Clinical and biochemical aspects of carnitine deficiency and insufficiency : transport defects and inborn errors of β-oxidationANGELINI, C; VERGANI, L; MARTINUZZI, A et al.Critical reviews in clinical laboratory sciences. 1992, Vol 29, Num 3-4, pp 217-242, issn 1040-8363Article

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathyYONEDA, M; CHOMYN, A; MARTINUZZI, A et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 23, pp 11164-11168, issn 0027-8424Article

Paralysis of innervated cultured human muscle fibers affects enzymes differntiallyMARTINUZZI, A; ASKANAS, V; KING ENGEL, W et al.Journal of neurochemistry. 1990, Vol 54, Num 1, pp 223-229, issn 0022-3042Article

De novo neuromuscular junction formation on human muscle fibres cultured in monolayer and innervated by foetal rat spinal cord: ultrastructural and ultrastructural-cytochemical studiesASKANAS, V; KWAN, H; ALVAREZ, R. B et al.Journal of neurocytology. 1987, Vol 16, Num 4, pp 523-537, issn 0300-4864Article

Coiling and neuroendoscopy : a new perspective in the treatment of intraventricular haemorrhages due to bleeding aneurysmsLONGATTI, P; FIORINDI, A; DI PAOLA, F et al.Journal of neurology, neurosurgery and psychiatry. 2006, Vol 77, Num 12, pp 1354-1358, issn 0022-3050, 5 p.Article

McArdle's disease : The unsolved mystery of the reappearing enzymeMARTINUZZI, A; SCHIEVANO, G; NASCIMBENI, A et al.The American journal of pathology. 1999, Vol 154, Num 6, pp 1893-1897, issn 0002-9440Article

Molecular characterization of myophosphorylase deficiency in a group of patients from Northern ItalyMARTINUZZI, A; TSUJINO, S; ANGELINI, C et al.Journal of the neurological sciences. 1996, Vol 137, Num 1, pp 14-19, issn 0022-510XArticle

Expression of muscle-gene-specific isozymes of phosphorylase and creatine kinase in innervated cultured human muscleMARTINUZZI, A; ASKANAS, V; KOBAYASHI, T et al.The Journal of cell biology. 1986, Vol 103, Num 4, pp 1423-1429, issn 0021-9525Article

Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: studies with malonyl-CoA suggest absence of only CPT-IITREVISAN, C. P; ANGELINI, C; FREDDO, L et al.Neurology. 1984, Vol 34, Num 3, pp 353-356, issn 0028-3878Article

Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2CRIMELLA, C; BASCHIROTTO, C; BENEDETTI, S et al.Clinical genetics. 2012, Vol 82, Num 2, pp 157-164, issn 0009-9163, 8 p.Article

Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosumCRIMELLA, C; ARNOLDI, A; TOSCANO, A et al.Journal of medical genetics. 2009, Vol 46, Num 5, pp 345-351, issn 0022-2593, 7 p.Article

Failure of endoscopic third ventriculostomy in the treatment of idiopathic normal pressure hydrocephalusLONGATTI, P. L; FIORINDI, A; MARTINUZZI, A et al.Minimally invasive neurosurgery. 2004, Vol 47, Num 6, pp 342-345, issn 0946-7211, 4 p.Article

Endoscopic treatment of colloid cysts of the third ventricle : 9 consecutive casesLONGATTI, P; MARTINUZZI, A; MORO, M et al.Minimally invasive neurosurgery. 2000, Vol 43, Num 3, pp 118-123, issn 0946-7211Article

Myophosphorylase deficiency affects muscle mitochondrial respiration as shown by ³¹P-MR spectroscopy in a case with associated multifocal encephalopathySICILIANO, G; ROSSI, B; MARTINI, A et al.Journal of the neurological sciences. 1995, Vol 128, Num 1, pp 84-91, issn 0022-510XArticle

Hypertrophic cardiomyopathy with mitochondrial myopathy : a new phenotype of complex II defectANGELINI, C; MELACINI, P; VALENTE, M. L et al.Japanese heart journal. 1993, Vol 34, Num 1, pp 63-77, issn 0021-4868Article

Correlation between clinical and molecular features in two MELAS familiesMARTINUZZI, A; BARTOLOMEI, L; CARROZZO, R et al.Journal of the neurological sciences. 1992, Vol 113, Num 2, pp 222-229, issn 0022-510XArticle

MELAS : clinical features, biochemistry and molecular geneticsCIAFALONI, E; RICCI, E; MARTINUZZI, A et al.Annals of neurology. 1992, Vol 31, Num 4, pp 391-398, issn 0364-5134Article

blood staining of the cornea following radial keratotomyRAPIZZI, A; PROSDOCIMO, G; GORLA, C et al.Refractive & corneal surgery. 1991, Vol 7, Num 2, pp 188-189, 2 p.Article

L-carnitine uptake in differentiating human cultured muscleMARTINUZZI, A; VERGANI, L; ROSA, M et al.Biochimica et biophysica acta. Molecular cell research. 1991, Vol 1095, Num 3, pp 217-222, issn 0167-4889Article

Asynchronous regulation of muscle specific isozymes of creatine kinase, glycogen phosphorylase, lactic dehydrogenase and phosphoglycerate mutase in innervated and non-innervated cultured human muscleMARTINUZZI, A; ASKANAS, V; KOBAYASHI, T et al.Neuroscience letters. 1988, Vol 89, Num 2, pp 216-222, issn 0304-3940Article

Developmental expression of the muscle-specific isozyme of phosphoglycerate mutase in human muscle cultured in monolayer and innervated by fetal rat spinal cordMARTINUZZI, A; ASKANAS, V; KOBAYASHI, T et al.Experimental neurology (Print). 1987, Vol 96, Num 2, pp 365-375, issn 0014-4886Article

Histoenzymatic profile of human muscle cultured in monolayer and innervated de novo by fetal rat spinal cordVITA, G; ASKANAS, V; MARTINUZZI, A et al.Muscle & nerve. 1987, Vol 11, Num 1, pp 1-9, issn 0148-639XArticle