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Martin Ritzen
Martin Ritzen
Karolinska Institutet
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Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH
P Burman, EM Ritzen, AC Lindgren
Endocrine reviews 22 (6), 787-799, 2001
5042001
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation
A Wedell, A Thilén, EM Ritzén, B Stengler, H Luthman
The Journal of Clinical Endocrinology & Metabolism 78 (5), 1145-1152, 1994
4491994
Nordic consensus on treatment of undescended testes
E Martin Ritzén, A Bergh, R Bjerknes, P Christiansen, D Cortes, ...
Acta paediatrica 96 (5), 638-643, 2007
4402007
Androgen transport and receptor mechanisms in testis and epididymis
FS French, WS McLean, AA Smith, DJ Tindall, SC Weddington, P Petrusz, ...
Hormone Binding and Target Cell Activation in the Testis, 265-285, 1974
3551974
Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins pediatric Endocrine Society and the European Society for Paediatric Endocrinology
Joint LwPes/esPe CAH working Group
The Journal of Clinical Endocrinology & Metabolism 87 (9), 4048-4053, 2002
3052002
A high-affinity androgen-binding protein (ABP) in rat testis: evidence for secretion into efferent duct fluid and absorption by epididymis
FS FRENCH, E MARTIN RITZfiN
Endocrinology 93 (1), 88-95, 1973
2751973
Steroid binding in polyacrylamide gels: quantitation at steady state conditions
EM Ritzén, FS French, SC Weddington, SN Nayfeh, V Hansson
Journal of Biological Chemistry 249 (20), 6597-6604, 1974
2631974
Consensus statement on 21-hydroxylase deficiency from the European society for paediatric endocrinology and the Lawson Wilkins pediatric endocrine society
S Berenbaum, G Chrousos, P Clayton, G Cutler, SD Keizer-Schrama, ...
Hormone research 58 (4), 188-195, 2002
2492002
Cognitive functions in children at risk for congenital adrenal hyperplasia treated prenatally with dexamethasone
T Hirvikoski, A Nordenstrom, T Lindholm, F Lindblad, EM Ritzén, A Wedell, ...
The Journal of Clinical Endocrinology & Metabolism 92 (2), 542-548, 2007
2412007
Surgical treatment of unilaterally undescended testes: testicular growth after randomization to orchiopexy at age 9 months or 3 years
C Kollin, B Karpe, U Hesser, T Granholm, EM Ritzén
The Journal of urology 178 (4S), 1589-1593, 2007
2382007
Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia
S Lajic, A Wedell, TH Bui, EM Ritzén, M Holst
The Journal of Clinical Endocrinology & Metabolism 83 (11), 3872-3880, 1998
2201998
Undescended testes: a consensus on management
EM Ritzén
European journal of endocrinology 159 (Supplement_1), S87-S90, 2008
2012008
Eating behavior in Prader-Willi syndrome, normal weight, and obese control groups
AC Lindgren, B Barkeling, A Hägg, EM Ritzén, C Marcus, S Rössner
The Journal of pediatrics 137 (1), 50-55, 2000
1852000
Dose-dependent effect of growth hormone on final height in children with short stature without growth hormone deficiency
K Albertsson-Wikland, AS Aronson, J Gustafsson, L Hagenas, ...
The Journal of Clinical Endocrinology & Metabolism 93 (11), 4342-4350, 2008
1762008
Growth hormone treatment of children with Prader‐Willi syndrome affects linear growth and body composition favourably
AC Lindgren, L Hagenäs, J Müller, S Blichfeldt, M Rosenborg, T Brismar, ...
Acta paediatrica 87 (1), 28-31, 1998
1741998
The Sertoli cell
EM Ritzen, V Hansson, FS French
The testis 8, 171-194, 1981
1731981
Demonstration of androgen-binding components in rat epididymis cytosol and comparison with binding components in prostate and other tissues
E MARTIN RITZÉN, SN Nayfeh, FS French, M CATHERINE DOBBINS
Endocrinology 89 (1), 143-151, 1971
1721971
Localization of estrogen receptor-alpha and-beta and androgen receptor in the human growth plate at different pubertal stages
O Nilsson, D Chrysis, O Pajulo, A Boman, M Holst, J Rubinstein, ...
Journal of Endocrinology 177 (2), 319-326, 2003
1682003
FSH stimulation of testicular androgen binding protein
V Hansson, E Reusch, O Trygstad, O Torgersen, EM Ritzen, FS French
Nature New Biology 246 (150), 56-58, 1973
1681973
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.
A Wedell, EM Ritzén, B Haglund-Stengler, H Luthman
Proceedings of the National Academy of Sciences 89 (15), 7232-7236, 1992
1671992
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Artiklar 1–20