Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Eeva-Maria Laitinen"'
Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations.
Autor:
Eeva-Maria Laitinen, Johanna Tommiska, Timo Sane, Kirsi Vaaralahti, Jorma Toppari, Taneli Raivio
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e39450 (2012)
BACKGROUND: Congenital hypogonadotropic hypogonadism (HH) is a rare cause for delayed or absent puberty. These patients may recover from HH spontaneously in adulthood. To date, it is not possible to predict who will undergo HH reversal later in life.
Externí odkaz:
https://doaj.org/article/8c2dfa59e87148d483d7fbd5979adf7f
Autor:
Matti Hero, Kirsi Vaaralahti, Eeva-Maria Laitinen, Johanna Tommiska, Taneli Raivio, Tero Varimo
Publikováno v:
Clinical Endocrinology. 82:122-126
OBJECTIVE In search of phenotypic cues that would allow early detection of Kallmann syndrome (KS), we evaluated the paediatric phenotypes in a series of females with KS. DESIGN, PATIENTS AND MEASUREMENTS In this retrospective cohort study, we investi
Publikováno v:
International Journal of Andrology. 35:534-540
Patients with congenital hypogonadotropic hypogonadism (HH) may have reduced peak bone mass in early adulthood, and increased risk for osteoporosis despite long-term hormonal replacement therapy (HRT). To investigate the relationship between HRT hist
Autor:
Taneli Raivio, Kirsi Vaaralahti, R. Koivu, Eeva-Maria Laitinen, Johanna Tommiska, Leena Valanne
Publikováno v:
Europe PubMed Central
Patients with Kallmann syndrome (KS; congenital hypogonadotropic hypogonadism and decreased/absent sense of smell), septo-optic dysplasia (SOD), or holoprosencephaly (HPE) reportedly have midline defects. In this study, we investigate a genetic overl
Autor:
Johanna Tommiska, Eeva-Maria Laitinen, Karoliina Wehkalampi, Taneli Raivio, Kirsi Vaaralahti, Leo Dunkel
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 95:3063-3066
Background: Recently variation in LIN28B, a human ortholog of the gene-regulating processing of micro-RNAs (miRNAs) controlling the timing of major developmental events in the nematode Caenorhabtidis elegans, was reported to be associated with timing
Autor:
Päivi J. Miettinen, Eeva-Maria Laitinen, Johanna Tommiska, Taneli Raivio, Tero Varimo, Anders Juul, Matti Hero, Johanna Känsäkoski
Publikováno v:
Pediatric research. 79(5)
We describe childhood growth patterns in a series of well-characterized patients with congenital hypogonadotropic hypogonadism (CHH) with special emphasis on genotype–phenotype correlation. We retrospectively evaluated the growth charts of 36 males
Publikováno v:
Clinical endocrinology. 83(1)
Autor:
Nelly Pitteloud, Peter Hackman, Johanna Känsäkoski, Eeva-Maria Laitinen, Taneli Raivio, Kirsi Vaaralahti, Johanna Tommiska, Rainer Fagerholm
Publikováno v:
Pediatric research. 75(5)
Congenital hypogonadotropic hypogonadism (HH), a rare disorder characterized by absent, partial, or delayed puberty, can be caused by the lack or deficient number of hypothalamic gonadotropin-releasing hormone (GnRH) neurons. SEMA3A was recently impl
Autor:
Anne Kinnala, Parinya Noisa, Johanna Känsäkoski, Taneli Raivio, Jorma Toppari, Johanna Tommiska, Harri Niinikoski, Kirsi Vaaralahti, Eeva-Maria Laitinen
Publikováno v:
Fertility and sterility. 99(3)
Objective To investigate the inheritance pattern of two missense PROKR2 changes within a single family. Design This is a descriptive study. Setting Tertiary referral center. Patient(s) The proband and his brother, both with congenital hypogonadotropi
Autor:
Timo Sane, Johanna Tommiska, Eeva-Maria Laitinen, Kirsi Vaaralahti, Taneli Raivio, Jorma Toppari
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e39450 (2012)
PLoS ONE
PLoS ONE
BACKGROUND: Congenital hypogonadotropic hypogonadism (HH) is a rare cause for delayed or absent puberty. These patients may recover from HH spontaneously in adulthood. To date, it is not possible to predict who will undergo HH reversal later in life.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d724628419d0ecacdf8bb1d697528c0f
http://hdl.handle.net/10138/165771
http://hdl.handle.net/10138/165771