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Anna-Pauliina Iivonen

Showing results (1-10 of 8) with videos related to

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Endocrine Connections|April 19, 2019
Screening for mutations in selected miRNA genes in hypogonadotropic hypogonadism patientsAnna-Pauliina Iivonen, Johanna Känsäkoski, Kirsi Vaaralahti, et al.
European Journal of Endocrinology|April 28, 2021
Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2Anna-Pauliina Iivonen, Juho Kärkinen, Venkatram Yellapragada, et al.
Endocrine Connections|April 29, 2018
Screening for germline <i>KCNQ1</i> and <i>KCNE2</i> mutations in a set of somatotropinoma patientsAnna-Pauliina Iivonen, Johanna Känsäkoski, Atte Karppinen, et al.
Plos One|November 29, 2017
GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiencyJohanna Hietamäki, Matti Hero, Elina Holopainen, et al.
Pediatric Research|November 20, 2020
Familial central precocious puberty: two novel MKRN3 mutationsTero Varimo, Anna-Pauliina Iivonen, Johanna Känsäkoski, et al.
Eclinicalmedicine|July 25, 2022
Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 yearsJohanna Hietamäki, Juho Kärkinen, Anna-Pauliina Iivonen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic HypopituitarismJohanna Hietamäki, Louise C Gregory, Sandy Ayoub, et al.
JCI Insight|May 22, 2024
A splice site variant in MADD affects hormone expression in pancreatic β cells and pituitary gonadotropesKristiina Pulli, Jonna Saarimäki-Vire, Pekka Ahonen, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Endocrine Connections|April 19, 2019
Screening for mutations in selected miRNA genes in hypogonadotropic hypogonadism patientsAnna-Pauliina Iivonen, Johanna Känsäkoski, Kirsi Vaaralahti, et al.
European Journal of Endocrinology|April 28, 2021
Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2Anna-Pauliina Iivonen, Juho Kärkinen, Venkatram Yellapragada, et al.
Endocrine Connections|April 29, 2018
Screening for germline <i>KCNQ1</i> and <i>KCNE2</i> mutations in a set of somatotropinoma patientsAnna-Pauliina Iivonen, Johanna Känsäkoski, Atte Karppinen, et al.
Plos One|November 29, 2017
GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiencyJohanna Hietamäki, Matti Hero, Elina Holopainen, et al.
Pediatric Research|November 20, 2020
Familial central precocious puberty: two novel MKRN3 mutationsTero Varimo, Anna-Pauliina Iivonen, Johanna Känsäkoski, et al.
Eclinicalmedicine|July 25, 2022
Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 yearsJohanna Hietamäki, Juho Kärkinen, Anna-Pauliina Iivonen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic HypopituitarismJohanna Hietamäki, Louise C Gregory, Sandy Ayoub, et al.
JCI Insight|May 22, 2024
A splice site variant in MADD affects hormone expression in pancreatic β cells and pituitary gonadotropesKristiina Pulli, Jonna Saarimäki-Vire, Pekka Ahonen, et al.
Pageof 1