152 related articles for article (PubMed ID: 35854182)
1. MKRN3 circulating levels in Prader-Willi syndrome: a pilot study.
Mariani M; Fintini D; Cirillo G; Palumbo S; Del Giudice EM; Bocchini S; Manco M; Cappa M; Grandone A
J Endocrinol Invest; 2022 Nov; 45(11):2165-2170. PubMed ID: 35854182
[TBL] [Abstract][Full Text] [Related]
2. Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome.
Meader BN; Albano A; Sekizkardes H; Delaney A
J Clin Endocrinol Metab; 2020 Aug; 105(8):2732-9. PubMed ID: 32480405
[TBL] [Abstract][Full Text] [Related]
3. MKRN3 levels in girls with central precocious puberty and correlation with sexual hormone levels: a pilot study.
Grandone A; Cirillo G; Sasso M; Capristo C; Tornese G; Marzuillo P; Luongo C; Rosaria Umano G; Festa A; Coppola R; Miraglia Del Giudice E; Perrone L
Endocrine; 2018 Jan; 59(1):203-208. PubMed ID: 28299573
[TBL] [Abstract][Full Text] [Related]
4. Advances in genetic mechanisms of hypothalamic dysfunction in Prader-Willi syndrome.
Wang XY; Sun R; Gao YQ
Yi Chuan; 2022 Oct; 44(10):899-912. PubMed ID: 36384726
[TBL] [Abstract][Full Text] [Related]
5. Multiple forms of hypogonadism of central, peripheral or combined origin in males with Prader-Willi syndrome.
Radicioni AF; Di Giorgio G; Grugni G; Cuttini M; Losacco V; Anzuini A; Spera S; Marzano C; Lenzi A; Cappa M; Crinò A
Clin Endocrinol (Oxf); 2012 Jan; 76(1):72-7. PubMed ID: 21718342
[TBL] [Abstract][Full Text] [Related]
6. Sexual dichotomy of gonadal function in Prader-Willi syndrome from early infancy through the fourth decade.
Hirsch HJ; Eldar-Geva T; Bennaroch F; Pollak Y; Gross-Tsur V
Hum Reprod; 2015 Nov; 30(11):2587-96. PubMed ID: 26345685
[TBL] [Abstract][Full Text] [Related]
7. An update on the genetic causes of central precocious puberty.
Shin YL
Ann Pediatr Endocrinol Metab; 2016 Jun; 21(2):66-9. PubMed ID: 27462581
[TBL] [Abstract][Full Text] [Related]
8. Hypothalamic and gonadal components of hypogonadism in boys with Prader-Labhart- Willi syndrome.
Eiholzer U; l'Allemand D; Rousson V; Schlumpf M; Gasser T; Girard J; Grüters A; Simoni M
J Clin Endocrinol Metab; 2006 Mar; 91(3):892-8. PubMed ID: 16352691
[TBL] [Abstract][Full Text] [Related]
9. An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.
Wu MY; Jiang M; Zhai X; Beaudet AL; Wu RC
PLoS One; 2012; 7(4):e34348. PubMed ID: 22496793
[TBL] [Abstract][Full Text] [Related]
10. A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.
Grandone A; Cantelmi G; Cirillo G; Marzuillo P; Luongo C; Miraglia del Giudice E; Perrone L
BMC Endocr Disord; 2015 Oct; 15():60. PubMed ID: 26499472
[TBL] [Abstract][Full Text] [Related]
11. Comparison of Makorin Ring Finger Protein 3 Levels Between Obese and Normal Weight Patients with Central Precocious Puberty.
Eren SE; Şimşek E
J Clin Res Pediatr Endocrinol; 2023 May; 15(2):182-189. PubMed ID: 36728292
[TBL] [Abstract][Full Text] [Related]
12. Circulating MKRN3 levels decline prior to pubertal onset and through puberty: a longitudinal study of healthy girls.
Hagen CP; Sørensen K; Mieritz MG; Johannsen TH; Almstrup K; Juul A
J Clin Endocrinol Metab; 2015 May; 100(5):1920-6. PubMed ID: 25695892
[TBL] [Abstract][Full Text] [Related]
13. Central precocious puberty caused by mutations in the imprinted gene MKRN3.
Abreu AP; Dauber A; Macedo DB; Noel SD; Brito VN; Gill JC; Cukier P; Thompson IR; Navarro VM; Gagliardi PC; Rodrigues T; Kochi C; Longui CA; Beckers D; de Zegher F; Montenegro LR; Mendonca BB; Carroll RS; Hirschhorn JN; Latronico AC; Kaiser UB
N Engl J Med; 2013 Jun; 368(26):2467-75. PubMed ID: 23738509
[TBL] [Abstract][Full Text] [Related]
14. A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
Kanber D; Giltay J; Wieczorek D; Zogel C; Hochstenbach R; Caliebe A; Kuechler A; Horsthemke B; Buiting K
Eur J Hum Genet; 2009 May; 17(5):582-90. PubMed ID: 19066619
[TBL] [Abstract][Full Text] [Related]
15. Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience.
Yang A; Kim J; Cho SY; Jin DK
Orphanet J Rare Dis; 2017 Aug; 12(1):146. PubMed ID: 28854950
[TBL] [Abstract][Full Text] [Related]
16. Hypogonadism in females with Prader-Willi syndrome from infancy to adulthood: variable combinations of a primary gonadal defect and hypothalamic dysfunction.
Eldar-Geva T; Hirsch HJ; Benarroch F; Rubinstein O; Gross-Tsur V
Eur J Endocrinol; 2010 Feb; 162(2):377-84. PubMed ID: 19946044
[TBL] [Abstract][Full Text] [Related]
17. Methylation status of hypothalamic
Fanis P; Morrou M; Tomazou M; Michailidou K; Spyrou GM; Toumba M; Skordis N; Neocleous V; Phylactou LA
Front Endocrinol (Lausanne); 2022; 13():1075341. PubMed ID: 36714607
[TBL] [Abstract][Full Text] [Related]
18. Gonadal Hormone Substitution in People with Prader-Labhart-Willi Syndrome: An International Prader-Willi Syndrome Organisation Survey.
Eiholzer U; Stephan A; Fritz C; Katschnig C; Noordam C;
Horm Res Paediatr; 2021; 94(5-6):176-185. PubMed ID: 34348303
[TBL] [Abstract][Full Text] [Related]
19. Testicular failure in boys with Prader-Willi syndrome: longitudinal studies of reproductive hormones.
Siemensma EP; de Lind van Wijngaarden RF; Otten BJ; de Jong FH; Hokken-Koelega AC
J Clin Endocrinol Metab; 2012 Mar; 97(3):E452-9. PubMed ID: 22188746
[TBL] [Abstract][Full Text] [Related]
20. [The reproductive system in Prader-Willi syndrome].
Eldar-Geva T; Hirsch HJ; Gross-Tsur V
Harefuah; 2015 Mar; 154(3):178-82, 211. PubMed ID: 25962248
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
