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Results of search for 'au:"Ionǎşescu, V"', page 6 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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Topics
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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Your search returned 138 results.
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101.
Protein synthesis in muscle cultures from patients with Duchenne muscular dystrophy. Calcium and A23187 ionophore dependent changes.
[electronic resource]
by
Ionasescu, V
Zellweger, H
Ionasescu, R
Lara-Braud, C
Cancilla, P A
Producer:
19761020
In:
Acta neurologica Scandinavica
vol. 54
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102.
Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy.
[electronic resource]
by
Ionasescu, V V
Trofatter, J
Haines, J L
Ionasescu, R
Searby, C
Producer:
19920520
In:
Neurology
vol. 42
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103.
Glycogenosis. IV. A new cause of infantile hypotonia.
[electronic resource]
by
Zellweger, H
Mueller, S
Ionasescu, V
Schochet, S S
McCormick, W F
Producer:
19720621
In:
The Journal of pediatrics
vol. 80
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104.
Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2).
[electronic resource]
by
Ionasescu, V
Anderson, R
Burns, T L
Searby, C
Ionasescu, R
Ferrell, R
Producer:
19880223
In:
American journal of human genetics
vol. 42
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105.
Late-onset oculogastrointestinal muscular dystrophy.
[electronic resource]
by
Ionasescu, V V
Thompson, H S
Aschenbrener, C
Anuras, S
Risk, W S
Producer:
19841115
In:
American journal of medical genetics
vol. 18
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106.
Small intestinal motility in myotonic dystrophy patients.
[electronic resource]
by
Nowak, T V
Anuras, S
Brown, B P
Ionasescu, V
Green, J B
Producer:
19840511
In:
Gastroenterology
vol. 86
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107.
Hypokalemic periodic paralysis. Low activity of sarcoplasmic reticulum and muscle ribosomes during an induced attack.
[electronic resource]
by
Ionasescu, V
Schochet, S S
Powers, J M
Koob, K
Conway, T W
Producer:
19740612
In:
Journal of the neurological sciences
vol. 21
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108.
Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).
[electronic resource]
by
Ionasescu, V
Searby, C
Sheffield, V C
Roklina, T
Nishimura, D
Ionasescu, R
Producer:
19970108
In:
Human molecular genetics
vol. 5
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109.
Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene.
[electronic resource]
by
Ionasescu, V V
Searby, C C
Ionasescu, R
Reisin, R
Ruggieri, V
Arberas, C
Producer:
19971023
In:
Muscle & nerve
vol. 20
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110.
A mitochondrial tRNA anticodon swap associated with a muscle disease.
[electronic resource]
by
Moraes, C T
Ciacci, F
Bonilla, E
Ionasescu, V
Schon, E A
DiMauro, S
Producer:
19930924
In:
Nature genetics
vol. 4
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111.
Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene.
[electronic resource]
by
Ionasescu, V V
Searby, C C
Ionasescu, R
Chatkupt, S
Patel, N
Koenigsberger, R
Producer:
19970213
In:
Muscle & nerve
vol. 20
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112.
Linkage studies of X-linked recessive spastic paraplegia using DNA probes.
[electronic resource]
by
Kenwrick, S
Ionasescu, V
Ionasescu, G
Searby, C
King, A
Dubowitz, M
Davies, K E
Producer:
19860917
In:
Human genetics
vol. 73
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113.
Alterations in lipid incorporation in Duchenne muscular dystrophy. Studies of fresh and cultured muscle.
[electronic resource]
by
Ionasescu, V
Monaco, L
Sandra, A
Ionasescu, R
Burmeister, L
Deprosse, C
Stern, L Z
Producer:
19810723
In:
Journal of the neurological sciences
vol. 50
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114.
Alterations in creatine kinase in fresh muscle and cell cultures in Duchenne dystrophy.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
Feld, R
Witte, D
Cancilla, P
Kaeding, L
Stern, L Z
Producer:
19810625
In:
Annals of neurology
vol. 9
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115.
X-linked recessive Charcot-Marie-Tooth neuropathy: clinical and genetic study.
[electronic resource]
by
Ionasescu, V V
Trofatter, J
Haines, J L
Summers, A M
Ionasescu, R
Searby, C
Producer:
19920507
In:
Muscle & nerve
vol. 15
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116.
Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.
[electronic resource]
by
Ionasescu, V V
Trofatter, J
Haines, J L
Summers, A M
Ionasescu, R
Searby, C
Producer:
19910626
In:
American journal of human genetics
vol. 48
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117.
Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I).
[electronic resource]
by
Ionasescu, V
Murray, J C
Burns, T L
Ionasescu, R
Ferrell, R
Searby, C
Chirgwin, J
Producer:
19870918
In:
Journal of the neurological sciences
vol. 80
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118.
Magnetic resonance imaging of children with Duchenne muscular dystrophy.
[electronic resource]
by
Schreiber, A
Smith, W L
Ionasescu, V
Zellweger, H
Franken, E A
Dunn, V
Ehrhardt, J
Producer:
19880113
In:
Pediatric radiology
vol. 17
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119.
Altered protein synthesis and creatine kinase in breast muscle cell cultures from dystrophic chick embryos.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
White, D
Feld, R
Cancilla, P
Kaeding, L
Kraus, L
Stern, L
Producer:
19800815
In:
Journal of the neurological sciences
vol. 46
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120.
A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8.
[electronic resource]
by
Ionasescu, V V
Kimura, J
Searby, C C
Smith, W L
Ross, M A
Ionasescu, R
Producer:
19960522
In:
Muscle & nerve
vol. 19
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