Treatment of Men with Paraphilia with a Long-Acting Analogue of Gonadotropin-Releasing Hormone von Rösler, Ariel, Witztum, Eliezer

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Prolonged Remission of Severe Cushing Syndrome without Adrenalectomy in an Infant with McCune-Albright Syndrome von Gillis, David, MD, Rösler, Ariel, MD, Hannon, Tamara S., MD, Koplewitz, Benjamin Z., MD, Hirsch, Harry J., MD

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Mutations in the Human CYP11B2 (Aldosterone Synthase) Gene Causing Corticosterone Methyloxidase II Deficiency von Pascoe, Leigh, Curnow, Kathleen M., Slutsker, Liliya, Rosler, Ariel, White, Perrin C.

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Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1 von Chang, Sue S, Grunder, Stefan, Hanukoglu, Aaron, Rösler, Ariel, Mathew, P.M, Hanukoglu, Israel, Schild, Laurent, Lu, Yin, Shimkets, Richard A, Nelson-Williams, Carol, Rossier, Bernard C, Lifton, Richard P

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Congenitally defective aldosterone biosynthesis in humans : the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients von MITSUUCHI, Y, KAWAMOTO, T, NAKAO, K, IMURA, H, ULICK, S, SHIZUTA, Y, RÖSLER, A, NAIKI, Y, MIYAHARA, K, TODA, K, KURIBAYASHI, I, ORII, T, YASUDA, K, MIURA, K

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Subclinical hypothyroidism in infertile women: The importance of continuous monitoring and the role of the thyrotropin-releasing hormone stimulation test von Eldar-Geva, Talia, Shoham, Michal, Rösler, Ariel, Margalioth, Ehud J., Livne, Keren, Meirow, Dror

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Pharmacotherapy of paraphilias in the next millennium von Rösler, Ariel, Witztum, Eliezer

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A (R80Q) mutation in 17 beta-hydroxysteroid dehydrogenase type 3 gene among Arabs of Israel is associated with pseudohermaphroditism in males and normal asymptomatic females von Rösler, A, Silverstein, S, Abeliovich, D

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A mutation in CYP11B1 (Arg-448→ His) associated with steroid 11β-hydroxylase deficiency in jews of Moroccan origin von WHITE, P. C, DUPONT, J, NEW, M. I, LEIBERMAN, E, HOCHBERG, Z, ROSLER, A

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Secondary Biosynthetic Defects in Women with Late-Onset Congenital Adrenal Hyperplasia von Eldar-Geva, Talia, Hurwitz, Arye, Vecsei, Paul, Palti, Zvi, Milwidsky, Ariel, Rösler, Ariel

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Steroid 17β-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism von Roesler, A

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Somatostatin Receptor Scintigraphy for Early Detection of Regional and Distant Metastases of Medullary Carcinoma of the Thyroid von KRAUSZ, YODPHAT, ROSLER, ARIEL, GUTTMANN, HADASSAH, ISH-SHALOM, SOPHIA, SHIBLEY, NAZEEH, CHISIN, ROLAND, GLASER, BENJAMIN

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Reply von Gillis, David, Rosler, Ariel, Koplewitz, Benjamin Z., Hannon, Tamara S., Hirsch, Harry J.

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Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression von ACHERMANNT, John C, ITO, Masafumi, SILVERMAN, Bernard L, HABIBY, Reema L, SONGYA PANG, ROSLER, Ariel, JAMESON, J. Larry

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Reply von Gillis, David, MD, Rosler, Ariel, MD, Koplewitz, Benjamin Z., MD, Hannon, Tamara S., MD, Hirsch, Harry J., MD

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Mutations in human 11β-hydroxylase genes: 11β-hydroxylase deficiency in Jews of Morocco and corticosterone methyl-oxidase II deficiency in Jews of Iran von Rösler, Ariel, White, Perrin C.

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Inborn errors of aldosterone biosynthesis in humans von Shizuta, Yutaka, Kawamoto, Takeshi, Mitsuuchi, Yasuhiro, Miyahara, Kaoru, Rösler, Ariel, Ulick, Stanley, Imura, Hiroo

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MAGNESIUM-INDUCED REVERSAL OF VITAMIN-D RESISTANCE IN HYPOPARATHYROIDISM von Rösler, Ariel, Rabinowitz, David

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Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes von White, Perrin C., Pascoe, Leigh, Curnow, Kathleen M., Tannin, Grace, Rösler, Ariel

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An Inherited Defect in Aldosterone Biosynthesis Caused by a Mutation in or near the Gene for Steroid 11-Hydroxylase von Globerman, Hadas, Rösler, Ariel, Theodor, Rachel, New, Maria I, White, Perrin C

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