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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, ISSN 0882-5963, 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
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... 
Recovery of Function - physiology | Female | Hypogonadism - physiopathology | Male | Remission, Spontaneous | Humans
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 06/2016, Volume 174, Issue 6, p. R267
Congenital hypogonadotropic hypogonadism (CHH) is characterized by lack of puberty and infertility. Traditionally, it has been considered a life-long condition... 
Puberty | Phenotypes | Infertility | Gonadotropin-releasing hormone | Mutation | Patients | Hypogonadism
Journal Article
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
International Journal of Nursing Studies, ISSN 0020-7489, 02/2018, Volume 78, p. 61
ObjectivesTo identify and summarize the common clinical settings, interventions, and outcomes of nurse practitioner care specific to older people.DesignScoping... 
Health care | Intervention | Home care | Nurse practitioners | Unmet needs | Service provision | Long term health care | Public policy | Primary care | Patients | Clinical outcomes | Quality of life | Databases | Health status | Health care expenditures | Inferiority | Older people | Systematic reviews | Work roles | Geriatrics | Length of stay
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
The Journal of Bone and Joint Surgery, ISSN 0021-9355, 09/2019, Volume 101, Issue 18, pp. 1645 - 1653
BACKGROUND:As guidelines and payers increasingly recommend use of patient decision aids (DAs), evidence about the comparative effectiveness of available DAs is... 
Journal Article
The Journal of Bone and Joint Surgery, ISSN 0021-9355, 09/2019, Volume 101, Issue 18, pp. 1645 - 1653
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 03/2018, Volume 178, Issue 3, p. R55
Congenital hypogonadotropic hypogonadism (CHH) and Kallmann syndrome (KS) are rare, related diseases that prevent normal pubertal development and cause... 
Genetic counseling | Congenital diseases | Infertility | Heredity | Children | Hypogonadism
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... 
Hypogonadism - genetics | Multifactorial Inheritance - genetics | Kallmann Syndrome - genetics | Humans | Penetrance | High-Throughput Nucleotide Sequencing | Genetic Counseling | Sequence Analysis, DNA | Hypogonadism - congenital | Infertility - genetics
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
Journal of advanced nursing, ISSN 0309-2402, 08/2019
The aim of the management of systemic sclerosis (MANOSS) study described in this protocol is to develop a chronic care model, based on a contextual analysis... 
Journal Article