Kongressberichte

ordine alfabetico / ordine cronologico

Contenuto, in ordine alfabetico


	American Society of Human Genetics / 50th Annual Meeting
	Colloquium on Mitochondria and Myopathies
	Euromit 4, "The Fourth European Meeting on Mitochondrial Pathology, "
	Euromit 5, "The Fourth European Meeting on Mitochondrial Pathology, Venice"
	European Federation of Neurological Societies / 5th Congress of the

	European Human Genetics Conference 2000
	Mitochondria 2003
	Mitochondria in cell life and cell death
	SSIEM Cambridge 2000
	The Third Albany Conference on Frontiers of Mitochondrial Research

Contenuto, in ordine cronologico


June 2003	Mitochondria 2003

Sept. 2001	Euromit 5, "The Fourth European Meeting on Mitochondrial Pathology"

Oct. 2000	European Federation of Neurological Societies / 5th Congress of the

	American Society of Human Genetics / 50th Annual Meeting
Sept. 2000	The Third Albany Conference on Frontiers of Mitochondrial Research
	SSIEM Cambridge 2000
May 2000	European Human Genetics Conference 2000
Apr. 2000	Colloquium on Mitochondria and Myopathies
	Mitochondria in cell life and cell death
Sept. 1999	Euromit 4, "The Fourth European Meeting on Mitochondrial Pathology"


Giugno 2003	Mitochondria 2003
	San Diego, CA USA


	www.mitosoc.org www.mitoresearch.org Program: http://www.mitosoc.org/mito 2003/ScientificProgram.htm


Sett. 2001	Euromit 5, "The Fifth European Meeting on Mitochondrial Pathology" Venice International University - San Servolo Island
	Venice, Italy


	Submitted sbstracts

14. - 18.10. 2000 5th Congress of the European Federation of Neurological Societies

Copenhagen, Denmark

Selected abstacts:

High dose oxygen therapy in stroke

Mitochondrial encephalopathies: insights from advance in cell biology and MR spectroscopy

New in vivo PET and MR evidence of regulation of brain oxygen and glucose metabolism in health and disease

Rapidly progressive neurodegeneration in a patient with familial hearing loss and heteroplasmic mitochondrial tRNASer(UCN) mutation, mimicking a subacute progressive encephalitis


15. - 18.10.2000	50th Annual Meeting - The American Society of Human Genetics
	Boston, MA USA

congress homepage

Selected abstracts can be found in Am J Hum Genet 2000 Oct;67(4) Suppl 2
under abstract number:

53, 55, 60, 78, 88, 233, 280, 281, 439, 533, 556, 1017, 1018, 1161, 1163, 1166, 1183, 1275, 1282, 1357, 1401, 1484, 1501, 1612, 1613, 1614, 1615, 1618, 1621, 1878, 2008, 2009, 2011, 2013, 2014, 2015, 2106, 2218, 2436

(the respective volume is not available on internet)


Sett. 2000	The Third Albany Conference on Frontiers of Mitochondrial Research
	Rensselaerville, New York


	Archive of the meeting


Sett. 2000	SSIEM Cambridge 2000
	Cambride, UK


	Program of the VIII. International Congress Of Inborn Errors Of Metabolism Abstracts have been published in a suppl. of J Inherit Metab Dis.


Maggio 2000	EUROPEAN HUMAN GENETICS CONFERENCE 2000
	Amsterdam, The Netherlands

	congress homepage

selected abstracts (not available through the congress homepage any more):

Encephalomyopathy and dilated cardiomyopathy associated with a large deletion of mitochondrial DNA in a 6 month-old infant

A novel mitochondrial DNA mutation (T12297C) affecting an highly conserved base of tRNALeu(CUN) associated with Dilated Cardiomyopathy

Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus

Denaturing gradient gel electrophoresis (DGGE) screening for mutations in mitochondrial DNA from a family with a clinical presentation consistent with MERRF syndrome

Analysis of the mutation A1555G in mitochondrial DNA in Greek patients with sensorineural deafness

Application of Mitochondrial DNA (mtDNA) sequence analysis to special forensic genetics problems

Molecular Beacon based Real-Time Fluorescence PCR for high throughput mitochondrial point mutation detection

Genetic mapping of Autosomal Dominant Progressive External Ophthalmoplegia (adPEO) in a Belgian family

Genetic analysis of mitochondrial DNA markers from archeological bones and modern Hungarian populations

Mitochondrial DNA diversity in East Slavs

Mitochondrial disorders

Mutation in the heme A: farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency

The Human ABC7 Transporter: Gene Structure and Mutation in X-Linked Sideroblastic Anemia with Ataxia (XLSA/A) Causing Disruption of Cytosolic Iron-Sulfur Protein Biogenesis


Aprile 2000	Colloquium on Mitochondria and Myopathies
	Halle/Saale, Deutschland

Program, participants and abstracts of the Colloquium in April 2000
Program and abstracts have been published in Eur J Med Res 5 (Suppl I)

Publication of the PR-office of the University Halle


Aprile 2000	Mitochondria in cell life and cell death (FASEB Experimental Biology 2000 meeting)
	San Diego

	Summary in the J Physiol 2000 Nov:

Duchen MR. Symposium Overview. J Physiol 2000 Nov 15;529(Pt 1):2

Crompton M. Mitochondrial intermembrane junctional complexes and their role in cell death. J Physiol 2000 Nov 15;529(Pt 1):11-21

O'Rourke B. Pathophysiological and protective roles of mitochondrial ion channels. J Physiol 2000 Nov 15;529(Pt 1):23-36

Ricquier D, et al. Mitochondrial uncoupling proteins: from mitochondria to the regulation of energy balance. J Physiol 2000 Nov 15;529(Pt 1):3-10

Rizzuto R, et al. Mitochondria as all-round players of the calcium game.
J Physiol 2000 Nov 15;529(Pt 1):37-47

Maechler P, et al. Mitochondrial signals in glucose-stimulated insulin secretion in the beta cell. J Physiol 2000 Nov 15;529(Pt 1):49-56

Duchen MR. Mitochondria and calcium: from cell signalling to cell death.
J Physiol 2000 Nov 15;529(Pt 1):57-68


Sett. 1999	Euromit 4, "The Fourth European Meeting on Mitochondrial Pathology" Queens' College, Cambridge 1999
	Cambridge, UK


	Submitted sbstracts

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	© MITO^NET 2001		Aggiornato al: 25.03.2002