Suchergebnisse - "Hypogonadism diagnosis"

Hypogonadism is frequent in very old men with multimorbidity and is associated with anemia and sarcopenia

Autoren: Schluessel, Sabine Bidlingmaier, Martin Martini, Sebastian et al.

Quelle: Z Gerontol Geriatr

Schlagwörter: Male, 2. Zero hunger, Sarcopenia, Hand Strength, Geriatrics, Primärer und sekundärer Hypogonadismus, Aged [MeSH], Hypogonadism/complications [MeSH], Hand Strength [MeSH], Hypogonadism/epidemiology [MeSH], Original Contributions, Testosterone [MeSH], Osteoporose, Osteoporosis/diagnosis [MeSH], Dual-energy X-ray absorptiometry, Anemia/diagnosis [MeSH], Osteoporosis/epidemiology [MeSH], Male [MeSH], Sarcopenia/complications [MeSH], Sarcopenia/epidemiology [MeSH], Osteoporosis/complications [MeSH], Primary and secondary hypogonadism, Humans [MeSH], Cross-Sectional Studies [MeSH], Osteoporosis, Anemia/complications [MeSH], Geriatrie, Hypogonadism/diagnosis [MeSH], Testosteron, Multimorbidity [MeSH], Testosterone, Sarcopenia/diagnosis [MeSH], Anemia/epidemiology [MeSH], Dual-Röntgen-Absorptiometrie, Hypogonadism, Multimorbidity, Anemia, 16. Peace & justice, 3. Good health, Cross-Sectional Studies, Humans, Aged

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/37674061
https://repository.publisso.de/resource/frl:6524218
https://epub.ub.uni-muenchen.de/116519/

Hypergonadotropic hypogonadism and chromosomal aberrations: clinical heterogeneity and implications on the health of elderly men, case series

Autoren: Tarik Elhadd Ahmad Majzoub Charlotte Wilson et al.

Quelle: BMC Endocr Disord
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-6 (2023)

Schlagwörter: Male, Chromosome Aberrations, Male hypogonadism, Chromosomal abnormalities, Hypogonadism, Hypergonadotropic hypogonadism, Case Report, RC648-665, Hypogonadism/diagnosis, Diseases of the endocrine glands. Clinical endocrinology, 3. Good health, Elderly, Klinefelter Syndrome, Karyotyping, Humans, Gynecomastia, Klinefelter Syndrome/diagnosis, Aged

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/37198592
https://doaj.org/article/6b70206e095b4b68a35067825e456c0b

Kisspeptin-54 Accurately Identifies Hypothalamic Gonadotropin-Releasing Hormone Neuronal Dysfunction in Men with Congenital Hypogonadotropic Hypogonadism.

Autoren: Abbara, A. Eng, P.C. Phylactou, M. et al.

Schlagwörter: Adult, Gonadotropin-Releasing Hormone/administration & dosage, Gonadotropin-Releasing Hormone/pharmacology, Humans, Hypogonadism/blood, Hypogonadism/congenital, Hypogonadism/diagnosis, Kallmann Syndrome/blood, Kallmann Syndrome/diagnosis, Kisspeptins/administration & dosage, Kisspeptins/pharmacology, Luteinizing Hormone/blood, Luteinizing Hormone/drug effects, Male, Congenital hypogonadotropic hypogonadism, Gonadotropin-releasing hormone, Kallmann, Kisspeptin

Relation: Neuroendocrinology; https://iris.unil.ch/handle/iris/99845; serval:BIB_13E1C6F18B1B; 000700096800001

Verfügbarkeit: https://iris.unil.ch/handle/iris/99845
https://doi.org/10.1159/000513248

Etiology and Secular Trends in Primary Amenorrhea in 856 Patients: A 17-Year Retrospective Multicenter Study in Korea

Autoren: Hoon Kim Mee-Hwa Lee Dong-Yun Lee et al.

Weitere Verfasser: Hoon Kim Mee-Hwa Lee Dong-Yun Lee et al.

Quelle: J Korean Med Sci

Schlagwörter: Amenorrhea / epidemiology, Etiology, 46, XX Disorders of Sex Development, Mullerian Ducts / abnormalities, Hypogonadism, Primary Amenorrhea, Hypogonadism* / diagnosis, Gonadal Dysgenesis, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Amenorrhea / etiology, XX Disorders of Sex Development* / complications, Humans, Original Article, Female, Müllerian Agenesis, Prospective Studies, Hypogonadism* / complications, Hypogonadism* / epidemiology, Amenorrhea, Mullerian Ducts

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/35880506

Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures

Autoren: Cassatella, D Howard, SR Acierno, JS et al.

Quelle: Eur J Endocrinol
European journal of endocrinology, vol. 178, no. 4, pp. 377-388
Cassatella, Daniele; Howard, Sasha R; Acierno, James S; Xu, Cheng; Papadakis, Georgios E; Santoni, Federico A; Dwyer, Andrew A; Santini, Sara; Sykiotis, Gerasimos P; Chambion, Caroline; Meylan, Jenny; Marino, Laura; Favre, Lucie; Li, Jiankang; Liu, Xuanzhu; Zhang, Jianguo; Bouloux, Pierre-Marc; Geyter, Christian De; Paepe, Anne De; Dhillo, Waljit S; ... (2018). Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures. European journal of endocrinology, 178(4), pp. 377-388. BioScientifica Ltd. 10.1530/EJE-17-0568 <http://dx.doi.org/10.1530/EJE-17-0568>

Schlagwörter: Adult, Male, Puberty, Delayed, 0301 basic medicine, Aged, Cohort Studies, Female, Finland/epidemiology, Growth Disorders/diagnosis, Growth Disorders/epidemiology, Growth Disorders/genetics, Humans, Hypogonadism/diagnosis, Hypogonadism/epidemiology, Hypogonadism/genetics, Middle Aged, Mutation/genetics, Puberty, Delayed/diagnosis, Puberty, Delayed/epidemiology, Puberty, Delayed/genetics, Hypogonadism, 610 Medicine & health, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Mutation, Clinical Study, 10. No inequality, Finland, Growth Disorders

Dateibeschreibung: application/pdf

Zugangs-URL: https://eje.bioscientifica.com/downloadpdf/journals/eje/178/4/EJE-17-0568.pdf
https://boris.unibe.ch/123702/1/%5B1479683X%20-%20European%20Journal%20of%20Endocrinology%5D%20Congenital%20hypogonadotropic%20hypogonadism%20and%20constitutional%20delay%20of%20growth%20and%20puberty%20have%20distinct%20genetic%20architectures.pdf
https://pubmed.ncbi.nlm.nih.gov/29419413
http://www.espeyearbook.org/ey/0015/ey0015.7-8.htm
https://www.zora.uzh.ch/id/eprint/157982/
https://eprints.ncl.ac.uk/file_store/production/247417/CB8C0EB6-47AC-4044-AD95-9075E16ADFBC.pdf
https://boris.unibe.ch/123702/
https://www.eje-online.org/content/178/4/377.full
https://discovery.ucl.ac.uk/10051503/
https://doi.org/10.1530/EJE-17-0568
https://avesis.gazi.edu.tr/publication/details/f55047ec-e54c-448f-acec-c5c1c413896b/oai
http://hdl.handle.net/10044/1/107031
https://serval.unil.ch/notice/serval:BIB_92D278111021
https://serval.unil.ch/resource/serval:BIB_92D278111021.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_92D2781110219
https://boris.unibe.ch/123702/
https://discovery-pp.ucl.ac.uk/id/eprint/10051503/

Gonadotropin-releasing hormone receptor mutations in ageing men.

Autoren: Tommiska, J. Känsäkoski, J. Pitteloud, N. et al.

Schlagwörter: Aged, Aging/genetics, DNA Mutational Analysis/methods, Genetic Predisposition to Disease/genetics, Humans, Hypogonadism/blood, Hypogonadism/diagnosis, Hypogonadism/genetics, Male, Mutation, Receptors, LHRH/genetics, Testosterone/blood

Relation: Clinical Endocrinology; https://iris.unil.ch/handle/iris/129039; serval:BIB_4E6F725FAB7A

Verfügbarkeit: https://iris.unil.ch/handle/iris/129039
https://doi.org/10.1111/cen.12833

Obesity and Aging in Late-Onset Hypogonadism

Autoren: RASTRELLI, GIULIA Wu, Frederick C. W. Winters, Stephen J. et al.

Weitere Verfasser: RASTRELLI, GIULIA Wu, Frederick C. W. Winters, Stephen J. et al.

Quelle: Male Hypogonadism ISBN: 9783319532967
Rastrelli, G & Wu, F 2017, Obesity and Aging in Late-onset Hypogonadism. in S J Winters & I Huhtaniemi (eds), Male Hypogonadism: Basic, Clinical and Therapeutic Principles . 2 edn, Springer Nature.

Schlagwörter: 2. Zero hunger, Testosterone - Age - Obesity - Late-onset hypogonadism - Diagnosis - Free testosterone - Sexual symptoms - Body composition - Insulin resistance - Mortality, 10. No inequality, 3. Good health

Zugangs-URL: https://research.manchester.ac.uk/en/publications/9ee63529-bbd4-4ea5-9979-a5f5fea13d69
https://core.ac.uk/display/74202152
https://link.springer.com/chapter/10.1007/978-3-319-53298-1_17/fulltext.html
https://www.research.manchester.ac.uk/portal/en/publications/obesity-and-aging-in-lateonset-hypogonadism(9ee63529-bbd4-4ea5-9979-a5f5fea13d69)/export.html
https://link.springer.com/chapter/10.1007%2F978-3-319-53298-1_17
https://rd.springer.com/chapter/10.1007/978-3-319-53298-1_17

A Short Version of the ADAM Questionnaire for Androgen Deficiency in Chinese Men

Autoren: Lam, TP Kung, AWC Chu, LW et al.

Quelle: The Journals of Gerontology Series A: Biological Sciences and Medical Sciences. 63:426-431

Schlagwörter: Questionnaires, Adult, Cross-Cultural Comparison, Male, Aging, Adolescent, European Continental Ancestry Group - statistics & numerical data, Androgens - blood - deficiency, Andropause, White People, 03 medical and health sciences, 0302 clinical medicine, Asian People, Predictive Value of Tests, Surveys and Questionnaires, 80 and over, Humans, Mass Screening, Testosterone, ADAM questionnaire, Aged, Aged, 80 and over, Chinese, Hypogonadism, Hypogonadism - diagnosis - ethnology, Age Factors, Reproducibility of Results, Men, Middle Aged, Cross-Sectional Studies, Asian Continental Ancestry Group - statistics & numerical data, Androgens, Androgen deficiency, Testosterone - blood

Zugangs-URL: https://academic.oup.com/biomedgerontology/article-pdf/63/4/426/1738591/426.pdf
https://pubmed.ncbi.nlm.nih.gov/18426968
http://biomedgerontology.oxfordjournals.org/content/63/4/426.abstract
http://hub.hku.hk/handle/10722/77655
https://pubmed.ncbi.nlm.nih.gov/18426968/
https://digital.library.adelaide.edu.au/dspace/handle/2440/53933
https://www.ncbi.nlm.nih.gov/pubmed/18426968
https://academic.oup.com/biomedgerontology/article-abstract/63/4/426/625654
http://hdl.handle.net/10722/77655

Novel FGFR1 Mutations in Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: Evidence for the Involvement of an Alternatively Spliced Isoform

Autoren: Gonçalves, C Bastos, M Pignatelli, D et al.

Schlagwörter: HCC END, Alternative Splicing, Computer Simulation, Cross-Sectional Studies, DNA Mutational Analysis, Databases, Genetic, Exons, Gene Frequency, Genetic Predisposition to Disease, Hypogonadism/diagnosis, Hypogonadism/genetics, Hypogonadism/metabolism, Kallmann Syndrome/diagnosis, Kallmann Syndrome/genetics, Kallmann Syndrome/metabolism, Mutation, Missense, Protein Conformation, Receptor, Fibroblast Growth Factor, Type 1/chemistry, Type 1/genetics, Type 1/metabolism, Structure-Activity Relationship

Dateibeschreibung: application/pdf

Relation: https://hdl.handle.net/10400.17/2465

Verfügbarkeit: https://hdl.handle.net/10400.17/2465
https://doi.org/10.1016/j.fertnstert.2015.07.1142

New case of primrose syndrome with mild intellectual disability

Autoren: Leśniewicz, Ryszard

Quelle: American Journal of Medical Genetics Part A. 155:2838-2840

Schlagwörter: Adult, Intellectual disability - pathology, Male, Calcinosis - pathology, Ear diseases - pathology, Hypogonadism - pathology, heterotopic - pathology, Ear diseases - diagnosis, Hypogonadism - diagnosis, heterotopic - diagnosis, Intellectual disability - diagnosis, Muscular atrophy - diagnosis, multiple - pathology, Ossification, Cataract - pathology, Rare diseases - pathology, Muscular atrophy - pathology, Phenotype, Calcinosis - diagnosis, Humans, Abnormalities, Rare diseases - diagnosis, multiple - diagnosis

The key role of testosterone in male hypogonadism / Testosteron i nyckelroll vid hypogonadism hos män

Autoren: Arver, S Lehtihet, M

Quelle: Läkartidningen. 106(39):2460

Posttraumatic hypopituitarism / Posttraumatisk hypopituitarisme

Autoren: Topstad, T K Quist Paulsen, A

Quelle: Tidsskrift for Den Norske Laegeforening. 111(14):1718

Absence d'hypogonadisme chez un patient masculin avec prolactinome géant : un paradoxe clinique

Autoren: Tamagno, Gianluca Daly, Adrian Deprez, Manuel et al.

Schlagwörter: Male, LH, Cabergoline, Biopsy, Sciences de la santé humaine, Endocrinology, metabolism & nutrition, Prolactinome, Pituitary Neoplasms/diagnosis/pathology, Humans, Prolactinoma, Testosterone, Human health sciences, Testostérone, Middle Aged, Hypogonadism/diagnosis, Immunohistochemistry, Magnetic Resonance Imaging, 3. Good health, Prolactin/blood, Luteinizing Hormone/blood, Giant, Prolactinoma/diagnosis/pathology, Testosterone/blood, Géant, Follow-Up Studies, Endocrinologie, métabolisme & nutrition

Zugangs-URL: https://hdl.handle.net/2268/7198

Clinical Management of Congenital Hypogonadotropic Hypogonadism.

Autoren: Young, J. Xu, C. Papadakis, G.E. et al.

Quelle: Endocrine reviews, vol. 40, no. 2, pp. 669-710

Schlagwörter: Adolescent, Adult, Female, Gonadotropin-Releasing Hormone/administration & dosage, Gonadotropin-Releasing Hormone/deficiency, Gonadotropin-Releasing Hormone/metabolism, Gonadotropins/administration & dosage, Humans, Hypogonadism/congenital, Hypogonadism/diagnosis, Hypogonadism/drug therapy, Hypogonadism/metabolism, Infant, Newborn, Male

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/30698671; info:eu-repo/semantics/altIdentifier/eissn/1945-7189; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_87D1B3A2F09F3; https://serval.unil.ch/notice/serval:BIB_87D1B3A2F09F; https://serval.unil.ch/resource/serval:BIB_87D1B3A2F09F.P001/REF.pdf

Verfügbarkeit: https://serval.unil.ch/notice/serval:BIB_87D1B3A2F09F
https://doi.org/10.1210/er.2018-00116
https://serval.unil.ch/resource/serval:BIB_87D1B3A2F09F.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_87D1B3A2F09F3

Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism.

Autoren: Xu, C. Lang-Muritano, M. Phan-Hug, F. et al.

Schlagwörter: Congenital Abnormalities/diagnosis, Congenital Abnormalities/genetics, Congenital Abnormalities/physiopathology, Cryptorchidism/genetics, Cryptorchidism/physiopathology, Fibroblast Growth Factor 8/genetics, Genetic Testing, Gonadotropin-Releasing Hormone/deficiency, Gonadotropin-Releasing Hormone/genetics, Humans, Hypogonadism/diagnosis, Hypogonadism/genetics, Hypogonadism/physiopathology, Infant, Newborn, Male, Receptor, Fibroblast Growth Factor, Type 1/genetics, Signal Transduction, congenital hypogonadotropic hypogonadism, exome sequencing, fibroblast growth factor receptor 1, minipuberty

Relation: Clinical Genetics; https://iris.unil.ch/handle/iris/78624; serval:BIB_2FA37B7AE074; 000405588000013

Verfügbarkeit: https://iris.unil.ch/handle/iris/78624
https://doi.org/10.1111/cge.12996

Increased human chorionic gonadotropin due to hypogonadism after treatment of a testicular seminoma

Autoren: Lempiäinen, Anna Hotakainen, Kristina Blomqvist, Carl et al.

Quelle: Clinical Chemistry. 53(8):1560-1561

Schlagwörter: Adult, Chorionic Gonadotropin/*blood, Diagnosis, Differential, Hormone Replacement Therapy, Humans, Hypogonadism/*diagnosis/drug therapy/etiology, Male, Neoplasm Recurrence, Local/diagnosis, Seminoma/complications/*diagnosis/therapy, Testicular Neoplasms/complications/*diagnosis/therapy, Testosterone/therapeutic use, Tumor Markers, Biological/blood, MEDICINE, MEDICIN

Dateibeschreibung: print

Zugangs-URL: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-17444

High Rates of Depression and Depressive Symptoms among Men Referred for Borderline Testosterone Levels.

Autoren: Westley, Christopher J Amdur, Richard L. Irwig, Michael S.

Quelle: Surgery Faculty Publications

Schlagwörter: Depression--diagnosis, Hypogonadism--diagnosis, Penile Erection--psychology, Sexual Behavior--psychology, Testosterone--blood, Surgery

Relation: https://hsrc.himmelfarb.gwu.edu/smhs_surgery_facpubs/298; http://dx.doi.org/10.1111/jsm.12937

Verfügbarkeit: https://hsrc.himmelfarb.gwu.edu/smhs_surgery_facpubs/298
https://doi.org/10.1111/jsm.12937

More than hypomyelination in pol-III disorder

Autoren: Vanderver, Adeline Tonduti, Davide Bernard, Genevieve et al.

Quelle: Neurology Faculty Publications

Schlagwörter: Anodontia--diagnosis, Anodontia--genetics, Ataxia--diagnosis, Ataxia--genetics, DNA Polymerase III--genetics, Hypogonadism--diagnosis, Hypogonadism--genetics, Leukoencephalopathies--diagnosis, Leukoencephalopathies--genetics, Neurology

Relation: https://hsrc.himmelfarb.gwu.edu/smhs_neuro_facpubs/19; http://www.ncbi.nlm.nih.gov/pubmed?holding=dcgwulib_fft_ndi&dr=abstract&otool=dcgwulib&term=23242285

Verfügbarkeit: https://hsrc.himmelfarb.gwu.edu/smhs_neuro_facpubs/19
http://www.ncbi.nlm.nih.gov/pubmed?holding=dcgwulib_fft_ndi&dr=abstract&otool=dcgwulib&term=23242285

Swedish Andrological Society on testosterone: Misunderstood, mythical and a part of men's health / Svensk andrologisk förening om testosteron: Missförstått, mytomspunnet och en del av mannens hälsa

Autoren: Giwercman, Aleksander Link, Katarina Pousette, Åke et al.

Quelle: Läkartidningen. 108(50):2665

'Hipogonadismo hipogonadotrófico: diagnóstico pré-puberal e papel das isoformas e variantes gênicas do hormônio luteinizante no fenótipo da doença'

Hypogonadotropic hypogonadism : pre-pubertal diagnosis and the role of the isoforms and allelic variants of the luteinizing hormone in the disease phenotype

Autoren: Berger, Karina

Thesis Advisors: Mendonca, Berenice Bilharinho de

Schlagwörter: Chromatography, Cromatografia, Fluorimunoensaio, Fluoroimmunoassay, Freqüência do gene, Gene frequency, Glicoproteínas, Glycoprotein hormones alpha subunit/genetics, Glycoproteins, Hipogonadismo/diagnóstico, Hipopituitarismo, Hormônio luteinizante subunidade beta/genética, Hypogonadism/diagnosis, Hypopituitarism

Dateibeschreibung: application/pdf

Verfügbarkeit: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-07082006-134343/