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Results:
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Results: 13
Authors:
VALANNE L
KETONEN L
MAJANDER A
SUOMALAINEN A
PIHKO H
Citation: L. Valanne et al., NEURORADIOLOGIC FINDINGS IN CHILDREN WITH MITOCHONDRIAL DISORDERS, American journal of neuroradiology, 19(2), 1998, pp. 369-377
Authors:
SUOMALAINEN A
MAJANDER A
WALLIN M
SETALA K
KONTULA K
LEINONEN H
SALMI T
PAETAU A
HALTIA M
VALANNE L
LONNQVIST J
PELTONEN L
SOMER H
Citation: A. Suomalainen et al., AUTOSOMAL-DOMINANT PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MULTIPLEDELETIONS OF MTDNA - CLINICAL, BIOCHEMICAL, AND MOLECULAR-GENETIC FEATURES OF THE 10Q-LINKED DISEASE, Neurology, 48(5), 1997, pp. 1244-1253
Authors:
MAJANDER A
LAMMINEN T
JUVONEN V
AULA P
NIKOSKELAINEN E
SAVONTAUS ML
WIKSTROM M
Citation: A. Majander et al., MUTATIONS IN SUBUNIT-6 OF THE F1F0-ATP SYNTHASE CAUSE 2 ENTIRELY DIFFERENT DISEASES, FEBS letters, 412(2), 1997, pp. 351-354
Authors:
TYNI T
MAJANDER A
KALIMO H
RAPOLA J
PIHKO H
Citation: T. Tyni et al., PATHOLOGY OF SKELETAL-MUSCLE AND IMPAIRED RESPIRATORY-CHAIN FUNCTION IN LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY WITH THE G1528C MUTATION, Neuromuscular disorders, 6(5), 1996, pp. 327-337
Authors:
FELLMAN V
PIHKO H
MAJANDER A
SEYBERTH HW
Citation: V. Fellman et al., SEVERE HYPERPROSTAGLANDIN-E SYNDROME WITH HYPERTHYROIDISM - STUDIES OF PATHOGENETIC MECHANISMS, Journal of inherited metabolic disease, 19(5), 1996, pp. 687-694
Authors:
MAJANDER A
FINEL M
SAVONTAUS ML
NIKOSKELAINEN E
WIKSTROM M
Citation: A. Majander et al., CATALYTIC ACTIVITY OF COMPLEX-I IN CELL-LINES THAT POSSESS REPLACEMENT MUTATIONS IN THE ND GENES IN LEBERS HEREDITARY OPTIC NEUROPATHY, European journal of biochemistry, 239(1), 1996, pp. 201-207
Authors:
MAJANDER A
PIHKO H
SANTAVUORI P
Citation: A. Majander et al., PALMITATE OXIDATION IN MUSCLE MITOCHONDRIA OF PATIENTS WITH THE JUVENILE FORM OF NEURONAL CEROID-LIPOFUSCINOSIS, American journal of medical genetics, 57(2), 1995, pp. 298-300
Authors:
MAKELABENGS P
SUOMALAINEN A
MAJANDER A
RAPOLA J
KALIMO H
NUUTILA A
PIHKO H
Citation: P. Makelabengs et al., CORRELATION BETWEEN THE CLINICAL SYMPTOMS AND THE PROPORTION OF MITOCHONDRIAL-DNA CARRYING THE 8993-POINT MUTATION IN THE NARP SYNDROME, Pediatric research, 37(5), 1995, pp. 634-639
Authors:
MAJANDER A
RAPOLA J
SARIOLA H
SUOMALAINEN A
POHJAVUORI M
PIHKO H
Citation: A. Majander et al., DIAGNOSIS OF FATAL INFANTILE DEFECTS OF THE MITOCHONDRIAL RESPIRATORY-CHAIN - AGE-DEPENDENCE AND POSTMORTEM ANALYSIS OF ENZYME-ACTIVITIES, Journal of the neurological sciences, 134(1-2), 1995, pp. 95-102
Authors:
LAMMINEN T
MAJANDER A
JUVONEN V
WIKSTROM M
AULA P
NIKOSKELAINEN E
SAVONTAUS ML
Citation: T. Lamminen et al., A MITOCHONDRIAL MUTATION AT NT-9101 IN THE ATP SYNTHASE-6 GENE ASSOCIATED WITH DEFICIENT OXIDATIVE-PHOSPHORYLATION IN A FAMILY WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY, American journal of human genetics, 56(5), 1995, pp. 1238-1240
Authors:
MAJANDER A
FINEL M
WIKSTROM M
Citation: A. Majander et al., DIPHENYLENEIODONIUM INHIBITS REDUCTION OF IRON-SULFUR CLUSTERS IN THEMITOCHONDRIAL NADH-UBIQUINONE OXIDOREDUCTASE (COMPLEX-I), The Journal of biological chemistry, 269(33), 1994, pp. 21037-21042
Authors:
FINEL M
MAJANDER A
Citation: M. Finel et A. Majander, STUDIES ON THE PROTON-TRANSLOCATING NADH-UBIQUINONE OXIDOREDUCTASES OF MITOCHONDRIA AND ESCHERICHIA-COLI USING THE INHIBITOR, 1,10-PHENANTHROLINE, FEBS letters, 339(1-2), 1994, pp. 142-146
Authors:
SUOMALAINEN A
MAJANDER A
PIHKO H
PELTONEN L
SYVANEN AC
Citation: A. Suomalainen et al., QUANTIFICATION OF TRANSFER RNA(3243)(LEU) POINT MUTATION OF MITOCHONDRIAL-DNA IN MELAS PATIENTS AND ITS EFFECTS ON MITOCHONDRIAL TRANSCRIPTION, Human molecular genetics, 2(5), 1993, pp. 525-534
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