243 related articles for article (PubMed ID: 27225315)
21. Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty.
Simon D; Ba I; Mekhail N; Ecosse E; Paulsen A; Zenaty D; Houang M; Jesuran Perelroizen M; de Filippo GP; Salerno M; Simonin G; Reynaud R; Carel JC; Léger J; de Roux N
Eur J Endocrinol; 2016 Jan; 174(1):1-8. PubMed ID: 26431553
[TBL] [Abstract][Full Text] [Related]
22. The genetic etiology is a relevant cause of central precocious puberty.
Canton APM; Seraphim CE; Montenegro LR; Krepischi ACV; Mendonca BB; Latronico AC; Brito VN
Eur J Endocrinol; 2024 Jun; 190(6):479-488. PubMed ID: 38857188
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Pioneering studies on monogenic central precocious puberty.
Canton APM; Seraphim CE; Brito VN; Latronico AC
Arch Endocrinol Metab; 2019 Aug; 63(4):438-444. PubMed ID: 31460623
[TBL] [Abstract][Full Text] [Related]
25. A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty.
Känsäkoski J; Raivio T; Juul A; Tommiska J
Pediatr Res; 2015 Dec; 78(6):709-11. PubMed ID: 26331766
[TBL] [Abstract][Full Text] [Related]
26. Clinical and Genetic Characterization of Familial Central Precocious Puberty.
Tinano FR; Canton APM; Montenegro LR; de Castro Leal A; Faria AG; Seraphim CE; Brauner R; Jorge AA; Mendonca BB; Argente J; Brito VN; Latronico AC
J Clin Endocrinol Metab; 2023 Jun; 108(7):1758-1767. PubMed ID: 36611250
[TBL] [Abstract][Full Text] [Related]
27. A novel heterozygous MKRN3 nonsense mutation in a Chinese girl with idiopathic central precocious puberty: A case report.
Liu M; Fan L; Gong CX
Medicine (Baltimore); 2020 Sep; 99(38):e22295. PubMed ID: 32957387
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Idiopathic central precocious puberty in 28 boys.
Pigneur B; Trivin C; Brauner R
Med Sci Monit; 2008 Jan; 14(1):CR10-14. PubMed ID: 18160938
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.
Montenegro L; Labarta JI; Piovesan M; Canton APM; Corripio R; Soriano-Guillén L; Travieso-Suárez L; Martín-Rivada Á; Barrios V; Seraphim CE; Brito VN; Latronico AC; Argente J
J Clin Endocrinol Metab; 2020 Oct; 105(10):. PubMed ID: 32676665
[TBL] [Abstract][Full Text] [Related]
33. MKRN3 and KISS1R mutations in precocious and early puberty.
Pagani S; Calcaterra V; Acquafredda G; Montalbano C; Bozzola E; Ferrara P; Gasparri M; Villani A; Bozzola M
Ital J Pediatr; 2020 Mar; 46(1):39. PubMed ID: 32228714
[TBL] [Abstract][Full Text] [Related]
34. Clinical Exome Sequencing Reveals MKRN3 Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty.
Ortiz-Cabrera NV; Riveiro-Álvarez R; López-Martínez MÁ; Pérez-Segura P; Aragón-Gómez I; Trujillo-Tiebas MJ; Soriano-Guillén L
Horm Res Paediatr; 2017; 87(2):88-94. PubMed ID: 27931036
[TBL] [Abstract][Full Text] [Related]
35. Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty.
Aycan Z; Savaş-Erdeve Ş; Çetinkaya S; Kurnaz E; Keskin M; Muratoğlu Şahin N; Bayramoğlu E; Ceylaner G
J Clin Res Pediatr Endocrinol; 2018 Jul; 10(3):223-229. PubMed ID: 29537379
[TBL] [Abstract][Full Text] [Related]
36. Identification of rare missense mutations in
Lee HS; Jeong HR; Rho JG; Kum CD; Kim KH; Kim DW; Cheong JY; Jeong SY; Hwang JS
Gynecol Endocrinol; 2020 Aug; 36(8):682-686. PubMed ID: 32400230
[No Abstract] [Full Text] [Related]
37. Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious Puberty.
Simsek E; Demiral M; Ceylaner S; Kırel B
Horm Res Paediatr; 2017; 87(6):405-411. PubMed ID: 27798941
[TBL] [Abstract][Full Text] [Related]
38. New causes of central precocious puberty: the role of genetic factors.
Bulcao Macedo D; Nahime Brito V; Latronico AC
Neuroendocrinology; 2014; 100(1):1-8. PubMed ID: 25116033
[TBL] [Abstract][Full Text] [Related]
39. MKRN3 role in regulating pubertal onset: the state of art of functional studies.
Palumbo S; Cirillo G; Aiello F; Papparella A; Miraglia Del Giudice E; Grandone A
Front Endocrinol (Lausanne); 2022; 13():991322. PubMed ID: 36187104
[TBL] [Abstract][Full Text] [Related]
40. [Recent advances in the genetic etiology of central precocious puberty].
Zhang YY; Luo FH
Zhongguo Dang Dai Er Ke Za Zhi; 2024 Mar; 26(3):302-307. PubMed ID: 38557384
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
