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Results of search for 'au:"Ionâşescu, V"', page 5 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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81.
Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature.
[electronic resource]
by
Schochet, S S
Zellweger, H
Ionasescu, V
McCormick, W F
Producer:
19720822
In:
Journal of the neurological sciences
vol. 16
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82.
Considerations on periarteritis nodosa; neurological aspects.
[electronic resource]
by
KREINDLER, A
IONESCU, I
MESTES, D
IONASESCU, V
GOLDENBERG, M
Producer:
20000701
In:
Rumanian medical review
vol. 1
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83.
Biochemical abnormalities of muscle ribosomes during attacks of hyperkalemic periodic paralysis.
[electronic resource]
by
Ionasescu, V
Zellweger, H
Schochet, S S
Conway, T W
Producer:
19731014
In:
Journal of the neurological sciences
vol. 19
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84.
The role of collagen in the pathogenesis of idiopathic clubfoot. Biochemical and electron microscopic correlations.
[electronic resource]
by
Ionasescu, V
Maynard, J A
Ponseti, I V
Zellweger, H
Producer:
19750201
In:
Helvetica paediatrica acta
vol. 29
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85.
Inherited metabolic myopathy with storage of glycoproteins and glycosaminoglycans.
[electronic resource]
by
Ionasescu, V
Pedrini, V
Aschenbrener, C
Ionasescu, R
Searby, C
Producer:
19840827
In:
American journal of medical genetics
vol. 18
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86.
Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplication.
[electronic resource]
by
Ionasescu, V V
Ionasescu, R
Searby, C
Barker, D F
Producer:
19930702
In:
Human molecular genetics
vol. 2
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87.
Protein synthesis in muscle cultures from patients with myotonic dystrophy. Influence of A23187 ionophore and calcium: preliminary investigation.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
Cancilla, P
Kahn, L
Zellweger, H
Producer:
19781025
In:
European neurology
vol. 16
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88.
Duchenne muscular dystrophy in monozygotic twins: deletion of 5' fragments of the gene.
[electronic resource]
by
Ionasescu, V V
Searby, C C
Ionasescu, R
Patil, S
Producer:
19890814
In:
American journal of medical genetics
vol. 33
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89.
Fibroblast cultures in Duchenne muscular dystrophy. Alterations in synthesis and secretion of collagen and noncollagen proteins.
[electronic resource]
by
Ionasescu, V
Lara-Braud, C
Zellweger, H
Ionasescu, R
Burmeister, L
Producer:
19770611
In:
Acta neurologica Scandinavica
vol. 55
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90.
Muscle ribosomal protein synthesis in normal pregnancy: implication for carrier detection in Duchenne muscular dystrophy.
[electronic resource]
by
Ionasescu, V
White, C
Zellweger, H
Lewis, R
Conway, T W
Producer:
19740917
In:
Journal of medical genetics
vol. 11
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91.
The human connexin32 gene is transcribed from two tissue-specific promoters.
[electronic resource]
by
Neuhaus, I M
Bone, L
Wang, S
Ionasescu, V
Werner, R
Producer:
19961217
In:
Bioscience reports
vol. 16
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92.
Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation.
[electronic resource]
by
Rummelt, V
Folberg, R
Ionasescu, V
Yi, H
Moore, K C
Producer:
19940119
In:
Ophthalmology
vol. 100
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93.
Cardiac manifestations of the mucopolysaccharidoses.
[electronic resource]
by
Schieken, R M
Kerber, R E
Ionasescu, V V
Zellweger, H
Producer:
19751126
In:
Circulation
vol. 52
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94.
Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1.
[electronic resource]
by
Ionasescu, V
Burns, T
Searby, C
Ionasescu, R
Whitehead, A S
Producer:
19880727
In:
Cytogenetics and cell genetics
vol. 47
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95.
[Duchenne's muscular dystrophy: also in girls?].
[electronic resource]
by
Ludescher, E
Müller, G
Ketelsen, U P
Zellweger, H
Ionasescu, V
Producer:
19840613
In:
Padiatrie und Padologie
vol. 19
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96.
Frequency of cerebral infarction in patients with inherited neuromuscular diseases.
[electronic resource]
by
Biller, J
Ionasescu, V
Zellweger, H
Adams, H P
Schultz, D T
Producer:
19870817
In:
Stroke
vol. 18
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97.
Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy.
[electronic resource]
by
Ionasescu, V V
Searby, C
Ionasescu, R
Neuhaus, I M
Werner, R
Producer:
19961126
In:
Neurology
vol. 47
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98.
Muscle ribosome detachment factor. Does it have a role in the pathogenesis of Duchenne muscular dystrophy?
[electronic resource]
by
Ionasescu, V
Braga, S
Kaeding, L
Rubenstein, P
Kalnitsky, G
Chatterjee, R
Producer:
19820313
In:
Acta neurologica Scandinavica
vol. 64
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99.
Charcot-Marie-Tooth neuropathy related to chromosome 1.
[electronic resource]
by
Ionasescu, V V
Trofatter, J
Haines, J L
Ionasescu, R
Searby, C
Producer:
19920818
In:
American journal of medical genetics
vol. 42
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100.
Giant axonal neuropathy: normal protein composition of neurofilaments.
[electronic resource]
by
Ionasescu, V
Searby, C
Rubenstein, P
Sandra, A
Cancilla, P
Robillard, J
Producer:
19830920
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 46
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