Nonclassical 21-Hydroxylase Deficiency
New, Maria I.·2006·The Journal of Clinical Endocrinology & Metabolism
Cited by (314)
Items 101–200 of 314
- Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency: An Update on Genetic Analysis of CYP21A2 GeneBerta Carvalho, Cristina Joana Marques, Rita Santos Silva, Manuel Fontoura, Davide Maurício Carvalho, Filipa Carvalho · 2020 · Experimental and Clinical Endocrinology & Diabetes
- Hyperinsulinemic-Euglycemic Clamp Strengthens the Insulin Resistance in Nonclassical Congenital Adrenal HyperplasiaAriane 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
- Substitution therapy in adult patients with congenital adrenal hyperplasiaNicole Reisch · 2014 · Best Practice & Research Clinical Endocrinology & Metabolism
- Absence of clinically relevant growth acceleration in untreated children with non-classical congenital adrenal hyperplasiaPijnenburg-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
- Obesity and Cardiometabolic Risk Factors in Children and Young Adults With Non-classical 21-Hydroxylase DeficiencyLiat de Vries, Yael Lebenthal, Moshe Phillip, Shlomit Shalitin, Ariel Tenenbaum, Rachel Bello · 2019 · Frontiers in Endocrinology
- 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
- Pregnancy and Prenatal Management of Congenital Adrenal HyperplasiaGianluca 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
- Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriersFrançoise Paris, Véronique Tardy, Anne Chalançon, Marie‐Christine Picot, Yves Morel, Charles Sultan · 2010 · Gynecological Endocrinology
- Hyperandrogénie féminineMaëliss Peigné, Anne Villers-Capelle, Geoffroy Robin, Didier Dewailly · 2013 · La Presse Médicale
- The Adrenal CortexPaul M. Stewart, John D C Newell-Price · 2016 · Elsevier eBooks
- MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosisMICHEL M. PUGEAT, Ingrid Plotton, Aude Brac de la Perrière, Gérald Raverot, Henri Déchaud, Véronique Raverot · 2018 · European Journal of Endocrinology
- Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary SyndromeGiovana 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
- Refractory Acne and 21-Hydroxylase Deficiency in a Selected Group of Female PatientsValentina Caputo, Santi Fiorella, Salvatrice Curiale, Alfredo Caputo, Marcello Niceta · 2010 · Dermatology
- Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and ChildhoodKenichi Kashimada, Makoto ONO, Toshikazu ONISHI, Satimi KOYAMA, Takio Toyoura, Kazuhide Imai, Sumitaka Saisho, Shuki Mizutani · 2008 · Endocrine Journal
- 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
- Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal HyperplasiaMalgorzata 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
- Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testingGuillaume 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
- Dynamic Testing for Evaluation of Adrenal and Gonadal Function in Pediatric and Adult Endocrinology: An OverviewAlpesh Goyal, Suraj Kubihal, Yashdeep Gupta, Viveka P. Jyotsna, Rajesh Khadgawat · 2019 · Indian Journal of Endocrinology and Metabolism
- Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyChen, Wuyan, Xu, Zhi, Nishitani, Miki, Van Ryzin, Carol, McDonnell, Nazli B., Merke, Deborah P. · 2012 · Human Genetics
- Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 PatientsBanu 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
- Defects of Adrenal SteroidogenesisMabel Yau, Ahmed Khattab, Christian Pina, Tony Yuen, Heino F. L. Meyer‐Bahlburg, Maria I. New · 2015 · Elsevier eBooks
- Sperm retrieval and concomitant tumor resection in azoospermic men with congenital adrenal hyperplasia and bilateral testicular adrenal rest tumors: a case reportKavoussi, 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
- 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
- Hyperandrogenism, Hirsutism, and Polycystic Ovary SyndromeRobert L. Rosenfield, Randall B. Barnes, David A. Ehrmann · 2015 · Elsevier eBooks
- Clinical, biochemical, and genetic features of non-classical 21-hydroxylase deficiency in Japanese childrenKenichi Kashimada, Tomohiro Ishii, Keisuke Nagasaki, Makoto Ono, Toshihiro Tajima, Ichiro Yokota, Yukihiro Hasegawa · 2015 · Endocrine Journal
- New developments in prenatal diagnosis of congenital adrenal hyperplasiaDiya Kazmi, Jack Bailey, Maggie LY. Yau, Wahid Abu‐Amer, Ameet Kumar, Merly Low, Tony Yuen · 2016 · The Journal of Steroid Biochemistry and Molecular Biology
- Low-Dose Dexamethasone Therapy from Infancy of Virilizing Congenital Adrenal HyperplasiaScott A. Rivkees, Kerry Stephenson · 2009 · International Journal of Pediatric Endocrinology
- The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian populationAyca 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
- 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 InteractionFelix G. Riepe, Olaf Hiort, Joachim Grötzinger, Wolfgang G. Sippell, Nils Peter Krone, Paul‐Martin Holterhus · 2008 · The Journal of Clinical Endocrinology & Metabolism
- Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyDörr, 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
- High-resolution melting curve (HRM) analysis to establish CYP21A2 mutations converted from the CYP21A1P in congenital adrenal hyperplasiaYi-Ching Lin, Yu‐Chih Lin, Ta‐Chih Liu, Jan‐Gowth Chang, Hsien-Hsiung Lee · 2011 · Clinica Chimica Acta
- No. 350-Hirsutism: Evaluation and TreatmentKimberly E. Liu, Tarek Motan, Paul Claman · 2017 · Journal of Obstetrics and Gynaecology Canada
- 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
- Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasiaIngeborg Brønstad, Lars Breivik, Paal Methlie, Anette S. B. Wolff, Eirik Bratland, Ingrid Nermoen, Kristian Løvås, Eystein S. Husebye · 2014 · Endocrine Connections
- Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolitesKoyama, Yuhei, Homma, Keiko, Fukami, Maki, Miwa, Masayuki, Ikeda, Kazushige, Ogata, Tsutomu, Murata, Mitsuru, Hasegawa, Tomonobu · 2016 · Clinical Pediatric Endocrinology
- Neonatal screening for congenital adrenal hyperplasia: transitory elevation of 17-hydroxyprogesteroneBelén 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
- A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook EffectTülay Güran, Gözde Yeşil, Ömer Güran, Suna Cesur, Oktav Bosnalı, Ayşenur Cerrah Celayir, Sevilay Topçuoğlu, Abdullah Bereket · 2012 · Journal of Clinical Research in Pediatric Endocrinology
- Non-classical 21-hydroxylase deficiency: prevalence in males with unexplained abnormal sperm analysisHaim Pinkas, Sonia Fuchs, Y Aurbach-Klipper, Alex Zvulunov, Hila Raanani, Galit Sheffer-Mimouni, Benjamin Fisch, Naomi Weintrob · 2009 · Fertility and Sterility
- Incidental Finding of Bilateral Ovarian Adrenal Rest Tumor in a Patient With Congenital Adrenal Hyperplasia: A Case Report and Brief ReviewLobna Bouzidi, Meriam Triki, Slim Charfi, Hana Ben Ameur, Mahdi Ben Dhaou, Touraya Bouaziz, Tahya Sallemi Boudawara · 2021 · Pediatric and Developmental Pathology
- Prevalence of non classical congenital adrenal hyperplasia due to 21‐hydroxylase deficiency in Greek women with acne: a hospital‐based cross‐sectional studyEftihios 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
- Application of the DHPLC method for mutational detection of the CYP21A2 gene in congenital adrenal hyperplasiaLi‐Ping Tsai, Ching‐Feng Cheng, Jo-Ping Hsieh, Ming‐Sheng Teng, Hsien-Hsiung Lee · 2009 · Clinica Chimica Acta
- Hirsutism and quality of life with aspects on social support, anxiety and depressionMaria Ekbäck · 2013 · Örebro University Library (Örebro University)
- LC-MS/MS improves screening towards 21-hydroxylase deficiencyUrszula 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
- Lack of correlation between phenotype and genotype in untreated 21‐hydroxylase‐deficient Indonesian patientsKristel Goossens, Achmad Zulfa Juniarto, Marianna A. Timmerman, Sultana MH Faradz, Katja P. Wolffenbuttel, Stenvert L. S. Drop, Frank H. de Jong · 2009 · Clinical Endocrinology
- 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
- Two novel CYP21A2 missense mutations in Italian patients with 21‐hydroxylase deficiency: Identification and functional characterisationPaola Concolino, Francesca Vendittelli, Enrica Mello, Cristiana Carelli Alinovi, Angelo Minucci, Cinzia Carrozza, Stefano Angelo Santini, Cecilia Zuppi, Ettore Capoluongo · 2009 · IUBMB Life
- Development of Graves' Hyperthyroidism Caused an Adrenal Crisis in a Patient with Previously Unrecognized Non-classical 21-hydroxylase DeficiencyNobuyuki Takasu, Ken Nakachi, Haruyo Higa · 2010 · Internal Medicine
- Basal 17‐hydroxyprogesterone cannot accurately predict nonclassical congenital adrenal hyperplasia in children and adolescentsRachel Bello, Yael Lebenthal, Liora Lazar, Shlomit Shalitin, Ariel Tenenbaum, Moshe Phillip, Liat de Vries · 2016 · Acta Paediatrica
- Low-Dose Dexamethasone Therapy from Infancy of Virilizing Congenital Adrenal HyperplasiaScottA Rivkees, Kerry Stephenson · 2009 · International Journal of Pediatric Endocrinology
- Clinical Management of Male InfertilityH.W.G. Baker · 2010 · Elsevier eBooks
- POLYCYSTIC OVARY SYNDROME: ORIGINS AND IMPLICATIONS: The significance of functional adrenal hyperandrogenism in polycystic ovary syndrome across the lifespanLaura Christine Torchen, Meng‐Hsing Wu, Brianna Thompson, Andi Beaudouin · 2025 · Reproduction
- Congenital Adrenal Hyperplasia: Unresolved IssuesMabel Yau, Ahmed Khattab, Dix Phillip Poppas, Lucia Ghizzoni, Maria I. New · 2016 · Frontiers of hormone research
- Developmental programming: postnatal estradiol modulation of prenatally organized reproductive neuroendocrine function in sheepMuraly Puttabyatappa, Rodolfo C. Cardoso, Carol Herkimer, Almudena Veiga‐Lopez, Vasantha Padmanabhan · 2016 · Reproduction
- Cortisol and Aldosterone Responses to Hypoglycemia and Na Depletion in Women With Non-Classic 21-Hydroxylase DeficiencyPeter 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
- 21‐Hydroxylase Deficiency and Klinefelter Syndrome in an Adult Man: Striking a Balance Between Androgen Excess and InsufficiencyA. Balestrieri, Lucia Zirilli, Bruno Madeo, Elisa Pignatti, Giulio Rossi, Cesare Carani, Vincenzo Rochira · 2008 · Journal of Andrology
- Natural History of Idiopathic Advanced Bone Age Diagnosed in Childhood: Pattern of Growth and PubertyLiora Lazar, Yael Lebenthal, Shlomit Shalitin, Moshe Phillip · 2010 · Hormone Research in Paediatrics
- Pubarquia precoz: Experience in 173 casesFrancisca C. Eyzaguirre, Rodrigo E. Bancalari, Ronald Youlton, Rossana Román, Ricardo Oliveira Silva, Hernán García, Verónica Mericq G · 2009 · Revista médica de Chile
- Clinical Patterns and Linear Growth in Children with Congenital Adrenal Hyperplasia, an 11-Year ExperienceAdnan M. Al Shaikh, Yasser. Alghanmi., Saniah Awidah, Abdullah Bahha, MohamedE Ahmed, Ashraf Tawfik Soliman · 2019 · Indian Journal of Endocrinology and Metabolism
- A Multiclassifier System to Identify and Subtype Congenital Adrenal Hyperplasia Based on Circulating Steroid HormonesLei 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
- High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screeningPatrícia 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
- 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
- Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in JapanTakashi Shinagawa, Reiko Horikawa, Tsuyoshi Isojima, Yasuhiro Naiki, Toshiaki Tanaka, Noriyuki Katsumata · 2007 · Endocrine Journal
- Premature Pubarche: Time to Revise the Diagnostic Approach?Federico Baronio, Alice Marzatico, Rosaria DE IASIO, Rita Ortolano, Antonio Fanolla, Giorgio Radetti, Antonio Balsamo, Andrea Pession, Alessandra Cassio · 2023 · Journal of Clinical Medicine
- Genome editing in the adrenal gland: a novel strategy for treating congenital adrenal hyperplasiaEva B. van Dijk, Samantha L. Ginn, Ian E. Alexander, Lara E. Graves · 2024 · Exploration of Endocrine and Metabolic Diseases
- Prenatal and Pregnancy Management of Congenital Adrenal HyperplasiaHanna Franziska Nowotny, Lea Tschaidse, Matthias K. Auer, Nicole Reisch · 2024 · Clinical Endocrinology
- The impact of genetic steroid disorders on human fertilityDavid Reichman, Zev Rosenwaks · 2016 · The Journal of Steroid Biochemistry and Molecular Biology
- Bilateral ovarian cysts in a neonate with salt-wasting congenital adrenal hyperplasiaRaghu Shankar, Jai Kumar Mahajan, Sanat Khanna, Katragadda L. N. Rao · 2010 · Journal of Pediatric Surgery
- Ultralow-dose Dexamethasone to Preserve Endogenous Cortisol Stress Response in Nonclassical Congenital Adrenal Hyperplasia: a New Promising TreatmentDaniëlle van der Kaay, Erica L T van den Akker · 2014 · Intern J Endocrinol Metab
- Ashwagandharoot in the treatment of non-classical adrenal hyperplasiaAmir Kalani, Gül Bahtiyar, Alan Scott Sacerdote · 2012 · BMJ Case Reports
- The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variantZhiyuan 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
- 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
- The Cycle Characteristics and Outcomes of Infertile Nonclassic 21-Hydroxylase Deficiency Patients Undergoing Ovarian Stimulation for In Vitro FertilizationShutian Jiang, Yanping Kuang · 2019 · Hormone and Metabolic Research
- Hyperandrogenism, Hirsutism, and Polycystic Ovary SyndromeRandall B. Barnes, David A. Ehrmann, Robert L. Rosenfield · 2010 · Elsevier eBooks
- Compromised Adult Height in Females with Non-Classical Congenital Adrenal Hyperplasia Diagnosed in ChildhoodRachel Bello, Liora Lazar, Moshe Phillip, Liat de Vries · 2023 · Hormone Research in Paediatrics
- Basal levels of 17-hydroxyprogesterone can distinguish children with isolated precocious pubarcheAnna Grandone, Pierluigi Marzuillo, Caterina Luongo, Roberto Toraldo, Michela Mariani, Emanuele Miraglia del Giudice, Laura Perrone · 2018 · Pediatric Research
- Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian populationZorana Grubić, Marija Maskalan, Katarina Štingl Janković, Sabina Zvečić, Katja Dumić Kubat, Nevena Krnić, Renata Žunec, Jasenka Ille, Vesna Kuŝec, Miro Dumić · 2016 · HLA
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- Utilidad del análisis molecular en el diagnóstico diferencial del déficit congénito de 21-hidroxilasa detectado en el cribado neonatalLeandro Soriano Guillén, M. Velázquez de Cuéllar Paracchi, Begoña Ezquieta · 2009 · Medicina Clínica
- Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn ScreenBonnie McCann‐Crosby, Mark C. Liang, Mitchell E. Geffner, Christina M. Koppin, Nicole R. Fraga, Vernon Reid Sutton, Lefkothea P. Karaviti, Gagandeep Bhullar, Mimi S. Kim · 2023 · International Journal of Neonatal Screening
- Genetics of gynaecological disordersDragana J. Josifova · 2017 · Best Practice & Research Clinical Obstetrics & Gynaecology
- 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 literatureAlessia Aureli, Sarah Bocchini, Michela Mariani, Antonino Crinò, Marco Cappa, Danilo Fintini · 2023 · Frontiers in Endocrinology
- The way toward adulthood for females with nonclassic congenital adrenal hyperplasiaGeorgia Ntali, Sokratis Charisis, Christo F. Kylafi, Evangelia Vogiatzi, Lina Michala · 2021 · Endocrine
- Cardiac tamponade as a presentation of primary adrenal insufficiencyJoseph William Page, Joshua Drinkwater, Guy Furniss, Mohammad Sahebjalal · 2022 · BMJ Case Reports
- Hiperplasia adrenal congênita em mulheres adultas: manejo de antigos e novos desafiosFlavia Amanda Costa‐Barbosa, Mariana Telles Silveira, Claudio Elias Kater · 2014 · Arquivos Brasileiros de Endocrinologia & Metabologia
- Inadequate testosterone suppression after medical and subsequent surgical castration in a patient with prostate cancerÓskar Ragnarsson, Gudmundur Johannsson, Kjell Geterud, Pär Lodding, Per Mikael Dahlqvist · 2013 · BMJ Case Reports
- Hiperplasia congénita da suprarrenal não clássica – aspetos relevantes para a prática clínicaTeresa Azevedo, Teresa Martins, Manuel Carlos Lemos, Fernando Rodrigues · 2014 · Revista Portuguesa de Endocrinologia Diabetes e Metabolismo
- The human genital tubercle is steroidogenic organ at early pregnancyIuliia Savchuk, Marie‐Line Morvan, Jean‐Philippe Antignac, Kristina Gemzell‐Danielsson, Bruno Le Bizec, Olle Söder, Konstantin Svechnikov · 2018 · Molecular and Cellular Endocrinology
- The Endocrinology of Sexual Behavior and Gender IdentityLouis J. Gooren · 2015 · Elsevier eBooks
- Hyperplasie congénitale des surrénales par déficit en 21-hydroxylaseAnne Bachelot · 2019 · Elsevier eBooks
- Updates on Hirsutism: A Narrative ReviewRamadan Hussein, Walid Kamal Abdelbasset · 2022 · International Journal of Biomedicine
- AcneAlison Layton, E. Anne Eady, Christos C. Zouboulis · 2016 · Wiley eBooks
- Beyond endocrine features in non-classical congenital adrenal hyperplasia: a narrative review of psychoneuro-social perspectives in pediatric and adolescent patientsRoberto Paparella, Fabiola Panvino, Ida Pucarelli, Marcello Niceta, Matteo Spaziani, Alberto Spalice, Francesco Pisani, Ignazio Ardizzone, Luigi Tarani · 2025 · European Journal of Pediatrics
- Tercer Consenso Argentino sobre Patologías endocrinológicasHugo Boquete · 2009 · Revista Argentina de Endocrinología y Metabolismo
- 17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in CYP21A2 Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analysesSeher Polat, Yusuf Kemal Arslan · 2022 · Journal of Clinical Research in Pediatric Endocrinology
- Androgens and Hirsutism in a Large Cohort of Portuguese WomenJoana Pinto, Nicoletta Cera, Claudia Camerino, Jorge Beires, Duarte Pignatelli · 2025 · Journal of Clinical Medicine
- Regulation of Aldosterone ProductionWilliam E. Rainey, Wendy Bollinger Bollag, Carlos M. Isales · 2009 · Elsevier eBooks
- Dépistage et prise en charge du déficit en 21-hydroxylase à révélation tardive chez les femmes avec hyperandrogénieJacques Young, Véronique Tardy, Aude Brac de la Perrière, Anne Bachelot, Yves Morel · 2010 · Annales d Endocrinologie
- Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a siblingYılmaz Kör, Minjing Zou, Roua A. Al‐Rijjal, Dorota Monies, Brian F. Meyer, Yufei Shi · 2018 · BMC Medical Genetics
- Hyperplasie congénitale des surrénales par déficit en 21-hydroxylaseAnne Bachelot · 2012 · Elsevier eBooks
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrierSara Ahmadi, Saadia Alvi, Randall J. Urban · 2013 · Expert Review of Endocrinology & Metabolism