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Tytuł:
Unveiling the spectrum: A cross-sectional exploration of hirsutism causes in women.
Autorzy:
Ansari RT; Rana Tabassum Ansari, FCPS. Fellow Endocrine, Baqai Institute of Diabetology and Endocrinology, Baqai Medical University, Karachi, Pakistan.
Syed U; Uneeba Syed, FCPS. Assistant Professor, Consultant Endocrinologist, Allama Iqbal Medical College, Jinnah hospital, Lahore, Pakistan.
Riaz M; Musarrat Riaz, FCPS. Department of Medicine, Associate Professor, Consultant Endocrinologist, Baqai Institute of Diabetology and Endocrinology, Baqai Medical University, Karachi, Pakistan.
Askari S; Saima Askari, FCPS. Department of Endocrinology/Medicine, Assistant Professor, Consultant Endocrinologist, Baqai Institute of Diabetology and Endocrinology, Baqai Medical University, Karachi, Pakistan.
Anjum S; Sarwat Anjum, FCPS. Consultant Endocrinologist, Baqai Institute of Diabetology and Endocrinology, Baqai Medical University, Karachi, Pakistan.
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Źródło:
Pakistan journal of medical sciences [Pak J Med Sci] 2024 Mar-Apr; Vol. 40 (4), pp. 736-740.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Nonclassic Congenital Adrenal Hyperplasia Metabolic Resolution Post Roux-en-Y Gastric Bypass and Associated Weight Loss.
Autorzy:
Romo KG; Division of Endocrinology, Cedars-Sinai, Los Angeles, CA 90048, USA.
Shu SW; University of Queensland-Ochsner Clinical School, Brisbane, QLD 4072, Australia.
Iqbal QZ; Endocrinology Division, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Uwaifo GI; Endocrinology Division, Department of Medicine, Southern Illinois University School of Medicine, Springfield, IL 62702, USA.
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Źródło:
JCEM case reports [JCEM Case Rep] 2024 Feb 23; Vol. 2 (3), pp. luae018. Date of Electronic Publication: 2024 Feb 23 (Print Publication: 2024).
Typ publikacji:
Case Reports
Raport
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Evidence of the Role of Inflammation and the Hormonal Environment in the Pathogenesis of Adrenal Myelolipomas in Congenital Adrenal Hyperplasia.
Autorzy:
Kolli V; National Institutes of Health Clinical Center, 10 Center Drive, Bethesda, MD 20892, USA.
Frucci E; National Institutes of Health Clinical Center, 10 Center Drive, Bethesda, MD 20892, USA.
da Cunha IW; Laboratory of Pathology, National Cancer Institute, Bethesda, MD 20892, USA.; D'Or Institute for Research and Education (IDOR), São Paulo 05403, Brazil.
Iben JR; The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
Kim SA; Laboratory of Pathology, National Cancer Institute, Bethesda, MD 20892, USA.
Mallappa A; National Institutes of Health Clinical Center, 10 Center Drive, Bethesda, MD 20892, USA.
Li T; The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
Faucz FR; The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
Kebebew E; Division of General Surgery, Department of Surgery, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Nilubol N; National Cancer Institute, Bethesda, MD 20892, USA.
Quezado MM; Laboratory of Pathology, National Cancer Institute, Bethesda, MD 20892, USA.
Merke DP; National Institutes of Health Clinical Center, 10 Center Drive, Bethesda, MD 20892, USA.; The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Feb 22; Vol. 25 (5). Date of Electronic Publication: 2024 Feb 22.
Typ publikacji:
Journal Article
MeSH Terms:
Adrenal Hyperplasia, Congenital*
Myelolipoma*/pathology
Adrenal Gland Neoplasms*/genetics
Lipoma*
Leukemia, Myeloid, Acute*
Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Clinical applications of genetic analysis and liquid chromatography tandem-mass spectrometry in rare types of congenital adrenal hyperplasia.
Autorzy:
Li Z; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.; Department of Endocrinology, Shenzhen Children's Hospital, Shenzhen, China.
Liang Y; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Du C; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yu X; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hou L; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Wu W; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Ying Y; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Luo X; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. .
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Źródło:
BMC endocrine disorders [BMC Endocr Disord] 2021 Nov 25; Vol. 21 (1), pp. 237. Date of Electronic Publication: 2021 Nov 25.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromatography, Liquid*
Tandem Mass Spectrometry*
Adrenal Hyperplasia, Congenital/*blood
Adrenal Hyperplasia, Congenital/*genetics
Child ; Child, Preschool ; China ; Disorder of Sex Development, 46,XY/blood ; Disorder of Sex Development, 46,XY/genetics ; Female ; Gonadal Steroid Hormones/blood ; Humans ; Infant, Newborn ; Male ; Retrospective Studies ; Sequence Analysis, DNA ; Spectrometry, Mass, Electrospray Ionization ; Steroid 11-beta-Hydroxylase/genetics
SCR Disease Name:
Adrenal hyperplasia 2; Lipoid congenital adrenal hyperplasia
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Newborn screening for congenital hypothyroidism, congenital adrenal hyperplasia and glucose-6-phosphate dehydrogenase deficiency in Bihar: A pressing priority in today's time.
Autorzy:
Kumari B; Department of Biochemistry, AIIMS, Patna, Bihar, India.
Raj K; Department of Biochemistry, AIIMS, Patna, Bihar, India.
Sharma S; Department of Biochemistry, AIIMS, Patna, Bihar, India.
Kumar S; Department of Biochemistry, AIIMS, Patna, Bihar, India.
Chowdhry BK; Department of Neonatology, AIIMS, Patna, Bihar, India.
Kumar A; Department of Pediatrics, Mahavir Vatsalya Hospital, Patna, Bihar, India.
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Źródło:
Journal of family medicine and primary care [J Family Med Prim Care] 2023 Dec; Vol. 12 (12), pp. 3332-3338. Date of Electronic Publication: 2023 Dec 21.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX: a case report and literature review.
Autorzy:
Chen H; Department of Endocrinology and Metabolism, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, China.
Chen Y; Department of Endocrinology and Metabolism, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, China.
Mao H; Department of Endocrinology and Metabolism, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, China.
Huang H; Department of Endocrinology and Metabolism, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, China.
Lou X; Department of Endocrinology and Metabolism, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, China.
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Źródło:
Blood pressure [Blood Press] 2023 Dec; Vol. 32 (1), pp. 2195008.
Typ publikacji:
Review; Case Reports; Journal Article
MeSH Terms:
Hypokalemia*
Hypertension*/genetics
Female ; Humans ; Adult ; Steroid 17-alpha-Hydroxylase/genetics ; Progesterone ; Amenorrhea/genetics ; Mutation, Missense
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Continuous Glucose Monitoring in Children and Adolescents with Congenital Adrenal Hyperplasia
Autorzy:
Dubinski I; Dr. von Hauner Children’s Hospital; Ludwig Maximilian University, Department of Paediatrics, Division of Paediatric Endocrinology, Munich, Germany
Bechtold-Dalla Pozza S; Dr. von Hauner Children’s Hospital; Ludwig Maximilian University, Department of Paediatrics, Division of Paediatric Endocrinology, Munich, Germany
Debor B; Dr. von Hauner Children’s Hospital; Ludwig Maximilian University, Department of Paediatrics, Division of Paediatric Endocrinology, Munich, Germany
Nowotny HF; Ludwig Maximilian University, Department of Medicine IV, Munich, Germany
Reisch N; Ludwig Maximilian University, Department of Medicine IV, Munich, Germany
Tschaidse L; Ludwig Maximilian University, Department of Medicine IV, Munich, Germany
Schmidt H; Dr. von Hauner Children’s Hospital; Ludwig Maximilian University, Department of Paediatrics, Division of Paediatric Endocrinology, Munich, Germany
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Źródło:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2023 Nov 22; Vol. 15 (4), pp. 380-389. Date of Electronic Publication: 2023 May 23.
Typ publikacji:
Observational Study; Journal Article
MeSH Terms:
Adrenal Hyperplasia, Congenital*/diagnosis
Adrenal Hyperplasia, Congenital*/drug therapy
Adrenal Hyperplasia, Congenital*/complications
Hypoglycemia*/complications
Infant ; Humans ; Child ; Adolescent ; Blood Glucose ; Prospective Studies ; Blood Glucose Self-Monitoring ; Hydrocortisone ; Glucose/therapeutic use
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Screening for Anxiety and Depression in Children with Congenital Adrenal Hyperplasia
Autorzy:
Jacob M; Cooperman Barnabas Medical Center, Division of Pediatric Endocrinology, New Jersey, USA
Lin-Su K; NewYork-Presbyterian Hospital, Weill Cornell Medicine, Division of Pediatric Endocrinology, New York, USA
Catarozoli C; NewYork-Presbyterian Hospital, Weill Cornell Medicine, Department of Child and Adolescent Psychiatry, New York, USA
Thomas C; Weill Cornell Medicine, Department of Population Health Sciences, New York, USA
Poppas D; NewYork-Presbyterian Hospital, Weill Cornell Medicine, Division of Pediatric Urology, New York, USA
Lekarev O; NewYork-Presbyterian Hospital, Weill Cornell Medicine, Division of Pediatric Endocrinology, New York, USA
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Źródło:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2023 Nov 22; Vol. 15 (4), pp. 406-416. Date of Electronic Publication: 2023 Jul 20.
Typ publikacji:
Journal Article
MeSH Terms:
Adrenal Hyperplasia, Congenital*/complications
Adrenal Hyperplasia, Congenital*/diagnosis
Adrenal Hyperplasia, Congenital*/epidemiology
Adolescent ; Child ; Humans ; Female ; Male ; Depression/diagnosis ; Depression/epidemiology ; Depression/etiology ; Cross-Sectional Studies ; Anxiety/diagnosis ; Anxiety/epidemiology ; Anxiety/etiology
SCR Disease Name:
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Case report: Coexistence of Jacobs syndrome, congenital adrenal hyperplasia, and ambiguous genitalia in a male infant.
Autorzy:
Khan QA; Khyber Teaching Hospital MTI KTH Peshawar Pakistan.
Amatul-Hadi F; Mercer University School of Medicine Macon Georgia USA.
Kooner A; Chicago College of Osteopathic Medicine Downers Grove Illinois USA.
Lee A; Arkansas College of Osteopathic Medicine Fort Smith Arkansas USA.
Ahmed R; Kennesaw State University Kennesaw Georgia USA.
Nadella A; Nanjing Medical University Nanjing China.
Pande H; Saint Louis University St. Louis Missouri USA.
Levin-Carrion Y; Rutgers New Jersey Medical School Newark New Jersey USA.
Afzal M; St. George's University School of Medicine True Blue Grenada.
Alfaro M; Long School of Medicine at the University of Texas Health Science Center San Antonio San Antonio Texas USA.
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Źródło:
Clinical case reports [Clin Case Rep] 2023 Nov 09; Vol. 11 (11), pp. e8097. Date of Electronic Publication: 2023 Nov 09 (Print Publication: 2023).
Typ publikacji:
Case Reports
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Isotretinoin-unresponsive acne as a sign of a congenital disorder: a case of 21-hydroxylase deficiency.
Autorzy:
Marzola E; Department of Medical Sciences, Section of Dermatology and Infectious Diseases, University of Ferrara, Italy.
Bettoli V; Department of Medical Sciences, Section of Dermatology and Infectious Diseases, University of Ferrara, Italy.
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Źródło:
Dermatology reports [Dermatol Reports] 2023 Aug 24; Vol. 16 (1), pp. 9717. Date of Electronic Publication: 2023 Aug 24 (Print Publication: 2024).
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Congenital adrenal hyperplasia disorder due to 17 α-hydroxylase deficiency: a case report.
Autorzy:
Tian Y; Department of Endocrinology and Metabolic, The First Hospital of Lanzhou University, Lanzhou, Gansu, P.R.China.
Hou L; Department of Endocrinology and Metabolic, The First Hospital of Lanzhou University, Lanzhou, Gansu, P.R.China.
Xiang S; Department of General Family Medicine, The First Hospital of Lanzhou University, Lanzhou, Gansu, P.R.China.
Tian X; Lintao Country People's Hospital, Lintao, Dingxi, Gansu, P.R.China.
Xu J; Department of Respiratory medicine, The First Hospital of Lanzhou University, Lanzhou, Gansu, P.R.China.
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Źródło:
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology [Gynecol Endocrinol] 2023 Aug 18; Vol. 39 (1), pp. 2250001.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Adrenal Hyperplasia, Congenital*/complications
Adrenal Hyperplasia, Congenital*/diagnosis
Adrenal Hyperplasia, Congenital*/drug therapy
Female ; Humans ; Young Adult ; Adult ; Steroid 17-alpha-Hydroxylase/genetics ; Adrenocorticotropic Hormone ; Estradiol
SCR Disease Name:
Adrenal hyperplasia, congenital, type 5
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera.
Autorzy:
Lao Q; National Institutes of Health Clinical Center, Bethesda, Maryland, USA.
Burkardt DD; National Institutes of Health Clinical Center, Bethesda, Maryland, USA.
Kollender S; National Institutes of Health Clinical Center, Bethesda, Maryland, USA.
Faucz FR; The Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
Merke DP; National Institutes of Health Clinical Center, Bethesda, Maryland, USA.; The Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Jul; Vol. 11 (7), pp. e2195. Date of Electronic Publication: 2023 May 08.
Typ publikacji:
Case Reports; Journal Article; Research Support, N.I.H., Intramural
MeSH Terms:
Adrenal Hyperplasia, Congenital*/genetics
Female ; Humans ; Alleles ; Genetic Testing ; Steroid 21-Hydroxylase/genetics ; Young Adult
SCR Disease Name:
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Endocrine profiles and cycle characteristics of infertile 17α-hydroxylase/17,20-lyase Deficiency Patients undergoing assisted Reproduction Treatment: a retrospective cohort study.
Autorzy:
Pan P; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China.
Zheng L; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China.
Huang J; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China.
Chen X; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China.
Ni R; Department of Reproductive Medicine, Kunming Angel Women's and Children's Hospital, Kunming, Yunnan, China.
Zhang Q; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China.
Yang D; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China. .
Li Y; Reproductive Medicine Centre, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 West Yan Jiang Road, Guangzhou, 510120, Guangdong, China. .
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Źródło:
Journal of ovarian research [J Ovarian Res] 2023 Jun 14; Vol. 16 (1), pp. 111. Date of Electronic Publication: 2023 Jun 14.
Typ publikacji:
Journal Article
MeSH Terms:
Infertility, Female*/genetics
Infertility, Female*/therapy
Adrenal Hyperplasia, Congenital*/genetics
Pregnancy ; Humans ; Female ; Steroid 17-alpha-Hydroxylase/genetics ; Retrospective Studies ; Mixed Function Oxygenases
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome.
Autorzy:
Kim JH; Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Kim GH; Medical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Yoo HW; Department of Pediatrics, Bundang CHA Medical Center, CHA University, Seongnam, Korea.
Choi JH; Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
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Źródło:
Annals of pediatric endocrinology & metabolism [Ann Pediatr Endocrinol Metab] 2023 Jun; Vol. 28 (2), pp. 77-86. Date of Electronic Publication: 2023 Jun 30.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation.
Autorzy:
Bakkar AA; Alhada Armed Forces Hospital, Taif, Saudi Arabia.
Alsaedi A; Alhada Armed Forces Hospital, Taif, Saudi Arabia.
Kamal NM; Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.
Althobaiti E; Alhada Armed Forces Hospital, Taif, Saudi Arabia.
Aboulkhair LA; Ministry of Health, Madinah, Saudi Arabia.
Almalki AM; Alhada Armed Forces Hospital, Taif, Saudi Arabia.
Alsalmi SA; Alhada Armed Forces Hospital, Taif, Saudi Arabia.
Alharthi Q; Ministry of Health, Taif, Saudi Arabia.
Abosabie SA; Faculty of Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Abosabie SA; Faculty of Medicine, Julius-Maximilians-Universität Würzburg, Bavaria, Germany.
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Źródło:
Clinical medicine insights. Endocrinology and diabetes [Clin Med Insights Endocrinol Diabetes] 2023 May 26; Vol. 16, pp. 11795514231167059. Date of Electronic Publication: 2023 May 26 (Print Publication: 2023).
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Clinical Update on Congenital Adrenal Hyperplasia: Recommendations from a Multidisciplinary Adrenal Program.
Autorzy:
Uslar T; Program for Adrenal Disorders CETREN-UC, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.; Department of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.
Olmos R; Program for Adrenal Disorders CETREN-UC, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.; Department of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.
Martínez-Aguayo A; Program for Adrenal Disorders CETREN-UC, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.; Division of Pediatrics, School of Medicine, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.
Baudrand R; Program for Adrenal Disorders CETREN-UC, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.; Department of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago 8330077, Chile.
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Źródło:
Journal of clinical medicine [J Clin Med] 2023 Apr 26; Vol. 12 (9). Date of Electronic Publication: 2023 Apr 26.
Typ publikacji:
Journal Article; Review
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Successful Treatment of Infertility in a Patient with Probable 17 Hydroxylase Deficiency and Particularities of Association with Adrenal Autoimmunity-A Case Report and Review of the Literature.
Autorzy:
Albu AI; Department of Endocrinology, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.; Endocrinology Department, Elias Hospital, 011461 Bucharest, Romania.
Iancu ME; Endocrinology Department, ARTHOPE SRL, 077190 Bucharest, Romania.
Albu DN; Department of Obstetrics and Gynecology, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.; Reproductive Medicine Department, Medlife Hospital, 010719 Bucharest, Romania.
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Źródło:
Life (Basel, Switzerland) [Life (Basel)] 2023 Mar 31; Vol. 13 (4). Date of Electronic Publication: 2023 Mar 31.
Typ publikacji:
Case Reports
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Model-Informed Target Morning 17α-Hydroxyprogesterone Concentrations in Dried Blood Spots for Pediatric Congenital Adrenal Hyperplasia Patients.
Autorzy:
Stachanow V; Department of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universitaet Berlin, Kelchstr 31, 12169 Berlin, Germany.; Graduate Research Training Program, PharMetrX, 12169 Berlin, Germany.
Neumann U; Charité-Universitätsmedizin, Freie Universität Berlin, 13353 Berlin, Germany.
Blankenstein O; Charité-Universitätsmedizin, Freie Universität Berlin, 13353 Berlin, Germany.; Labor Berlin, Charité Vivantes GmbH, 13353 Berlin, Germany.
Alder-Baerens N; Labor Berlin, Charité Vivantes GmbH, 13353 Berlin, Germany.
Bindellini D; Department of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universitaet Berlin, Kelchstr 31, 12169 Berlin, Germany.; Graduate Research Training Program, PharMetrX, 12169 Berlin, Germany.
Hindmarsh P; Developmental Endocrinology Research Group, UCL Institute of Child Health, London WC1E 6BT, UK.
Ross RJ; Department of Oncology and Metabolism, University of Sheffield, Sheffield S10 2TN, UK.
Whitaker MJ; Department of Oncology and Metabolism, University of Sheffield, Sheffield S10 2TN, UK.
Melin J; Department of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universitaet Berlin, Kelchstr 31, 12169 Berlin, Germany.; Graduate Research Training Program, PharMetrX, 12169 Berlin, Germany.
Huisinga W; Institute of Mathematics, Universität Potsdam, 14476 Potsdam, Germany.
Michelet R; Department of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universitaet Berlin, Kelchstr 31, 12169 Berlin, Germany.
Kloft C; Department of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universitaet Berlin, Kelchstr 31, 12169 Berlin, Germany.
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Źródło:
Pharmaceuticals (Basel, Switzerland) [Pharmaceuticals (Basel)] 2023 Mar 21; Vol. 16 (3). Date of Electronic Publication: 2023 Mar 21.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Premature Pubarche: Time to Revise the Diagnostic Approach?
Autorzy:
Baronio F; Department Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna Policlinico di S.Orsola, 40138 Bologna, Italy.
Marzatico A; Department Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna Policlinico di S.Orsola, 40138 Bologna, Italy.
De Iasio R; Metropolitan Laboratory, AUSL Bologna, 40124 Bologna, Italy.
Ortolano R; Department Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna Policlinico di S.Orsola, 40138 Bologna, Italy.
Fanolla A; Observatory for Health Provincial Government, 39100 Bolzano, Italy.
Radetti G; Marienklinik, 39100 Bolzano, Italy.
Balsamo A; Department of Medical and Surgical Sciences, University of Bologna, 40126 Bologna, Italy.
Pession A; Department Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna Policlinico di S.Orsola, 40138 Bologna, Italy.; Department of Medical and Surgical Sciences, University of Bologna, 40126 Bologna, Italy.
Cassio A; Department Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna Policlinico di S.Orsola, 40138 Bologna, Italy.; Department of Medical and Surgical Sciences, University of Bologna, 40126 Bologna, Italy.
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Źródło:
Journal of clinical medicine [J Clin Med] 2023 Mar 11; Vol. 12 (6). Date of Electronic Publication: 2023 Mar 11.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Weight Loss During Topiramate Treatment in a Severely Obese Adolescent with Congenital Adrenal Hyperplasia and Migraine
Autorzy:
Seagroves A; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA
Ross HM; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA
Vidmar AP; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA; University of Southern California, Keck School of Medicine, Department of Pediatrics, California, USA
Geffner ME; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA; University of Southern California, Keck School of Medicine, Department of Pediatrics, California, USA; The Saban Research Institute, California, USA
Kim WS; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA
Hwang D; University of Southern California, Keck School of Medicine, Department of Pediatrics, California, USA
Borzutzky C; University of Southern California, Keck School of Medicine, Department of Pediatrics, California, USA; Children’s Hospital Los Angeles, Clinic of Adolescent and Young Adult Medicine, California, USA
Fraga NR; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA
Kim MS; Children’s Hospital Los Angeles, Center for Endocrinology, Diabetes and Metabolism, California, USA; University of Southern California, Keck School of Medicine, Department of Pediatrics, California, USA; The Saban Research Institute, California, USA
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Źródło:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2023 Feb 27; Vol. 15 (1), pp. 81-85. Date of Electronic Publication: 2021 Aug 23.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 1-20 z 177

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