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Results of search for 'au:"THILEN, A"'
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Authors
Andersson Gäre, B
Andersson, J
BERGSTRAND, C G
BLOMBACK, M
Berglund, G
Eeg-Olofsson, O
Ekström, H
Eriksson, M
FAHLEN, T
FRANCKEN, I V
Fasth, A
HERRLIN, K M
Hagenfeldt, L
Hammarén, L
Larsson, A
Ritzén, E M
THILEN, A
Thilen, A
Thilén, A
Wedell, A
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Topics
Adolescent
Adrenal Hyperplasia, Congenital
Child
Child, Preschool
Female
Follow-Up Studies
Genotype
Hemophilia A
Humans
Infant
Infant, Newborn
Male
Neonatal Screening
Prognosis
Retrospective Studies
Steroid 21-Hydroxylase
Sweden
analysis
epidemiology
genetics
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Languages
English
Swedish
Your search returned 14 results.
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1.
Congenital adrenal hyperplasia in Sweden 1969-1986. Prevalence, symptoms and age at diagnosis.
[electronic resource]
by
Thilén, A
Larsson, A
Producer:
19900509
In:
Acta paediatrica Scandinavica
vol. 79
Online resources:
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2.
A study on the onset and prognosis of acute vascular purpura (the Schoenlein-Henoch syndrome) in children.
[electronic resource]
by
STERKY, G
THILEN, A
Producer:
19981101
In:
Acta paediatrica
vol. 49
Online resources:
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3.
[An evaluation of health care program proposal of the Health Care Planning and Realization Institute. Chemical criteria as a control of illness in juvenile diabetes].
[electronic resource]
by
Thalme, B
Thilén, A
Producer:
19860818
In:
Lakartidningen
vol. 83
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No items available.
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4.
Antihemophilic activity in Cohn's fraction I prepared from postpartum serum.
[electronic resource]
by
HERRLIN, K M
THILEN, A
Producer:
20030501
In:
Scandinavian journal of clinical and laboratory investigation
vol. 7
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5.
A follow-up study of children treated for acute purulent meningitis.
[electronic resource]
by
BERGSTRAND, C G
FAHLEN, T
THILEN, A
Producer:
20020501
In:
Acta paediatrica
vol. 46
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6.
Familial leukaemia--three cases of acute leukaemia in four siblings.
[electronic resource]
by
Lundmark, K M
Thilén, A
Vahlquist, B
Producer:
19671120
In:
Acta paediatrica Scandinavica
p. Suppl 172:200+
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7.
Carriers of hemophilia A: a laboratory study.
[electronic resource]
by
NILSSON, I M
BLOMBACK, M
THILEN, A
FRANCKEN, I V
Producer:
19981101
In:
Acta medica Scandinavica
vol. 165
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8.
Fanconi's anaemia associated with haemophilia A.
[electronic resource]
by
Ljung, R
Holmberg, L
Nilsson, K O
Thilén, A
Producer:
19800324
In:
Clinical genetics
vol. 16
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9.
Granulopoiesis in infantile genetic agranulocytosis. In vitro cloning of marrow cells in agar culture.
[electronic resource]
by
Olofsson, T
Olsson, I
Kostmann, R
Malmström, S
Thilen, A
Producer:
19760430
In:
Scandinavian journal of haematology
vol. 16
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10.
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
[electronic resource]
by
Nordenström, A
Thilén, A
Hagenfeldt, L
Larsson, A
Wedell, A
Producer:
19990527
In:
The Journal of clinical endocrinology and metabolism
vol. 84
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11.
[Neurofibromatosis in children].
[electronic resource]
by
Eeg-Olofsson, O
Lindskog, U
Lundell, K H
Thilén, A
Wettrell, G
Producer:
19820222
In:
Lakartidningen
vol. 78
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12.
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation.
[electronic resource]
by
Wedell, A
Thilén, A
Ritzén, E M
Stengler, B
Luthman, H
Producer:
19940608
In:
The Journal of clinical endocrinology and metabolism
vol. 78
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13.
Early growth is not increased in untreated moderately severe 21-hydroxylase deficiency.
[electronic resource]
by
Thilén, A
Woods, K A
Perry, L A
Savage, M O
Wedell, A
Ritzén, E M
Producer:
19960103
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 84
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14.
Incidence and prevalence of juvenile chronic arthritis: a population survey.
[electronic resource]
by
Andersson Gäre, B
Fasth, A
Andersson, J
Berglund, G
Ekström, H
Eriksson, M
Hammarén, L
Holmquist, L
Ronge, E
Thilen, A
Producer:
19870716
In:
Annals of the rheumatic diseases
vol. 46
Online resources:
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