Plewnia K - Search Results

1

Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study.

Federico A, Dotti MT, Cardaioli E, Grieco G, Malandrini A, Manneschi L, Plewnia K, Rufa A, Renieri A, Bruttini M, Perticoni GF. Federico A, et al. Among authors: plewnia k. J Submicrosc Cytol Pathol. 1998 Oct;30(4):521-6. J Submicrosc Cytol Pathol. 1998. PMID: 9851061

2

A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case.

Plewnia K, Dotti MT, Malandrini A, Manneschi L, Battisti C, De Stefano N, Rufa A, Motolese E, Federico A. Plewnia K, et al. J Submicrosc Cytol Pathol. 1997 Jul;29(3):335-8. J Submicrosc Cytol Pathol. 1997. PMID: 9267042

3

Palpebral ptosis and muscle fatiguability associated with perineurial cell ensheathment of muscle fibers: a new disease of the neuromuscular junction?

Federico A, Plewnia K, Battisti C, Cavallaro T, Dotti MT, Malandrini A, Manneschi L. Federico A, et al. Among authors: plewnia k. J Neurol Sci. 1997 Aug;149(2):147-50. doi: 10.1016/s0022-510x(97)05381-1. J Neurol Sci. 1997. PMID: 9171322

4

Cerebrotendinous xanthomatosis: evidence of lipomatous hypertrophy of the atrial septum.

Dotti MT, Mondillo S, Plewnia K, Agricola E, Federico A. Dotti MT, et al. Among authors: plewnia k. J Neurol. 1998 Nov;245(11):723-6. doi: 10.1007/s004150050274. J Neurol. 1998. PMID: 9808240

5

Mosaicism for full mutation and normal-sized allele of the FMR1 gene: a new case.

Orrico A, Galli L, Dotti MT, Plewnia K, Censini S, Federico A. Orrico A, et al. Among authors: plewnia k. Am J Med Genet. 1998 Jul 24;78(4):341-4. Am J Med Genet. 1998. PMID: 9714436

6

Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.

Stromillo ML, Dotti MT, Battaglini M, Mortilla M, Bianchi S, Plewnia K, Pantoni L, Inzitari D, Federico A, De Stefano N. Stromillo ML, et al. Among authors: plewnia k. J Neurol Neurosurg Psychiatry. 2009 Jan;80(1):41-7. doi: 10.1136/jnnp.2008.155853. Epub 2008 Oct 1. J Neurol Neurosurg Psychiatry. 2009. PMID: 18829627

7

A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778.

Dotti MT, Plewnia K, Cardaioli E, Manneschi L, Rufa A, Alemà G, Federico A. Dotti MT, et al. Among authors: plewnia k. J Neurol. 1998 May;245(5):302-3. doi: 10.1007/s004150050223. J Neurol. 1998. PMID: 9617713 No abstract available.

8

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.

Marconi R, De Fusco M, Aridon P, Plewnia K, Rossi M, Carapelli S, Ballabio A, Morgante L, Musolino R, Epifanio A, Micieli G, De Michele G, Casari G. Marconi R, et al. Among authors: plewnia k. Ann Neurol. 2003 Mar;53(3):376-81. doi: 10.1002/ana.10464. Ann Neurol. 2003. PMID: 12601705

9

Complete clinical and functional recovery following low-dose methotrexate related paraparesis in a patient with compound c.1298A>C AND c.677C>T MTHFR polymorphism: A case report.

Saviola G, Abdi-Ali L, Sacco S, Comini L, Plewnia K, Rossi M, Orrico A. Saviola G, et al. Among authors: plewnia k. Medicine (Baltimore). 2018 Dec;97(49):e13350. doi: 10.1097/MD.0000000000013350. Medicine (Baltimore). 2018. PMID: 30544400 Free PMC article.

10

Detection of disability worsening in relapsing-remitting multiple sclerosis patients: a real-world roving Expanded Disability Status Scale reference analysis from the Italian Multiple Sclerosis Register.

Lepore V, Bosetti C, Santucci C, Iaffaldano P, Trojano M, Mosconi P; Italian Multiple Sclerosis Register Centers Group, the Scientific Committee of Italian SM Register. Lepore V, et al. Eur J Neurol. 2021 Feb;28(2):567-578. doi: 10.1111/ene.14589. Epub 2020 Nov 6. Eur J Neurol. 2021. PMID: 33058344

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