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Strategies, ISSN 0892-4562, 03/2017, Volume 30, Issue 2, pp. 42 - 44
This article present nine strategies that have been used successfully to improve activity levels in PE classes. These strategies comprise small-sided games,... 
Journal Article
Journal of pediatric nursing, 08/2019
Journal Article
06/2018, Endocrine Development, ISBN 9783318061420, Volume 33, 17
Passage from childhood to adult life involves biological changes culminating in full reproductive capacity as well as psychosocial development. For patients... 
Chapter
Book Chapter
Journal of Vascular Nursing, ISSN 1062-0303, 05/2019
Journal Article
Frontiers of hormone research, 2018, Volume 49, p. 156
The metabolic syndrome (MetS) is a term used to describe the constellation of cardiometabolic risk factors including central adiposity, dyslipidemia, insulin... 
Testosterone - metabolism | Hypogonadism - metabolism | Humans | Testosterone - deficiency | Male | Metabolic Syndrome - metabolism
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 06/2016, Volume 174, Issue 6, pp. R267 - R274
Congenital hypogonadotropic hypogonadism (CHH) is characterized by lack of puberty and infertility. Traditionally, it has been considered a life-long condition... 
DELAYED PUBERTY | GONADOTROPIN-RELEASING-HORMONE | ENDOCRINOLOGY & METABOLISM | FERTILE EUNUCH | LINKED KALLMANN-SYNDROME | RECEPTOR GENE | HOMOZYGOUS R262Q MUTATION | CANDIDATE GENE | INDUCTION | DEFICIENCY | PULSATILE
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 07/2015, Volume 173, Issue 1, pp. R15 - R24
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 05/2005, Volume 90, Issue 5, pp. 2636 - 2641
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 03/2018, Volume 178, Issue 3, pp. R55 - R80
Congenital hypogonadotropic hypogonadism (CHH) and Kallmann syndrome (KS) are rare, related diseases that prevent normal pubertal development and cause... 
FIBROBLAST-GROWTH-FACTOR-RECEPTOR-1 GENE | GONADOTROPIN-RELEASING-HORMONE | DAX1/NR0B1 MUTATION | ENDOCRINOLOGY & METABOLISM | ADRENAL HYPOPLASIA CONGENITA | DIGENIC MUTATIONS | OF-FUNCTION MUTATIONS | PRIMARY AMENORRHEA | BETA-SUBUNIT | PHENOTYPIC SPECTRUM | LUTEINIZING-HORMONE
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 12/2018, Volume 89, Issue 6, pp. 712 - 718
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2010, Volume 107, Issue 34, pp. 15140 - 15144
Between the genetic extremes of rare monogenic and common polygenic diseases lie diverse oligogenic disorders involving mutations in more than one locus in... 
Deficiency diseases | Sex hormones | Nervous system diseases | Disease models | Medical genetics | Genetic diseases | Genetic mutation | Kallmann syndrome | Human genetics | Hypogonadism | Rare variant | Digenic | Idiopathic hypogonadotropic hypogonadism | FGFR1 | idiopathic hypogonadotropic hypogonadism | GPR54 | MULTIDISCIPLINARY SCIENCES | CLINICAL HETEROGENEITY | MISSENSE MUTATIONS | PUBERTY | digenic | GENE | BARDET-BIEDL-SYNDROME | LINKED KALLMANN-SYNDROME | FIBROBLAST-GROWTH-FACTOR-RECEPTOR-1 | GNRH RECEPTOR | rare variant | Receptors, LHRH - genetics | Humans | Male | Gene Regulatory Networks | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Case-Control Studies | Receptors, Peptide - genetics | Genetic Variation | DNA Mutational Analysis | Female | Neuropeptides - genetics | Fibroblast Growth Factor 8 - genetics | Kallmann Syndrome - genetics | Extracellular Matrix Proteins - genetics | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Hypogonadism - genetics | Homozygote | Phenotype | Pedigree | Gastrointestinal Hormones - genetics | Heterozygote | Models, Genetic | Receptors, G-Protein-Coupled - genetics | Mutation | Receptors, Kisspeptin-1 | Gonadotropin-Releasing Hormone - deficiency | Cohort Studies | Multifactorial diseases | Genetic aspects | Hormones | Gonadotropin | Health aspects | Pathogens | Genetics | Genetic disorders | Pathogenesis | Index Medicus | Biological Sciences
Journal Article
Diabetes Care, ISSN 0149-5992, 07/2005, Volume 28, Issue 7, pp. 1636 - 1642
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2013, Volume 92, Issue 5, pp. 725 - 743
Journal Article