Bone density and risk of osteoporosis in Klinefelter syndrome. - Wikidata - awgldk - TriplyDB

Bone density and risk of osteoporosis in Klinefelter syndrome.

Bone density and risk of osteoporosis in Klinefelter syndrome.

http://www.wikidata.org/entity/Q37826806

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Recognizing and treating secondary osteoporosis The Sex Chromosome Trisomy mouse model of XXY and XYY: metabolism and motor performance.The importance of having two X chromosomes.Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome.Clinical and hormonal status of infants with nonmosaic XXY karyotype.47,XXY Klinefelter syndrome: clinical characteristics and age-specific recommendations for medical management.Melatonin and the skeleton.Testicular parenchymal abnormalities in Klinefelter syndrome: a question of cancer? Examination of 40 consecutive patients Low INSL3 in Klinefelter syndrome is related to osteocalcin, testosterone treatment and body composition, as well as measures of the hypothalamic-pituitary-gonadal axis.

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Bone density and risk of osteoporosis in Klinefelter syndrome.

http://www.wikidata.org/entity/Q37826806

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 10 February 2011

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Bone density and risk of osteoporosis in Klinefelter syndrome.

@en

Bone density and risk of osteoporosis in Klinefelter syndrome.

@nl

type

label

Bone density and risk of osteoporosis in Klinefelter syndrome.

@en

Bone density and risk of osteoporosis in Klinefelter syndrome.

@nl

prefLabel

Bone density and risk of osteoporosis in Klinefelter syndrome.

@en

Bone density and risk of osteoporosis in Klinefelter syndrome.

@nl

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J.1651-2227.2010.02138.X

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Acta Paediatrica

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Bone density and risk of osteoporosis in Klinefelter syndrome.

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P2860

Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man

Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene

Targeted disruption of the Insl3 gene causes bilateral cryptorchidism

Mutations in the insulin-like factor 3 receptor are associated with osteoporosis.

Gonadal dysgenesis and bone metabolism.

Normal bone mineral content but unfavourable muscle/fat ratio in Klinefelter syndrome.

The INSL3-LGR8/GREAT ligand-receptor pair in human cryptorchidism.

Official positions of the International Society for Clinical Densitometry.

X-chromosome inactivation patterns and androgen receptor functionality influence phenotype and social characteristics as well as pharmacogenetics of testosterone therapy in Klinefelter patients.

Estrogens and bone health in men.

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878-884

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