Novel methods in adrenal research: a metabolomics approach
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A. Walch | L. Guasti | N. Sun | G. Eisenhofer | S. Richter | W. Arlt | A. Taylor | G. Ruiz-Babot | T. Papathomas | V. Chortis | Vasileios Chortis
[1] Martin Fassnacht,et al. Plasma steroid metabolome profiling for the diagnosis of adrenocortical carcinoma. , 2019, European journal of endocrinology.
[2] M. Manzoni,et al. Molecular signatures of medullary thyroid carcinoma by matrix-assisted laser desorption/ionisation mass spectrometry imaging. , 2019, Journal of proteomics.
[3] Carsten Denkert,et al. MALDI‐Imaging for Classification of Epithelial Ovarian Cancer Histotypes from a Tissue Microarray Using Machine Learning Methods , 2018, Proteomics. Clinical applications.
[4] V. Chortis,et al. The role of steroid metabolome analysis for the diagnosis and follow-up of adrenocortical tumors. , 2018, Minerva endocrinologica.
[5] M. Speicher,et al. Current and future perspectives of liquid biopsies in genomics-driven oncology , 2018, Nature Reviews Genetics.
[6] A. Ewing,et al. On-Tissue Chemical Derivatization of Catecholamines Using 4-( N-Methyl)pyridinium Boronic Acid for ToF-SIMS and LDI-ToF Mass Spectrometry Imaging. , 2018, Analytical chemistry.
[7] R. Casadonte,et al. Digital PCR After MALDI–Mass Spectrometry Imaging to Combine Proteomic Mapping and Identification of Activating Mutations in Pulmonary Adenocarcinoma , 2018, Proteomics. Clinical applications.
[8] B. Heijs,et al. Mass spectrometry imaging: How will it affect clinical research in the future? , 2018, Expert review of proteomics.
[9] Jay-Jiguang Zhu,et al. Analysis of cerebrospinal fluid metabolites in patients with primary or metastatic central nervous system tumors , 2018, Acta neuropathologica communications.
[10] P. Romagnoli,et al. Human fetal adrenal cells retain age‐related stem‐ and endocrine‐differentiation potential in culture , 2018, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[11] T. MacDonald,et al. Rapid discrimination of pediatric brain tumors by mass spectrometry imaging , 2018, Journal of Neuro-Oncology.
[12] H. Olsson,et al. Endogenous expression mapping of malignant melanoma by mass spectrometry imaging , 2018, Clinical and Translational Medicine.
[13] D. Aust,et al. Metabolome-guided genomics to identify mutations in isocitrate dehydrogenase, fumarate hydratase and succinate dehydrogenase genes in pheochromocytoma and paraganglioma , 2018, Genetics in Medicine.
[14] T. Pons,et al. Role of MDH2 pathogenic variant in pheochromocytoma and paraganglioma patients , 2018, Genetics in Medicine.
[15] B. Shuch,et al. Krebs Cycle-Deficient Hereditary Cancer Syndromes are Defined by Homologous Recombination DNA Repair Defects , 2018, Nature Genetics.
[16] W. Arlt,et al. Monogenic Disorders of Adrenal Steroidogenesis , 2018, Hormone Research in Paediatrics.
[17] S. Tevosian,et al. Pheochromocytoma/Paraganglioma: A Poster Child for Cancer Metabolism , 2018, The Journal of clinical endocrinology and metabolism.
[18] Zhongming Zhao,et al. Molecular Characterization and Clinical Relevance of Metabolic Expression Subtypes in Human Cancers , 2018, Cell reports.
[19] P. de Vos,et al. Long-term viability and function of transplanted islets macroencapsulated at high density are achieved by enhanced oxygen supply , 2018, Scientific Reports.
[20] R. Crystal,et al. Biology of the Adrenal Gland Cortex Obviates Effective Use of Adeno-Associated Virus Vectors to Treat Hereditary Adrenal Disorders. , 2018, Human gene therapy.
[21] C. Ludwig,et al. Oncogenic IDH1 Mutations Promote Enhanced Proline Synthesis through PYCR1 to Support the Maintenance of Mitochondrial Redox Homeostasis , 2018, Cell reports.
[22] Aubry K. Miller,et al. Rapid detection of 2-hydroxyglutarate in frozen sections of IDH mutant tumors by MALDI-TOF mass spectrometry , 2018, Acta neuropathologica communications.
[23] Na Sun,et al. High-Resolution Tissue Mass Spectrometry Imaging Reveals a Refined Functional Anatomy of the Human Adult Adrenal Gland , 2018, Endocrinology.
[24] Graeme Eisenhofer,et al. Plasma Steroid Metabolome Profiling for Diagnosis and Subtyping Patients with Cushing Syndrome. , 2018, Clinical chemistry.
[25] Ó. Pozo,et al. SULFATION PATHWAYS: Alternate steroid sulfation pathways targeted by LC-MS/MS analysis of disulfates: application to prenatal diagnosis of steroid synthesis disorders. , 2018, Journal of molecular endocrinology.
[26] U. Srirangalingam,et al. Modeling Congenital Adrenal Hyperplasia and Testing Interventions for Adrenal Insufficiency Using Donor-Specific Reprogrammed Cells , 2018, Cell reports.
[27] F. Beuschlein,et al. The impact of Connshing's syndrome - mild cortisol excess in primary aldosteronism drives diabetes risk. , 2017, Journal of hypertension.
[28] P. Kapur,et al. Oncometabolites: A New Paradigm for Oncology, Metabolism, and the Clinical Laboratory. , 2017, Clinical chemistry.
[29] Dylan Lewis,et al. A 13-Steroid Serum Panel Based on LC-MS/MS: Use in Detection of Adrenocortical Carcinoma. , 2017, Clinical chemistry.
[30] W. Young,et al. High-Resolution, Accurate-Mass (HRAM) Mass Spectrometry Urine Steroid Profiling in the Diagnosis of Adrenal Disorders. , 2017, Clinical chemistry.
[31] Li Zhang,et al. Delivery strategies of the CRISPR‐Cas9 gene‐editing system for therapeutic applications , 2017, Journal of controlled release : official journal of the Controlled Release Society.
[32] Morgan R Alexander,et al. The 3D OrbiSIMS—label-free metabolic imaging with subcellular lateral resolution and high mass-resolving power , 2017, Nature Methods.
[33] Roman Jaksik,et al. Proteome profiles of different types of thyroid cancers , 2017, Molecular and Cellular Endocrinology.
[34] C. Haglund,et al. N‐Glycomic Profiling of Pheochromocytomas and Paragangliomas Separates Metastatic and Nonmetastatic Disease , 2017, The Journal of clinical endocrinology and metabolism.
[35] Martin J. Lohse,et al. Single-molecule imaging reveals receptor–G protein interactions at cell surface hot spots , 2017, Nature.
[36] M. Lohse,et al. Internalized TSH receptors en route to the TGN induce local Gs-protein signaling and gene transcription , 2017, Nature Communications.
[37] Adam K. Glaser,et al. Multiplexed Optical Imaging of Tumor-Directed Nanoparticles: A Review of Imaging Systems and Approaches , 2017, Nanotheranostics.
[38] Yen-Hung Lin,et al. Risk of new-onset diabetes mellitus in primary aldosteronism: a population study over 5 years , 2017, Journal of hypertension.
[39] M. Esteller,et al. Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer–Predisposing Mutations in Pheochromocytomas and Paragangliomas , 2017, Clinical Cancer Research.
[40] A. Longatto-Filho,et al. GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior , 2017, OncoTarget.
[41] Joanna Polanska,et al. Molecular profiles of thyroid cancer subtypes: Classification based on features of tissue revealed by mass spectrometry imaging. , 2017, Biochimica et biophysica acta. Proteins and proteomics.
[42] S. Ellis,et al. Laser post-ionisation combined with a high resolving power orbitrap mass spectrometer for enhanced MALDI-MS imaging of lipids. , 2017, Chemical communications.
[43] A. Lane,et al. Exploring cancer metabolism using stable isotope-resolved metabolomics (SIRM) , 2017, The Journal of Biological Chemistry.
[44] W. Arlt,et al. Diagnosis of a malignant adrenal mass: the role of urinary steroid metabolite profiling , 2017, Current opinion in endocrinology, diabetes, and obesity.
[45] Michael Biehl,et al. Steroid metabolome analysis reveals prevalent glucocorticoid excess in primary aldosteronism , 2017, JCI insight.
[46] Yen-Hung Lin,et al. Risk of Fracture in Primary Aldosteronism: A Population‐Based Cohort Study , 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[47] B. Klink,et al. Metabologenomics of Phaeochromocytoma and Paraganglioma: An Integrated Approach for Personalised Biochemical and Genetic Testing. , 2017, The Clinical biochemist. Reviews.
[48] R. Caprioli,et al. Imaging mass spectrometry assists in the classification of diagnostically challenging atypical Spitzoid neoplasms. , 2016, Journal of the American Academy of Dermatology.
[49] Marissa Fessenden,et al. Metabolomics: Small molecules, single cells , 2016, Nature.
[50] Na Sun,et al. High-mass-resolution MALDI mass spectrometry imaging of metabolites from formalin-fixed paraffin-embedded tissue , 2016, Nature Protocols.
[51] E. Bessonova,et al. Different Types of Urinary Steroid Profiling Obtained by High-Performance Liquid Chromatography and Gas Chromatography-Mass Spectrometry in Patients with Adrenocortical Carcinoma , 2016, Hormones and Cancer.
[52] Erwin G. Van Meir,et al. Selective Detection of the D-enantiomer of 2-Hydroxyglutarate in the CSF of Glioma Patients with Mutated Isocitrate Dehydrogenase , 2016, Clinical Cancer Research.
[53] Hans Clevers,et al. Modeling Development and Disease with Organoids , 2016, Cell.
[54] R. Langer,et al. How Suitable is Matrix-Assisted Laser Desorption/Ionization-Time-of-Flight for Metabolite Imaging from Clinical Formalin-Fixed and Paraffin-Embedded Tissue Samples in Comparison to Matrix-Assisted Laser Desorption/Ionization-Fourier Transform Ion Cyclotron Resonance Mass Spectrometry? , 2016, Analytical chemistry.
[55] Steven A. Brown,et al. Circadian Metabolomics: Insights for Biology and Medicine , 2016 .
[56] U. Schubert,et al. Multigrid MALDI mass spectrometry imaging (mMALDI MSI) , 2016, Analytical and Bioanalytical Chemistry.
[57] Nick Barker,et al. Organoids as an in vitro model of human development and disease , 2016, Nature Cell Biology.
[58] B. Klink,et al. Epigenetic Mutation of the Succinate Dehydrogenase C Promoter in a Patient With Two Paragangliomas. , 2016, The Journal of clinical endocrinology and metabolism.
[59] Stefan R Bornstein,et al. Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline. , 2016, The Journal of clinical endocrinology and metabolism.
[60] C. Thompson,et al. The Emerging Hallmarks of Cancer Metabolism. , 2016, Cell metabolism.
[61] L. McDonnell,et al. Mass spectrometry imaging of amino neurotransmitters: a comparison of derivatization methods and application in mouse brain tissue , 2016, Metabolomics.
[62] Graeme Eisenhofer,et al. Genotype-Specific Steroid Profiles Associated With Aldosterone-Producing Adenomas , 2016, Hypertension.
[63] M. Blankenstein,et al. Comparison of 7 Published LC-MS/MS Methods for the Simultaneous Measurement of Testosterone, Androstenedione, and Dehydroepiandrosterone in Serum. , 2015, Clinical chemistry.
[64] A. Longatto-Filho,et al. Metabolic reprogramming: a new relevant pathway in adult adrenocortical tumors , 2015, Oncotarget.
[65] Christian M. Metallo,et al. Loss of succinate dehydrogenase activity results in dependency on pyruvate carboxylation for cellular anabolism , 2015, Nature Communications.
[66] F. Beuschlein,et al. Increased prevalence of diabetes mellitus and the metabolic syndrome in patients with primary aldosteronism of the German Conn's Registry. , 2015, European journal of endocrinology.
[67] P. Bénit,et al. In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma , 2015, Clinical Cancer Research.
[68] R. Langer,et al. High‐resolution MALDI‐FT‐ICR MS imaging for the analysis of metabolites from formalin‐fixed, paraffin‐embedded clinical tissue samples , 2015, The Journal of pathology.
[69] B. Keevil,et al. Mass spectrometry and immunoassay: how to measure steroid hormones today and tomorrow. , 2015, European journal of endocrinology.
[70] I. Norton,et al. MALDI mass spectrometry imaging analysis of pituitary adenomas for near-real-time tumor delineation , 2015, Proceedings of the National Academy of Sciences.
[71] A. Tischler,et al. SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T) , 2015, Modern Pathology.
[72] M. Loda,et al. Innovation in metabolomics to improve personalized healthcare , 2015, Annals of the New York Academy of Sciences.
[73] I. Kema,et al. Diagnostic Value of Urinary Steroid Profiling in the Evaluation of Adrenal Tumors , 2015, Hormones and Cancer.
[74] L. Guasti,et al. New Directions for the Treatment of Adrenal Insufficiency , 2015, Front. Endocrinol..
[75] Juan F. García,et al. Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene. , 2015, Journal of the National Cancer Institute.
[76] K. Dreisewerd,et al. Mass spectrometry imaging with laser-induced postionization , 2015, Science.
[77] C. Stratakis,et al. Metabolome Profiling by HRMAS NMR Spectroscopy of Pheochromocytomas and Paragangliomas Detects SDH Deficiency: Clinical and Pathophysiological Implications12 , 2015, Neoplasia.
[78] E. Letouzé,et al. Oncometabolites‐driven tumorigenesis: From genetics to targeted therapy , 2014, International journal of cancer.
[79] S. Wiemann,et al. Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad. , 2014, Endocrine-related cancer.
[80] Juergen A. Knoblich,et al. Organogenesis in a dish: Modeling development and disease using organoid technologies , 2014, Science.
[81] F. Beuschlein,et al. Krebs cycle metabolite profiling for identification and stratification of pheochromocytomas/paragangliomas due to succinate dehydrogenase deficiency. , 2014, The Journal of clinical endocrinology and metabolism.
[82] H. Bayır,et al. Improved spatial resolution of matrix-assisted laser desorption/ionization imaging of lipids in the brain by alkylated derivatives of 2,5-dihydroxybenzoic acid. , 2014, Rapid communications in mass spectrometry : RCM.
[83] C. Borchers,et al. Comprehensive imaging of porcine adrenal gland lipids by MALDI-FTMS using quercetin as a matrix. , 2014, Analytical chemistry.
[84] P. Bachellier,et al. Metabolomic profile of the adrenal gland: from physiology to pathological conditions. , 2013, Endocrine-related cancer.
[85] Malte Buchholz,et al. MALDI mass spectrometric imaging based identification of clinically relevant signals in prostate cancer using large‐scale tissue microarrays , 2013, International journal of cancer.
[86] G. Schackert,et al. Accumulation of 2-hydroxyglutarate is not a biomarker for malignant progression in IDH-mutated low-grade gliomas. , 2013, Neuro-oncology.
[87] R. Rodenburg,et al. Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma , 2013, Clinical Cancer Research.
[88] A. Chan,et al. Diagnosis of 5α–reductase 2 deficiency: is measurement of dihydrotestosterone essential? , 2013, International Journal of Pediatric Endocrinology.
[89] W. Linehan,et al. Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. , 2012, The Journal of urology.
[90] Kazuwa Nakao,et al. Differentiation of human embryonic stem cells and human induced pluripotent stem cells into steroid-producing cells. , 2012, Endocrinology.
[91] G. Siuzdak,et al. Innovation: Metabolomics: the apogee of the omics trilogy , 2012, Nature Reviews Molecular Cell Biology.
[92] Ovidiu C. Andronesi,et al. Detection of 2-Hydroxyglutarate in IDH-Mutated Glioma Patients by In Vivo Spectral-Editing and 2D Correlation Magnetic Resonance Spectroscopy , 2012, Science Translational Medicine.
[93] C. Shackleton,et al. A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency , 2011, The Journal of clinical endocrinology and metabolism.
[94] M. Dattani,et al. Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency , 2011, The Journal of clinical endocrinology and metabolism.
[95] Michael Biehl,et al. Urine Steroid Metabolomics as a Biomarker Tool for Detecting Malignancy in Adrenal Tumors , 2011, The Journal of clinical endocrinology and metabolism.
[96] A. Wallace,et al. Pitfalls in the Diagnosis of 5α-Reductase Type 2 Deficiency during Early Infancy , 2011, Hormone Research in Paediatrics.
[97] G. Fava,et al. Psychological assessment of primary aldosteronism: a controlled study. , 2011, Journal of Clinical Endocrinology and Metabolism.
[98] D. Hanahan,et al. Hallmarks of Cancer: The Next Generation , 2011, Cell.
[99] V. Montori,et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. , 2010, The Journal of clinical endocrinology and metabolism.
[100] G. Lavery,et al. Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS) , 2010, The Journal of Steroid Biochemistry and Molecular Biology.
[101] E. van Marck,et al. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. , 2009, The Lancet. Oncology.
[102] S. Hahner,et al. Therapeutic management of adrenal insufficiency. , 2009, Best practice & research. Clinical endocrinology & metabolism.
[103] J. Svartberg,et al. Normal overall mortality rate in Addison's disease, but young patients are at risk of premature death. , 2008, European journal of endocrinology.
[104] O. Kämpe,et al. Increased death risk and altered cancer incidence pattern in patients with isolated or combined autoimmune primary adrenocortical insufficiency , 2008, Clinical endocrinology.
[105] R. Lifton,et al. A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism. , 2008, The Journal of clinical endocrinology and metabolism.
[106] V. Montori,et al. The diagnosis of Cushing's syndrome: an Endocrine Society Clinical Practice Guideline. , 2008, The Journal of clinical endocrinology and metabolism.
[107] Z. Hochberg,et al. Metabolic evidence for impaired 17alpha-hydroxylase activity in a kindred bearing the E305G mutation for isolate 17,20-lyase activity. , 2008, European journal of endocrinology.
[108] G. Johannsson,et al. Premature mortality in patients with Addison's disease: a population-based study. , 2006, The Journal of clinical endocrinology and metabolism.
[109] M. Ermani,et al. Prevalence and characteristics of the metabolic syndrome in primary aldosteronism. , 2006, The Journal of clinical endocrinology and metabolism.
[110] Jacques Simard,et al. Molecular Biology of the 3-Hydroxysteroid Dehydrogenase/5-4 Isomerase Gene Family , 2005 .
[111] C. Shackleton,et al. Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study , 2004, The Lancet.
[112] E. Jabs,et al. Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome , 2004, Nature Genetics.
[113] Kenneth L. Jones,et al. The diagnosis of congenital adrenal hyperplasia in the newborn by gas chromatography/mass spectrometry analysis of random urine specimens. , 2002, The Journal of clinical endocrinology and metabolism.
[114] E. Husebye,et al. Subjective health status in Norwegian patients with Addison’s disease * , 2002, Clinical endocrinology.
[115] J. Milbrandt,et al. Nuclear receptor steroidogenic factor 1 directs embryonic stem cells toward the steroidogenic lineage , 1997, Molecular and cellular biology.
[116] C. Shackleton,et al. Urinary free cortisone and the assessment of 11β‐hydroxysteroid dehydrogenase activity in man , 1996, Clinical endocrinology.
[117] B. Walker,et al. 11 beta-Hydroxysteroid dehydrogenase activity in Cushing's syndrome: explaining the mineralocorticoid excess state of the ectopic adrenocorticotropin syndrome. , 1995, The Journal of clinical endocrinology and metabolism.
[118] T. Pickering,et al. Cortisol inactivation overload: a mechanism of mineralocorticoid hypertension in the ectopic adrenocorticotropin syndrome. , 1992, The Journal of clinical endocrinology and metabolism.
[119] R. Tedde,et al. Defective ring A reduction of cortisol as the major metabolic error in the syndrome of apparent mineralocorticoid excess. , 1992, The Journal of clinical endocrinology and metabolism.
[120] C. Edwards,et al. Syndrome of apparent mineralocorticoid excess. A defect in the cortisol-cortisone shuttle. , 1988, The Journal of clinical investigation.
[121] G. E. Joannou. Identification of 15β-hydroxylated c21 steroids in the neo-natal period: The role of 3α, 15β,17α-trihydroxy-5β-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (cah) due to a 21-hydroxylase deficiency , 1981 .
[122] C. Gomez-Sanchez,et al. DIAGNOSIS OF ENDOCRINE DISEASE 18-Oxocortisol and 18-hydroxycortisol: is there clinical utility of these steroids? , 2017 .
[123] N. Zelinska. Вроджена гіперплазія надниркових залоз внаслідок дефіциту 21-гідроксилази. Клінічні практичні настанови Ендокринологічного Товариства. Частина 1 , 2018 .
[124] I. Dunn,et al. Rapid Mass Spectrometry Imaging to Assess the Biochemical Profile of Pituitary Tissue for Potential Intraoperative Usage. , 2017, Advances in cancer research.
[125] E. Patel,et al. Fresh Frozen Versus Formalin-Fixed Paraffin Embedded for Mass Spectrometry Imaging. , 2017, Methods in molecular biology.
[126] A. Walch,et al. In Situ Metabolomics in Cancer by Mass Spectrometry Imaging , 2017, Advances in cancer research.
[127] K. Pacak,et al. Succinate-to-fumarate ratio as a new metabolic marker to detect the presence of SDHB/D-related paraganglioma: initial experimental and ex vivo findings. , 2014, Endocrinology.
[128] F. Beuschlein,et al. Mitotane therapy in adrenocortical cancer induces CYP 3 A 4 and inhibits 5-reductase , explaining the need for personalized glucocorticoid and androgen replacement , 2012 .
[129] W. Kaelin,et al. Cancer and altered metabolism: potential importance of hypoxia-inducible factor and 2-oxoglutarate-dependent dioxygenases. , 2011, Cold Spring Harbor symposia on quantitative biology.
[130] R. Cooks,et al. Molecular imaging of adrenal gland by desorption electrospray ionization mass spectrometry. , 2010, The Analyst.
[131] Jacques Simard,et al. Molecular biology of the 3beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family. , 2005, Endocrine reviews.
[132] E. Moszczyńska,et al. Definitive diagnosis of enzymatic deficiencies of steroidogenesis in at-risk newborns and infants by urinary marker analysis using GC/MS-SIM. , 1997, Hormone Research.
[133] J. Trottier,et al. Book Review: Mass Spectrometry: Principles and Applications. E. de Hoffman, J. Charette and W. Stroobant. Wiley, Chichester 1996. ISBN 0 471 96697 5 , 1997 .
[134] S. Ulick,et al. Hypersecretion of a new corticosteroid, 18-hydroxycortisol in two types of adrenocortical hypertension. , 1982, Clinical and experimental hypertension. Part A, Theory and practice.
[135] G. E. Joannou. Identification of 15 beta-hydroxylated C21 steroids in the neo-natal period: the role of 3 alpha,15 beta,17 alpha-trihydroxy-5 beta-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (CAH) due to a 21-hydroxylase deficiency. , 1981, Journal of Steroid Biochemistry.