Klassische 21-OHD CAH (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Klassische 21-OHD CAH" in German language version.

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W. Höller, S. Scholz, D. Knorr, F. Bidlingmaier, E. Keller, E. D. Albert: Genetic differences between the salt-wasting, simple virilizing, and nonclassical types of congenital adrenal hyperplasia. In: The Journal of clinical endocrinology and metabolism. Bd. 60, Nr. 4, April 1985, S. 757–763, doi:10.1210/jcem-60-4-757, PMID 2982907.
M. I. New: An update of congenital adrenal hyperplasia. In: Annals of the New York Academy of Sciences. Bd. 1038, Dezember 2004, S. 14–43, doi:10.1196/annals.1315.009, PMID 15838095.
C. H. Houben, S. Y. Tsui, J. W. Mou, K. W. Chan, Y. H. Tam, K. H. Lee: Reconstructive surgery for females with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review from the Prince of Wales Hospital. In: Hong Kong medical journal = Xianggang yi xue za zhi. Bd. 20, Nr. 6, Dezember 2014, S. 481–485, doi:10.12809/hkmj144227, PMID 25045882.

W. Höller, S. Scholz, D. Knorr, F. Bidlingmaier, E. Keller, E. D. Albert: Genetic differences between the salt-wasting, simple virilizing, and nonclassical types of congenital adrenal hyperplasia. In: The Journal of clinical endocrinology and metabolism. Bd. 60, Nr. 4, April 1985, S. 757–763, doi:10.1210/jcem-60-4-757, PMID 2982907.
M. I. New: An update of congenital adrenal hyperplasia. In: Annals of the New York Academy of Sciences. Bd. 1038, Dezember 2004, S. 14–43, doi:10.1196/annals.1315.009, PMID 15838095.
C. H. Houben, S. Y. Tsui, J. W. Mou, K. W. Chan, Y. H. Tam, K. H. Lee: Reconstructive surgery for females with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review from the Prince of Wales Hospital. In: Hong Kong medical journal = Xianggang yi xue za zhi. Bd. 20, Nr. 6, Dezember 2014, S. 481–485, doi:10.12809/hkmj144227, PMID 25045882.
L. G. Gomes, G. Madureira, B. B. Mendonca, T. A. Bachega: Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. In: Clinics. Bd. 68, Nr. 2, 2013, S. 147–152, PMID 23525308, PMC 3584273 (freier Volltext)