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Results of search for 'au:"EMERY, A E"', page 5 of 9
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Authors
Anand, R
Black, I
Bolton, C E
Brooks, A P
Burt, D
Clack, E R
Davie, A M
EMERY, A E
Eccleston, D
Emery, A E
Emery, M L
Holloway, S
King, B
Lumb, E M
Nelson, M M
Scrimgeour, J B
Skinner, R
Smith, C
Timson, J
Vassilopoulos, D
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Adolescent
Adult
Aged
Child
Child, Preschool
Creatine Kinase
Female
Genetic Counseling
Humans
Male
Middle Aged
Muscles
Muscular Dystrophies
Pregnancy
Prenatal Diagnosis
analysis
blood
diagnosis
enzymology
genetics
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81.
Leucocyte fatty acid oxidation in hereditary neuromuscular disorders. A preliminary report.
[electronic resource]
by
King, B
Emery, A E
Producer:
19740212
In:
Journal of the neurological sciences
vol. 20
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82.
Calcium stimulated enzyme efflux from human skeletal muscle.
[electronic resource]
by
Anand, R
Emery, A E
Producer:
19801021
In:
Research communications in chemical pathology and pharmacology
vol. 28
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83.
Medicine and art: diagnosis and medical treatment.
[electronic resource]
by
Emery, A E
Emery, M
Producer:
19921217
In:
Proceedings of the Royal College of Physicians of Edinburgh
vol. 22
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84.
A neurogenic component in muscular dystrophy.
[electronic resource]
by
Emery, A E
Gosden, C
Producer:
19740827
In:
Journal of medical genetics
vol. 11
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85.
Bloch-Sulzberger Syndrome (incontinentia pigmenti).
[electronic resource]
by
Shotts, N
Emery, A E
Producer:
19670526
In:
Journal of medical genetics
vol. 3
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86.
Verapamil and calcium-stimulated enzyme efflux from skeletal muscle.
[electronic resource]
by
Anand, R
Emery, A E
Producer:
19820814
In:
Clinical chemistry
vol. 28
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87.
Erythrocyte spectrin in Duchenne muscular dystrophy.
[electronic resource]
by
Anand, R
Emery, A E
Producer:
19820322
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 117
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88.
Muscle histology in fetuses at risk for Duchenne muscular dystrophy.
[electronic resource]
by
Toop, J
Emery, A E
Producer:
19740828
In:
Clinical genetics
vol. 5
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89.
[The importance of biomicroscopic examination of the lens in the detection of heterozygotes for certain hereditary diseases, in particular, myotonic dystrophy].
[electronic resource]
by
Pescia, G
Emery, A E
Producer:
19770224
In:
Journal de genetique humaine
vol. 24
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90.
Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).
[electronic resource]
by
Fried, K
Emery, A E
Producer:
19720628
In:
Clinical genetics
vol. 2
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91.
Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy.
[electronic resource]
by
Emery, A E
Spikesman, A
Producer:
19700807
In:
Journal of the neurological sciences
vol. 10
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92.
Ascertainment and prevention of genetic disease.
[electronic resource]
by
Emery, A E
Smith, C
Producer:
19701201
In:
British medical journal
vol. 3
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93.
Pregnancy and serum-creatine-kinase levels in potential carriers of Duchenne X-linked muscular dystrophy.
[electronic resource]
by
Emery, A E
King, B
Producer:
19710630
In:
Lancet (London, England)
vol. 1
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94.
Genetics in art.
[electronic resource]
by
Emery, A E
Emery, M
Producer:
19940922
In:
Journal of medical genetics
vol. 31
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95.
Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy.
[electronic resource]
by
Davie, A M
Emery, A E
Producer:
19790425
In:
Journal of medical genetics
vol. 15
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96.
The genetics of muscular dystrophy.
[electronic resource]
by
Emery, A E
Walton, J N
Producer:
19700220
In:
Progress in medical genetics
vol. 5
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97.
Limb blood flow in patients and carriers of Duchenne muscular dystrophy.
[electronic resource]
by
Emery, A E
Schelling, J L
Producer:
19660925
In:
Acta genetica et statistica medica
vol. 15
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98.
Long-chain esters in clover wax.
[electronic resource]
by
Emery, A E
Gear, J R
Producer:
19700220
In:
Canadian journal of biochemistry
vol. 47
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99.
Amniotic fluid cell cultures.
[electronic resource]
by
Nelson, M M
Emery, A E
Producer:
19730611
In:
Journal of medical genetics
vol. 10
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100.
Serum creatine kinase levels.
[electronic resource]
by
Emery, A E
Spikesman, A M
Producer:
19700831
In:
British medical journal
vol. 2
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