Zobrazeno 1 - 10
of 16
pro vyhledávání: '"M. R. Balestrini"'
Publikováno v:
Scopus-Elsevier
We report the cases of two siblings both affected by inherited sensory-motor neuropathy of a demyelinative nature but with markedly different severity and pathological findings. The clinical, neurophysiological and morphological features in these two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625aa25fb717d32692def1ae93fdc3bb
https://doi.org/10.1055/s-2008-1071419
https://doi.org/10.1055/s-2008-1071419
Publikováno v:
Child's Nervous System. 6:143-147
A series of 64 consecutive cases of children with neuroepthelial tumors of the cerebral hemispheres operated on from 1966 to 1983 is analyzed with regard to the long-term survival rate and the quality of life at late follow-up. At the time of the dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::701312769e64b56634a06a176794708b
https://doi.org/10.1007/bf00308491
https://doi.org/10.1007/bf00308491
Autor:
M. Fornari, M. R. Balestrini, Giovanni Lasio, S. Lodrini, F. Pluchino, S. Visintini, C. Cimino, C. L. Solero
Publikováno v:
Child's Nervous System. 6:66-70
Between 1956 and 1987 operations were performed on 36 patients below the age of 20 years for epidermoid and dermoid cysts of the central nervous system. Seventeen tumors were intracranial intradural lesions (47%): 12 were located in the supratentoria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e010ea267e21ef49d132f5080fa73ce
https://doi.org/10.1007/bf00307923
https://doi.org/10.1007/bf00307923
Autor:
Graziella Uziel, Isabella Moroni, Marianna Bugiani, Massimo Zeviani, M. R. Balestrini, Eman Bakhsh, Eleonora Lamantea, Alberto Bizzi, S. Al Shahwan
Publikováno v:
Neurology. 67(2)
Background: Pelizaeus-Merzbacher-like disease (PMLD) is an inherited hypomyelinating leukoencephalopathy with onset in early infancy. Like Pelizaeus-Merzbacher disease (PMD), PMLD is characterized clinically by nystagmus, cerebellar ataxia, and spast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::608fd5f718a7459def09f626eba2a956
https://pubmed.ncbi.nlm.nih.gov/16707726
https://pubmed.ncbi.nlm.nih.gov/16707726
Autor:
Amerigo Boiardi, Antonio Silvani, Giovanni Broggi, Laura Fariselli, Bianca Pollo, Maurizio Gelati, Marica Eoli, C. Marras, M. R. Balestrini, Andrea Salmaggi
Publikováno v:
Journal of neuro-oncology. 74(3)
The clinical course of 50 patients with low-grade glioma (31 male, 19 female) undergoing surgery at a single Institution from 1992 to 1996 was analyzed in relationship with known prognostic factors as far as time to tumor progression (TTP) and surviv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daf096e17c8eaf34d8c1c694208c29e3
https://pubmed.ncbi.nlm.nih.gov/16132525
https://pubmed.ncbi.nlm.nih.gov/16132525
Autor:
M. R. Balestrini, Laura Grazia Valentini, Giovanni Lasio, S. Giombini, L. Giordano, M. Grisoli, C. L. Solero, S. Visintini
Publikováno v:
Child's Nervous System. 11:170-172
The authors review 71 patients with triventricular hydrocephalus in whom a contrast-enhanced CT scan did not show any tumoral or vascular lesion that could have caused the hydrocephalus. The patients were subdivided into three age groups. The results
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d607e96f149e450dfbb70382f4401f2a
https://doi.org/10.1007/bf00570259
https://doi.org/10.1007/bf00570259
Publikováno v:
Minerva pediatrica. 48(3)
Twenty-eight children (mean age 8 years) with neurofibromatosis type 1 (NF1) and cerebral tumor were studied from 1975 to 1992 (mean follow-up 8.1 years) considering the biological behaviour of the tumor and the patient's quality of life, in order to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29b8f0927ad4e3c8e63cdc2edfc7bf62
https://pubmed.ncbi.nlm.nih.gov/8766674
https://pubmed.ncbi.nlm.nih.gov/8766674
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 10(2)
Eighty children who in the first 2 years of life had signs and symptoms relating to a cerebral neoplasm were studied over an 18-year period (1970–1987), the mean follow-up being 8.2 years. In each case age at onset, clinical presentation, tumor loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f33afd8cc52dab57cd533a598c4bb367
https://pubmed.ncbi.nlm.nih.gov/8033157
https://pubmed.ncbi.nlm.nih.gov/8033157
Autor:
M. R. Balestrini, Emilia Bellone, Davide Pareyson, A. Sghirlanzoni, R. Marazzi, D. Riva, Paola Mandich, Guido Cavaletti
We compared 25 autosomal dominant hereditary motor and sensory neuropathy (HMSN) type I patients with 7 subjects affected by hypertrophic HMSN with non-dominant inheritance. All the autosomal dominant HMSN I cases carried the chromosome 17p11.2 dupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7cdfda34cd29f393e96659c93c1fc31
http://hdl.handle.net/10281/44779
http://hdl.handle.net/10281/44779
Autor:
R. Micheli, M. R. Balestrini, L. Giordano, C. L. Solero, F. Pluchino, L. Rottoli, A. Allegranza
Publikováno v:
Pediatric Neurology. 8:381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1473388a793b8b9017272305f78b102e
https://doi.org/10.1016/0887-8994(92)90236-r
https://doi.org/10.1016/0887-8994(92)90236-r