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Astrid Thilén
Observed names:
A Thilen,
A Thilén,
A. THILÉN,
A. THILéN,
A. Thilen,
ASTRID THILÉN,
Astrid Thilen,
Astrid Thilén
show all 8
Observed institutions:
Uppsala University,
Karolinska University Hospital,
Uppsala University Hospital,
Lund University,
Karolinska Institutet,
Ryhov Hospital Jönköping,
Royal Manchester Children's Hospital,
Norrköping Hospital,
University of Gothenburg
show all 9
OpenAlex ID:
A5074313862
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation
1994
·
A Wedell
, A Thilén
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
370
One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study
2013
·
Sebastian Gidlöf
, Henrik Falhammar
, et al.
·
The Lancet Diabetes & Endocrinology
·
187
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder
1993
·
Songya Pang
, Anastasia Clark
, et al.
·
Screening
·
162
Benefits of Neonatal Screening for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in Sweden
1998
·
Astrid Thilén
, Anna Nordenström
, et al.
·
PEDIATRICS
·
151
Genotyping Is a Valuable Diagnostic Complement to Neonatal Screening for Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency1
1999
·
Anna Nordenström
, Astrid Thilén
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
99
Incidence and prevalence of juvenile chronic arthritis: a population survey.
1987
·
B Andersson Gäre
, A Fasth
, et al.
·
Annals of the Rheumatic Diseases
·
67
PDF
Congenital Adrenal Hyperplasia in Sweden 1969‐1986 Prevalence, Symptoms and Age at Diagnosis
1990
·
A. THILÉN
, A. LARSSON
·
Acta Paediatrica
·
66
Carriers of Hemophilia A
1959
·
Inga Marie Nilsson
, Margareta Blombäck
, et al.
·
Acta Medica Scandinavica
·
55
Early growth is not increased in untreated moderately severe 21‐hydroxylase deficiency
1995
·
A Thilén
, KA Woods
, et al.
·
Acta Paediatrica
·
53
A Study on the Onset and Prognosis of Acute Vascular Purpura (the Schönlein‐Henoch Syndrome) in Children
1960
·
GÖRAN STERKY
, ASTRID THILÉN
·
Acta Paediatrica
·
46
Granulopoiesis in Infantile Genetic Agranulocytosis In vitro Cloning of Marrow Cells in Agar Culture
1976
·
Tor Olofsson
, Inge Olsson
, et al.
·
Scandinavian Journal of Haematology
·
18
Screening of half a million Swedish newborn infants for congenital adrenal hyperplasia
1992
·
Agne Larsson
, Astrid Thilén
, et al.
·
Screening
·
17
A Follow‐up Study of Children Treated for Acute Purulent Meningitis
1957
·
C. G. BERGSTRAND
, T. FAHLéN
, et al.
·
Acta Paediatrica
·
17
Familial Leukaemia — Three Cases of Acute Leukaemia in Four Siblings
1967
·
K. M. LUNDMARK
, ASTRID THILÉN
, et al.
·
Acta Paediatrica
·
7
Mutational Spectrum of the Steroid 21-Hydroxylase Gene In Sweden
1994
·
Anna Wedell
, Astrid Thilén
, et al.
·
Obstetrical & Gynecological Survey
·
4
Antihemophilic Activity in Cohn's Fraction I Prepared from Postpartum Serum
1955
·
K. M. Herrlin
, A. Thilen
·
Scandinavian Journal of Clinical and Laboratory Investigation
·
4
[Neurofibromatosis in children].
1981
·
O Eeg-Olofsson
, U Lindskog
, et al.
·
PubMed
·
3
Fanconi's anaemia associated with haemophilia A
1979
·
Rolf Ljung
, Lars Holmberg
, et al.
·
Clinical Genetics
·
2
Are infants insensitive to androgen? Comments on a letter by Arisaka et al.
1996
·
EM Ritzén
, A Thilén
, et al.
·
Acta Paediatrica
Screening of 0.7 Million Swedish Newborn Infants for Congenital Adrenal Hyperplasia
1992
·
Agne Larsson
, Astrid Thilén
, et al.
·
Pediatric Research
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Works count:
20
Citation count:
1,328
H-index:
13
I10-index:
13
Year
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