Association of MICA alleles and HLA-B51 in Italian patients with Behçet's disease.

…, F Cantini, F Salvi, R Malatesta, C Molinotti… - The Journal of …, 2001 - jrheum.org
OBJECTIVE: To evaluate the distribution of the MHC class I chain related gene A transmembrane
(MICA-TM) alleles in Italian patients with Behçet's disease (BD), and to investigate the …

Retinitis pigmentosa, ataxia, and mental retardation associated with mitochondrial DNA mutation in an Italian family.

…, A Cerullo, M Bragliani, C Molinotti… - British journal of …, 1993 - bjo.bmj.com
… PTP, 1 FtM of each primer and 2 5 units ilymerase(Perkin Elmer-Cetus, Norwalk, Each cycle
consisted of 94C denaturation seconds, 55C annealing for 150 seconds C extension for4 …

Optic neuropathy in Behçet's disease. Report of two cases

…, M Mascalchi, R Malatesta, I Olivieri, C Molinotti… - The Italian Journal of …, 1999 - Springer
Orbital magnetic resonance imaging demonstrated increased signal of the optic nerve in short
time inversion recovery (STIR) images of two young women with unilateral visual blurring. …

One-step purification by high-performance liquid chromatography of retinal S-antigen

C Molinotti, P Puddu, S Perugini, P Barboni… - Research in Clinic and …, 1989 - Springer
… The retinal homogenate was centrifuged (Beckman 75rB) at 48,000 g for 15 min at 4 C and
the clear supernatant was collected. The sediment was resuspended and the same operation …

Neuroophthalmological implications of the radiological finding of the transverse sinus.

…, R Lodi, A Mularoni, C Molinotti - Metabolic, Pediatric, and …, 1989 - europepmc.org
Visualization of transverse intracranial sinuses by means of standard radiograms of the skill
is a rather unusual finding. In order to detect the radiological evidence of this important …

[CITATION][C] Isolation and purification of soluble antigens from the bovine retina

…, L Rossi, S Peruguni, P Puddu, C Molinotti… - … Della Societa Italiana …, 1986 - europepmc.org
[Isolation and purification of soluble antigens from the bovine retina] - Abstract - Europe PMC
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[HTML][HTML] Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit a

A Baracca, S Barogi, V Carelli, G Lenaz… - Journal of Biological …, 2000 - ASBMB
C; 29 cycles each consisting of denaturation for 80 s at 94 C, annealing for 100 s at 56 C,
and extension for 120 s at 72 C; and a final cycle of “superextension” for 5 min at 72 C. This last …

an Italian family PieroPuddu, PieroBarboni, Vilma Mantovani, Pasquale Montagna, Angelina Cerullo, Michela Bragliani, Carla Molinotti, Roberto Caramazza

G JostBjonas, J Cazenave, PV Poirier, JB Cheyrou… - bjo.bmj.com
… , Angelina Cerullo, Michela Bragliani, Carla Molinotti, Roberto Caramazza 89 Influence of a
… to bilateral sequential optic neuropathyJF Acheson, 0 C Cockerell, CR Bentley, MD Sanders …

Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome

P Mäkelä-Bengs, A Suomalainen, A Majander… - Pediatric …, 1995 - nature.com
ABSTRACT: We describe a four-generation family with a maternally inherited mitochondrial
disorder. The symptoms were restricted to the CNS and muscle, the most common features …

Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G …

G Sgarbi, A Baracca, G Lenaz, LM Valentino… - Biochemical …, 2006 - portlandpress.com
Mutations in the ATP6 gene of mtDNA (mitochondrial DNA) have been shown to cause
several different neurological disorders. The product of this gene is ATPase 6, an essential …