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Results of search for 'au:"Rötig, A"', page 1 of 8
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Authors
Barrientos, A
Boddaert, N
Bonnefont, J P
Bourgeron, T
Chretien, D
Chrétien, D
Cormier, V
Cormier-Daire, V
Desguerre, I
Lebre, A S
Munnich, A
Niaudet, P
Parfait, B
Rabier, D
Rotig, A
Rustin, P
Rötig, A
Saudubray, J M
de Lonlay, P
von Kleist-Retzow, J C
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Adult
Base Sequence
Child
Child, Preschool
DNA, Mitochondrial
Electron Transport
Female
Humans
Infant
Infant, Newborn
Male
Mitochondria
Molecular Sequence Data
Mutation
complications
deficiency
diagnosis
enzymology
genetics
metabolism
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Your search returned 143 results.
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1.
[Mitochondrial cytopathies].
[electronic resource]
by
Rötig, A
Producer:
19961028
In:
Pathologie-biologie
vol. 44
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2.
Genetics of mitochondrial respiratory chain deficiencies.
[electronic resource]
by
Rötig, A
Producer:
20150110
In:
Revue neurologique
vol. 170
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3.
[Metabolic, enzymological and molecular assessment of mitochondrial cytopathies].
[electronic resource]
by
Munnich, A
Rotig, A
Producer:
19920311
In:
Pediatrie
vol. 46
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4.
Renal involvement in mitochondrial cytopathies.
[electronic resource]
by
Niaudet, P
Rötig, A
Producer:
19961204
In:
Pediatric nephrology (Berlin, Germany)
vol. 10
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5.
The kidney in mitochondrial cytopathies.
[electronic resource]
by
Niaudet, P
Rotig, A
Producer:
19970620
In:
Kidney international
vol. 51
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6.
Homologous and heterologous expression of a ribosomal protein gene in Podospora anserina requires an intron.
[electronic resource]
by
Dequard-Chablat, M
Rötig, A
Producer:
19970331
In:
Molecular & general genetics : MGG
vol. 253
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7.
Quinone analogs prevent enzymes targeted in Friedreich ataxia from iron-induced injury in vitro.
[electronic resource]
by
Rustin, P
Munnich, A
Rötig, A
Producer:
19990908
In:
BioFactors (Oxford, England)
vol. 9
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8.
[Friedreich's ataxia and mitochondria: the puzzle reconstructed].
[electronic resource]
by
Rötig, A
Munnich, A
Rustin, P
Producer:
19990729
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 6 Suppl 2
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9.
Kearns-Sayre's syndrome developing in a boy who survived pearson's syndrome caused by mitochondrial DNA deletion.
[electronic resource]
by
Simonsz, H J
Bärlocher, K
Rötig, A
Producer:
19930715
In:
Documenta ophthalmologica. Advances in ophthalmology
vol. 82
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10.
Mitochondrial diabetes mellitus.
[electronic resource]
by
Rötig, A
Bonnefont, J P
Munnich, A
Producer:
19961203
In:
Diabetes & metabolism
vol. 22
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11.
[Mitochondrial diabetes].
[electronic resource]
by
Rötig, A
Bonnefont, J P
Munnich, A
Producer:
19970917
In:
Journees annuelles de diabetologie de l'Hotel-Dieu
p. 33-42
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12.
Renal involvement in mitochondrial cytopathies.
[electronic resource]
by
Grünfeld, J P
Niaudet, P
Rötig, A
Producer:
19961008
In:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
vol. 11
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13.
Phenotypic expression of mitochondrial genotypes in cultured skin fibroblasts and in Epstein-Barr virus-transformed lymphocytes in Pearson syndrome.
[electronic resource]
by
Rötig, A
Bourgeron, T
Rustin, P
Munnich, A
Producer:
19950808
In:
Muscle & nerve. Supplement
vol. 3
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14.
Co-amplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations.
[electronic resource]
by
Parfait, B
Rustin, P
Munnich, A
Rötig, A
Producer:
19980701
In:
Biochemical and biophysical research communications
vol. 247
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15.
Expression study of genes involved in iron metabolism in human tissues.
[electronic resource]
by
Rötig, A
Chantrel-Groussard, K
Munnich, A
Rustin, P
Producer:
20010419
In:
Biochemical and biophysical research communications
vol. 281
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16.
The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscle.
[electronic resource]
by
Chretien, D
Bourgeron, T
Rötig, A
Munnich, A
Rustin, P
Producer:
19910124
In:
Biochemical and biophysical research communications
vol. 173
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17.
Isolation and characterization of mitochondria from human B lymphoblastoid cell lines.
[electronic resource]
by
Bourgeron, T
Chretien, D
Rötig, A
Munnich, A
Rustin, P
Producer:
19920814
In:
Biochemical and biophysical research communications
vol. 186
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18.
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome.
[electronic resource]
by
Rötig, A
Bourgeron, T
Chretien, D
Rustin, P
Munnich, A
Producer:
19951215
In:
Human molecular genetics
vol. 4
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19.
Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte cultures.
[electronic resource]
by
Bourgeron, T
Chretien, D
Rötig, A
Munnich, A
Rustin, P
Producer:
19931007
In:
The Journal of biological chemistry
vol. 268
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20.
Nicotinamide adenine dinucleotides permeate through mitochondrial membranes in human Epstein-Barr virus-transformed lymphocytes.
[electronic resource]
by
Rustin, P
Chretien, D
Parfait, B
Rötig, A
Munnich, A
Producer:
19971103
In:
Molecular and cellular biochemistry
vol. 174
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