-
1دورية أكاديمية
المؤلفون: Tragantzopoulou, Panagiota1 (AUTHOR) g.tragantzopoulou@westminster.ac.uk, Giannouli, Vaitsa2 (AUTHOR) giannouliv@hotmail.com
المصدر: Pediatric Reports. Jun2024, Vol. 16 Issue 2, p420-431. 12p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *CHILD patients, *SYNDROMES in children, *ATTENTION-deficit hyperactivity disorder, *GENETIC disorders, *VERBAL learning
-
2دورية أكاديمية
المؤلفون: García-Payá, Elena1 (AUTHOR), Sirera Sirera, Paula1 (AUTHOR), Huertas-García, Isabel1 (AUTHOR), Hernández Romero, Sofía Daniela1 (AUTHOR), Olivas García, Julia1 (AUTHOR)
المصدر: Cytogenetic & Genome Research. 2024, Vol. 163 Issue 5/6, p295-300. 6p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *DELETION mutation, *GENETIC variation, *SINGLE nucleotide polymorphisms, *INTELLECTUAL development, *GAIT in humans
-
3دورية أكاديمية
المؤلفون: Ahmadi, Aslan1, Torkan, Mohammad Hossein2, Sanaei, Ayda1, Naseri, Reza3 dr.rezanaseri@sbmu.ac.ir
المصدر: Iranian Journal of Neonatology. Apr2024, Vol. 15 Issue 2, p63-69. 7p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *BRAIN abnormalities, *GENETIC disorders, *CHROMOSOME abnormalities, *HUMAN abnormalities, *SPERMATOGENESIS
-
4دورية أكاديمية
المؤلفون: Paparella, Roberto1 (AUTHOR) roberto.paparella@uniroma1.it, Ferraguti, Giampiero2 (AUTHOR) giampiero.ferraguti@uniroma1.it, Fiore, Marco3 (AUTHOR) marco.fiore@cnr.it, Menghi, Michela1 (AUTHOR) michela.menghi@uniroma1.it, Micangeli, Ginevra1 (AUTHOR) ginevra.micangeli@uniroma1.it, Tarani, Francesca1 (AUTHOR) francesca.tarani@uniroma1.it, Ligotino, Aurora1 (AUTHOR) marisapatrizia.messina@uniroma1.it, Messina, Marisa Patrizia1 (AUTHOR) luigi.tarani@uniroma1.it, Ceccanti, Mauro4 (AUTHOR) mauro.ceccanti@uniroma1.it, Minni, Antonio5,6 (AUTHOR) antonio.minni@uniroma1.it, Barbato, Christian3 (AUTHOR) christian.barbato@cnr.it, Lucarelli, Marco2,7 (AUTHOR) marco.lucarelli@uniroma1.it, Tarani, Luigi1 (AUTHOR), Petrella, Carla3 (AUTHOR) carla.petrella@cnr.it
المصدر: International Journal of Molecular Sciences. Feb2024, Vol. 25 Issue 4, p2214. 11p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *LIPOCALIN-2, *INHIBIN, *X chromosome, *PILOT projects, *ENDOCRINE diseases, *CHOLESTERYL ester transfer protein, *SERUM
-
5دورية أكاديمية
العنوان البديل: MALE INFERTILITY : MICRODISSECTION TESTICULAR SPERM EXTRACTION FROM PATIENTS WITH KLINEFELTER'S SYNDROME.
المصدر: Nishinihon Journal of Urology. Dec2023, Vol. 86 Issue 2, p39-45. 7p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *MALE infertility, *INTRACYTOPLASMIC sperm injection, *AZOOSPERMIA, *INFERTILITY
-
6دورية أكاديمية
المؤلفون: Li-Hsin Tai1,2 lihsin081550@gmail.com, Sheau-Fang Yang3,4, Yu-Li Chen5, Yoon Bin Chong5, Ta-Chih Yu5, Ann-Shung Lieu5,6 e791125@gmail.com
المصدر: British Journal of Neurosurgery. Dec2023, Vol. 37 Issue 6, p1853-1858. 6p.
مصطلحات موضوعية: *MEDULLA oblongata, *KLINEFELTER'S syndrome, *TEENAGERS
-
7دورية أكاديمية
المؤلفون: Birch, Sophie1
المصدر: Trends in Urology & Men's Health. Nov2023, Vol. 14 Issue 6, p23-26. 4p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *THROMBOEMBOLISM, *HYPOGONADISM, *KALLMANN syndrome, *INFERTILITY, *SYNDROMES
-
8دورية أكاديمية
المؤلفون: Willems, Stien1 (AUTHOR), David, Karel2,3 (AUTHOR), Decallonne, Brigitte2,3 (AUTHOR), Marcq, Philippe2 (AUTHOR), Antonio, Leen2,3 (AUTHOR), Vanderschueren, Dirk2,3 (AUTHOR) dirk.vanderschueren@uzleuven.be
المصدر: Andrology. Oct2023, Vol. 11 Issue 7, p1295-1302. 8p.
مصطلحات موضوعية: *BONE density, *KLINEFELTER'S syndrome, *TREATMENT effectiveness, *OSTEOPOROSIS, *BONE health
-
9دورية أكاديمية
المؤلفون: Fjermestad, K. W.1,2 (AUTHOR) kfj@frambu.no, Finnbakk, R. R.1 (AUTHOR), Solbakk, A.-K.1,3,4,5 (AUTHOR), Gravholt, C. H.6,7,8 (AUTHOR), Huster, R. J.1,9 (AUTHOR)
المصدر: Orphanet Journal of Rare Diseases. 9/1/2023, Vol. 18 Issue 1, p1-8. 8p.
مصطلحات موضوعية: *KLINEFELTER'S syndrome, *SLEEP latency, *SLEEP interruptions, *SLEEP quality, *SLEEP, *MENTAL health
-
10دورية أكاديمية
المؤلفون: Chaoli Tan, Jing Guo, Jialiang Huang, Yaoxi Mo, Youqiong Li
المصدر: Clinical Laboratory; 2024, Vol. 70 Issue 6, p1196-1200, 5p
مصطلحات موضوعية: KLINEFELTER'S syndrome, GLUCOSE-6-phosphate dehydrogenase deficiency, SEX chromosome abnormalities, KARYOTYPES, Y chromosome, GLUCOSE-6-phosphate dehydrogenase, X chromosome