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Molecular and gene network analysis of thyroid transcription factor 1 (TTF1) and enhanced at puberty (EAP1) genes in patients with GnRH-dependent pubertal disorders. [electronic resource] by
- Cukier, Priscilla
- Wright, Hollis
- Rulfs, Tomke
- Silveira, Leticia Ferreira Gontijo
- Teles, Milena Gurgel
- Mendonca, Berenice Bilharinho
- Arnhold, Ivo J P
- Heger, Sabine
- Latronico, Ana Claudia
- Ojeda, Sergio R
- Brito, Vinicius Nahime
Producer: 20140609
In:
Hormone research in paediatrics vol. 80
Availability: No items available.
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The benign spectrum of hypothalamic hamartomas: infrequent epilepsy and normal cognition in patients presenting with central precocious puberty. [electronic resource] by
- Cukier, Priscilla
- Castro, Luiz Henrique Martins
- Banaskiwitz, Natalie
- Teles, Leandro Roberto
- Ferreira, Luiz Roberto Kobuti
- Adda, Carla Cristina
- da Costa Leite, Claudia
- Arnhold, Ivo J P
- Mendonca, Berenice Bilharinho
- Latronico, Ana Claudia
- Brito, Vinicius Nahime
Producer: 20130701
In:
Seizure vol. 22
Availability: No items available.
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[Nelson's Syndrome: a case report]. [electronic resource] by
- Cukier, Priscilla
- Duch, Flávia Moretti
- Teixeira, Manoel Jacobsen
- Fragoso, Maria Candida B V
- Pereira, Maria Adelaide A
- Freire, Daniel Soares
- Fonoff, Erich Talamoni
- Costa, Márcia Helena Soares
- Domenice, Sorahia
- Lucon, Antonio Marmo
- de Mendonça, Berenice B
Producer: 20080506
In:
Arquivos brasileiros de endocrinologia e metabologia vol. 51
Availability: No items available.
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11.
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Central precocious puberty caused by mutations in the imprinted gene MKRN3. [electronic resource] by
- Abreu, Ana Paula
- Dauber, Andrew
- Macedo, Delanie B
- Noel, Sekoni D
- Brito, Vinicius N
- Gill, John C
- Cukier, Priscilla
- Thompson, Iain R
- Navarro, Victor M
- Gagliardi, Priscila C
- Rodrigues, Tânia
- Kochi, Cristiane
- Longui, Carlos Alberto
- Beckers, Dominique
- de Zegher, Francis
- Montenegro, Luciana R
- Mendonca, Berenice B
- Carroll, Rona S
- Hirschhorn, Joel N
- Latronico, Ana Claudia
- Kaiser, Ursula B
Producer: 20130716
In:
The New England journal of medicine vol. 368
Availability: No items available.
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Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3. [electronic resource] by
- Macedo, Delanie B
- Abreu, Ana Paula
- Reis, Ana Claudia S
- Montenegro, Luciana R
- Dauber, Andrew
- Beneduzzi, Daiane
- Cukier, Priscilla
- Silveira, Leticia F G
- Teles, Milena G
- Carroll, Rona S
- Junior, Gil Guerra
- Filho, Guilherme Guaragna
- Gucev, Zoran
- Arnhold, Ivo J P
- de Castro, Margaret
- Moreira, Ayrton C
- Martinelli, Carlos Eduardo
- Hirschhorn, Joel N
- Mendonca, Berenice B
- Brito, Vinicius N
- Antonini, Sonir R
- Kaiser, Ursula B
- Latronico, Ana Claudia
Producer: 20140808
In:
The Journal of clinical endocrinology and metabolism vol. 99
Availability: No items available.
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