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Titlebook: Klinefelter’s Syndrome; From a Disabling Con Andrea Garolla,Giovanni Corona Book 2020 Springer Nature Switzerland AG 2020 Genetic disorders

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樓主: SCOWL
41#
發(fā)表于 2025-3-28 18:24:30 | 只看該作者
Klinefelter Syndrome: Cardiovascular Characteristics,alformation. Metabolic syndrome and type 2 diabetes, which are highly prevalent in KS patients, may contribute to the increased cardiovascular mortality. The few available studies on cardiac damage in KS have provided conflicting results. Aside from increased prevalence of valvular abnormalities, su
42#
發(fā)表于 2025-3-28 21:55:10 | 只看該作者
Savina Dipresa,Andrea Garolla in Sect.?.. The requirement that entropy must be maximum possible is analyzed in Sect.?.. The extremum in energy, namely that energy must be the minimum possible, is discussed in Sect.?.. The fact that the physical consequences of both these extrema are similar is noted and emphasized. Of course, a
43#
發(fā)表于 2025-3-29 02:55:57 | 只看該作者
44#
發(fā)表于 2025-3-29 03:26:09 | 只看該作者
45#
發(fā)表于 2025-3-29 07:16:16 | 只看該作者
Franz Sesti,Riccardo Pofi,Andrea M. Isidorinsivist familiar with ultrasound, it specifically details findings of immediate clinical relevance throughout its approx. 220 pages. Through a whole-body approach, this book considers new emergency applications regarding the abdomen, venous system, head, heart, and the most original topic, the lung.
46#
發(fā)表于 2025-3-29 12:32:50 | 只看該作者
Andrea Garolla,Giovanni CoronaFirst book covering all physiological and pathological aspects of Klinefelter‘s syndrome.Appeals to both professionals and non-experts.Written by leading experts in the field
47#
發(fā)表于 2025-3-29 18:00:22 | 只看該作者
Trends in Andrology and Sexual Medicinehttp://image.papertrans.cn/k/image/543490.jpg
48#
發(fā)表于 2025-3-29 22:32:34 | 只看該作者
49#
發(fā)表于 2025-3-30 02:54:05 | 只看該作者
Klinefelter’s Syndrome978-3-030-51410-5Series ISSN 2367-0088 Series E-ISSN 2367-0096
50#
發(fā)表于 2025-3-30 06:00:30 | 只看該作者
Early Developmental Pathways and Communication Good Practices,ccording to the studies of the literature. Behavioural phenotype of this genetic condition is wide and heterogenous for both clinical and neuropsychiatric aspects. The spread of prenatal diagnosis demonstrated that the outcomes are much better than those described in the original literature.
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