Zobrazeno 1 - 10
of 643
pro vyhledávání: '"XXY"'
Autor:
Qiliang Ding, Abigail L. Bronson, Kyna A. Byerly, Anna A. Essendrup, Elyse B. Mitchell, Cassandra K. Runke, Ross A. Rowsey, Nicole L. Hoppman
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-6 (2024)
Abstract Background Interphase fluorescence in situ hybridization (FISH) is commonly used for rapid aneuploidy detection in clinical settings. While FISH-based aneuploidy detection provides rapid results desirable for patient management, it usually o
Externí odkaz:
https://doaj.org/article/de3c40ccc0fd493fa7bf0c2e0556d1a8
Autor:
Julia Spiekermann, Jakob Höppner, Eliena Ibnukhsein, Kathrin Sinningen, Beatrice Hanusch, Cordula Kiewert, Heide Siggelkow, Corinna Grasemann
Publikováno v:
Molecular and Cellular Pediatrics, Vol 11, Iss 1, Pp 1-9 (2024)
Abstract Background In adults with Klinefelter syndrome (KS), impaired bone health with reduced bone mineral density (BMD) has been described even in the presence of testosterone replacement therapy. The aim of the present study was to characterize b
Externí odkaz:
https://doaj.org/article/d5ac7849c7fd4d9e9cd932f84c29b189
Autor:
Olivera, Guillermo1
Publikováno v:
Chasqui (01458973). nov2017, Vol. 46 Issue 2, p207-226. 20p.
Akademický článek
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Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Objectives To investigate sleep among men with Klinefelter syndrome (KS). Method We compared the sleep domains latency, disturbance, and efficiency in 30 men with KS (M age = 36.7 years, SD = 10.6) to 21 age-matched non-KS controls (M age =
Externí odkaz:
https://doaj.org/article/95564dbc783349628ee8367745ffb614
Autor:
Alan D Rogol
Publikováno v:
Endocrine Connections, Vol 12, Iss 9, Pp 1-10 (2023)
The overall incidence of sex chromosome aneuploidies is approximately 1 per 500 live-born infants, but far more common at conception. I shall review the fertility aspects of the sex chromosome trisomies, XXY, XYY, and XXX, with special reference to t
Externí odkaz:
https://doaj.org/article/e83273e09f8a44b2bfc77b48d0358ab2
Autor:
René J. Huster, Christina Thunberg, Anne-Kristin Solbakk, Claus H. Gravholt, Krister Fjermestad
Publikováno v:
NeuroImage: Clinical, Vol 44, Iss , Pp 103674- (2024)
Deficits in several cognitive domains are prevalent in men with Klinefelter Syndrome (KS). Verbal deficits are among the most characteristic cognitive impairments of KS, yet other cognitive domains also exhibit deficits. Executive functions, especial
Externí odkaz:
https://doaj.org/article/25761494509146dba1d2899bc9258821
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 12, Pp 3406-3408 (2023)
Reviewed here is a case of Klinefelter Syndrome (KS) diagnosed by a primary care physician after recognition of key features of KS, confirmed by karyotype, along with a discussion of factors associated with this patient's diagnosis and care. Recognit
Externí odkaz:
https://doaj.org/article/48392f83ac574ef4ad43c034f68c6942
Autor:
Fradinger, Moira1 moira.fradinger@yale.edu
Publikováno v:
Cuadernos de Literatura. jul-dec2016, Vol. 20 Issue 40, p357-381. 25p.
Autor:
Corbatta, Jorgelina (AUTHOR) aa1690@wayne.edu
Publikováno v:
Psychoanalytic Inquiry. Nov/Dec2015, Vol. 35 Issue 8, p823-831. 9p.