Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders (2012)
- Authors:
- USP affiliated authors: XAVIER, ANA CLAUDIA LATRÔNICO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: PUBERDADE PRECOCE; MUTAÇÃO GENÉTICA; FENÓTIPOS; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Publisher place: Chevy Chase
- Date published: 2012
- Source:
- Título: Endocrine Reviews
- ISSN: 0163-769X
- Volume/Número/Paginação/Ano: v. 33, 03_meetingAbstracts, Res. SUN-619, 2012
- Conference titles: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo
-
ABNT
TUSSET, Cintia et al. Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-619. Acesso em: 12 mar. 2026. -
APA
Tusset, C., Noel, S., Silveira, L., Trarbach, E., Gianetti, E., Seminara, S., et al. (2012). Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-619 -
NLM
Tusset C, Noel S, Silveira L, Trarbach E, Gianetti E, Seminara S, Kaiser U, Latronico AC, Mendonca BB. Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders [Internet]. Endocrine Reviews. 2012 ; 33[citado 2026 mar. 12 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-619 -
Vancouver
Tusset C, Noel S, Silveira L, Trarbach E, Gianetti E, Seminara S, Kaiser U, Latronico AC, Mendonca BB. Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders [Internet]. Endocrine Reviews. 2012 ; 33[citado 2026 mar. 12 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-619 - Fatores determinantes da estatura final normal em meninas com puberdade precoce dependente de gonadotrofinas tratadas com análogos de GnRII depot
- Análise dos valares de LH 2 horas após acetato de leuprolide depot na monitorização do tratamento da puberdade precoce dependente de gonadotrofinas
- Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD)
- Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders
- Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction
- XAF1 as a modifier of p53 function and cancer susceptibility
- Localization of Occult Adrenal Tissue with Cosyntropin-Stimulated 18F-FDG-PET/CT in a Patient with Metachronous Adrenocortical Tumor Who Presented with Persistently Elevated DHEAS after Bilateral Adrenalectomy
- A novel missense variant in the Necdin gene in a male patient with kallmann syndrome
- Molecular analysis of the neuropeptide Y1 receptor gene in human idiopathic gonadotropin-dependent precocious puberty and isolated hypogonadotropic hypogonadism
- Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
