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Results of search for 'au:"Tulinius, M"', page 1 of 3
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Authors
Andersen, O
Andersson, S
Darin, N
Eriksson, B O
Holme, E
Holmgren, D
Houshmand, M
Karlsson, J
Kimber, E
Kristiansson, B
Kroksmark, A K
Kroksmark, A-K
Larsson, N G
Magnusson, P
Moslemi, A R
Moslemi, A-R
Oldfors, A
Swolin-Eide, D
Tulinius, M
Tulinius, M H
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Topics
Acidosis, Lactic
Adolescent
Adult
Child
Child, Preschool
Chromosome Deletion
DNA Mutational Analysis
DNA, Mitochondrial
Female
Humans
Infant
Infant, Newborn
Male
Mitochondria, Muscle
Mutation
complications
diagnosis
enzymology
genetics
metabolism
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Languages
English
Swedish
Your search returned 44 results.
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1.
Mitochondrial myopathies. Clinical and diagnostic aspects.
[electronic resource]
by
Tulinius, M H
Producer:
19990805
In:
Scandinavian journal of rehabilitation medicine. Supplement
vol. 39
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2.
Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden.
[electronic resource]
by
Darin, N
Tulinius, M
Producer:
20000307
In:
Neuromuscular disorders : NMD
vol. 10
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3.
EEG findings in children and adolescents with mitochondrial encephalomyopathies: a study of 25 cases.
[electronic resource]
by
Tulinius, M H
Hagne, I
Producer:
19911121
In:
Brain & development
vol. 13
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4.
Early-onset myopathy with tubular aggregates.
[electronic resource]
by
Tulinius, M H
Lundberg, A
Oldfors, A
Producer:
19970206
In:
Pediatric neurology
vol. 15
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5.
Muscle strength and motor function in children and adolescents with spinal muscular atrophy II and III.
[electronic resource]
by
Kroksmark, A K
Beckung, E
Tulinius, M
Producer:
20011205
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
vol. 5
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6.
[DNA diagnosis of mitochondrial diseases is now possible].
[electronic resource]
by
Larsson, N G
Holme, E
Tulinius, M H
Producer:
19900117
In:
Lakartidningen
vol. 86
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7.
[Mitochondrial diseases in children--a review].
[electronic resource]
by
Holme, E
Kristiansson, B
Oldfors, A
Tulinius, M
Producer:
19871014
In:
Lakartidningen
vol. 84
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8.
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibres.
[electronic resource]
by
Oldfors, A
Holme, E
Tulinius, M
Larsson, N G
Producer:
19960119
In:
Acta neuropathologica
vol. 90
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9.
Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibres.
[electronic resource]
by
Moslemi, A R
Tulinius, M
Holme, E
Oldfors, A
Producer:
19981021
In:
Neuromuscular disorders : NMD
vol. 8
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10.
Inheritance and expression of mitochondrial DNA point mutations.
[electronic resource]
by
Holme, E
Tulinius, M H
Larsson, N G
Oldfors, A
Producer:
19950807
In:
Biochimica et biophysica acta
vol. 1271
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11.
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas.
[electronic resource]
by
Larsson, N G
Tulinius, M H
Holme, E
Oldfors, A
Producer:
19950808
In:
Muscle & nerve. Supplement
vol. 3
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12.
A case of Kearns-Sayre syndrome with metaphyseal dysplasia.
[electronic resource]
by
Wilson, B
Claësson, I
Forsell, C
Tulinius, M
Hagberg, B
Producer:
19930722
In:
Pediatric radiology
vol. 23
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13.
Cytochrome c oxidase deficiency in infancy.
[electronic resource]
by
Oldfors, A
Sommerland, H
Holme, E
Tulinius, M
Kristiansson, B
Producer:
19890418
In:
Acta neuropathologica
vol. 77
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14.
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation.
[electronic resource]
by
Tajsharghi, H
Kimber, E
Holmgren, D
Tulinius, M
Oldfors, A
Producer:
20070322
In:
Neurology
vol. 68
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15.
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.
[electronic resource]
by
Larsson, N G
Holme, E
Kristiansson, B
Oldfors, A
Tulinius, M
Producer:
19901011
In:
Pediatric research
vol. 28
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16.
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities.
[electronic resource]
by
Darin, N
Oldfors, A
Moslemi, A R
Holme, E
Tulinius, M
Producer:
20010419
In:
Annals of neurology
vol. 49
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17.
Two new mutations in the MTATP6 gene associated with Leigh syndrome.
[electronic resource]
by
Moslemi, A-R
Darin, N
Tulinius, M
Oldfors, A
Holme, E
Producer:
20060117
In:
Neuropediatrics
vol. 36
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18.
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis.
[electronic resource]
by
Kimber, E
Tajsharghi, H
Kroksmark, A-K
Oldfors, A
Tulinius, M
Producer:
20060913
In:
Neurology
vol. 67
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19.
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne.
[electronic resource]
by
Houshmand, M
Larsson, N G
Oldfors, A
Tulinius, M
Holme, E
Producer:
19960920
In:
Human genetics
vol. 97
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20.
Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes.
[electronic resource]
by
Tulinius, M H
Holme, E
Kristiansson, B
Larsson, N G
Oldfors, A
Producer:
19910904
In:
The Journal of pediatrics
vol. 119
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