1: Abstract Ghelli A, Porcelli AM, Zanna C, Martinuzzi A, Carelli V, Rugolo M.
Protection against Oxidant-Induced Apoptosis by Exogenous Glutathione in Leber Hereditary Optic Neuropathy Cybrids.
Invest Ophthalmol Vis Sci. 2008 Feb;49(2):671-6.
PMID: 18235013 [PubMed - in process]
2: Abstract
OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion.
Brain. 2008 Feb;131(Pt 2):352-67.
PMID: 18222991 [PubMed - in process]
3: Abstract
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.
Neurology. 2008 Jan 23; [Epub ahead of print]
PMID: 18216301 [PubMed - as supplied by publisher]
4: Abstract Hudson G, Carelli V, Horvath R, Zeviani M, Smeets HJ, Chinnery PF.
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy.
Mol Vis. 2007 Dec 21;13:2339-43.
PMID: 18199976 [PubMed - in process]
5: Abstract Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K, Letournel F, Liguori R, La Morgia C, Montagna P, Liguori M, Zanna C, Rugolo M, Cossarizza A, Wissinger B, Verny C, Schwarzenbacher R, Martín MA, Arenas J, Ayuso C, Garesse R, Lenaers G, Bonneau D, Carelli V.
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.
Brain. 2008 Feb;131(Pt 2):338-51. Epub 2007 Dec 24.
PMID: 18158317 [PubMed - in process]
6: Abstract D'Aguanno S, Barassi A, Lupisella S, d'eril GM, Del Boccio P, Pieragostino D, Pallotti F, Carelli V, Valentino ML, Liguori R, Avoni P, Bernardini S, Gambi D, Urbani A, Federici G.
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.
J Neuroimmunol. 2008 Jan;193(1-2):156-60. Epub 2007 Dec 3.
PMID: 18061280 [PubMed - in process]
7: Abstract Zeviani M, Carelli V.
Mitochondrial disorders.
Curr Opin Neurol. 2007 Oct;20(5):564-71. Review.
PMID: 17885446 [PubMed - indexed for MEDLINE]
8: Abstract Hudson G, Carelli V, Spruijt L, Gerards M, Mowbray C, Achilli A, Pyle A, Elson J, Howell N, La Morgia C, Valentino ML, Huoponen K, Savontaus ML, Nikoskelainen E, Sadun AA, Salomao SR, Belfort R Jr, Griffiths P, Man PY, de Coo RF, Horvath R, Zeviani M, Smeets HJ, Torroni A, Chinnery PF.
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Am J Hum Genet. 2007 Aug;81(2):228-33. Epub 2007 Jun 4.
PMID: 17668373 [PubMed - indexed for MEDLINE]
9: Abstract Genasetti A, Valentino ML, Carelli V, Vigetti D, Viola M, Karousou EG, Melzi d'Eril GV, De Luca G, Passi A, Pallotti F.
Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach.
J Mol Diagn. 2007 Sep;9(4):538-45. Epub 2007 Jul 25.
PMID: 17652639 [PubMed - indexed for MEDLINE]
10: Abstract Valentino ML, Martí R, Tadesse S, López LC, Manes JL, Lyzak J, Hahn A, Carelli V, Hirano M.
Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
FEBS Lett. 2007 Jul 24;581(18):3410-4. Epub 2007 Jun 27.
PMID: 17612528 [PubMed - indexed for MEDLINE]
11: Abstract

Baracca A, Sgarbi G, Mattiazzi M, Casalena G, Pagnotta E, Valentino ML, Moggio M, Lenaz G, Carelli V, Solaini G.

Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993.
Biochim Biophys Acta. 2007 Jul;1767(7):913-9. Epub 2007 May 18.
PMID: 17568559 [PubMed - indexed for MEDLINE]
12: Abstract Gasparre G, Porcelli AM, Bonora E, Pennisi LF, Toller M, Iommarini L, Ghelli A, Moretti M, Betts CM, Martinelli GN, Ceroni AR, Curcio F, Carelli V, Rugolo M, Tallini G, Romeo G.
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.
Proc Natl Acad Sci U S A. 2007 May 22;104(21):9001-6. Epub 2007 May 15.
PMID: 17517629 [PubMed - indexed for MEDLINE]
13: Abstract

Carelli V, La Morgia C, Iommarini L, Carroccia R, Mattiazzi M, Sangiorgi S, Farne' S, Maresca A, Foscarini B, Lanzi L, Amadori M, Bellan M, Valentino ML.

Mitochondrial optic neuropathies: how two genomes may kill the same cell type?
Biosci Rep. 2007 Jun;27(1-3):173-84. Review.
PMID: 17479363 [PubMed - indexed for MEDLINE]
14: Abstract Sadun AA, Salomao SR, Berezovsky A, Sadun F, Denegri AM, Quiros PA, Chicani F, Ventura D, Barboni P, Sherman J, Sutter E, Belfort R Jr, Carelli V.
Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study.
Trans Am Ophthalmol Soc. 2006;104:51-61.
PMID: 17471325 [PubMed - indexed for MEDLINE]
15: Abstract

Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.

Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
Invest Ophthalmol Vis Sci. 2007 May;48(5):2362-70.
PMID: 17460303 [PubMed - indexed for MEDLINE]
     
     
     
     
     
     
     
 
 
 
 
16:
 
Abstract
Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy?
Environ Health Perspect. 2007 Jan;115(1):113-5.
PMID: 17366829 [PubMed - indexed for MEDLINE]
17:
 
Abstract
Leber hereditary optic neuropathy possibly triggered by exposure to tire fire.
J Neuroophthalmol. 2006 Dec;26(4):268-72.
PMID: 17204920 [PubMed - indexed for MEDLINE]
18:
 
Abstract
Leber's hereditary optic neuropathy with childhood onset.
Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5303-9.
PMID: 17122117 [PubMed - indexed for MEDLINE]
19:
 
No Abstract
Optic nerve structure in healthy subjects.
Arch Ophthalmol. 2006 Oct;124(10):1507; author reply 1508-9. No abstract available. Erratum in: Arch Ophthalmol. 2006 Dec;124(12):1700. Zannini, Maurizio [corrected to Zanini, Maurizio].
PMID: 17030731 [PubMed - indexed for MEDLINE]
20:
 
Abstract
Detection and quantification of retinal nerve fiber layer thickness in optic disc edema using stratus OCT.
Arch Ophthalmol. 2006 Aug;124(8):1111-7.
PMID: 16908813 [PubMed - indexed for MEDLINE]
21:
 
Abstract
Choline pivaloyl ester strengthened the benefit effects of Tacrine and Galantamine on electroencephalographic and cognitive performances in nucleus basalis magnocellularis-lesioned and aged rats.
Pharmacol Biochem Behav. 2006 Jul;84(3):453-67. Epub 2006 Jul 21.
PMID: 16859739 [PubMed - indexed for MEDLINE]
22:
 
Abstract
The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype.
J Med Genet. 2006 Jul;43(7):e38.
PMID: 16816025 [PubMed - indexed for MEDLINE]
23:
 
Abstract
Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts.
Mitochondrion. 2006 Aug;6(4):161-75. Epub 2006 May 24.
PMID: 16815102 [PubMed - in process]
24:
 
No Abstract
The role of mitochondria in health, ageing, and diseases affecting vision.
Br J Ophthalmol. 2006 Jul;90(7):809-10. No abstract available.
PMID: 16782943 [PubMed - indexed for MEDLINE]
25:
 
Abstract
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Cancer Res. 2006 Jun 15;66(12):6087-96.
PMID: 16778181 [PubMed - indexed for MEDLINE]
26:
 
No Abstract
Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate.
Mitochondrion. 2006 Apr;6(2):102-3. Epub 2006 Apr 3. No abstract available.
PMID: 16581312 [PubMed - indexed for MEDLINE]
27:
 
Abstract
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.
Am J Hum Genet. 2006 Apr;78(4):564-74. Epub 2006 Jan 27.
PMID: 16532388 [PubMed - indexed for MEDLINE]
28:
 
Abstract
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.
Gastroenterology. 2006 Mar;130(3):893-901.
PMID: 16530527 [PubMed - indexed for MEDLINE]
29:
 
Abstract
Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
Br J Ophthalmol. 2006 Feb;90(2):150-3.
PMID: 16424523 [PubMed - indexed for MEDLINE]
30:
 
Abstract
Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA.
Biochem J. 2006 May 1;395(3):493-500.
PMID: 16402916 [PubMed - indexed for MEDLINE]
31:
 
Abstract
Complex I deficiency primes Bax-dependent neuronal apoptosis through mitochondrial oxidative damage.
Proc Natl Acad Sci U S A. 2005 Dec 27;102(52):19126-31. Epub 2005 Dec 19.
PMID: 16365298 [PubMed - indexed for MEDLINE]
32:
 
Abstract
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy.
Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4809-14.
PMID: 16303983 [PubMed - indexed for MEDLINE]
33:
 
Abstract
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G.
Apoptosis. 2005 Oct;10(5):997-1007.
PMID: 16151635 [PubMed - indexed for MEDLINE]
34:
 
Abstract
Relative post-mortem sparing of afferent pupil fibers in a patient with 3460 Leber's hereditary optic neuropathy.
Graefes Arch Clin Exp Ophthalmol. 2005 Nov;243(11):1175-9. Epub 2005 Jul 8.
PMID: 16003516 [PubMed - indexed for MEDLINE]
35:
 
Abstract
Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy.
Br J Ophthalmol. 2005 Jul;89(7):825-7.
PMID: 15965159 [PubMed - indexed for MEDLINE]
36:
 
Abstract
A site-specific controlled-release system for metformin.
J Pharm Pharmacol. 2005 May;57(5):565-71.
PMID: 15901345 [PubMed - indexed for MEDLINE]
37:
 
Abstract
Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids.
Arch Neurol. 2005 May;62(5):730-6.
PMID: 15883259 [PubMed - indexed for MEDLINE]
38:
 
Abstract
Dominance in mitochondrial disorders.
J Inherit Metab Dis. 2005;28(3):287-99. Review.
PMID: 15868464 [PubMed - indexed for MEDLINE]
39:
 
Abstract
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.
Eur J Hum Genet. 2005 Jun;13(6):748-52.
PMID: 15827561 [PubMed - indexed for MEDLINE]
40:
 
Abstract
Correlation between retinal nerve fibre layer thickness and optic nerve head size: an optical coherence tomography study.
Br J Ophthalmol. 2005 Apr;89(4):489-92.
PMID: 15774930 [PubMed - indexed for MEDLINE]
41:
 
Abstract
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization process.
Brain. 2005 May;128(Pt 5):1026-37. Epub 2005 Feb 23.
PMID: 15728653 [PubMed - indexed for MEDLINE]
42:
 
Abstract
Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.
FEBS J. 2005 Mar;272(5):1124-35.
PMID: 15720387 [PubMed - indexed for MEDLINE]
43:
 
Abstract
Matrices for site-specific controlled-delivery of 5-fluorouracil to descending colon.
J Control Release. 2005 Feb 16;102(3):669-77.
PMID: 15681088 [PubMed - indexed for MEDLINE]
44:
 
Abstract
Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.
Ophthalmology. 2005 Jan;112(1):127-31.
PMID: 15629832 [PubMed - indexed for MEDLINE]
45:
 
Abstract
Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy.
Ophthalmology. 2005 Jan;112(1):120-6.
PMID: 15629831 [PubMed - indexed for MEDLINE]
46:
 
Abstract
Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy.
Ann Neurol. 2004 Nov;56(5):719-23.
PMID: 15505825 [PubMed - indexed for MEDLINE]
47:
 
Abstract
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.
Ann Neurol. 2004 Nov;56(5):631-41.
PMID: 15505787 [PubMed - indexed for MEDLINE]
48:
 
Abstract
Methyl-DEAE-dextran: a candidate biomaterial.
Biomed Mater Eng. 2004;14(4):411-7.
PMID: 15472389 [PubMed - indexed for MEDLINE]
49:
 
Abstract
Visual electrophysiologic findings in patients from an extensive Brazilian family with Leber's hereditary optic neuropathy.
Doc Ophthalmol. 2004 Mar;108(2):147-55.
PMID: 15455797 [PubMed - indexed for MEDLINE]
50:
 
Abstract
The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool.
Am J Hum Genet. 2004 Nov;75(5):910-8. Epub 2004 Sep 20.
PMID: 15382008 [PubMed - indexed for MEDLINE]
51:
 
Abstract
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.
Brain. 2004 Oct;127(Pt 10):2183-92. Epub 2004 Sep 1.
PMID: 15342361 [PubMed - indexed for MEDLINE]
52:
 
Abstract
Electroencephalographic effects induced by choline pivaloyl esters in scopolamine-treated or nucleus basalis magnocellularis lesioned rats.
Pharmacol Biochem Behav. 2004 Aug;78(4):667-73.
PMID: 15301920 [PubMed - indexed for MEDLINE]
53:
 
Abstract
Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration.
Biochim Biophys Acta. 2004 Jul 23;1658(1-2):172-9. Review.
PMID: 15282189 [PubMed - indexed for MEDLINE]
54:
 
Abstract
Bioenergetics of mitochondrial diseases associated with mtDNA mutations.
Biochim Biophys Acta. 2004 Jul 23;1658(1-2):89-94. Review.
PMID: 15282179 [PubMed - indexed for MEDLINE]
55:
 
Abstract
Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report.
Graefes Arch Clin Exp Ophthalmol. 2004 Oct;242(10):878-80. Epub 2004 Mar 24.
PMID: 15042378 [PubMed - indexed for MEDLINE]
56:
 
Abstract
Choline pivaloyl esters improve in rats cognitive and memory performances impaired by scopolamine treatment or lesions of the nucleus basalis of Meynert.
Neurosci Lett. 2004 Feb 19;356(3):199-202.
PMID: 15036629 [PubMed - indexed for MEDLINE]
57:
 
Abstract
Apoptotic cell death of cybrid cells bearing Leber's hereditary optic neuropathy mutations is caspase independent.
Ann N Y Acad Sci. 2003 Dec;1010:213-7.
PMID: 15033723 [PubMed - indexed for MEDLINE]
58:
 
Abstract
Ophthalmologic findings in a large pedigree of 11778/Haplogroup J Leber hereditary optic neuropathy.
Am J Ophthalmol. 2004 Feb;137(2):271-7. Erratum in: Am J Ophthalmol. 2004 Apr;137(4):following 793.
PMID: 14962416 [PubMed - indexed for MEDLINE]
59:
 
Abstract
Mitochondrial dysfunction as a cause of optic neuropathies.
Prog Retin Eye Res. 2004 Jan;23(1):53-89. Review.
PMID: 14766317 [PubMed - indexed for MEDLINE]
60:
 
Abstract
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
Neurology. 2004 Jan 27;62(2):316-8.
PMID: 14745080 [PubMed - indexed for MEDLINE]
61:
 
Abstract
Synthesis and biological evaluation of GABA derivatives able to cross the blood-brain barrier in rats.
Bioorg Med Chem Lett. 2003 Nov 3;13(21):3765-9.
PMID: 14552775 [PubMed - indexed for MEDLINE]
62:
 
Abstract
Mitochondrial disorders.
Curr Opin Neurol. 2003 Oct;16(5):585-94. Review.
PMID: 14501842 [PubMed - indexed for MEDLINE]
63:
 
No Abstract
Mitochondrial function and dysfunction within the optic nerve.
Arch Ophthalmol. 2003 Sep;121(9):1342-3. No abstract available.
PMID: 12963627 [PubMed - indexed for MEDLINE]
64:
 
Abstract
Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathy.
Am J Ophthalmol. 2003 Aug;136(2):231-8.
PMID: 12888043 [PubMed - indexed for MEDLINE]
65:
 
Abstract
Nuclear genes in mitochondrial disorders.
Curr Opin Genet Dev. 2003 Jun;13(3):262-70. Review.
PMID: 12787788 [PubMed - indexed for MEDLINE]
66:
 
Abstract
Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction.
Trends Genet. 2003 May;19(5):257-62. Review.
PMID: 12711217 [PubMed - indexed for MEDLINE]
67:
 
Abstract
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients.
Am J Med Genet A. 2003 May 15;119(1):37-40.
PMID: 12707956 [PubMed - indexed for MEDLINE]
68:
 
Abstract
A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
Trans Am Ophthalmol Soc. 2002;100:169-78; discussion 178-9.
PMID: 12545691 [PubMed - indexed for MEDLINE]
69:
 
Abstract
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium.
J Biol Chem. 2003 Feb 7;278(6):4145-50. Epub 2002 Nov 21.
PMID: 12446713 [PubMed - indexed for MEDLINE]
70:
 
Abstract
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy.
Ann Neurol. 2002 Nov;52(5):534-42.
PMID: 12402249 [PubMed - indexed for MEDLINE]
71:
 
Abstract
Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy.
Biochim Biophys Acta. 2002 Oct 9;1588(1):7-14.
PMID: 12379308 [PubMed - indexed for MEDLINE]
72:
 
Abstract
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.
Ann Neurol. 2002 Jun;51(6):774-8.
PMID: 12112086 [PubMed - indexed for MEDLINE]
73:
 
Abstract
First application of extremely high-resolution magnetic resonance imaging to study microscopic features of normal and LHON human optic nerve.
Ophthalmology. 2002 Jun;109(6):1085-91.
PMID: 12045048 [PubMed - indexed for MEDLINE]
74:
 
Abstract
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy.
J Neurol Neurosurg Psychiatry. 2002 Jun;72(6):805-7.
PMID: 12023431 [PubMed - indexed for MEDLINE]
75:
 
Abstract
Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies.
Neurochem Int. 2002 May;40(6):573-84. Review.
PMID: 11850115 [PubMed - indexed for MEDLINE]
76:
 
Abstract
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation.
Arch Neurol. 2002 Feb;59(2):264-70.
PMID: 11843698 [PubMed - indexed for MEDLINE]
77:
 
Abstract
Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis.
J Biol Chem. 2002 Feb 22;277(8):5810-5. Epub 2001 Dec 11.
PMID: 11741983 [PubMed - indexed for MEDLINE]
78:
 
Abstract
Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases.
J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):813-6.
PMID: 11723211 [PubMed - indexed for MEDLINE]
79:
 
No Abstract
Optic neuropathy in Lhon and Leigh syndrome.
Ophthalmology. 2001 Jul;108(7):1172-3. No abstract available.
PMID: 11425664 [PubMed - indexed for MEDLINE]
80:
 
Abstract
Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve.
Trans Am Ophthalmol Soc. 2000;98:223-32; discussion 232-5.
PMID: 11190025 [PubMed - indexed for MEDLINE]
81:
 
Abstract
'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.
Brain. 2000 Sep;123 ( Pt 9):1896-902.
PMID: 10960053 [PubMed - indexed for MEDLINE]
82:
 
Abstract
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family.
Ital J Neurol Sci. 1998 Feb;19(1):41-4.
PMID: 10935859 [PubMed - indexed for MEDLINE]
83:
 
Abstract
Polyoxyethylene-poly(methacrylic acid-co-methyl methacrylate) compounds for site-specific peroral delivery.
Int J Pharm. 2000 Jul 20;202(1-2):103-12.
PMID: 10915932 [PubMed - indexed for MEDLINE]
84:
 
Abstract
Colpocephaly in two siblings: further evidence of a genetic transmission.
Dev Med Child Neurol. 2000 Apr;42(4):280-2.
PMID: 10795569 [PubMed - indexed for MEDLINE]
85:
 
Abstract
Congenital encephalomyopathy with epilepsy, chorioretinitis, basal ganglia involvement, and muscle minicores.
Ann Neurol. 2000 Mar;47(3):395-9.
PMID: 10716265 [PubMed - indexed for MEDLINE]
86:
 
Abstract
Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit a.
J Biol Chem. 2000 Feb 11;275(6):4177-82.
PMID: 10660580 [PubMed - indexed for MEDLINE]
87:
 
Abstract
Low brain intracellular free magnesium in mitochondrial cytopathies.
J Cereb Blood Flow Metab. 1999 May;19(5):528-32.
PMID: 10326720 [PubMed - indexed for MEDLINE]
88:
 
Abstract
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy.
Ann Neurol. 1999 Mar;45(3):320-8.
PMID: 10072046 [PubMed - indexed for MEDLINE]
89:
 
Abstract
Silicone microspheres for pH-controlled gastrointestinal drug delivery.
Int J Pharm. 1999 Mar 1;179(1):73-83.
PMID: 10053204 [PubMed - indexed for MEDLINE]
90:
 
Abstract
Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient.
J Neurol Sci. 1998 Oct 8;160(2):183-8.
PMID: 9849804 [PubMed - indexed for MEDLINE]
91:
 
Abstract
Childhood Leber's hereditary optic neuropathy (ND1/3460) with visual recovery.
Pediatr Neurol. 1998 Oct;19(4):308-12.
PMID: 9831004 [PubMed - indexed for MEDLINE]
92:
 
Abstract
Effect of vehicles on yohimbine permeation across excised hairless mouse skin.
Pharm Acta Helv. 1998 Aug;73(3):127-34.
PMID: 9713257 [PubMed - indexed for MEDLINE]
93:
 
Abstract
Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia.
J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):574-80. Review.
PMID: 9219741 [PubMed - indexed for MEDLINE]
94:
 
Abstract
Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.
Neurology. 1997 Jun;48(6):1623-32.
PMID: 9191778 [PubMed - indexed for MEDLINE]
95:
 
Abstract
Familial Unverricht-Lundborg disease: a clinical, neurophysiologic, and genetic study.
Epilepsia. 1997 Jun;38(6):637-41.
PMID: 9186245 [PubMed - indexed for MEDLINE]
96:
 
Abstract
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.
Am J Hum Genet. 1997 May;60(5):1107-21.
PMID: 9150158 [PubMed - indexed for MEDLINE]
97:
 
Abstract
Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study.
J Neurol Sci. 1997 May 1;148(1):25-31.
PMID: 9125387 [PubMed - indexed for MEDLINE]
98:
 
Abstract
Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON).
Mol Aspects Med. 1997;18 Suppl:S263-7.
PMID: 9266534 [PubMed - indexed for MEDLINE]
99:
 
No Abstract
Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.
Am J Hum Genet. 1996 Jul;59(1):248-52. No abstract available.
PMID: 8659531 [PubMed - indexed for MEDLINE]
100:
 
Abstract
The interaction of Q analogs, particularly hydroxydecyl benzoquinone (idebenone), with the respiratory complexes of heart mitochondria.
Arch Biochem Biophys. 1996 Jun 15;330(2):395-400.
PMID: 8660670 [PubMed - indexed for MEDLINE]
101:
 
Abstract
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.
Am J Med Genet. 1996 Feb 2;61(4):356-62.
PMID: 8834048 [PubMed - indexed for MEDLINE]
102:
 
Abstract
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.
Biochem Biophys Res Commun. 1995 May 25;210(3):880-8.
PMID: 7763260 [PubMed - indexed for MEDLINE]
103:
 
No Abstract
Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy.
J Neurol Neurosurg Psychiatry. 1995 May;58(5):640-1. No abstract available.
PMID: 7745422 [PubMed - indexed for MEDLINE]
104:
 
No Abstract
Lack of association between mitochondrial tRNA(Leu(UUR)) point mutation and cluster headache.
Lancet. 1995 Apr 29;345(8957):1120-1. No abstract available.
PMID: 7715370 [PubMed - indexed for MEDLINE]
105:
 
Abstract
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.
FEBS Lett. 1994 Oct 3;352(3):375-9.
PMID: 7926004 [PubMed - indexed for MEDLINE]
106:
 
No Abstract
Ceftriaxone is ineffective in ALS.
Ital J Neurol Sci. 1994 Feb;15(1):66. No abstract available.
PMID: 8206750 [PubMed - indexed for MEDLINE]
107:
 
Abstract
Testing models for genetic determination in migraine.
Cephalalgia. 1993 Dec;13(6):389-94.
PMID: 8313452 [PubMed - indexed for MEDLINE]
108:
 
Abstract
1H-NMR study and structure determination of 4,4- and 4,6-dimers from electrochemical reduction of NADP+.
Biochim Biophys Acta. 1991 Jan 8;1076(1):37-48.
PMID: 1986794 [PubMed - indexed for MEDLINE]
109:
 
Abstract
Adriamycin-catalyzed aerobic photooxidation of NAD dimers to NAD+.
Biochim Biophys Acta. 1989 Apr 25;991(1):25-9.
PMID: 2540842 [PubMed - indexed for MEDLINE]
110:
 
No Abstract
Zero-order drug release from monolithic polydimethylsiloxane matrices through controlled polymer cracking.
Farmaco [Prat]. 1988 Apr;43(4):121-35. No abstract available.
PMID: 3208877 [PubMed - indexed for MEDLINE]
111:
 
Abstract
Photocatalyzed anaerobic oxidation of nicotinamide coenzyme dimers to NAD+ by adriamycin.
Free Radic Res Commun. 1988;4(6):397-402.
PMID: 3243503 [PubMed - indexed for MEDLINE]
112:
 
Abstract
Oxidation of nicotinamide coenzyme dimers by one-electron-accepting proteins.
Biochem J. 1986 Aug 1;237(3):919-22.
PMID: 3026335 [PubMed - indexed for MEDLINE]
113:
 
No Abstract
A study of molecular interactions in a petrolatum-based gel containing nonionic surfactants.
Pharm Acta Helv. 1986;61(7):198-204. No abstract available.
PMID: 3737620 [PubMed - indexed for MEDLINE]
114:
 
Abstract
Oxidation of NAD dimers by horseradish peroxidase.
Biochem J. 1985 Mar 1;226(2):391-5.
PMID: 3994664 [PubMed - indexed for MEDLINE]
115:
 
No Abstract
Release of osmotically active drugs from silicone rubber matrixes.
Farmaco [Prat]. 1984 Sep;39(9):310-9. No abstract available.
PMID: 6500025 [PubMed - indexed for MEDLINE]
116:
 
No Abstract
Effect of different water-soluble additives on the sustained release of sulfanilamide from silicone rubber matrices.
Farmaco [Prat]. 1983 Dec;37(12):377-89. No abstract available.
PMID: 6822285 [PubMed - indexed for MEDLINE]
117:
 
No Abstract
A study of drug-vehicle interactions in anhydrous polyethylene glycol ointments.
Farmaco [Prat]. 1983 Sep;38(9):323-33. No abstract available.
PMID: 6641920 [PubMed - indexed for MEDLINE]
118:
 
Abstract
Effect of different water-soluble additives on water sorption into silicone rubber.
J Pharm Sci. 1983 Mar;72(3):316-7.
PMID: 6842386 [PubMed - indexed for MEDLINE]
119:
 
Abstract
Evidence for binding of NAD dimers to NAD-dependent dehydrogenases.
Biochim Biophys Acta. 1981 Sep 15;661(1):120-3.
PMID: 7028119 [PubMed - indexed for MEDLINE]
120:
 
Abstract
Effect of tissue degeneration on drug transfer across in vitro rat intestine.
Farmaco [Sci]. 1981 Mar;36(3):166-80.
PMID: 7227503 [PubMed - indexed for MEDLINE]
121:
 
Abstract
Vehicle effects in percutaneous absorption: in vitro study of influence of solvent power and microscopic viscosity of vehicle on benzocaine release from suspension hydrogels.
J Pharm Sci. 1980 Apr;69(4):387-91.
PMID: 7373530 [PubMed - indexed for MEDLINE]
122:
 
No Abstract
A method for studying drug complexation in semisolid vehicles.
Farmaco [Prat]. 1978 Jan;33(1):3-21. No abstract available.
PMID: 624378 [PubMed - indexed for MEDLINE]
123:
 
No Abstract
Release of drugs from ointment bases. III. Influence of the membrane and receiving phase on in vitro release of progesterone from two different vehicles.
Farmaco [Prat]. 1977 Dec;32(12):591-610. No abstract available.
PMID: 590491 [PubMed - indexed for MEDLINE]
124:
 
No Abstract
The self-inhibited leaky integrator: transfer functions and steady state relations.
Biol Cybern. 1975 Oct 1;20(1):51-9. No abstract available.
PMID: 171005 [PubMed - indexed for MEDLINE]
125:
 
No Abstract
A new reaction of bis(o-aminopheyl)disulfide with keto-compounds. II. Reaction with 17-beta-hydroxy-5-alpha-androstan-3-one.
Tetrahedron Lett. 1968 Jun;32:3561-4. No abstract available.
PMID: 5654064 [PubMed - indexed for MEDLINE]
126:
 
No Abstract
Synthesis of pyrrolo[1,2-a]benzo[f]indole derivatives.
Tetrahedron Lett. 1967 Mar;9:765-9. No abstract available.
PMID: 6040275 [PubMed - indexed for MEDLINE]
127:
 
No Abstract
[Separation of some constituents of the ether extracts of male fern by chromatography of polyamides.]
Farmaco [Prat]. 1961 Jul;16:318-23. Italian. No abstract available.
PMID: 14448608 [PubMed - indexed for MEDLINE]
128:
 
No Abstract
[N-Picoline-substituted anilides with local anesthetic action.]
Farmaco [Sci]. 1961 Jun;16:375-86. Italian. No abstract available.
PMID: 14448605 [PubMed - indexed for MEDLINE]
129:
 
No Abstract
[Picoline derivatives of ethylenediamine with local anesthetic activity.]
Farmaco [Sci]. 1960 Dec;15:803-8. Italian. No abstract available.
PMID: 14448607 [PubMed - indexed for MEDLINE]
130:
 
No Abstract
[On the N-picolyl-N-diethylaminoethylsulfanilamides and their penicillin salts.]
Farmaco [Sci]. 1960 Dec;15:797-802. Italian. No abstract available.
PMID: 14448606 [PubMed - indexed for MEDLINE]
131:
 
No Abstract
[Separation of the principle anthraquinone compounds of rhubarb my means of chromatography on polyamides.]
Farmaco [Prat]. 1957 Apr;12(4):184-91. Italian. No abstract available.
PMID: 13438024 [PubMed - indexed for MEDLINE]
132:
 
No Abstract
[X-ray analysis in the toxicological research on alkaloids and synthetic narcotics.]
Farmaco [Sci]. 1956;11(4):317-35. Italian. No abstract available.
PMID: 13330859 [PubMed - indexed for MEDLINE]
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