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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 | 449 | 1994 |
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 | 440 | 2007 |
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 | 355 | 1974 |
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 | 305 | 2002 |
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 | 275 | 1973 |
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 | 263 | 1974 |
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 | 249 | 2002 |
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 | 241 | 2007 |
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 | 238 | 2007 |
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 | 220 | 1998 |
Undescended testes: a consensus on management EM Ritzén European journal of endocrinology 159 (Supplement_1), S87-S90, 2008 | 201 | 2008 |
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 | 185 | 2000 |
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 | 176 | 2008 |
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 | 174 | 1998 |
The Sertoli cell EM Ritzen, V Hansson, FS French The testis 8, 171-194, 1981 | 173 | 1981 |
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 | 172 | 1971 |
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 | 168 | 2003 |
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 | 168 | 1973 |
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 | 167 | 1992 |