about
Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutationsLIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious pubertyExome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathyDigenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadismMANAGEMENT OF ENDOCRINE DISEASE: Reversible hypogonadotropic hypogonadismHigh-sensitivity C-reactive protein in paediatric inflammatory bowel disease.Comparison of solution-based exome capture methods for next generation sequencingBone mineral density, body composition and bone turnover in patients with congenital hypogonadotropic hypogonadism.Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.Serum angiopoietin-like 4 protein levels and expression in adipose tissue are inversely correlated with obesity in monozygotic twins.Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland.Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.Genetic Overlap between Holoprosencephaly and Kallmann Syndrome.Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor geneImpaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadismNeural crest cells: from developmental biology to clinical interventions.Gonadotrophin replacement for induction of fertility in hypogonadal men.Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome.Congenital hypogonadotropic hypogonadism, functional hypogonadotropism or constitutional delay of growth and puberty? An analysis of a large patient series from a single tertiary center.Neural Progenitor Cells Derived from Human Embryonic Stem Cells as an Origin of Dopaminergic Neurons.Precocious Puberty or Premature Thelarche: Analysis of a Large Patient Series in a Single Tertiary Center with Special Emphasis on 6- to 8-Year-Old Girls.Combined negative effect of donor age and time in culture on the reprogramming efficiency into induced pluripotent stem cells.Development of Gonadotropin-Releasing Hormone-Secreting Neurons from Human Pluripotent Stem Cells.Idiopathic hypogonadotropic hypogonadism in a mother and her monozygotic twins born after a single embryo transfer.Serum glucocorticoids and adiponectin associate with insulin resistance in children born small for gestational age.Glucocorticoid bioactivity does not predict response to steroid therapy in severe pediatric ulcerative colitis.PROKR2 mutations in autosomal recessive Kallmann syndrome.A homozygous R262Q mutation in the gonadotropin-releasing hormone receptor presenting as reversal of hypogonadotropic hypogonadism and late-onset hypogonadism.Termination of pregnancy with mifepristone and prostaglandin suppresses transiently circulating glucocorticoid bioactivity.Serum androgen bioactivity in adolescence: a longitudinal study of boys with constitutional delay of puberty.Circulating glucocorticoid bioactivity in the preterm newborn after antenatal betamethasone treatment.Hereditary myopathy with early respiratory failure: occurrence in various populations.Late follicular phase administration of mifepristone suppresses circulating leptin and FSH - mechanism(s) of action in emergency contraception?Circulating antiandrogenic activity in children with congenital adrenal hyperplasia during peroral flutamide treatment.Identification of glucocorticoid-response genes in children with acute lymphoblastic leukemia.Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis.The Role of Sequential BMP Signaling in Directing Human Embryonic Stem Cells to Bipotential Gonadal Cells.Health-related quality of life in male patients with congenital hypogonadotropic hypogonadism.
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description
Finnish researcher, professor of translational pediatrics at the University of Helsinki
@en
finnischer Professor
@de
suomalainen tutkija, Helsingin yliopiston translationaalisen lastentautiopin professori
@fi
name
Taneli Raivio
@ast
Taneli Raivio
@ca
Taneli Raivio
@en
Taneli Raivio
@es
Taneli Raivio
@fi
Taneli Raivio
@fr
Taneli Raivio
@ga
Taneli Raivio
@nl
Taneli Raivio
@sl
Taneli Raivio
@sq
type
label
Taneli Raivio
@ast
Taneli Raivio
@ca
Taneli Raivio
@en
Taneli Raivio
@es
Taneli Raivio
@fi
Taneli Raivio
@fr
Taneli Raivio
@ga
Taneli Raivio
@nl
Taneli Raivio
@sl
Taneli Raivio
@sq
prefLabel
Taneli Raivio
@ast
Taneli Raivio
@ca
Taneli Raivio
@en
Taneli Raivio
@es
Taneli Raivio
@fi
Taneli Raivio
@fr
Taneli Raivio
@ga
Taneli Raivio
@nl
Taneli Raivio
@sl
Taneli Raivio
@sq
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1076507115
P27
P31
P496
0000-0001-5385-434X
P569
1970-09-21T00:00:00Z
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P735
P7859
viaf-317090214