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Results of search for 'au:"Ionǎşescu, V"', page 2 of 7
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Authors
Anuras, S
Burmeister, L
Burns, T
Burns, T L
Cancilla, P
Conway, T W
Fischbeck, K H
Haines, J L
Hart, M
IONASESCU, V
Ionasescu, R
Ionasescu, V
Ionasescu, V V
Ionăşescu, V
LUCA, N
Luca, N
Sandra, A
Searby, C
Simpson, J
Zellweger, H
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Adolescent
Adult
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Collagen
Creatine Kinase
Female
Genetic Linkage
Humans
Male
Middle Aged
Muscle Proteins
Muscles
Muscular Dystrophies
Pedigree
X Chromosome
biosynthesis
genetics
metabolism
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21.
STUDIES ON CARBOHYDRATE METABOLISM IN AMYOTROPHIC LATERAL SCLEROSIS AND HEREDITARY PROXIMAL SPINAL MUSCULAR ATROPHY.
[electronic resource]
by
Ionǎşescu, V
Luca, N
Producer:
19961201
In:
Acta neurologica Scandinavica
vol. 40
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22.
Electroencephalographic findings in two families with Friedreich's ataxia.
[electronic resource]
by
CRIGHEL, E
IONASESCU, V
Producer:
19981101
In:
Confinia neurologica
vol. 22
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23.
Duchenne muscular dystrophy in young girls?
[electronic resource]
by
Ionasescu, V
Zellweger, H
Producer:
19750127
In:
Acta neurologica Scandinavica
vol. 50
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24.
Variant of Bixler syndrome.
[electronic resource]
by
Ionasescu, V
Roberts, R J
Producer:
19750110
In:
Journal de genetique humaine
vol. 22
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25.
Alterations in lipid turnover in developing muscle.
[electronic resource]
by
Sandra, A
Ionasescu, V V
Producer:
19800815
In:
Biochemical and biophysical research communications
vol. 93
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26.
Fetal serum-creatine-phosphokinase not a valid predictor of Duchenne muscular dystrophy.
[electronic resource]
by
Ionasescu, V
Zelleger, H
Cancilla, P
Producer:
19790221
In:
Lancet (London, England)
vol. 2
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27.
Detection of carriers and genetic counseling in duchenne muscular dystrophy by ribosomal protein synthesis.
[electronic resource]
by
Ionasescu, V
Zellweger, H
Burmeister, L
Producer:
19770129
In:
Acta neurologica Scandinavica
vol. 54
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28.
Frequency of new mutants among boys with Duchenne muscular dystrophy.
[electronic resource]
by
Bucher, K
Ionasescu, V
Hanson, J
Producer:
19810528
In:
American journal of medical genetics
vol. 7
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29.
Twenty years-Iowa muscle clinic: reminiscences and prospects.
[electronic resource]
by
Zellweger, H
Simpson, J
Ionasescu, V
Producer:
19820708
In:
European journal of pediatrics
vol. 138
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30.
Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
Searby, C
Producer:
19961209
In:
American journal of medical genetics
vol. 63
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31.
Teratogenic effect of anticonvulsant drugs.
[electronic resource]
by
Waziri, M
Ionasescu, V
Zellweger, H
Producer:
19761101
In:
American journal of diseases of children (1960)
vol. 130
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32.
Trisomy 22.
[electronic resource]
by
Zellweger, H
Ionasescu, V
Simpson, J
Producer:
19751211
In:
Journal de genetique humaine
vol. 23
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33.
Neurogenic control of muscle ribosomal protein synthesis.
[electronic resource]
by
Ionasescu, V
Lewis, R
Schottelius, B
Producer:
19760410
In:
Acta neurologica Scandinavica
vol. 51
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34.
Respiratory control and oxidative phosphorylation in the dystrophic muscle.
[electronic resource]
by
Ionăşescu, V
Luca, N
Vuia, O
Producer:
19680428
In:
Acta neurologica Scandinavica
vol. 43
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35.
Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy.
[electronic resource]
by
Ionasescu, V
Searby, C
Ionasescu, R
Producer:
19940718
In:
Human molecular genetics
vol. 3
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36.
Trisomy 22.
[electronic resource]
by
Zellweger, H
Ionasescu, V
Simpson, J
Producer:
19760410
In:
Journal de genetique humaine
vol. 23 SUPPL
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37.
Intestinal pseudo-obstruction in adult spinal muscular atrophy.
[electronic resource]
by
Ionasescu, V
Christensen, J
Hart, M
Producer:
19940823
In:
Muscle & nerve
vol. 17
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38.
Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophy.
[electronic resource]
by
Zellweger, H
Ionasescu, V
Simpson, J
Producer:
19810327
In:
Helvetica paediatrica acta
vol. 35
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39.
Fibroblast clones for detection of Duchenne carriers.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
Searby, C
Producer:
19830729
In:
The New England journal of medicine
vol. 309
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40.
Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.
[electronic resource]
by
Ionasescu, V
Hug, G
Hoppel, C
Producer:
19810129
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 43
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