21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase DeficiencyTonetto-Fernandes, V.; Lemos-Marini, S.H.V.; De Mello, M.P.; Ribeiro-Neto, L.M.; Kater, C.E. · Journal of Pediatric Endocrinology and Metabolism · 2008

152 DIURNAL SALIVARY SIEROIO PATTERNS AS AN INDEX OF ADEQUACY OF TREATMENT IN 21-HYDROXYLASE DEFICIENCY (21-HD) QUANCY OF TREATEMENT IN 21-HYDROXYLASE DEFICIENCY (21-HD)Otten, B J; Rijken, J C; Stoelinga, G B A; Enruad, Th J; Van den Brande, J L · Pediatric Research · 1988

Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndromeElizabeth A. Parker; Karine Hovanes; John Germak; Forbes Porter; Deborah P. Merke · 2006

Clinical heterogeneity of 21-hydroxylase deficiency of sibs with identical 21-hydroxylase genesBormann, M.; Kochhan, L.; Knorr, D.; Bidlingmaier, F.; Olek, K. · European Journal of Endocrinology · 1992

Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.Haglund-Stengler, B.; Martin Ritzen, E.; Gustafsson, J.; Luthman, H. · Proceedings of the National Academy of Sciences · 1991

The chimericCYP21P/CYP21gene and 21-hydroxylase deficiencyHsien-Hsiung Lee · 2004

Haplotypes of the Steroid 21-Hydroxylase Gene Region Encoding Mild Steroid 21-Hydroxylase DeficiencyBarbro Haglund-Stengler, E. Martin Ritzen, Jan Gustafsson and Holger Luthman · Proceedings of the National Academy of Sciences of the United States of America · 1991

Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients with 21-Hydroxylase DeficiencyNAKURA, JUN; MIKI, TETSURO; FUKUCHI, KEN-ICHIRO; SHIMIZU, KAZUO; NOSE, OSAMU; TAKAI, SHIN-ICHIRO; WHITE, PERRIN C.; HONJO, TASUKU; KUMAHARA, YUICHI · Endocrinologia Japonica · 1987

Thyroid abnormalities in children infected with human immunodeficiency virusSteven Hirschfeld; Louisa Laue; Gordon B. Cutler Jr.; Philip A. Pizzo · 1996

Growth and neuroendocrine dysfunction in children with acquired immunodeficiency syndromeLouisa Laue; Philip A. Pizzo; Karina Butler; Gordon B. Cutler Jr. · 1990

Treatment of Familial Male Precocious Puberty with Spironolactone and TestolactoneLaue, Louisa; Kenigsberg, Daniel; Pescovitz, Ora H.; Hench, Karen D.; Barnes, Kevin M.; Loriaux, D. Lynn; Cutler, Gordon B. · New England Journal of Medicine · 1989

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious pubertyShenker, Andrew; Laue, Louisa; Kosugi, Shinji; Merendino, John J.; Minegishi, Takashi; Cutler, Gordon B. · 1993

Heterogeneity of Activating Mutations of the Human Luteinizing Hormone Receptor in Male-Limited Precocious PubertyLouisa Laue; Shao-Ming Wu; Masataka Kudo; Aaron J.W. Hsueh; Gordon B. Cutler; Jr.; David H. Jelly; Frank B. Diamond; Wai-Yee Chan · 1996

Genetic Heterogeneity of Constitutively Activating Mutations of the Human Luteinizing Hormone Receptor in Familial Male-Limited Precocious PubertyLouisa Laue, Wai-Yee Chan, Aaron J. W. Hsueh, M. Kudo, Sheau Yu Hsu, Shao-Ming Wu, LeAnn Blomberg and Gordon B. Cutler, Jr. · Proceedings of the National Academy of Sciences of the United States of America · 1995

Hypomagnesemic TetanyRajput, Rajesh; Kumar, Kamlesh; Dhingra, Atul · The Endocrinologist · 2009

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Evaluation Form May/June 2010&NA;, · The Endocrinologist · 2010

Prolonged Treatment With Antithyroid DrugsNelson, Peggy; Gossain, Ved V. · The Endocrinologist · 2010

Endocrinologic Diseases in HemoglobinopathiesEl Baba, Khaled; Zantout, Mira S.; Azar, Sami T. · The Endocrinologist · 2009

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Isolated ACTH DeficiencyYamamoto, Toshihide · The Endocrinologist · 2009

Hyper- and HypocalcemiaRehman, Habib Ur; Michaels, Clara E. · The Endocrinologist · 2010