di Gregorio E, Rossi V, Parnetti L, Rossi A, Donti E, Brusco A, Calabresi P, Tambasco N. Castrioto A, et al. Among authors: donti e. Eur J Neurol. 2011 Oct;18(10):1263-5. doi: 10.1111/j.1468-1331.2011.03366.x. Epub 2011 Mar 7. Eur J Neurol. 2011. PMID: 21382133

5

Xq12-q13.3 duplication: evidence of a recurrent syndrome.

Prontera P, Ottaviani V, Isidori I, Stangoni G, Donti E. Prontera P, et al. Among authors: donti e. Ann Neurol. 2012 Nov;72(5):821-2; author reply 822-3. doi: 10.1002/ana.23754. Ann Neurol. 2012. PMID: 23280798 No abstract available.

6

Hypothesis: gonadal temperature influences sex-specific imprinting.

Prontera P, Donti E. Prontera P, et al. Among authors: donti e. Front Genet. 2014 Aug 25;5:294. doi: 10.3389/fgene.2014.00294. eCollection 2014. Front Genet. 2014. PMID: 25202325 Free PMC article.

7

Hot water epilepsy and Mccune-Albright syndrome: a case report.

Belcastro V, Parnetti L, Prontera P, Donti E, Rossi A, Tambasco N. Belcastro V, et al. Among authors: donti e. Seizure. 2009 Mar;18(2):161-2. doi: 10.1016/j.seizure.2008.07.005. Epub 2008 Aug 15. Seizure. 2009. PMID: 18706835 Free article.

8

A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.

Costa C, Prontera P, Sarchielli P, Tonelli A, Bassi MT, Cupini LM, Caproni S, Siliquini S, Donti E, Calabresi P. Costa C, et al. Among authors: donti e. Cephalalgia. 2014 Jan;34(1):68-72. doi: 10.1177/0333102413498941. Epub 2013 Aug 5. Cephalalgia. 2014. PMID: 23918834

9

Encephalocraniocutaneous lipomatosis (ECCL) in a patient with history of familial multiple lipomatosis (FML).

Prontera P, Stangoni G, Manes I, Mencarelli A, Donti E. Prontera P, et al. Among authors: donti e. Am J Med Genet A. 2009 Mar;149A(3):543-5. doi: 10.1002/ajmg.a.32692. Am J Med Genet A. 2009. PMID: 19215040 No abstract available.

10

Obstruction of the tricuspid valve orifice by a huge right atrial myxoma associated with the Carney complex: a case report.

Affronti A, Di Bella I, Prontera P, Da Col U, Ramoni E, Donti E, Paris M, Ragni T. Affronti A, et al. Among authors: donti e. J Card Surg. 2010 Nov;25(6):674-6. doi: 10.1111/j.1540-8191.2010.01114.x. Epub 2010 Sep 29. J Card Surg. 2010. PMID: 20880078

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