Comi GP - Search Results

1

Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG.

Villa D, Cinnante C, Valcamonica G, Manenti G, Lanfranconi S, Colombi A, Ghione I, Saetti MC, D'Amico M, Bonato S, Bresolin N, Comi GP, Ronchi D. Villa D, et al. Among authors: comi gp. BMC Neurol. 2020 Aug 26;20(1):316. doi: 10.1186/s12883-020-01890-2. BMC Neurol. 2020. PMID: 32847536 Free PMC article.

2

Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility.

Moroni I, Gonano EF, Comi GP, Tegazzin V, Prelle A, Bordoni A, Bresolin N, Scarlato G. Moroni I, et al. Among authors: comi gp. J Neurol. 1995 Feb;242(3):127-33. doi: 10.1007/BF00936884. J Neurol. 1995. PMID: 7751854

3

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Bet L, Moggio M, Comi GP, Mariani C, Prelle A, Checcarelli N, Bordoni A, Bresolin N, Scarpini E, Scarlato G. Bet L, et al. Among authors: comi gp. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

4

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferro MT, Bordoni A, et al. Comi GP, et al. Brain. 1994 Feb;117 ( Pt 1):1-14. doi: 10.1093/brain/117.1.1-a. Brain. 1994. PMID: 8149204

5

Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency.

Bresolin N, Comi GP, Fortunato F, Meola G, Gallanti A, Tajana A, Velicogna M, Gonano EF, Ninfali P, Pifferi S, et al. Bresolin N, et al. Among authors: comi gp. J Neurol. 1993 May;240(5):272-7. doi: 10.1007/BF00838160. J Neurol. 1993. PMID: 8326330

6

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G. Comi GP, et al. Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119. Ann Neurol. 1998. PMID: 9450776

7

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

Papadimitriou A, Comi GP, Hadjigeorgiou GM, Bordoni A, Sciacco M, Napoli L, Prelle A, Moggio M, Fagiolari G, Bresolin N, Salani S, Anastasopoulos I, Giassakis G, Divari R, Scarlato G. Papadimitriou A, et al. Among authors: comi gp. Neurology. 1998 Oct;51(4):1086-92. doi: 10.1212/wnl.51.4.1086. Neurology. 1998. PMID: 9781534

8

Lack of apoptosis in mitochondrial encephalomyopathies.

Sciacco M, Fagiolari G, Lamperti C, Messina S, Bazzi P, Napoli L, Chiveri L, Prelle A, Comi GP, Bresolin N, Scarlato G, Moggio M. Sciacco M, et al. Among authors: comi gp. Neurology. 2001 Apr 24;56(8):1070-4. doi: 10.1212/wnl.56.8.1070. Neurology. 2001. PMID: 11320180

9

Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria.

Cagliani R, Comi GP, Tancredi L, Sironi M, Fortunato F, Giorda R, Bardoni A, Moggio M, Prelle A, Bresolin N, Scarlato G. Cagliani R, et al. Among authors: comi gp. Neuromuscul Disord. 2001 May;11(4):389-94. doi: 10.1016/s0960-8966(00)00207-8. Neuromuscul Disord. 2001. PMID: 11369190

10

Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis.

Comi GP, Fortunato F, Lucchiari S, Bordoni A, Prelle A, Jann S, Keller A, Ciscato P, Galbiati S, Chiveri L, Torrente Y, Scarlato G, Bresolin N. Comi GP, et al. Ann Neurol. 2001 Aug;50(2):202-7. doi: 10.1002/ana.1095. Ann Neurol. 2001. PMID: 11506403

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