X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (86) 86
humans (83) 83
male (70) 70
endocrinology & metabolism (55) 55
gonadotropin-releasing-hormone (45) 45
female (44) 44
adult (38) 38
mutation (37) 37
hypogonadism - genetics (34) 34
abridged index medicus (33) 33
kallmann-syndrome (31) 31
idiopathic hypogonadotropic hypogonadism (25) 25
hypogonadism (24) 24
deficiency (23) 23
gonadotropin-releasing hormone - deficiency (23) 23
luteinizing-hormone (23) 23
phenotype (22) 22
animals (20) 20
kallmann syndrome - genetics (20) 20
pedigree (20) 20
middle aged (19) 19
mutations (17) 17
puberty (17) 17
receptor, fibroblast growth factor, type 1 - genetics (17) 17
kallmann syndrome (16) 16
adolescent (15) 15
cohort studies (15) 15
gene (15) 15
genetic aspects (14) 14
gonadotropin-releasing hormone - genetics (14) 14
nerve tissue proteins - genetics (14) 14
research (14) 14
mice (13) 13
receptors, g-protein-coupled - genetics (13) 13
hypogonadism - physiopathology (12) 12
receptors, lhrh - genetics (12) 12
extracellular matrix proteins - genetics (11) 11
follicle-stimulating-hormone (11) 11
genotype (11) 11
heterozygote (11) 11
receptor (11) 11
testosterone - blood (11) 11
endocrine system (10) 10
expression (10) 10
gastrointestinal hormones - genetics (10) 10
genetics & heredity (10) 10
hypogonadotropic hypogonadism (10) 10
luteinizing hormone - blood (10) 10
neuropeptides - genetics (10) 10
pituitary (10) 10
receptors, peptide - genetics (10) 10
testosterone (10) 10
aged (9) 9
genetic disorders (9) 9
gonadotropin-releasing hormone - therapeutic use (9) 9
hypogonadism - drug therapy (9) 9
jcem online (9) 9
reproduction (9) 9
signal transduction (9) 9
advances in genetics (8) 8
article (8) 8
congenital hypogonadotropic hypogonadism (8) 8
fibroblast growth factor 8 - genetics (8) 8
follicle stimulating hormone - blood (8) 8
gonadotropin-releasing hormone (8) 8
hormones (8) 8
hormones, hormone substitutes, and hormone antagonists (8) 8
hypogonadism - congenital (8) 8
of-function mutations (8) 8
olfactory-bulb (8) 8
original (8) 8
original article (8) 8
physiological aspects (8) 8
pituitary hormones (8) 8
analysis (7) 7
child (7) 7
dna mutational analysis (7) 7
fibroblast growth factor (7) 7
genes (7) 7
genetic association studies (7) 7
genetics (7) 7
gonadotropin-releasing hormone - metabolism (7) 7
heterogeneity (7) 7
jcem online: advances in genetics (7) 7
molecular sequence data (7) 7
multidisciplinary sciences (7) 7
neurons (7) 7
neurons - metabolism (7) 7
receptors, kisspeptin-1 (7) 7
secretion (7) 7
biological sciences (6) 6
cell biology (6) 6
delayed puberty (6) 6
fgfr1 (6) 6
fibroblast growth factor receptor 1 (6) 6
gene mutations (6) 6
gonadotropin (6) 6
gonadotropins (6) 6
hypogonadism - complications (6) 6
hypogonadism - metabolism (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


BMJ : British Medical Journal, ISSN 1756-1833, 12/2012, Volume 345, Issue 7889, pp. e7913 - e7913
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
The New England Journal of Medicine, ISSN 0028-4793, 08/2007, Volume 357, Issue 9, pp. 863 - 873
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
Journal of Clinical Investigation, ISSN 0021-9738, 08/2008, Volume 118, Issue 8, pp. 2822 - 2831
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2011, Volume 364, Issue 3, pp. 215 - 225
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 02/2013, Volume 78, Issue 2, pp. 291 - 296
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 02/2007, Volume 117, Issue 2, pp. 457 - 463
Journal Article