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Results of search for 'au:"Ionǎşescu, V"', page 3 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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41.
Discriminant analysis of ribosomal protein synthesis findings in carrier detection of Duchenne muscular dystrophy.
[electronic resource]
by
Ionasescu, V
Burmeister, L
Hanson, J
Producer:
19800923
In:
American journal of medical genetics
vol. 5
Online resources:
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42.
Prenatal diagnosis of Duchenne muscular dystrophy based on Xp21.2 deletion.
[electronic resource]
by
Ionasescu, V V
Searby, C
Ionasescu, R
Producer:
19860917
In:
Neurology
vol. 36
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43.
Gastrointestinal manifestations of the muscular dystrophies.
[electronic resource]
by
Nowak, T V
Ionasescu, V
Anuras, S
Producer:
19820521
In:
Gastroenterology
vol. 82
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44.
Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B.
[electronic resource]
by
Hayasaka, K
Takada, G
Ionasescu, V V
Producer:
19931230
In:
Human molecular genetics
vol. 2
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45.
Ribosomal protein synthesis in Duchenne muscular dystrophy.
[electronic resource]
by
Ionasescu, V
Zellweger, H
Conway, T W
Producer:
19720113
In:
Archives of biochemistry and biophysics
vol. 144
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46.
[Genetic neurological diseases].
[electronic resource]
by
Ionăşescu, V
Roşianu, C
Drincă-Ionescu, M
Producer:
19680203
In:
Studii si cercetari de neurologie
vol. 12
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47.
[Muscular dystrophies].
[electronic resource]
by
Zellweger, H
Ionasescu, V
Conway, T W
Producer:
19720818
In:
Schweizerische medizinische Wochenschrift
vol. 102
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48.
Screening of dominantly inherited Charcot-Marie-Tooth neuropathies.
[electronic resource]
by
Ionasescu, V V
Ionasescu, R
Searby, C
Producer:
19931118
In:
Muscle & nerve
vol. 16
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49.
[Myasthenia with respiratory onset].
[electronic resource]
by
Ionăşescu, V
Nereanţiu, F
Patrichi-Macovei, M
Producer:
19671028
In:
Neurologia, psihiatria, neurochirurgia
vol. 11
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50.
[Current problems in genetics].
[electronic resource]
by
Ionăşescu, V
Roşianu, C
Drincă-Ionescu, M
Producer:
19680303
In:
Studii si cercetari de neurologie
vol. 12
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51.
A new approach for carrier detection in Duchenne muscular dystrophy. Protein synthesis of muscle polyribosomes in vitro.
[electronic resource]
by
Ionasescu, V
Zellweger, H
Conway, T W
Producer:
19711007
In:
Neurology
vol. 21
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52.
Becker muscular dystrophy recombinant DNA studies in identical twins.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
Searby, C
Burns, T
Producer:
19880830
In:
Muscle & nerve
vol. 11
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53.
The problem of trisomy 22. A case report and a discussion of the variant forms.
[electronic resource]
by
Zellweger, H
Ionasescu, V
Simpson, J
Burmeister, L
Producer:
19760901
In:
Clinical pediatrics
vol. 15
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54.
[Heterogeneity of muscular dystrophy].
[electronic resource]
by
Zellweger, H
Pavone, L
Ionasescu, V
Conway, T
Producer:
19720524
In:
Minerva medica
vol. 63
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55.
Biochemical and histopathological studies of the carrier state in Duchenne's muscular dystrophy.
[electronic resource]
by
Ionasescu, V
Vuia, O
Luca, N
Popa, P
Producer:
19690801
In:
Confinia neurologica
vol. 30
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56.
Collagen synthesis by Duchenne myogenic clones: pathogenic implications for the disease.
[electronic resource]
by
Ionasescu, V
Ionasescu, R
Massimini, G
Sandra, A
Producer:
19830127
In:
Birth defects original article series
vol. 18
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57.
Amino acid abnormality in Sjögren-Larsson syndrome.
[electronic resource]
by
Ionasescu, V
Stegink, L
Mueller, S
Weinstein, M
Producer:
19730329
In:
Archives of neurology
vol. 28
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58.
Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 gene.
[electronic resource]
by
Ionasescu, V V
Searby, C
Greenberg, S A
Producer:
19970326
In:
Journal of medical genetics
vol. 33
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59.
HEREDITARY PROXIMAL SPINAL MUSCULAR ATROPHY. BIOCHEMICAL INVESTIGATIONS.
[electronic resource]
by
IONASESCU, V
LUCA, N
PETRESCU, A
CALCAIANU, G
Producer:
19961201
In:
Confinia neurologica
vol. 25
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60.
Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies.
[electronic resource]
by
Ionasescu, V V
Searby, C C
Ionasescu, R
Producer:
19891023
In:
Acta neurologica Scandinavica
vol. 79
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