Nonclassical 21-Hydroxylase Deficiency

New, Maria I.·2006·The Journal of Clinical Endocrinology & Metabolism

Cited by (314)

Items 101–200 of 314

  1. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency: An Update on Genetic Analysis of CYP21A2 Gene
    Berta Carvalho, Cristina Joana Marques, Rita Santos Silva, Manuel Fontoura, Davide Maurício Carvalho, Filipa Carvalho · 2020 · Experimental and Clinical Endocrinology & Diabetes
  2. Hyperinsulinemic-Euglycemic Clamp Strengthens the Insulin Resistance in Nonclassical Congenital Adrenal Hyperplasia
    Ariane Delai, Patrícia Moreira Gomes, Maria Cristina Foss‐Freitas, Jorge Elías, Sonir Roberto Rauber Antonini, Margaret de Castro, Ayrton Custódio Moreira, Lívia M. Mermejo · 2021 · The Journal of Clinical Endocrinology & Metabolism
  3. Substitution therapy in adult patients with congenital adrenal hyperplasia
    Nicole Reisch · 2014 · Best Practice & Research Clinical Endocrinology & Metabolism
  4. Absence of clinically relevant growth acceleration in untreated children with non-classical congenital adrenal hyperplasia
    Pijnenburg-Kleizen, Karijn J., Borm, George F., Otten, Barto J., Schott, Dina A., van den Akker, Erica L., Stokvis-Brantsma, Wilhelmina H., Voorhoeve, Paul G., Bakker, Boudewijn, Claahsen-van der Grinten, Hedi L. · 2012 · Hormone Research in Paediatrics
  5. Obesity and Cardiometabolic Risk Factors in Children and Young Adults With Non-classical 21-Hydroxylase Deficiency
    Liat de Vries, Yael Lebenthal, Moshe Phillip, Shlomit Shalitin, Ariel Tenenbaum, Rachel Bello · 2019 · Frontiers in Endocrinology
  6. Russian clinical practice guidelines «congenital adrenal hyperplasia»
    Natalia G. Mokrysheva, Galina Afanas'evna Mel'nichenko, Leila V. Adamyan, Ekaterina Anatol'evna Troshina, Н В Молашенко, Сазонова Анна Игоревна, Elena V. Uvarova, Esayan R.M. Esayan, Elena Nikolaevna Andreeva, Ж. А. Ужегова et al. · 2021 · Obesity and metabolism
  7. Pregnancy and Prenatal Management of Congenital Adrenal Hyperplasia
    Gianluca Cera, Pietro Locantore, Roberto Novizio, Ettore Maggio, Vittoria Ramunno, Andrea Corsello, Caterina Policola, Paola Concolino, Rosa Maria Paragliola, Alfredo Pontecorvi · 2022 · Journal of Clinical Medicine
  8. Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers
    Françoise Paris, Véronique Tardy, Anne Chalançon, Marie‐Christine Picot, Yves Morel, Charles Sultan · 2010 · Gynecological Endocrinology
  9. Hyperandrogénie féminine
    Maëliss Peigné, Anne Villers-Capelle, Geoffroy Robin, Didier Dewailly · 2013 · La Presse Médicale
  10. The Adrenal Cortex
    Paul M. Stewart, John D C Newell-Price · 2016 · Elsevier eBooks
  11. MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosis
    MICHEL M. PUGEAT, Ingrid Plotton, Aude Brac de la Perrière, Gérald Raverot, Henri Déchaud, Véronique Raverot · 2018 · European Journal of Endocrinology
  12. Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary Syndrome
    Giovana De Nardo Maffazioli, Tânia A.S.S. Bachega, Sylvia Asaka Yamashita Hayashida, Larissa Garcia Gomes, Helena Panteliou Lima Valassi, José Antônio Miguel Marcondes, Berenice Bilharinho Mendonca, Edmund Chada Baracat, Gustavo Arantes Rosa Maciel · 2020 · The Journal of Clinical Endocrinology & Metabolism
  13. Refractory Acne and 21-Hydroxylase Deficiency in a Selected Group of Female Patients
    Valentina Caputo, Santi Fiorella, Salvatrice Curiale, Alfredo Caputo, Marcello Niceta · 2010 · Dermatology
  14. Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood
    Kenichi Kashimada, Makoto ONO, Toshikazu ONISHI, Satimi KOYAMA, Takio Toyoura, Kazuhide Imai, Sumitaka Saisho, Shuki Mizutani · 2008 · Endocrine Journal
  15. Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: further characterization of classic and non-classic patients and heterozygote carriers.
    Flavia Amanda Costa‐Barbosa, Valdemir Melechco Carvalho, Odete Hirata Nakamura, Tânia A.S.S. Bachega, José Gilberto H. Vieira, Claudio Elias Kater · 2011 · PubMed
  16. Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal Hyperplasia
    Malgorzata Gabriela Wasniewska, Letteria Anna Morabito, Federico Baronio, Silvia Einaudi, Mariacarolina Salerno, Carla Bizzarri, Gianni Russo, Mariangela Chiarito, Anna Grandone, Laura Guazzarotti et al. · 2020 · Hormone Research in Paediatrics
  17. Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing
    Guillaume Bachelot, Anne Bachelot, Marion Bonnier, Joe‐Elie Salem, Dominique Farabos, Séverine Trabado, Charlotte Dupont, Peter Kamenický, Muriel Houang, Jean Fiet et al. · 2022 · Human Reproduction
  18. Dynamic Testing for Evaluation of Adrenal and Gonadal Function in Pediatric and Adult Endocrinology: An Overview
    Alpesh Goyal, Suraj Kubihal, Yashdeep Gupta, Viveka P. Jyotsna, Rajesh Khadgawat · 2019 · Indian Journal of Endocrinology and Metabolism
  19. Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Chen, Wuyan, Xu, Zhi, Nishitani, Miki, Van Ryzin, Carol, McDonnell, Nazli B., Merke, Deborah P. · 2012 · Human Genetics
  20. Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients
    Banu Küçükemre Aydın, Nurçin Saka, Firdevs Baş, Yasin Yılmaz, Belma Haliloğlu, Tülay Güran, Serap Turan, Abdullah Bereket, Gül Yeşiltepe Mutlu, Filiz Çizmecioğlu et al. · 2017 · Journal of Pediatric and Adolescent Gynecology
  21. Defects of Adrenal Steroidogenesis
    Mabel Yau, Ahmed Khattab, Christian Pina, Tony Yuen, Heino F. L. Meyer‐Bahlburg, Maria I. New · 2015 · Elsevier eBooks
  22. Sperm retrieval and concomitant tumor resection in azoospermic men with congenital adrenal hyperplasia and bilateral testicular adrenal rest tumors: a case report
    Kavoussi, Parviz K., Summers-Colquitt, Roxanne B., Odenwald, Kate C., Kressin, Megan, Kavoussi, Keikhosrow M., Pool, Thomas B., Kavoussi, Shahryar K. · 2016 · Journal of Assisted Reproduction and Genetics
  23. A sequence variation in 3'UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.
    Soara Menabò, Antonio Balsamo, Lilia Baldazzi, Michela Barbaro, Annalisa Nicoletti, V Conti, P Pirazzoli, Anna Wedell, A Cicognani · 2012 · PubMed
  24. Hyperandrogenism, Hirsutism, and Polycystic Ovary Syndrome
    Robert L. Rosenfield, Randall B. Barnes, David A. Ehrmann · 2015 · Elsevier eBooks
  25. Clinical, biochemical, and genetic features of non-classical 21-hydroxylase deficiency in Japanese children
    Kenichi Kashimada, Tomohiro Ishii, Keisuke Nagasaki, Makoto Ono, Toshihiro Tajima, Ichiro Yokota, Yukihiro Hasegawa · 2015 · Endocrine Journal
  26. New developments in prenatal diagnosis of congenital adrenal hyperplasia
    Diya Kazmi, Jack Bailey, Maggie LY. Yau, Wahid Abu‐Amer, Ameet Kumar, Merly Low, Tony Yuen · 2016 · The Journal of Steroid Biochemistry and Molecular Biology
  27. Low-Dose Dexamethasone Therapy from Infancy of Virilizing Congenital Adrenal Hyperplasia
    Scott A. Rivkees, Kerry Stephenson · 2009 · International Journal of Pediatric Endocrinology
  28. 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
  29. Functional and Structural Consequences of a Novel Point Mutation in theCYP21A2Gene Causing Congenital Adrenal Hyperplasia: Potential Relevance of Helix C for P450 Oxidoreductase-21-Hydroxylase Interaction
    Felix G. Riepe, Olaf Hiort, Joachim Grötzinger, Wolfgang G. Sippell, Nils Peter Krone, Paul‐Martin Holterhus · 2008 · The Journal of Clinical Endocrinology & Metabolism
  30. Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Dörr, Helmuth-Günther, Schulze, Nadja, Bettendorf, Markus, Binder, Gerhard, Bonfig, Walter, Denzer, Christian, Dunstheimer, Desiree, Salzgeber, Kirsten, Schmidt, Heinrich, Schwab, Karl Otfried et al. · 2020 · Molecular and Cellular Pediatrics
  31. High-resolution melting curve (HRM) analysis to establish CYP21A2 mutations converted from the CYP21A1P in congenital adrenal hyperplasia
    Yi-Ching Lin, Yu‐Chih Lin, Ta‐Chih Liu, Jan‐Gowth Chang, Hsien-Hsiung Lee · 2011 · Clinica Chimica Acta
  32. No. 350-Hirsutism: Evaluation and Treatment
    Kimberly E. Liu, Tarek Motan, Paul Claman · 2017 · Journal of Obstetrics and Gynaecology Canada
  33. Genotype, phenotype and hormonal levels correlation in non-classical congenital adrenal hyperplasia.
    S. Einaudi, E Napolitano, Francesca Restivo, Giovanna Motta, Matteo Baldi, Gerdi Tuli, Enrico Grosso, Nicola Migone, Elisa Menegatti, Chiara Manieri · 2011 · PubMed
  34. Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia
    Ingeborg Brønstad, Lars Breivik, Paal Methlie, Anette S. B. Wolff, Eirik Bratland, Ingrid Nermoen, Kristian Løvås, Eystein S. Husebye · 2014 · Endocrine Connections
  35. Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites
    Koyama, Yuhei, Homma, Keiko, Fukami, Maki, Miwa, Masayuki, Ikeda, Kazushige, Ogata, Tsutomu, Murata, Mitsuru, Hasegawa, Tomonobu · 2016 · Clinical Pediatric Endocrinology
  36. Neonatal screening for congenital adrenal hyperplasia: transitory elevation of 17-hydroxyprogesterone
    Belén Huidobro Fernández, M. Echeverría Fernández, E. Dulín Íñiguez, Begoña Ezquieta Zubicaray, M.B. Roldán Martín, María Dolores Rodríguez Arnao, Amparo Rodríguez Sánchez · 2011 · Journal of Pediatric Endocrinology and Metabolism
  37. A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect
    Tülay Güran, Gözde Yeşil, Ömer Güran, Suna Cesur, Oktav Bosnalı, Ayşenur Cerrah Celayir, Sevilay Topçuoğlu, Abdullah Bereket · 2012 · Journal of Clinical Research in Pediatric Endocrinology
  38. Non-classical 21-hydroxylase deficiency: prevalence in males with unexplained abnormal sperm analysis
    Haim Pinkas, Sonia Fuchs, Y Aurbach-Klipper, Alex Zvulunov, Hila Raanani, Galit Sheffer-Mimouni, Benjamin Fisch, Naomi Weintrob · 2009 · Fertility and Sterility
  39. Incidental Finding of Bilateral Ovarian Adrenal Rest Tumor in a Patient With Congenital Adrenal Hyperplasia: A Case Report and Brief Review
    Lobna Bouzidi, Meriam Triki, Slim Charfi, Hana Ben Ameur, Mahdi Ben Dhaou, Touraya Bouaziz, Tahya Sallemi Boudawara · 2021 · Pediatric and Developmental Pathology
  40. Prevalence of non classical congenital adrenal hyperplasia due to 21‐hydroxylase deficiency in Greek women with acne: a hospital‐based cross‐sectional study
    Eftihios Trakakis, Evangelia Papadavid, Μaria Dalamaga, Dimitra Koumaki, Nicholas G. Stavrianeas, Dimitris Rigopoulos, George C. Creatsas, Demetrios P. Kassanos · 2012 · Journal of the European Academy of Dermatology and Venereology
  41. Application of the DHPLC method for mutational detection of the CYP21A2 gene in congenital adrenal hyperplasia
    Li‐Ping Tsai, Ching‐Feng Cheng, Jo-Ping Hsieh, Ming‐Sheng Teng, Hsien-Hsiung Lee · 2009 · Clinica Chimica Acta
  42. Hirsutism and quality of life with aspects on social support, anxiety and depression
    Maria Ekbäck · 2013 · Örebro University Library (Örebro University)
  43. LC-MS/MS improves screening towards 21-hydroxylase deficiency
    Urszula Ambroziak, Anna Kępczyńska‐Nyk, Alina Kuryłowicz, Aleksandra Wysłouch‐Cieszyńska, E Małunowicz, Zbigniew Bartoszewicz, Agnieszka Kondracka, Radosław Jaźwiec, Emilia Pawłowska, Magdalena Szcześniak et al. · 2014 · Gynecological Endocrinology
  44. Lack of correlation between phenotype and genotype in untreated 21‐hydroxylase‐deficient Indonesian patients
    Kristel Goossens, Achmad Zulfa Juniarto, Marianna A. Timmerman, Sultana MH Faradz, Katja P. Wolffenbuttel, Stenvert L. S. Drop, Frank H. de Jong · 2009 · Clinical Endocrinology
  45. Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiency.
    E Napolitano, Chiara Manieri, Francesca Restivo, E. Composto, Fabio Lanfranco, M Repici, Barbara Pasini, S. Einaudi, Elisa Menegatti · 2011 · PubMed
  46. Two novel CYP21A2 missense mutations in Italian patients with 21‐hydroxylase deficiency: Identification and functional characterisation
    Paola Concolino, Francesca Vendittelli, Enrica Mello, Cristiana Carelli Alinovi, Angelo Minucci, Cinzia Carrozza, Stefano Angelo Santini, Cecilia Zuppi, Ettore Capoluongo · 2009 · IUBMB Life
  47. Development of Graves' Hyperthyroidism Caused an Adrenal Crisis in a Patient with Previously Unrecognized Non-classical 21-hydroxylase Deficiency
    Nobuyuki Takasu, Ken Nakachi, Haruyo Higa · 2010 · Internal Medicine
  48. Basal 17‐hydroxyprogesterone cannot accurately predict nonclassical congenital adrenal hyperplasia in children and adolescents
    Rachel Bello, Yael Lebenthal, Liora Lazar, Shlomit Shalitin, Ariel Tenenbaum, Moshe Phillip, Liat de Vries · 2016 · Acta Paediatrica
  49. Low-Dose Dexamethasone Therapy from Infancy of Virilizing Congenital Adrenal Hyperplasia
    ScottA Rivkees, Kerry Stephenson · 2009 · International Journal of Pediatric Endocrinology
  50. Clinical Management of Male Infertility
    H.W.G. Baker · 2010 · Elsevier eBooks
  51. POLYCYSTIC OVARY SYNDROME: ORIGINS AND IMPLICATIONS: The significance of functional adrenal hyperandrogenism in polycystic ovary syndrome across the lifespan
    Laura Christine Torchen, Meng‐Hsing Wu, Brianna Thompson, Andi Beaudouin · 2025 · Reproduction
  52. Congenital Adrenal Hyperplasia: Unresolved Issues
    Mabel Yau, Ahmed Khattab, Dix Phillip Poppas, Lucia Ghizzoni, Maria I. New · 2016 · Frontiers of hormone research
  53. Developmental programming: postnatal estradiol modulation of prenatally organized reproductive neuroendocrine function in sheep
    Muraly Puttabyatappa, Rodolfo C. Cardoso, Carol Herkimer, Almudena Veiga‐Lopez, Vasantha Padmanabhan · 2016 · Reproduction
  54. Cortisol and Aldosterone Responses to Hypoglycemia and Na Depletion in Women With Non-Classic 21-Hydroxylase Deficiency
    Peter Kamenický, Anne Blanchard, Antonin Lamazière, Céline Piedvache, Bruno Donadille, Lise Duranteau, Hélène Bry, Jean–François Gautier, Sylvie Salenave, Marie‐Laure Raffin‐Sanson et al. · 2019 · The Journal of Clinical Endocrinology & Metabolism
  55. 21‐Hydroxylase Deficiency and Klinefelter Syndrome in an Adult Man: Striking a Balance Between Androgen Excess and Insufficiency
    A. Balestrieri, Lucia Zirilli, Bruno Madeo, Elisa Pignatti, Giulio Rossi, Cesare Carani, Vincenzo Rochira · 2008 · Journal of Andrology
  56. Natural History of Idiopathic Advanced Bone Age Diagnosed in Childhood: Pattern of Growth and Puberty
    Liora Lazar, Yael Lebenthal, Shlomit Shalitin, Moshe Phillip · 2010 · Hormone Research in Paediatrics
  57. Pubarquia precoz: Experience in 173 cases
    Francisca C. Eyzaguirre, Rodrigo E. Bancalari, Ronald Youlton, Rossana Román, Ricardo Oliveira Silva, Hernán García, Verónica Mericq G · 2009 · Revista médica de Chile
  58. Clinical Patterns and Linear Growth in Children with Congenital Adrenal Hyperplasia, an 11-Year Experience
    Adnan M. Al Shaikh, Yasser. Alghanmi., Saniah Awidah, Abdullah Bahha, MohamedE Ahmed, Ashraf Tawfik Soliman · 2019 · Indian Journal of Endocrinology and Metabolism
  59. A Multiclassifier System to Identify and Subtype Congenital Adrenal Hyperplasia Based on Circulating Steroid Hormones
    Lei Ye, Zhiyun Zhao, Huixia Ren, Wencui Wang, Wenzhong Zhou, Sichang Zheng, Jie Zhang, Jie Zhang, Haorong Li, Zhihan Wan et al. · 2022 · The Journal of Clinical Endocrinology & Metabolism
  60. High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening
    Patrícia S. Castro, Tatiana de Oliveira Rassi, Raquel Ferreira Araújo, Isabela Leite Pezzuti, Andresa S. Rodrigues, Tânia A.S.S. Bachega, Ivani Novato Silva · 2019 · Journal of Pediatric Endocrinology and Metabolism
  61. Classic virilizing congenital adrenal hyperplasia presenting late: case series from Pakistan.
    Aysha Habib Khan, Muniba Aban, Rameez-ul-Hassan, Naeem-ul-Haq, Jamal Raza, Abdul Jabbar, Tariq Moatter · 2009 · PubMed
  62. Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
    Takashi Shinagawa, Reiko Horikawa, Tsuyoshi Isojima, Yasuhiro Naiki, Toshiaki Tanaka, Noriyuki Katsumata · 2007 · Endocrine Journal
  63. Premature Pubarche: Time to Revise the Diagnostic Approach?
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  64. Genome editing in the adrenal gland: a novel strategy for treating congenital adrenal hyperplasia
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  65. Prenatal and Pregnancy Management of Congenital Adrenal Hyperplasia
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  66. The impact of genetic steroid disorders on human fertility
    David Reichman, Zev Rosenwaks · 2016 · The Journal of Steroid Biochemistry and Molecular Biology
  67. Bilateral ovarian cysts in a neonate with salt-wasting congenital adrenal hyperplasia
    Raghu Shankar, Jai Kumar Mahajan, Sanat Khanna, Katragadda L. N. Rao · 2010 · Journal of Pediatric Surgery
  68. Ultralow-dose Dexamethasone to Preserve Endogenous Cortisol Stress Response in Nonclassical Congenital Adrenal Hyperplasia: a New Promising Treatment
    Daniëlle van der Kaay, Erica L T van den Akker · 2014 · Intern J Endocrinol Metab
  69. Ashwagandharoot in the treatment of non-classical adrenal hyperplasia
    Amir Kalani, Gül Bahtiyar, Alan Scott Sacerdote · 2012 · BMJ Case Reports
  70. The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant
    Zhiyuan Zhao, Yinjie Gao, Lin Lü, Anli Tong, Shi Chen, Wei Zhang, Xiaoxia Zhang, Bang Sun, Xueyan Wu, Jiangfeng Mao et al. · 2023 · Frontiers in Endocrinology
  71. Testikuläre adrenale Resttumoren (TART) bei erwachsenen Männern mit klassischem adrenogenitalen Syndrom (AGS)
    Philipp Knape, Nicole Reisch, Helmuth G. Dörr, Martín Reincke, Severin V. Lenk, Marcus O. Quinkler · 2008 · Der Urologe
  72. The Cycle Characteristics and Outcomes of Infertile Nonclassic 21-Hydroxylase Deficiency Patients Undergoing Ovarian Stimulation for In Vitro Fertilization
    Shutian Jiang, Yanping Kuang · 2019 · Hormone and Metabolic Research
  73. Hyperandrogenism, Hirsutism, and Polycystic Ovary Syndrome
    Randall B. Barnes, David A. Ehrmann, Robert L. Rosenfield · 2010 · Elsevier eBooks
  74. Compromised Adult Height in Females with Non-Classical Congenital Adrenal Hyperplasia Diagnosed in Childhood
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  75. Basal levels of 17-hydroxyprogesterone can distinguish children with isolated precocious pubarche
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  76. Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population
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  79. Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn Screen
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  80. Genetics of gynaecological disorders
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  81. A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature
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  82. The way toward adulthood for females with nonclassic congenital adrenal hyperplasia
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  83. Cardiac tamponade as a presentation of primary adrenal insufficiency
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  84. Hiperplasia adrenal congênita em mulheres adultas: manejo de antigos e novos desafios
    Flavia Amanda Costa‐Barbosa, Mariana Telles Silveira, Claudio Elias Kater · 2014 · Arquivos Brasileiros de Endocrinologia & Metabologia
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  88. The Endocrinology of Sexual Behavior and Gender Identity
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  89. Hyperplasie congénitale des surrénales par déficit en 21-hydroxylase
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  90. Updates on Hirsutism: A Narrative Review
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  91. Acne
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  92. Beyond endocrine features in non-classical congenital adrenal hyperplasia: a narrative review of psychoneuro-social perspectives in pediatric and adolescent patients
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  93. Tercer Consenso Argentino sobre Patologías endocrinológicas
    Hugo Boquete · 2009 · Revista Argentina de Endocrinología y Metabolismo
  94. 17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in CYP21A2 Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analyses
    Seher Polat, Yusuf Kemal Arslan · 2022 · Journal of Clinical Research in Pediatric Endocrinology
  95. Androgens and Hirsutism in a Large Cohort of Portuguese Women
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  96. Regulation of Aldosterone Production
    William E. Rainey, Wendy Bollinger Bollag, Carlos M. Isales · 2009 · Elsevier eBooks
  97. Dépistage et prise en charge du déficit en 21-hydroxylase à révélation tardive chez les femmes avec hyperandrogénie
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  98. Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling
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  99. Hyperplasie congénitale des surrénales par déficit en 21-hydroxylase
    Anne Bachelot · 2012 · Elsevier eBooks
  100. Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
    Sara Ahmadi, Saadia Alvi, Randall J. Urban · 2013 · Expert Review of Endocrinology & Metabolism