The adrenogenital syndrome with deficiency of 3β-hydroxysteroid dehydrogenase

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1. SALT WASTAGE, RAISED PLASMA-RENIN ACTIVITY, AND NORMAL OR HIGH PLASMA-ALDOSTERONE: A FORM OF PSEUDOHYPOALDOSTERONISM
   Ariel Rösler, Ephraim Gazit, Rachel Theodor, H. Biochis, David L. Rabinowitz · 1973 · The Lancet
2. Hypothalamic-pituitary-gonadal axis function in pubertal male and female siblings with glucocorticoid-treated nonsalt-wasting 3 beta- hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia
   Ying Chang, Howard E. Kulin, LUIGI R. GARIBALDI, Mary Jean Suriano, K Bracki, Songya Pang · 1993 · The Journal of Clinical Endocrinology & Metabolism
3. Urinary excretion of pregnanetriol and Δ5-pregnenetriol in two forms of congenital adrenal hyperplasia
   Alfred M. Bongiovanni, Walter R. Eberlein, Thomas Moshang · 1971 · Journal of Clinical Investigation
4. History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology
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5. Clinical and molecular review of atypical congenital adrenal hyperplasia
   Taninee Sahakitrungruang · 2015 · Annals of Pediatric Endocrinology & Metabolism
6. Characterization of Two Novel Homozygous Missense Mutations Involving Codon 6 and 259 of Type II 3 -Hydroxysteroid Dehydrogenase (3 HSD) Gene Causing, Respectively, Nonsalt-Wasting and Salt-Wasting 3 HSD Deficiency Disorder
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7. Dynamic testing in reproductive endocrinology
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8. Male pseudohermaphroditism: Genetics and Clinical delineation
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9. The Adrenal Cortex and Its Disorders
   Walter L. Miller, John C. Achermann, Christa E. Flück · 2008 · Elsevier eBooks
10. Genetic disorders of steroid hormone synthesis and metabolism
    Maria I. New, Perrin C. White · 1995 · Baillière s Clinical Endocrinology and Metabolism
11. The in Vivo Metabolism of 16α-Hydroxyprogesterone*
    J. L. Ruse, S. Solomon · 1966 · Biochemistry
12. Congenital adrenal hyperplasia.
    G. H. Newns · 1974 · Archives of Disease in Childhood
13. A Novel Homozygous Q334X Mutation in the HSD3B2 Gene Causing Classic 3β-Hydroxysteroid Dehydrogenase Deficiency: An Unexpected Diagnosis after a Positive Newborn Screen for 21-Hydroxylase Deficiency
    Jeandron, Debra D., Sahakitrungruang, Taninee · 2012 · Hormone Research in Paediatrics
14. Hereditary Male Pseudohermaphroditism
    James E. Griffin, Jean D. Wilson · 1978 · Clinics in Obstetrics and Gynaecology
15. 3 : 21-Dihydroxypregn-5-ene-20-one in Urine of Normal Newborn Infants and in Third Day Urine of Child with Deficiency of 3 -hydroxysteroid-dehydrogenase
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16. The murine 3β-hydroxysteroid dehydrogenase multigene family: Structure, function and tissue-specific expression
    Payne, Anita H., Clarke, Trent R., Bain, Paul A. · 1995 · The Journal of Steroid Biochemistry and Molecular Biology
17. 5 Congenital adrenal hyperplasia
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18. The diagnosis and management of intersex
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19. The isolation of 16-ketoandrostenediol (3β,17β-dihydroxyandrost-5-en-16-one) from the urine of a newborn infant
    John V. Reynolds · 1964 · Steroids
20. Structure-function relationships and molecular genetics of the 3β-hydroxysteroid dehydrogenase gene family
    Simard, Jacques, Sanchez, Rocio, Durocher, Francine, Rhéaume, Eric, Turgeon, Carl, Labrie, Yvan, Luu-The, Van, Mebarki, Farida, Morel, Yves, de Launoit, Yvan et al. · 1995 · The Journal of Steroid Biochemistry and Molecular Biology
21. Nonclassical 3β-hydroxysteroid dehydrogenase deficiency: a review of our experience with 25 female patients
    Patricia Schram, Michele Zerah, Pushpa Mani, Ralphael Jewelewicz, Sharon B. Jaffe, Maria I. New · 1992 · Fertility and Sterility
22. Defects of steroidogenesis
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23. Genetic Disorders of Steroid Metabolism Diagnosed by Mass Spectrometry
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24. ABNORMALITIES OF GONADAL FUNCTION IN MEN
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25. Congenital adrenal hyperplasia
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26. Prenatal Therapy in Congenital Adrenal Hyperplasia Attempted Prevention of Abnormal External Genital Masculinization by Pharmacologic Suppression of the Fetal Adrenal Gland in Utero
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27. Congenital and acquired disorders of the adrenal cortex
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28. Monosulfates of 16-oxygenated ketonic C19 steroids in adult human urine
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29. Virilizing Adrenal Tumor in a Child Suppressed with Dexamethasone for Three Years. Effect of o, p′-DDD on Serum and Urinary Androgens
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30. The incidence of late‐onset congenital adrenal hyperplasia due to 3β‐hydroxysteroid dehydrogenase deficiency among hirsute women
    Jennifer J.I. Mathieson, Béatrice Couzinet, S. Wekstein‐Noel, K. Nahoui, Gérard Turpin, GILBERT SCHAISON · 1992 · Clinical Endocrinology
31. Metabolism of Steroids in Germfree and Conventional Rats Treated with a 3β‐Hydroxy‐δ5‐Steroid Oxidoreductase Inhibitor
    Ingemar Björkhem, Jan-Ακε Gustafsson, Sven A. Gustafsson · 1970 · European Journal of Biochemistry
32. The response of several adrenocortical steroids to the administration of ACTH in hirsute women
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33. Clinical Implications of Androgen Synthesis via 5&agr;-Reduced Precursors
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34. Detection of 3β-hydroxysteroid dehydrogenase deficiency in a newborn by means of urinary steroid analysis
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35. Familial Male Pseudohermaphroditism with Normal Leydig Cell Function at Puberty*
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36. Fetal-Placental-Maternal Interrelations Involving Steroid Hormones
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37. Urinary steroid pattern of the human newborn infant
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38. Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population
    Meshael M. Alswailem, Ohoud Alzahrani, Doha S. Alhomaidah, Rahma Alasmari, Ebtesam Qasem, Avaniyapuram Kannan Murugan, Afaf Alsagheir, Imad Addin Brema, Bassam Ben Abbas, Mohammed S. Almehthel et al. · 2017 · Molecular and Cellular Endocrinology
39. Urinary steroidal pattern of infants with congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
    Alfred M. Bongiovanni · 1980 · Journal of Steroid Biochemistry
40. Disorders of Sex Development
    Valerie A. Arboleda, Alice A. Fleming, Eric J. N. Vilain · 2010 · Elsevier eBooks
41. Defects of Adrenal Steroidogenesis
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42. Medical genetics 1962
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43. Non-classic adrenal hyperplasia in hyperandrogenism: A reappraisal
    Carlos Morán, Eric S. Knochenhauer, Ricardo Azziz · 1998 · Journal of Endocrinological Investigation
44. Bile acids and hormonal steroids in bile of a boy with 3β-hydroxysteroid dehydrogenase deficiency
    Tiina K. Laatikainen, Jaakko Perheentupa, R. Vihko, I. Makino, Jan Sjövall · 1972 · Journal of Steroid Biochemistry
45. Male hypogonadism.
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46. Disorders of Sexual Development
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47. Molecular medicine of steroid hormone biosynthesis
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48. The activation of microsomal steroid 21-hydroxylase by cytosol from the cortex of bovine adrenals.
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49. The adrenal cortex in childhood.
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50. The in Vivo Metabolism of 16α-Hydroxydehydroisoandrosterone in Man*
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51. The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population
    Ayca Dundar, Ruslan Bayramov, Müge Gülcihan Önal, Mustafa Akkus, Muhammet Ensar Doğan, Sercan Kenanoğlu, Meltem Cerrah Güneş, Ulviye Kazimli, Mehmet Nuri Özbek, Oya Ercan et al. · 2019 · Molecular Biology Reports
52. Male psuedohermaphroditism caused by nonsalt-losing congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase (3β-HSD) deficiency
    U. Heinrich, Markus Bettendorf, P. Vecsei · 1993 · The Journal of Steroid Biochemistry and Molecular Biology
53. The identification and quantification of δ5-androstenetriol (3β, 16α, 17β-trihydroxyandrost-5-ene) isolated from the urine of premature infants
    John Warren Reynolds · 1966 · Steroids
54. Normal ovarian function in a mild form of late-onset 3β-hydroxysteroid dehydrogenase deficiency
    Martha Medina, Joaquín Herrera, Mirza Flores, Orlando Martin, JOSE A. BERMUDEZ, Arturo Zárate · 1986 · Fertility and Sterility
55. The Biochemistry of the 3β—Hydroxy—∆ 5—Steroid Sulfates
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56. Congenital Adrenal Hyperplasia
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57. Primary and Secondary Hypogonadism
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58. Die Nebennierenrinde
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59. Separation, Identification, and Estimation of Human Steroid Hormones and Their Metabolites: Applications to Adrenocortical Steroids
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60. Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone
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61. Genotyping of the type II 3β-hydroxysteroid dehydrogenase gene (HSD3B2) in women with hirsutism and elevated ACTH-stimulated δ5-steroids
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62. The virilized female: endocrine background
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63. A New Homozygous Frameshift Mutation in the HSD3B2 Gene in an Apparently Nonconsanguineous Italian Family
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65. XY females with enzyme deficiencies of steroid metabolism
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67. Detection of 3β-hydroxysteroid-dehydrogenase deficiency by urinary steroid profiling: solvolysis of urinary samples should be a necessary prerequisite
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68. Bases Moleculares da Hiperplasia Adrenal Congênita
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69. Effect of age, obesity, starvation, and changes in adrenocortical and ovarian activity on the urinary excretion of dehydroepiandrosterone relative to androsterone + etiocholanolone: Relevance to the measurement of breast cancer discriminants in women
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70. METABOLIC CONJUGATION AND HYDROLYSIS OF STEROID HORMONES IN THE FETOPLACENTAL UNIT
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71. Genetic Disorders of Male Sexual Differentiation
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72. Steroid Metabolism in the Fetus and the Newborn Infant
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73. Human Steroid Biosynthesis
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74. AN AUTOPSY CASE OF CONGENITAL LIPOID HYPERPLASIA OF THE ADRENAL CORTEX
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75. Defects of Adrenal Steroidogenesis
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76. Congenital adrenal hyperplasia
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77. Disorders of Sexual Differentiation
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78. Adrenal Cortex
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79. Normal and Abnormal Embryo-Fetal Development in Mammals
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80. Congenital adrenal hyperplasia
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81. Ambiguous Genitalia in the Newborn
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82. Evidence that the same structural gene encodes testicular and adrenal 3?-hydroxysteroid dehydrogenase-isomerase
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83. Corticosteroid Therapy in the Neonatal Period
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84. Some Newer Inborn Errors of Metabolism
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85. Kongenitale Nebennierenrindenhyperplasie mit maximaler Virilisierung (penile urethra)
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87. Testicular Steroidogenesis
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88. Testicular Steroidogenesis
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89. Hyperandrogenism in Women
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93. Some Aspects of Endocrinology in the Fetus and the Newborn
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94. Late-Onset Adrenal Hyperplasia
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95. Lessons from Inborn Errors of Metabolism
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97. Causas raras de pseudo-hermafroditismo feminino: quando suspeitar?
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98. Pseudovaginal Perineoscrotal Hypospadias: Genetic Heterogeneity
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99. Pre- and Perinatal Endocrinology
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100. Die Nebennierenrinde
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