Botti S - Search Results

1

Kennedy's disease: clinical and molecular study of two Italian families.

Pareyson D, Castellotti B, Botti S, Defanti CA, Gellera C, Taroni F, Sghirlanzoni A. Pareyson D, et al. Among authors: botti s. Ital J Neurol Sci. 1995 Oct;16(7):467-71. doi: 10.1007/BF02229324. Ital J Neurol Sci. 1995. PMID: 8749704

2

Sexual function of adult long-term survivors and their partners after allogeneic hematopoietic cell transplantation in Europe (S-FAST): a study from the Transplant Complications Working Party and Nurses Group of the EBMT.

Gjærde LK, Eeltink C, Stringer J, Mooyaart J, Bosman P, Kenyon M, Liptrott S, Greenfield DM, Linke A, Turlure P, Botti S, Dzaferagic D, Sica S, Welsh L, Kisch A, Perić Z, Schoemans H, Murray J. Gjærde LK, et al. Among authors: botti s. Bone Marrow Transplant. 2023 Feb;58(2):195-202. doi: 10.1038/s41409-022-01869-2. Epub 2022 Nov 14. Bone Marrow Transplant. 2023. PMID: 36376470

3

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.

Pareyson D, Scaioli V, Taroni F, Botti S, Lorenzetti D, Solari A, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: botti s. Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133. Neurology. 1996. PMID: 8780105

4

PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.

Pareyson D, Botti S, Sghirlanzoni A, Taroni F. Pareyson D, et al. Among authors: botti s. Neurology. 1997 Nov;49(5):1478-9. doi: 10.1212/wnl.49.5.1478. Neurology. 1997. PMID: 9371959 No abstract available.

5

Facial nerve is liable to pressure palsy.

Poloni TE, Merlo IM, Alfonsi E, Marinou-Aktipi K, Botti S, Arrigo A, Taroni F, Ceroni M. Poloni TE, et al. Among authors: botti s. Neurology. 1998 Jul;51(1):320-2. doi: 10.1212/wnl.51.1.320. Neurology. 1998. PMID: 9674839 No abstract available.

6

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.

Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: botti s. Muscle Nerve. 1998 Dec;21(12):1686-91. doi: 10.1002/(sici)1097-4598(199812)21:12<1686::aid-mus10>3.0.co;2-z. Muscle Nerve. 1998. PMID: 9843070

7

Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F. Pareyson D, et al. Among authors: botti s. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

8

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation.

Pareyson D, Taroni F, Botti S, Morbin M, Baratta S, Lauria G, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: botti s. Neurology. 2000 Apr 25;54(8):1696-8. doi: 10.1212/wnl.54.8.1696. Neurology. 2000. PMID: 10762521 Free article.

9

Heterozygous Null Mutation in the P₀ Gene Associated with Mild Charcot-Marie-Tooth Disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F. Pareyson D, et al. Among authors: botti s. Ann N Y Acad Sci. 1999 Oct;883(1):477-480. doi: 10.1111/j.1749-6632.1999.tb08615.x. Ann N Y Acad Sci. 1999. PMID: 29086956 No abstract available.

10

Management of carbapenem resistant Klebsiella pneumoniae infections in stem cell transplant recipients: an Italian multidisciplinary consensus statement.

Girmenia C, Viscoli C, Piciocchi A, Cudillo L, Botti S, Errico A, Sarmati L, Ciceri F, Locatelli F, Giannella M, Bassetti M, Tascini C, Lombardini L, Majolino I, Farina C, Luzzaro F, Rossolini GM, Rambaldi A. Girmenia C, et al. Among authors: botti s. Haematologica. 2015 Sep;100(9):e373-6. doi: 10.3324/haematol.2015.125484. Epub 2015 Apr 10. Haematologica. 2015. PMID: 25862702 Free PMC article. No abstract available.

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